Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7669589_7676614del | CA2499224945 | TP53 | c.-19_*21del c.-21-1377_*21del c.-19_*310del c.-19_*222del c.-253_*21del c.-136_*222del c.-136_*21del c.-136_*310del c.-136_983+1021del | ClinVar |
17 | g.7669609_7676594del | CA2581463470 | TP53 | c.1_1182del c.-21-1358_786del c.1_903del c.1_1161del c.1_994-3365del c.1_782+4572del c.1_*289del c.1_*201del c.-234_1065del c.-117_*201del c.1_1149del c.-117_1065del c.-117_*289del c.-117_983+1000del | |
17 | g.7674218_7674967del | CA645588534 | TP53 | c.569_750del c.173_354del c.290_471del c.548_729del c.452_633del c.92_273del c.536_717del | COSMIC COSMIC COSMIC |
17 | g.7674797_7674852del | CA891842248 | TP53 | c.672+7_672+62del (n.672+7_672+62del) c.276+7_276+62del (n.276+7_276+62del) c.393+7_393+62del (n.393+7_393+62del) c.651+7_651+62del (n.651+7_651+62del) n.935_990del n.67+201_67+256del c.555+7_555+62del (n.555+7_555+62del) c.195+7_195+62del (n.195+7_195+62del) c.639+7_639+62del (n.639+7_639+62del) | |
17 | g.7674810A= | CA2245953705 | TP53 | c.672+49T= (n.672+49T=) c.276+49T= (n.276+49T=) c.393+49T= (n.393+49T=) c.651+49T= (n.651+49T=) n.977T= n.67+243T= c.555+49T= (n.555+49T=) c.195+49T= (n.195+49T=) c.639+49T= (n.639+49T=) | |
17 | g.7674810A>G | CA001985 | TP53 | c.672+49T>C (n.672+49T>C) c.276+49T>C (n.276+49T>C) c.393+49T>C (n.393+49T>C) c.651+49T>C (n.651+49T>C) n.977T>C n.67+243T>C c.555+49T>C (n.555+49T>C) c.195+49T>C (n.195+49T>C) c.639+49T>C (n.639+49T>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.7674810A>T | CA2732929139 | TP53 | c.672+49T>A (n.672+49T>A) c.276+49T>A (n.276+49T>A) c.393+49T>A (n.393+49T>A) c.651+49T>A (n.651+49T>A) n.977T>A n.67+243T>A c.555+49T>A (n.555+49T>A) c.195+49T>A (n.195+49T>A) c.639+49T>A (n.639+49T>A) | dbSNP |
17 | g.7674811C>A | CA001992 | TP53 | c.672+48G>T (n.672+48G>T) c.276+48G>T (n.276+48G>T) c.393+48G>T (n.393+48G>T) c.651+48G>T (n.651+48G>T) n.976G>T n.67+242G>T c.555+48G>T (n.555+48G>T) c.195+48G>T (n.195+48G>T) c.639+48G>T (n.639+48G>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7674811C= | CA2245953708 | TP53 | c.672+48G= (n.672+48G=) c.276+48G= (n.276+48G=) c.393+48G= (n.393+48G=) c.651+48G= (n.651+48G=) n.976G= n.67+242G= c.555+48G= (n.555+48G=) c.195+48G= (n.195+48G=) c.639+48G= (n.639+48G=) | |
17 | g.7674811C>G | CA2580606185 | TP53 | c.672+48G>C (n.672+48G>C) c.276+48G>C (n.276+48G>C) c.393+48G>C (n.393+48G>C) c.651+48G>C (n.651+48G>C) n.976G>C n.67+242G>C c.555+48G>C (n.555+48G>C) c.195+48G>C (n.195+48G>C) c.639+48G>C (n.639+48G>C) | dbSNP |
17 | g.7674811C>T | CA001993 | TP53 | c.672+48G>A (n.672+48G>A) c.276+48G>A (n.276+48G>A) c.393+48G>A (n.393+48G>A) c.651+48G>A (n.651+48G>A) n.976G>A n.67+242G>A c.555+48G>A (n.555+48G>A) c.195+48G>A (n.195+48G>A) c.639+48G>A (n.639+48G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7674813A>G | CA2733136358 | TP53 | c.672+46T>C (n.672+46T>C) c.276+46T>C (n.276+46T>C) c.393+46T>C (n.393+46T>C) c.651+46T>C (n.651+46T>C) n.974T>C n.67+240T>C c.555+46T>C (n.555+46T>C) c.195+46T>C (n.195+46T>C) c.639+46T>C (n.639+46T>C) | dbSNP |
17 | g.7674813A>T | CA2733136359 | TP53 | c.672+46T>A (n.672+46T>A) c.276+46T>A (n.276+46T>A) c.393+46T>A (n.393+46T>A) c.651+46T>A (n.651+46T>A) n.974T>A n.67+240T>A c.555+46T>A (n.555+46T>A) c.195+46T>A (n.195+46T>A) c.639+46T>A (n.639+46T>A) | dbSNP |
17 | g.7674814C>A | CA2635878436 | TP53 | c.672+45G>T (n.672+45G>T) c.276+45G>T (n.276+45G>T) c.393+45G>T (n.393+45G>T) c.651+45G>T (n.651+45G>T) n.973G>T n.67+239G>T c.555+45G>T (n.555+45G>T) c.195+45G>T (n.195+45G>T) c.639+45G>T (n.639+45G>T) | gnomAD v4 |
17 | g.7674814C= | CA2245953711 | TP53 | c.672+45G= (n.672+45G=) c.276+45G= (n.276+45G=) c.393+45G= (n.393+45G=) c.651+45G= (n.651+45G=) n.973G= n.67+239G= c.555+45G= (n.555+45G=) c.195+45G= (n.195+45G=) c.639+45G= (n.639+45G=) | |
17 | g.7674814C>T | CA624865040 | TP53 | c.672+45G>A (n.672+45G>A) c.276+45G>A (n.276+45G>A) c.393+45G>A (n.393+45G>A) c.651+45G>A (n.651+45G>A) n.973G>A n.67+239G>A c.555+45G>A (n.555+45G>A) c.195+45G>A (n.195+45G>A) c.639+45G>A (n.639+45G>A) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.7674815C>A | CA2635878438 | TP53 | c.672+44G>T (n.672+44G>T) c.276+44G>T (n.276+44G>T) c.393+44G>T (n.393+44G>T) c.651+44G>T (n.651+44G>T) n.972G>T n.67+238G>T c.555+44G>T (n.555+44G>T) c.195+44G>T (n.195+44G>T) c.639+44G>T (n.639+44G>T) | gnomAD v4 |
17 | g.7674815C>T | CA2733136361 | TP53 | c.672+44G>A (n.672+44G>A) c.276+44G>A (n.276+44G>A) c.393+44G>A (n.393+44G>A) c.651+44G>A (n.651+44G>A) n.972G>A n.67+238G>A c.555+44G>A (n.555+44G>A) c.195+44G>A (n.195+44G>A) c.639+44G>A (n.639+44G>A) | dbSNP |
17 | g.7674816A>C | CA2733136362 | TP53 | c.672+43T>G (n.672+43T>G) c.276+43T>G (n.276+43T>G) c.393+43T>G (n.393+43T>G) c.651+43T>G (n.651+43T>G) n.971T>G n.67+237T>G c.555+43T>G (n.555+43T>G) c.195+43T>G (n.195+43T>G) c.639+43T>G (n.639+43T>G) | dbSNP |
17 | g.7674816A>G | CA2733136363 | TP53 | c.672+43T>C (n.672+43T>C) c.276+43T>C (n.276+43T>C) c.393+43T>C (n.393+43T>C) c.651+43T>C (n.651+43T>C) n.971T>C n.67+237T>C c.555+43T>C (n.555+43T>C) c.195+43T>C (n.195+43T>C) c.639+43T>C (n.639+43T>C) | dbSNP |
17 | g.7674817C>A | CA2635878439 | TP53 | c.672+42G>T (n.672+42G>T) c.276+42G>T (n.276+42G>T) c.393+42G>T (n.393+42G>T) c.651+42G>T (n.651+42G>T) n.970G>T n.67+236G>T c.555+42G>T (n.555+42G>T) c.195+42G>T (n.195+42G>T) c.639+42G>T (n.639+42G>T) | dbSNP gnomAD v4 |
17 | g.7674817C>G | CA2733136365 | TP53 | c.672+42G>C (n.672+42G>C) c.276+42G>C (n.276+42G>C) c.393+42G>C (n.393+42G>C) c.651+42G>C (n.651+42G>C) n.970G>C n.67+236G>C c.555+42G>C (n.555+42G>C) c.195+42G>C (n.195+42G>C) c.639+42G>C (n.639+42G>C) | dbSNP |
17 | g.7674817C>T | CA2635878440 | TP53 | c.672+42G>A (n.672+42G>A) c.276+42G>A (n.276+42G>A) c.393+42G>A (n.393+42G>A) c.651+42G>A (n.651+42G>A) n.970G>A n.67+236G>A c.555+42G>A (n.555+42G>A) c.195+42G>A (n.195+42G>A) c.639+42G>A (n.639+42G>A) | gnomAD v4 |
17 | g.7674818C>A | CA002005 | TP53 | c.672+41G>T (n.672+41G>T) c.276+41G>T (n.276+41G>T) c.393+41G>T (n.393+41G>T) c.651+41G>T (n.651+41G>T) n.969G>T n.67+235G>T c.555+41G>T (n.555+41G>T) c.195+41G>T (n.195+41G>T) c.639+41G>T (n.639+41G>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.7674818C= | CA2245953716 | TP53 | c.672+41G= (n.672+41G=) c.276+41G= (n.276+41G=) c.393+41G= (n.393+41G=) c.651+41G= (n.651+41G=) n.969G= n.67+235G= c.555+41G= (n.555+41G=) c.195+41G= (n.195+41G=) c.639+41G= (n.639+41G=) | |
17 | g.7674818C>G | CA624865041 | TP53 | c.672+41G>C (n.672+41G>C) c.276+41G>C (n.276+41G>C) c.393+41G>C (n.393+41G>C) c.651+41G>C (n.651+41G>C) n.969G>C n.67+235G>C c.555+41G>C (n.555+41G>C) c.195+41G>C (n.195+41G>C) c.639+41G>C (n.639+41G>C) | dbSNP gnomAD v2 |
17 | g.7674818C>T | CA2732929491 | TP53 | c.672+41G>A (n.672+41G>A) c.276+41G>A (n.276+41G>A) c.393+41G>A (n.393+41G>A) c.651+41G>A (n.651+41G>A) n.969G>A n.67+235G>A c.555+41G>A (n.555+41G>A) c.195+41G>A (n.195+41G>A) c.639+41G>A (n.639+41G>A) | dbSNP |
17 | g.7674819C>A | CA645588690 | TP53 | c.672+40G>T (n.672+40G>T) c.276+40G>T (n.276+40G>T) c.393+40G>T (n.393+40G>T) c.651+40G>T (n.651+40G>T) n.968G>T n.67+234G>T c.555+40G>T (n.555+40G>T) c.195+40G>T (n.195+40G>T) c.639+40G>T (n.639+40G>T) | gnomAD v4 COSMIC |
17 | g.7674819C>T | CA2635878443 | TP53 | c.672+40G>A (n.672+40G>A) c.276+40G>A (n.276+40G>A) c.393+40G>A (n.393+40G>A) c.651+40G>A (n.651+40G>A) n.968G>A n.67+234G>A c.555+40G>A (n.555+40G>A) c.195+40G>A (n.195+40G>A) c.639+40G>A (n.639+40G>A) | dbSNP gnomAD v4 |
17 | g.7674820T>G | CA2576155453 | TP53 | c.672+39A>C (n.672+39A>C) c.276+39A>C (n.276+39A>C) c.393+39A>C (n.393+39A>C) c.651+39A>C (n.651+39A>C) n.967A>C n.67+233A>C c.555+39A>C (n.555+39A>C) c.195+39A>C (n.195+39A>C) c.639+39A>C (n.639+39A>C) | |
17 | g.7674821T>A | CA002012 | TP53 | c.672+38A>T (n.672+38A>T) c.276+38A>T (n.276+38A>T) c.393+38A>T (n.393+38A>T) c.651+38A>T (n.651+38A>T) n.966A>T n.67+232A>T c.555+38A>T (n.555+38A>T) c.195+38A>T (n.195+38A>T) c.639+38A>T (n.639+38A>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7674821T= | CA2245953718 | TP53 | c.672+38A= (n.672+38A=) c.276+38A= (n.276+38A=) c.393+38A= (n.393+38A=) c.651+38A= (n.651+38A=) n.966A= n.67+232A= c.555+38A= (n.555+38A=) c.195+38A= (n.195+38A=) c.639+38A= (n.639+38A=) | |
17 | g.7674821_7674854del | CA2579881560 | TP53 | c.672+5_672+38del (n.672+5_672+38del) c.276+5_276+38del (n.276+5_276+38del) c.393+5_393+38del (n.393+5_393+38del) c.651+5_651+38del (n.651+5_651+38del) n.933_966del n.67+199_67+232del c.555+5_555+38del (n.555+5_555+38del) c.195+5_195+38del (n.195+5_195+38del) c.639+5_639+38del (n.639+5_639+38del) | |
17 | g.7674822A= | CA2245953722 | TP53 | c.672+37T= (n.672+37T=) c.276+37T= (n.276+37T=) c.393+37T= (n.393+37T=) c.651+37T= (n.651+37T=) n.965T= n.67+231T= c.555+37T= (n.555+37T=) c.195+37T= (n.195+37T=) c.639+37T= (n.639+37T=) | |
17 | g.7674822A>G | CA624865042 | TP53 | c.672+37T>C (n.672+37T>C) c.276+37T>C (n.276+37T>C) c.393+37T>C (n.393+37T>C) c.651+37T>C (n.651+37T>C) n.965T>C n.67+231T>C c.555+37T>C (n.555+37T>C) c.195+37T>C (n.195+37T>C) c.639+37T>C (n.639+37T>C) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.7674822A>T | CA002020 | TP53 | c.672+37T>A (n.672+37T>A) c.276+37T>A (n.276+37T>A) c.393+37T>A (n.393+37T>A) c.651+37T>A (n.651+37T>A) n.965T>A n.67+231T>A c.555+37T>A (n.555+37T>A) c.195+37T>A (n.195+37T>A) c.639+37T>A (n.639+37T>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7674823_7674862del | CA645588691 | TP53 | c.670_672+37del c.274_276+37del c.391_393+37del c.649_651+37del n.926_965del n.67+192_67+231del c.553_555+37del c.193_195+37del c.637_639+37del | COSMIC |
17 | g.7674823A= | CA2245953727 | TP53 | c.672+36T= (n.672+36T=) c.276+36T= (n.276+36T=) c.393+36T= (n.393+36T=) c.651+36T= (n.651+36T=) n.964T= n.67+230T= c.555+36T= (n.555+36T=) c.195+36T= (n.195+36T=) c.639+36T= (n.639+36T=) | |
17 | g.7674823A>C | CA981210304 | TP53 | c.672+36T>G (n.672+36T>G) c.276+36T>G (n.276+36T>G) c.393+36T>G (n.393+36T>G) c.651+36T>G (n.651+36T>G) n.964T>G n.67+230T>G c.555+36T>G (n.555+36T>G) c.195+36T>G (n.195+36T>G) c.639+36T>G (n.639+36T>G) | dbSNP gnomAD v3 gnomAD v4 |
17 | g.7674823A>G | CA002027 | TP53 | c.672+36T>C (n.672+36T>C) c.276+36T>C (n.276+36T>C) c.393+36T>C (n.393+36T>C) c.651+36T>C (n.651+36T>C) n.964T>C n.67+230T>C c.555+36T>C (n.555+36T>C) c.195+36T>C (n.195+36T>C) c.639+36T>C (n.639+36T>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7674823A>T | CA2732929140 | TP53 | c.672+36T>A (n.672+36T>A) c.276+36T>A (n.276+36T>A) c.393+36T>A (n.393+36T>A) c.651+36T>A (n.651+36T>A) n.964T>A n.67+230T>A c.555+36T>A (n.555+36T>A) c.195+36T>A (n.195+36T>A) c.639+36T>A (n.639+36T>A) | dbSNP |
17 | g.7674824C>A | CA000327 | TP53 | c.672+35G>T (n.672+35G>T) c.276+35G>T (n.276+35G>T) c.393+35G>T (n.393+35G>T) c.651+35G>T (n.651+35G>T) n.963G>T n.67+229G>T c.555+35G>T (n.555+35G>T) c.195+35G>T (n.195+35G>T) c.639+35G>T (n.639+35G>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7674824C= | CA2245953732 | TP53 | c.672+35G= (n.672+35G=) c.276+35G= (n.276+35G=) c.393+35G= (n.393+35G=) c.651+35G= (n.651+35G=) n.963G= n.67+229G= c.555+35G= (n.555+35G=) c.195+35G= (n.195+35G=) c.639+35G= (n.639+35G=) | |
17 | g.7674824C>G | CA2732928833 | TP53 | c.672+35G>C (n.672+35G>C) c.276+35G>C (n.276+35G>C) c.393+35G>C (n.393+35G>C) c.651+35G>C (n.651+35G>C) n.963G>C n.67+229G>C c.555+35G>C (n.555+35G>C) c.195+35G>C (n.195+35G>C) c.639+35G>C (n.639+35G>C) | dbSNP |
17 | g.7674824C>T | CA624865043 | TP53 | c.672+35G>A (n.672+35G>A) c.276+35G>A (n.276+35G>A) c.393+35G>A (n.393+35G>A) c.651+35G>A (n.651+35G>A) n.963G>A n.67+229G>A c.555+35G>A (n.555+35G>A) c.195+35G>A (n.195+35G>A) c.639+35G>A (n.639+35G>A) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.7674827del | CA2635878448 | TP53 | c.672+35del (n.672+35del) c.276+35del (n.276+35del) c.393+35del (n.393+35del) c.651+35del (n.651+35del) n.963del n.67+229del c.555+35del (n.555+35del) c.195+35del (n.195+35del) c.639+35del (n.639+35del) | gnomAD v4 |
17 | g.7674825C>A | CA2739569346 | TP53 | c.672+34G>T (n.672+34G>T) c.276+34G>T (n.276+34G>T) c.393+34G>T (n.393+34G>T) c.651+34G>T (n.651+34G>T) n.962G>T n.67+228G>T c.555+34G>T (n.555+34G>T) c.195+34G>T (n.195+34G>T) c.639+34G>T (n.639+34G>T) | |
17 | g.7674825C= | CA2245953738 | TP53 | c.672+34G= (n.672+34G=) c.276+34G= (n.276+34G=) c.393+34G= (n.393+34G=) c.651+34G= (n.651+34G=) n.962G= n.67+228G= c.555+34G= (n.555+34G=) c.195+34G= (n.195+34G=) c.639+34G= (n.639+34G=) | |
17 | g.7674825C>G | CA002041 | TP53 | c.672+34G>C (n.672+34G>C) c.276+34G>C (n.276+34G>C) c.393+34G>C (n.393+34G>C) c.651+34G>C (n.651+34G>C) n.962G>C n.67+228G>C c.555+34G>C (n.555+34G>C) c.195+34G>C (n.195+34G>C) c.639+34G>C (n.639+34G>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.7674825C>T | CA002039 | TP53 | c.672+34G>A (n.672+34G>A) c.276+34G>A (n.276+34G>A) c.393+34G>A (n.393+34G>A) c.651+34G>A (n.651+34G>A) n.962G>A n.67+228G>A c.555+34G>A (n.555+34G>A) c.195+34G>A (n.195+34G>A) c.639+34G>A (n.639+34G>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7674826C>A | CA2508301611 | TP53 | c.672+33G>T (n.672+33G>T) c.276+33G>T (n.276+33G>T) c.393+33G>T (n.393+33G>T) c.651+33G>T (n.651+33G>T) n.961G>T n.67+227G>T c.555+33G>T (n.555+33G>T) c.195+33G>T (n.195+33G>T) c.639+33G>T (n.639+33G>T) | dbSNP |
17 | g.7674826C>G | CA2739569347 | TP53 | c.672+33G>C (n.672+33G>C) c.276+33G>C (n.276+33G>C) c.393+33G>C (n.393+33G>C) c.651+33G>C (n.651+33G>C) n.961G>C n.67+227G>C c.555+33G>C (n.555+33G>C) c.195+33G>C (n.195+33G>C) c.639+33G>C (n.639+33G>C) | |
17 | g.7674826C>T | CA2733136369 | TP53 | c.672+33G>A (n.672+33G>A) c.276+33G>A (n.276+33G>A) c.393+33G>A (n.393+33G>A) c.651+33G>A (n.651+33G>A) n.961G>A n.67+227G>A c.555+33G>A (n.555+33G>A) c.195+33G>A (n.195+33G>A) c.639+33G>A (n.639+33G>A) | dbSNP |
17 | g.7674827C>A | CA645588692 | TP53 | c.672+32G>T (n.672+32G>T) c.276+32G>T (n.276+32G>T) c.393+32G>T (n.393+32G>T) c.651+32G>T (n.651+32G>T) n.960G>T n.67+226G>T c.555+32G>T (n.555+32G>T) c.195+32G>T (n.195+32G>T) c.639+32G>T (n.639+32G>T) | dbSNP COSMIC |
17 | g.7674827C>G | CA2739569348 | TP53 | c.672+32G>C (n.672+32G>C) c.276+32G>C (n.276+32G>C) c.393+32G>C (n.393+32G>C) c.651+32G>C (n.651+32G>C) n.960G>C n.67+226G>C c.555+32G>C (n.555+32G>C) c.195+32G>C (n.195+32G>C) c.639+32G>C (n.639+32G>C) | |
17 | g.7674827C>T | CA2739569349 | TP53 | c.672+32G>A (n.672+32G>A) c.276+32G>A (n.276+32G>A) c.393+32G>A (n.393+32G>A) c.651+32G>A (n.651+32G>A) n.960G>A n.67+226G>A c.555+32G>A (n.555+32G>A) c.195+32G>A (n.195+32G>A) c.639+32G>A (n.639+32G>A) | |
17 | g.7674828T>A | CA2580606186 | TP53 | c.672+31A>T (n.672+31A>T) c.276+31A>T (n.276+31A>T) c.393+31A>T (n.393+31A>T) c.651+31A>T (n.651+31A>T) n.959A>T n.67+225A>T c.555+31A>T (n.555+31A>T) c.195+31A>T (n.195+31A>T) c.639+31A>T (n.639+31A>T) | |
17 | g.7674828T>C | CA000325 | TP53 | c.672+31A>G (n.672+31A>G) c.276+31A>G (n.276+31A>G) c.393+31A>G (n.393+31A>G) c.651+31A>G (n.651+31A>G) n.959A>G n.67+225A>G c.555+31A>G (n.555+31A>G) c.195+31A>G (n.195+31A>G) c.639+31A>G (n.639+31A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
17 | g.7674828T>G | CA2580606187 | TP53 | c.672+31A>C (n.672+31A>C) c.276+31A>C (n.276+31A>C) c.393+31A>C (n.393+31A>C) c.651+31A>C (n.651+31A>C) n.959A>C n.67+225A>C c.555+31A>C (n.555+31A>C) c.195+31A>C (n.195+31A>C) c.639+31A>C (n.639+31A>C) | |
17 | g.7674828T= | CA2245953745 | TP53 | c.672+31A= (n.672+31A=) c.276+31A= (n.276+31A=) c.393+31A= (n.393+31A=) c.651+31A= (n.651+31A=) n.959A= n.67+225A= c.555+31A= (n.555+31A=) c.195+31A= (n.195+31A=) c.639+31A= (n.639+31A=) | |
17 | g.7674829C>A | CA2732925632 | TP53 | c.672+30G>T (n.672+30G>T) c.276+30G>T (n.276+30G>T) c.393+30G>T (n.393+30G>T) c.651+30G>T (n.651+30G>T) n.958G>T n.67+224G>T c.555+30G>T (n.555+30G>T) c.195+30G>T (n.195+30G>T) c.639+30G>T (n.639+30G>T) | dbSNP |
17 | g.7674829C= | CA2245953750 | TP53 | c.672+30G= (n.672+30G=) c.276+30G= (n.276+30G=) c.393+30G= (n.393+30G=) c.651+30G= (n.651+30G=) n.958G= n.67+224G= c.555+30G= (n.555+30G=) c.195+30G= (n.195+30G=) c.639+30G= (n.639+30G=) | |
17 | g.7674829C>G | CA2739569350 | TP53 | c.672+30G>C (n.672+30G>C) c.276+30G>C (n.276+30G>C) c.393+30G>C (n.393+30G>C) c.651+30G>C (n.651+30G>C) n.958G>C n.67+224G>C c.555+30G>C (n.555+30G>C) c.195+30G>C (n.195+30G>C) c.639+30G>C (n.639+30G>C) | |
17 | g.7674829C>T | CA002059 | TP53 | c.672+30G>A (n.672+30G>A) c.276+30G>A (n.276+30G>A) c.393+30G>A (n.393+30G>A) c.651+30G>A (n.651+30G>A) n.958G>A n.67+224G>A c.555+30G>A (n.555+30G>A) c.195+30G>A (n.195+30G>A) c.639+30G>A (n.639+30G>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7674830C>A | CA2635878457 | TP53 | c.672+29G>T (n.672+29G>T) c.276+29G>T (n.276+29G>T) c.393+29G>T (n.393+29G>T) c.651+29G>T (n.651+29G>T) n.957G>T n.67+223G>T c.555+29G>T (n.555+29G>T) c.195+29G>T (n.195+29G>T) c.639+29G>T (n.639+29G>T) | gnomAD v4 |
17 | g.7674830C>G | CA2739569351 | TP53 | c.672+29G>C (n.672+29G>C) c.276+29G>C (n.276+29G>C) c.393+29G>C (n.393+29G>C) c.651+29G>C (n.651+29G>C) n.957G>C n.67+223G>C c.555+29G>C (n.555+29G>C) c.195+29G>C (n.195+29G>C) c.639+29G>C (n.639+29G>C) | |
17 | g.7674830C>T | CA2635878459 | TP53 | c.672+29G>A (n.672+29G>A) c.276+29G>A (n.276+29G>A) c.393+29G>A (n.393+29G>A) c.651+29G>A (n.651+29G>A) n.957G>A n.67+223G>A c.555+29G>A (n.555+29G>A) c.195+29G>A (n.195+29G>A) c.639+29G>A (n.639+29G>A) | gnomAD v4 |
17 | g.7674831T>A | CA2635878460 | TP53 | c.672+28A>T (n.672+28A>T) c.276+28A>T (n.276+28A>T) c.393+28A>T (n.393+28A>T) c.651+28A>T (n.651+28A>T) n.956A>T n.67+222A>T c.555+28A>T (n.555+28A>T) c.195+28A>T (n.195+28A>T) c.639+28A>T (n.639+28A>T) | gnomAD v4 |
17 | g.7674831T>C | CA2733136370 | TP53 | c.672+28A>G (n.672+28A>G) c.276+28A>G (n.276+28A>G) c.393+28A>G (n.393+28A>G) c.651+28A>G (n.651+28A>G) n.956A>G n.67+222A>G c.555+28A>G (n.555+28A>G) c.195+28A>G (n.195+28A>G) c.639+28A>G (n.639+28A>G) | dbSNP |
17 | g.7674832C>A | CA2635878461 | TP53 | c.672+27G>T (n.672+27G>T) c.276+27G>T (n.276+27G>T) c.393+27G>T (n.393+27G>T) c.651+27G>T (n.651+27G>T) n.955G>T n.67+221G>T c.555+27G>T (n.555+27G>T) c.195+27G>T (n.195+27G>T) c.639+27G>T (n.639+27G>T) | gnomAD v4 |
17 | g.7674832C>G | CA2741514602 | TP53 | c.672+27G>C (n.672+27G>C) c.276+27G>C (n.276+27G>C) c.393+27G>C (n.393+27G>C) c.651+27G>C (n.651+27G>C) n.955G>C n.67+221G>C c.555+27G>C (n.555+27G>C) c.195+27G>C (n.195+27G>C) c.639+27G>C (n.639+27G>C) | |
17 | g.7674832C>T | CA2733136371 | TP53 | c.672+27G>A (n.672+27G>A) c.276+27G>A (n.276+27G>A) c.393+27G>A (n.393+27G>A) c.651+27G>A (n.651+27G>A) n.955G>A n.67+221G>A c.555+27G>A (n.555+27G>A) c.195+27G>A (n.195+27G>A) c.639+27G>A (n.639+27G>A) | dbSNP |
17 | g.7674834del | CA2733136372 | TP53 | c.672+27del (n.672+27del) c.276+27del (n.276+27del) c.393+27del (n.393+27del) c.651+27del (n.651+27del) n.955del n.67+221del c.555+27del (n.555+27del) c.195+27del (n.195+27del) c.639+27del (n.639+27del) | dbSNP |
17 | g.7674833C>A | CA2739569352 | TP53 | c.672+26G>T (n.672+26G>T) c.276+26G>T (n.276+26G>T) c.393+26G>T (n.393+26G>T) c.651+26G>T (n.651+26G>T) n.954G>T n.67+220G>T c.555+26G>T (n.555+26G>T) c.195+26G>T (n.195+26G>T) c.639+26G>T (n.639+26G>T) | |
17 | g.7674833C>G | CA2739569353 | TP53 | c.672+26G>C (n.672+26G>C) c.276+26G>C (n.276+26G>C) c.393+26G>C (n.393+26G>C) c.651+26G>C (n.651+26G>C) n.954G>C n.67+220G>C c.555+26G>C (n.555+26G>C) c.195+26G>C (n.195+26G>C) c.639+26G>C (n.639+26G>C) | |
17 | g.7674833C>T | CA645588694 | TP53 | c.672+26G>A (n.672+26G>A) c.276+26G>A (n.276+26G>A) c.393+26G>A (n.393+26G>A) c.651+26G>A (n.651+26G>A) n.954G>A n.67+220G>A c.555+26G>A (n.555+26G>A) c.195+26G>A (n.195+26G>A) c.639+26G>A (n.639+26G>A) | COSMIC |
17 | g.7674833_7674834delinsTT | CA645588693 | TP53 | c.672+25_672+26delinsAA (n.672+25_672+26delinsAA) c.276+25_276+26delinsAA (n.276+25_276+26delinsAA) c.393+25_393+26delinsAA (n.393+25_393+26delinsAA) c.651+25_651+26delinsAA (n.651+25_651+26delinsAA) n.953_954delinsAA n.67+219_67+220delinsAA c.555+25_555+26delinsAA (n.555+25_555+26delinsAA) c.195+25_195+26delinsAA (n.195+25_195+26delinsAA) c.639+25_639+26delinsAA (n.639+25_639+26delinsAA) | COSMIC |
17 | g.7674834C>A | CA2733136374 | TP53 | c.672+25G>T (n.672+25G>T) c.276+25G>T (n.276+25G>T) c.393+25G>T (n.393+25G>T) c.651+25G>T (n.651+25G>T) n.953G>T n.67+219G>T c.555+25G>T (n.555+25G>T) c.195+25G>T (n.195+25G>T) c.639+25G>T (n.639+25G>T) | dbSNP |
17 | g.7674834C>G | CA645588696 | TP53 | c.672+25G>C (n.672+25G>C) c.276+25G>C (n.276+25G>C) c.393+25G>C (n.393+25G>C) c.651+25G>C (n.651+25G>C) n.953G>C n.67+219G>C c.555+25G>C (n.555+25G>C) c.195+25G>C (n.195+25G>C) c.639+25G>C (n.639+25G>C) | COSMIC |
17 | g.7674834C>T | CA645588695 | TP53 | c.672+25G>A (n.672+25G>A) c.276+25G>A (n.276+25G>A) c.393+25G>A (n.393+25G>A) c.651+25G>A (n.651+25G>A) n.953G>A n.67+219G>A c.555+25G>A (n.555+25G>A) c.195+25G>A (n.195+25G>A) c.639+25G>A (n.639+25G>A) | dbSNP COSMIC COSMIC |
17 | g.7674835A= | CA2245953751 | TP53 | c.672+24T= (n.672+24T=) c.276+24T= (n.276+24T=) c.393+24T= (n.393+24T=) c.651+24T= (n.651+24T=) n.952T= n.67+218T= c.555+24T= (n.555+24T=) c.195+24T= (n.195+24T=) c.639+24T= (n.639+24T=) | |
17 | g.7674835A>C | CA2635878464 | TP53 | c.672+24T>G (n.672+24T>G) c.276+24T>G (n.276+24T>G) c.393+24T>G (n.393+24T>G) c.651+24T>G (n.651+24T>G) n.952T>G n.67+218T>G c.555+24T>G (n.555+24T>G) c.195+24T>G (n.195+24T>G) c.639+24T>G (n.639+24T>G) | gnomAD v4 |
17 | g.7674835A>G | CA624865044 | TP53 | c.672+24T>C (n.672+24T>C) c.276+24T>C (n.276+24T>C) c.393+24T>C (n.393+24T>C) c.651+24T>C (n.651+24T>C) n.952T>C n.67+218T>C c.555+24T>C (n.555+24T>C) c.195+24T>C (n.195+24T>C) c.639+24T>C (n.639+24T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7674835A>T | CA645588697 | TP53 | c.672+24T>A (n.672+24T>A) c.276+24T>A (n.276+24T>A) c.393+24T>A (n.393+24T>A) c.651+24T>A (n.651+24T>A) n.952T>A n.67+218T>A c.555+24T>A (n.555+24T>A) c.195+24T>A (n.195+24T>A) c.639+24T>A (n.639+24T>A) | dbSNP COSMIC |
17 | g.7674836G>A | CA2733136376 | TP53 | c.672+23C>T (n.672+23C>T) c.276+23C>T (n.276+23C>T) c.393+23C>T (n.393+23C>T) c.651+23C>T (n.651+23C>T) n.951C>T n.67+217C>T c.555+23C>T (n.555+23C>T) c.195+23C>T (n.195+23C>T) c.639+23C>T (n.639+23C>T) | dbSNP |
17 | g.7674836G>C | CA2739569354 | TP53 | c.672+23C>G (n.672+23C>G) c.276+23C>G (n.276+23C>G) c.393+23C>G (n.393+23C>G) c.651+23C>G (n.651+23C>G) n.951C>G n.67+217C>G c.555+23C>G (n.555+23C>G) c.195+23C>G (n.195+23C>G) c.639+23C>G (n.639+23C>G) | |
17 | g.7674836G>T | CA2739569355 | TP53 | c.672+23C>A (n.672+23C>A) c.276+23C>A (n.276+23C>A) c.393+23C>A (n.393+23C>A) c.651+23C>A (n.651+23C>A) n.951C>A n.67+217C>A c.555+23C>A (n.555+23C>A) c.195+23C>A (n.195+23C>A) c.639+23C>A (n.639+23C>A) | |
17 | g.7674836_7674851delinsGAGACCCCAGTTGCAA | CA2245953755 | TP53 | c.672+8_672+23delinsTTGCAACTGGGGTCTC (n.672+8_672+23delinsTTGCAACTGGGGTCTC) c.276+8_276+23delinsTTGCAACTGGGGTCTC (n.276+8_276+23delinsTTGCAACTGGGGTCTC) c.393+8_393+23delinsTTGCAACTGGGGTCTC (n.393+8_393+23delinsTTGCAACTGGGGTCTC) c.651+8_651+23delinsTTGCAACTGGGGTCTC (n.651+8_651+23delinsTTGCAACTGGGGTCTC) n.936_951delinsTTGCAACTGGGGTCTC n.67+202_67+217delinsTTGCAACTGGGGTCTC c.555+8_555+23delinsTTGCAACTGGGGTCTC (n.555+8_555+23delinsTTGCAACTGGGGTCTC) c.195+8_195+23delinsTTGCAACTGGGGTCTC (n.195+8_195+23delinsTTGCAACTGGGGTCTC) c.639+8_639+23delinsTTGCAACTGGGGTCTC (n.639+8_639+23delinsTTGCAACTGGGGTCTC) | |
17 | g.7674837A>C | CA2739569356 | TP53 | c.672+22T>G (n.672+22T>G) c.276+22T>G (n.276+22T>G) c.393+22T>G (n.393+22T>G) c.651+22T>G (n.651+22T>G) n.950T>G n.67+216T>G c.555+22T>G (n.555+22T>G) c.195+22T>G (n.195+22T>G) c.639+22T>G (n.639+22T>G) | |
17 | g.7674837A>G | CA2733136381 | TP53 | c.672+22T>C (n.672+22T>C) c.276+22T>C (n.276+22T>C) c.393+22T>C (n.393+22T>C) c.651+22T>C (n.651+22T>C) n.950T>C n.67+216T>C c.555+22T>C (n.555+22T>C) c.195+22T>C (n.195+22T>C) c.639+22T>C (n.639+22T>C) | dbSNP |
17 | g.7674837A>T | CA2733136382 | TP53 | c.672+22T>A (n.672+22T>A) c.276+22T>A (n.276+22T>A) c.393+22T>A (n.393+22T>A) c.651+22T>A (n.651+22T>A) n.950T>A n.67+216T>A c.555+22T>A (n.555+22T>A) c.195+22T>A (n.195+22T>A) c.639+22T>A (n.639+22T>A) | dbSNP |
17 | g.7674838_7674852del | CA624865045 | TP53 | c.672+8_672+22del (n.672+8_672+22del) c.276+8_276+22del (n.276+8_276+22del) c.393+8_393+22del (n.393+8_393+22del) c.651+8_651+22del (n.651+8_651+22del) n.936_950del n.67+202_67+216del c.555+8_555+22del (n.555+8_555+22del) c.195+8_195+22del (n.195+8_195+22del) c.639+8_639+22del (n.639+8_639+22del) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7674838G>A | CA981210336 | TP53 | c.672+21C>T (n.672+21C>T) c.276+21C>T (n.276+21C>T) c.393+21C>T (n.393+21C>T) c.651+21C>T (n.651+21C>T) n.949C>T n.67+215C>T c.555+21C>T (n.555+21C>T) c.195+21C>T (n.195+21C>T) c.639+21C>T (n.639+21C>T) | dbSNP gnomAD v3 gnomAD v4 |
17 | g.7674838G>C | CA002066 | TP53 | c.672+21C>G (n.672+21C>G) c.276+21C>G (n.276+21C>G) c.393+21C>G (n.393+21C>G) c.651+21C>G (n.651+21C>G) n.949C>G n.67+215C>G c.555+21C>G (n.555+21C>G) c.195+21C>G (n.195+21C>G) c.639+21C>G (n.639+21C>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.7674838G= | CA2245953762 | TP53 | c.672+21C= (n.672+21C=) c.276+21C= (n.276+21C=) c.393+21C= (n.393+21C=) c.651+21C= (n.651+21C=) n.949C= n.67+215C= c.555+21C= (n.555+21C=) c.195+21C= (n.195+21C=) c.639+21C= (n.639+21C=) | |
17 | g.7674838G>T | CA2732929840 | TP53 | c.672+21C>A (n.672+21C>A) c.276+21C>A (n.276+21C>A) c.393+21C>A (n.393+21C>A) c.651+21C>A (n.651+21C>A) n.949C>A n.67+215C>A c.555+21C>A (n.555+21C>A) c.195+21C>A (n.195+21C>A) c.639+21C>A (n.639+21C>A) | dbSNP |
17 | g.7674838_7674882del | CA645588698 | TP53 | c.649_672+21del c.253_276+21del c.370_393+21del c.628_651+21del n.905_949del n.67+171_67+215del c.532_555+21del c.172_195+21del c.616_639+21del | COSMIC |
17 | g.7674838_7676615del | CA2843744559 | TP53 | c.-21_672+21del c.-21-1379_276+21del c.-21_393+21del c.-21_651+21del n.119_949del c.-255_555+21del c.-138_555+21del | |
17 | g.7674839A= | CA2245953767 | TP53 | c.672+20T= (n.672+20T=) c.276+20T= (n.276+20T=) c.393+20T= (n.393+20T=) c.651+20T= (n.651+20T=) n.948T= n.67+214T= c.555+20T= (n.555+20T=) c.195+20T= (n.195+20T=) c.639+20T= (n.639+20T=) | |
17 | g.7674839A>C | CA2739569357 | TP53 | c.672+20T>G (n.672+20T>G) c.276+20T>G (n.276+20T>G) c.393+20T>G (n.393+20T>G) c.651+20T>G (n.651+20T>G) n.948T>G n.67+214T>G c.555+20T>G (n.555+20T>G) c.195+20T>G (n.195+20T>G) c.639+20T>G (n.639+20T>G) | |
17 | g.7674839A>G | CA2739569358 | TP53 | c.672+20T>C (n.672+20T>C) c.276+20T>C (n.276+20T>C) c.393+20T>C (n.393+20T>C) c.651+20T>C (n.651+20T>C) n.948T>C n.67+214T>C c.555+20T>C (n.555+20T>C) c.195+20T>C (n.195+20T>C) c.639+20T>C (n.639+20T>C) | |
17 | g.7674839A>T | CA287488288 | TP53 | c.672+20T>A (n.672+20T>A) c.276+20T>A (n.276+20T>A) c.393+20T>A (n.393+20T>A) c.651+20T>A (n.651+20T>A) n.948T>A n.67+214T>A c.555+20T>A (n.555+20T>A) c.195+20T>A (n.195+20T>A) c.639+20T>A (n.639+20T>A) | ClinVar dbSNP |
17 | g.7674840C>A | CA2732957054 | TP53 | c.672+19G>T (n.672+19G>T) c.276+19G>T (n.276+19G>T) c.393+19G>T (n.393+19G>T) c.651+19G>T (n.651+19G>T) n.947G>T n.67+213G>T c.555+19G>T (n.555+19G>T) c.195+19G>T (n.195+19G>T) c.639+19G>T (n.639+19G>T) | dbSNP |
17 | g.7674840C= | CA2245953772 | TP53 | c.672+19G= (n.672+19G=) c.276+19G= (n.276+19G=) c.393+19G= (n.393+19G=) c.651+19G= (n.651+19G=) n.947G= n.67+213G= c.555+19G= (n.555+19G=) c.195+19G= (n.195+19G=) c.639+19G= (n.639+19G=) | |
17 | g.7674840C>G | CA2732957055 | TP53 | c.672+19G>C (n.672+19G>C) c.276+19G>C (n.276+19G>C) c.393+19G>C (n.393+19G>C) c.651+19G>C (n.651+19G>C) n.947G>C n.67+213G>C c.555+19G>C (n.555+19G>C) c.195+19G>C (n.195+19G>C) c.639+19G>C (n.639+19G>C) | dbSNP |
17 | g.7674840C>T | CA624865046 | TP53 | c.672+19G>A (n.672+19G>A) c.276+19G>A (n.276+19G>A) c.393+19G>A (n.393+19G>A) c.651+19G>A (n.651+19G>A) n.947G>A n.67+213G>A c.555+19G>A (n.555+19G>A) c.195+19G>A (n.195+19G>A) c.639+19G>A (n.639+19G>A) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
17 | g.7674841C>A | CA2732925633 | TP53 | c.672+18G>T (n.672+18G>T) c.276+18G>T (n.276+18G>T) c.393+18G>T (n.393+18G>T) c.651+18G>T (n.651+18G>T) n.946G>T n.67+212G>T c.555+18G>T (n.555+18G>T) c.195+18G>T (n.195+18G>T) c.639+18G>T (n.639+18G>T) | dbSNP |
17 | g.7674841C= | CA2245953777 | TP53 | c.672+18G= (n.672+18G=) c.276+18G= (n.276+18G=) c.393+18G= (n.393+18G=) c.651+18G= (n.651+18G=) n.946G= n.67+212G= c.555+18G= (n.555+18G=) c.195+18G= (n.195+18G=) c.639+18G= (n.639+18G=) | |
17 | g.7674841C>G | CA000324 | TP53 | c.672+18G>C (n.672+18G>C) c.276+18G>C (n.276+18G>C) c.393+18G>C (n.393+18G>C) c.651+18G>C (n.651+18G>C) n.946G>C n.67+212G>C c.555+18G>C (n.555+18G>C) c.195+18G>C (n.195+18G>C) c.639+18G>C (n.639+18G>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7674841C>T | CA2732925634 | TP53 | c.672+18G>A (n.672+18G>A) c.276+18G>A (n.276+18G>A) c.393+18G>A (n.393+18G>A) c.651+18G>A (n.651+18G>A) n.946G>A n.67+212G>A c.555+18G>A (n.555+18G>A) c.195+18G>A (n.195+18G>A) c.639+18G>A (n.639+18G>A) | dbSNP |
17 | g.7674842C>A | CA645588699 | TP53 | c.672+17G>T (n.672+17G>T) c.276+17G>T (n.276+17G>T) c.393+17G>T (n.393+17G>T) c.651+17G>T (n.651+17G>T) n.945G>T n.67+211G>T c.555+17G>T (n.555+17G>T) c.195+17G>T (n.195+17G>T) c.639+17G>T (n.639+17G>T) | COSMIC |
17 | g.7674842C= | CA2245953784 | TP53 | c.672+17G= (n.672+17G=) c.276+17G= (n.276+17G=) c.393+17G= (n.393+17G=) c.651+17G= (n.651+17G=) n.945G= n.67+211G= c.555+17G= (n.555+17G=) c.195+17G= (n.195+17G=) c.639+17G= (n.639+17G=) | |
17 | g.7674842C>G | CA645588701 | TP53 | c.672+17G>C (n.672+17G>C) c.276+17G>C (n.276+17G>C) c.393+17G>C (n.393+17G>C) c.651+17G>C (n.651+17G>C) n.945G>C n.67+211G>C c.555+17G>C (n.555+17G>C) c.195+17G>C (n.195+17G>C) c.639+17G>C (n.639+17G>C) | COSMIC |
17 | g.7674842C>T | CA645588700 | TP53 | c.672+17G>A (n.672+17G>A) c.276+17G>A (n.276+17G>A) c.393+17G>A (n.393+17G>A) c.651+17G>A (n.651+17G>A) n.945G>A n.67+211G>A c.555+17G>A (n.555+17G>A) c.195+17G>A (n.195+17G>A) c.639+17G>A (n.639+17G>A) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
17 | g.7674843C>A | CA2732963333 | TP53 | c.672+16G>T (n.672+16G>T) c.276+16G>T (n.276+16G>T) c.393+16G>T (n.393+16G>T) c.651+16G>T (n.651+16G>T) n.944G>T n.67+210G>T c.555+16G>T (n.555+16G>T) c.195+16G>T (n.195+16G>T) c.639+16G>T (n.639+16G>T) | dbSNP |
17 | g.7674843C= | CA2245953788 | TP53 | c.672+16G= (n.672+16G=) c.276+16G= (n.276+16G=) c.393+16G= (n.393+16G=) c.651+16G= (n.651+16G=) n.944G= n.67+210G= c.555+16G= (n.555+16G=) c.195+16G= (n.195+16G=) c.639+16G= (n.639+16G=) | |
17 | g.7674843C>T | CA658683988 | TP53 | c.672+16G>A (n.672+16G>A) c.276+16G>A (n.276+16G>A) c.393+16G>A (n.393+16G>A) c.651+16G>A (n.651+16G>A) n.944G>A n.67+210G>A c.555+16G>A (n.555+16G>A) c.195+16G>A (n.195+16G>A) c.639+16G>A (n.639+16G>A) | ClinVar dbSNP |
17 | g.7674844del | CA2697552071 | TP53 | c.672+15del (n.672+15del) c.276+15del (n.276+15del) c.393+15del (n.393+15del) c.651+15del (n.651+15del) n.943del n.67+209del c.555+15del (n.555+15del) c.195+15del (n.195+15del) c.639+15del (n.639+15del) | ClinVar |
17 | g.7674844A= | CA2245953794 | TP53 | c.672+15T= (n.672+15T=) c.276+15T= (n.276+15T=) c.393+15T= (n.393+15T=) c.651+15T= (n.651+15T=) n.943T= n.67+209T= c.555+15T= (n.555+15T=) c.195+15T= (n.195+15T=) c.639+15T= (n.639+15T=) | |
17 | g.7674844A>C | CA16607853 | TP53 | c.672+15T>G (n.672+15T>G) c.276+15T>G (n.276+15T>G) c.393+15T>G (n.393+15T>G) c.651+15T>G (n.651+15T>G) n.943T>G n.67+209T>G c.555+15T>G (n.555+15T>G) c.195+15T>G (n.195+15T>G) c.639+15T>G (n.639+15T>G) | ClinVar dbSNP |
17 | g.7674844A>G | CA002079 | TP53 | c.672+15T>C (n.672+15T>C) c.276+15T>C (n.276+15T>C) c.393+15T>C (n.393+15T>C) c.651+15T>C (n.651+15T>C) n.943T>C n.67+209T>C c.555+15T>C (n.555+15T>C) c.195+15T>C (n.195+15T>C) c.639+15T>C (n.639+15T>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7674844A>T | CA2732924680 | TP53 | c.672+15T>A (n.672+15T>A) c.276+15T>A (n.276+15T>A) c.393+15T>A (n.393+15T>A) c.651+15T>A (n.651+15T>A) n.943T>A n.67+209T>A c.555+15T>A (n.555+15T>A) c.195+15T>A (n.195+15T>A) c.639+15T>A (n.639+15T>A) | dbSNP |
17 | g.7674845G>A | CA645588702 | TP53 | c.672+14C>T (n.672+14C>T) c.276+14C>T (n.276+14C>T) c.393+14C>T (n.393+14C>T) c.651+14C>T (n.651+14C>T) n.942C>T n.67+208C>T c.555+14C>T (n.555+14C>T) c.195+14C>T (n.195+14C>T) c.639+14C>T (n.639+14C>T) | ClinVar dbSNP COSMIC |
17 | g.7674845G>C | CA658683989 | TP53 | c.672+14C>G (n.672+14C>G) c.276+14C>G (n.276+14C>G) c.393+14C>G (n.393+14C>G) c.651+14C>G (n.651+14C>G) n.942C>G n.67+208C>G c.555+14C>G (n.555+14C>G) c.195+14C>G (n.195+14C>G) c.639+14C>G (n.639+14C>G) | ClinVar dbSNP gnomAD v4 |
17 | g.7674845G= | CA2245953798 | TP53 | c.672+14C= (n.672+14C=) c.276+14C= (n.276+14C=) c.393+14C= (n.393+14C=) c.651+14C= (n.651+14C=) n.942C= n.67+208C= c.555+14C= (n.555+14C=) c.195+14C= (n.195+14C=) c.639+14C= (n.639+14C=) | |
17 | g.7674845_7674848del | CA2635878478 | TP53 | c.672+11_672+14del (n.672+11_672+14del) c.276+11_276+14del (n.276+11_276+14del) c.393+11_393+14del (n.393+11_393+14del) c.651+11_651+14del (n.651+11_651+14del) n.939_942del n.67+205_67+208del c.555+11_555+14del (n.555+11_555+14del) c.195+11_195+14del (n.195+11_195+14del) c.639+11_639+14del (n.639+11_639+14del) | gnomAD v4 |
17 | g.7674846T>A | CA2733136386 | TP53 | c.672+13A>T (n.672+13A>T) c.276+13A>T (n.276+13A>T) c.393+13A>T (n.393+13A>T) c.651+13A>T (n.651+13A>T) n.941A>T n.67+207A>T c.555+13A>T (n.555+13A>T) c.195+13A>T (n.195+13A>T) c.639+13A>T (n.639+13A>T) | dbSNP |
17 | g.7674846T>C | CA2573154666 | TP53 | c.672+13A>G (n.672+13A>G) c.276+13A>G (n.276+13A>G) c.393+13A>G (n.393+13A>G) c.651+13A>G (n.651+13A>G) n.941A>G n.67+207A>G c.555+13A>G (n.555+13A>G) c.195+13A>G (n.195+13A>G) c.639+13A>G (n.639+13A>G) | ClinVar dbSNP gnomAD v4 |
17 | g.7674846T>G | CA2733136383 | TP53 | c.672+13A>C (n.672+13A>C) c.276+13A>C (n.276+13A>C) c.393+13A>C (n.393+13A>C) c.651+13A>C (n.651+13A>C) n.941A>C n.67+207A>C c.555+13A>C (n.555+13A>C) c.195+13A>C (n.195+13A>C) c.639+13A>C (n.639+13A>C) | dbSNP |
17 | g.7674847T>A | CA2733136389 | TP53 | c.672+12A>T (n.672+12A>T) c.276+12A>T (n.276+12A>T) c.393+12A>T (n.393+12A>T) c.651+12A>T (n.651+12A>T) n.940A>T n.67+206A>T c.555+12A>T (n.555+12A>T) c.195+12A>T (n.195+12A>T) c.639+12A>T (n.639+12A>T) | dbSNP |
17 | g.7674847T>C | CA2517029599 | TP53 | c.672+12A>G (n.672+12A>G) c.276+12A>G (n.276+12A>G) c.393+12A>G (n.393+12A>G) c.651+12A>G (n.651+12A>G) n.940A>G n.67+206A>G c.555+12A>G (n.555+12A>G) c.195+12A>G (n.195+12A>G) c.639+12A>G (n.639+12A>G) | dbSNP |
17 | g.7674848del | CA2576155454 | TP53 | c.672+11del (n.672+11del) c.276+11del (n.276+11del) c.393+11del (n.393+11del) c.651+11del (n.651+11del) n.939del n.67+205del c.555+11del (n.555+11del) c.195+11del (n.195+11del) c.639+11del (n.639+11del) | |
17 | g.7674848G>A | CA645588703 | TP53 | c.672+11C>T (n.672+11C>T) c.276+11C>T (n.276+11C>T) c.393+11C>T (n.393+11C>T) c.651+11C>T (n.651+11C>T) n.939C>T n.67+205C>T c.555+11C>T (n.555+11C>T) c.195+11C>T (n.195+11C>T) c.639+11C>T (n.639+11C>T) | dbSNP COSMIC |
17 | g.7674848G>C | CA2733136393 | TP53 | c.672+11C>G (n.672+11C>G) c.276+11C>G (n.276+11C>G) c.393+11C>G (n.393+11C>G) c.651+11C>G (n.651+11C>G) n.939C>G n.67+205C>G c.555+11C>G (n.555+11C>G) c.195+11C>G (n.195+11C>G) c.639+11C>G (n.639+11C>G) | dbSNP |
17 | g.7674849C>A | CA2635878482 | TP53 | c.672+10G>T (n.672+10G>T) c.276+10G>T (n.276+10G>T) c.393+10G>T (n.393+10G>T) c.651+10G>T (n.651+10G>T) n.938G>T n.67+204G>T c.555+10G>T (n.555+10G>T) c.195+10G>T (n.195+10G>T) c.639+10G>T (n.639+10G>T) | gnomAD v4 |
17 | g.7674850A= | CA2245953801 | TP53 | c.672+9T= (n.672+9T=) c.276+9T= (n.276+9T=) c.393+9T= (n.393+9T=) c.651+9T= (n.651+9T=) n.937T= n.67+203T= c.555+9T= (n.555+9T=) c.195+9T= (n.195+9T=) c.639+9T= (n.639+9T=) | |
17 | g.7674850A>G | CA16607883 | TP53 | c.672+9T>C (n.672+9T>C) c.276+9T>C (n.276+9T>C) c.393+9T>C (n.393+9T>C) c.651+9T>C (n.651+9T>C) n.937T>C n.67+203T>C c.555+9T>C (n.555+9T>C) c.195+9T>C (n.195+9T>C) c.639+9T>C (n.639+9T>C) | ClinVar dbSNP |
17 | g.7674850A>T | CA2635878485 | TP53 | c.672+9T>A (n.672+9T>A) c.276+9T>A (n.276+9T>A) c.393+9T>A (n.393+9T>A) c.651+9T>A (n.651+9T>A) n.937T>A n.67+203T>A c.555+9T>A (n.555+9T>A) c.195+9T>A (n.195+9T>A) c.639+9T>A (n.639+9T>A) | gnomAD v4 |
17 | g.7674851A= | CA2245953808 | TP53 | c.672+8T= (n.672+8T=) c.276+8T= (n.276+8T=) c.393+8T= (n.393+8T=) c.651+8T= (n.651+8T=) n.936T= n.67+202T= c.555+8T= (n.555+8T=) c.195+8T= (n.195+8T=) c.639+8T= (n.639+8T=) | |
17 | g.7674851A>C | CA002087 | TP53 | c.672+8T>G (n.672+8T>G) c.276+8T>G (n.276+8T>G) c.393+8T>G (n.393+8T>G) c.651+8T>G (n.651+8T>G) n.936T>G n.67+202T>G c.555+8T>G (n.555+8T>G) c.195+8T>G (n.195+8T>G) c.639+8T>G (n.639+8T>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.7674851A>G | CA2732930213 | TP53 | c.672+8T>C (n.672+8T>C) c.276+8T>C (n.276+8T>C) c.393+8T>C (n.393+8T>C) c.651+8T>C (n.651+8T>C) n.936T>C n.67+202T>C c.555+8T>C (n.555+8T>C) c.195+8T>C (n.195+8T>C) c.639+8T>C (n.639+8T>C) | dbSNP |
17 | g.7674851A>T | CA2732930212 | TP53 | c.672+8T>A (n.672+8T>A) c.276+8T>A (n.276+8T>A) c.393+8T>A (n.393+8T>A) c.651+8T>A (n.651+8T>A) n.936T>A n.67+202T>A c.555+8T>A (n.555+8T>A) c.195+8T>A (n.195+8T>A) c.639+8T>A (n.639+8T>A) | dbSNP |
17 | g.7674851_7674853delinsAAC | CA2245953810 | TP53 | c.672+6_672+8delinsGTT (n.672+6_672+8delinsGTT) c.276+6_276+8delinsGTT (n.276+6_276+8delinsGTT) c.393+6_393+8delinsGTT (n.393+6_393+8delinsGTT) c.651+6_651+8delinsGTT (n.651+6_651+8delinsGTT) n.934_936delinsGTT n.67+200_67+202delinsGTT c.555+6_555+8delinsGTT (n.555+6_555+8delinsGTT) c.195+6_195+8delinsGTT (n.195+6_195+8delinsGTT) c.639+6_639+8delinsGTT (n.639+6_639+8delinsGTT) | |
17 | g.7674851_7674853delinsCAA | CA913203435 | TP53 | c.672+6_672+8delinsTTG (n.672+6_672+8delinsTTG) c.276+6_276+8delinsTTG (n.276+6_276+8delinsTTG) c.393+6_393+8delinsTTG (n.393+6_393+8delinsTTG) c.651+6_651+8delinsTTG (n.651+6_651+8delinsTTG) n.934_936delinsTTG n.67+200_67+202delinsTTG c.555+6_555+8delinsTTG (n.555+6_555+8delinsTTG) c.195+6_195+8delinsTTG (n.195+6_195+8delinsTTG) c.639+6_639+8delinsTTG (n.639+6_639+8delinsTTG) | ClinVar dbSNP |
17 | g.7674851_7674858del | CA2635878487 | TP53 | c.672+1_672+8del (n.672+1_672+8del) c.276+1_276+8del (n.276+1_276+8del) c.393+1_393+8del (n.393+1_393+8del) c.651+1_651+8del (n.651+1_651+8del) n.929_936del n.67+195_67+202del c.555+1_555+8del (n.555+1_555+8del) c.195+1_195+8del (n.195+1_195+8del) c.639+1_639+8del (n.639+1_639+8del) | gnomAD v4 |
17 | g.7674852A>C | CA2733136395 | TP53 | c.672+7T>G (n.672+7T>G) c.276+7T>G (n.276+7T>G) c.393+7T>G (n.393+7T>G) c.651+7T>G (n.651+7T>G) n.935T>G n.67+201T>G c.555+7T>G (n.555+7T>G) c.195+7T>G (n.195+7T>G) c.639+7T>G (n.639+7T>G) | dbSNP |
17 | g.7674852A>T | CA2733136394 | TP53 | c.672+7T>A (n.672+7T>A) c.276+7T>A (n.276+7T>A) c.393+7T>A (n.393+7T>A) c.651+7T>A (n.651+7T>A) n.935T>A n.67+201T>A c.555+7T>A (n.555+7T>A) c.195+7T>A (n.195+7T>A) c.639+7T>A (n.639+7T>A) | dbSNP |
17 | g.7674856_7674884del | CA645588704 | TP53 | c.651_672+7del c.255_276+7del c.372_393+7del c.630_651+7del n.907_935del n.67+173_67+201del c.534_555+7del c.174_195+7del c.618_639+7del | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674853C>A | CA002094 | TP53 | c.672+6G>T (n.672+6G>T) c.276+6G>T (n.276+6G>T) c.393+6G>T (n.393+6G>T) c.651+6G>T (n.651+6G>T) n.934G>T n.67+200G>T c.555+6G>T (n.555+6G>T) c.195+6G>T (n.195+6G>T) c.639+6G>T (n.639+6G>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7674853C= | CA2245953817 | TP53 | c.672+6G= (n.672+6G=) c.276+6G= (n.276+6G=) c.393+6G= (n.393+6G=) c.651+6G= (n.651+6G=) n.934G= n.67+200G= c.555+6G= (n.555+6G=) c.195+6G= (n.195+6G=) c.639+6G= (n.639+6G=) | |
17 | g.7674853C>G | CA2573154667 | TP53 | c.672+6G>C (n.672+6G>C) c.276+6G>C (n.276+6G>C) c.393+6G>C (n.393+6G>C) c.651+6G>C (n.651+6G>C) n.934G>C n.67+200G>C c.555+6G>C (n.555+6G>C) c.195+6G>C (n.195+6G>C) c.639+6G>C (n.639+6G>C) | ClinVar dbSNP gnomAD v4 |
17 | g.7674853C>T | CA002095 | TP53 | c.672+6G>A (n.672+6G>A) c.276+6G>A (n.276+6G>A) c.393+6G>A (n.393+6G>A) c.651+6G>A (n.651+6G>A) n.934G>A n.67+200G>A c.555+6G>A (n.555+6G>A) c.195+6G>A (n.195+6G>A) c.639+6G>A (n.639+6G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.7674854C>A | CA2580611967 | TP53 | c.672+5G>T (n.672+5G>T) c.276+5G>T (n.276+5G>T) c.393+5G>T (n.393+5G>T) c.651+5G>T (n.651+5G>T) n.933G>T n.67+199G>T c.555+5G>T (n.555+5G>T) c.195+5G>T (n.195+5G>T) c.639+5G>T (n.639+5G>T) | dbSNP |
17 | g.7674854C= | CA2245953823 | TP53 | c.672+5G= (n.672+5G=) c.276+5G= (n.276+5G=) c.393+5G= (n.393+5G=) c.651+5G= (n.651+5G=) n.933G= n.67+199G= c.555+5G= (n.555+5G=) c.195+5G= (n.195+5G=) c.639+5G= (n.639+5G=) | |
17 | g.7674854C>G | CA2580094923 | TP53 | c.672+5G>C (n.672+5G>C) c.276+5G>C (n.276+5G>C) c.393+5G>C (n.393+5G>C) c.651+5G>C (n.651+5G>C) n.933G>C n.67+199G>C c.555+5G>C (n.555+5G>C) c.195+5G>C (n.195+5G>C) c.639+5G>C (n.639+5G>C) | ClinVar gnomAD v4 |
17 | g.7674854C>T | CA497925274 | TP53 | c.672+5G>A (n.672+5G>A) c.276+5G>A (n.276+5G>A) c.393+5G>A (n.393+5G>A) c.651+5G>A (n.651+5G>A) n.933G>A n.67+199G>A c.555+5G>A (n.555+5G>A) c.195+5G>A (n.195+5G>A) c.639+5G>A (n.639+5G>A) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
17 | g.7674855A= | CA2245953827 | TP53 | c.672+4T= (n.672+4T=) c.276+4T= (n.276+4T=) c.393+4T= (n.393+4T=) c.651+4T= (n.651+4T=) n.932T= n.67+198T= c.555+4T= (n.555+4T=) c.195+4T= (n.195+4T=) c.639+4T= (n.639+4T=) | |
17 | g.7674855A>G | CA915949532 | TP53 | c.672+4T>C (n.672+4T>C) c.276+4T>C (n.276+4T>C) c.393+4T>C (n.393+4T>C) c.651+4T>C (n.651+4T>C) n.932T>C n.67+198T>C c.555+4T>C (n.555+4T>C) c.195+4T>C (n.195+4T>C) c.639+4T>C (n.639+4T>C) | ClinVar dbSNP |
17 | g.7674855A>T | CA2732965417 | TP53 | c.672+4T>A (n.672+4T>A) c.276+4T>A (n.276+4T>A) c.393+4T>A (n.393+4T>A) c.651+4T>A (n.651+4T>A) n.932T>A n.67+198T>A c.555+4T>A (n.555+4T>A) c.195+4T>A (n.195+4T>A) c.639+4T>A (n.639+4T>A) | dbSNP |
17 | g.7674856G>A | CA2499224964 | TP53 | c.672+3C>T (n.672+3C>T) c.276+3C>T (n.276+3C>T) c.393+3C>T (n.393+3C>T) c.651+3C>T (n.651+3C>T) n.931C>T n.67+197C>T c.555+3C>T (n.555+3C>T) c.195+3C>T (n.195+3C>T) c.639+3C>T (n.639+3C>T) | ClinVar dbSNP |
17 | g.7674856G>C | CA2733136399 | TP53 | c.672+3C>G (n.672+3C>G) c.276+3C>G (n.276+3C>G) c.393+3C>G (n.393+3C>G) c.651+3C>G (n.651+3C>G) n.931C>G n.67+197C>G c.555+3C>G (n.555+3C>G) c.195+3C>G (n.195+3C>G) c.639+3C>G (n.639+3C>G) | dbSNP |
17 | g.7674856G= | CA2245953832 | TP53 | c.672+3C= (n.672+3C=) c.276+3C= (n.276+3C=) c.393+3C= (n.393+3C=) c.651+3C= (n.651+3C=) n.931C= n.67+197C= c.555+3C= (n.555+3C=) c.195+3C= (n.195+3C=) c.639+3C= (n.639+3C=) | |
17 | g.7674856G>T | CA645588705 | TP53 | c.672+3C>A (n.672+3C>A) c.276+3C>A (n.276+3C>A) c.393+3C>A (n.393+3C>A) c.651+3C>A (n.651+3C>A) n.931C>A n.67+197C>A c.555+3C>A (n.555+3C>A) c.195+3C>A (n.195+3C>A) c.639+3C>A (n.639+3C>A) | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674857A= | CA2245953848 | TP53 | c.672+2T= (n.672+2T=) c.276+2T= (n.276+2T=) c.393+2T= (n.393+2T=) c.651+2T= (n.651+2T=) n.930T= n.67+196T= c.555+2T= (n.555+2T=) c.195+2T= (n.195+2T=) c.639+2T= (n.639+2T=) | |
17 | g.7674857A>C | CA397839766 | TP53 | c.672+2T>G (n.672+2T>G) c.276+2T>G (n.276+2T>G) c.393+2T>G (n.393+2T>G) c.651+2T>G (n.651+2T>G) n.930T>G n.67+196T>G c.555+2T>G (n.555+2T>G) c.195+2T>G (n.195+2T>G) c.639+2T>G (n.639+2T>G) | ClinVar dbSNP |
17 | g.7674857A>G | CA397839763 | TP53 | c.672+2T>C (n.672+2T>C) c.276+2T>C (n.276+2T>C) c.393+2T>C (n.393+2T>C) c.651+2T>C (n.651+2T>C) n.930T>C n.67+196T>C c.555+2T>C (n.555+2T>C) c.195+2T>C (n.195+2T>C) c.639+2T>C (n.639+2T>C) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674857A>T | CA397839761 | TP53 | c.672+2T>A (n.672+2T>A) c.276+2T>A (n.276+2T>A) c.393+2T>A (n.393+2T>A) c.651+2T>A (n.651+2T>A) n.930T>A n.67+196T>A c.555+2T>A (n.555+2T>A) c.195+2T>A (n.195+2T>A) c.639+2T>A (n.639+2T>A) | ClinVar dbSNP |
17 | g.7674857_7674858delinsAC | CA2245953856 | TP53 | c.672+1_672+2delinsGT (n.672+1_672+2delinsGT) c.276+1_276+2delinsGT (n.276+1_276+2delinsGT) c.393+1_393+2delinsGT (n.393+1_393+2delinsGT) c.651+1_651+2delinsGT (n.651+1_651+2delinsGT) n.929_930delinsGT n.67+195_67+196delinsGT c.555+1_555+2delinsGT (n.555+1_555+2delinsGT) c.195+1_195+2delinsGT (n.195+1_195+2delinsGT) c.639+1_639+2delinsGT (n.639+1_639+2delinsGT) | |
17 | g.7674860_7674880dup | CA1139665121 | TP53 | c.654_672+2dup c.258_276+2dup c.375_393+2dup c.633_651+2dup n.910_930dup n.67+176_67+196dup c.537_555+2dup c.177_195+2dup c.621_639+2dup | ClinVar dbSNP |
17 | g.7674860_7674880del | CA645588706 | TP53 | c.654_672+2del c.258_276+2del c.375_393+2del c.633_651+2del n.910_930del n.67+176_67+196del c.537_555+2del c.177_195+2del c.621_639+2del | COSMIC |
17 | g.7674858C>A | CA397839769 | TP53 | c.672+1G>T (n.672+1G>T) c.276+1G>T (n.276+1G>T) c.393+1G>T (n.393+1G>T) c.651+1G>T (n.651+1G>T) n.929G>T n.67+195G>T c.555+1G>T (n.555+1G>T) c.195+1G>T (n.195+1G>T) c.639+1G>T (n.639+1G>T) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674858C= | CA2245953865 | TP53 | c.672+1G= (n.672+1G=) c.276+1G= (n.276+1G=) c.393+1G= (n.393+1G=) c.651+1G= (n.651+1G=) n.929G= n.67+195G= c.555+1G= (n.555+1G=) c.195+1G= (n.195+1G=) c.639+1G= (n.639+1G=) | |
17 | g.7674858C>G | CA397839772 | TP53 | c.672+1G>C (n.672+1G>C) c.276+1G>C (n.276+1G>C) c.393+1G>C (n.393+1G>C) c.651+1G>C (n.651+1G>C) n.929G>C n.67+195G>C c.555+1G>C (n.555+1G>C) c.195+1G>C (n.195+1G>C) c.639+1G>C (n.639+1G>C) | ClinVar COSMIC COSMIC COSMIC COSMIC |
17 | g.7674858C>T | CA339249 | TP53 | c.672+1G>A (n.672+1G>A) c.276+1G>A (n.276+1G>A) c.393+1G>A (n.393+1G>A) c.651+1G>A (n.651+1G>A) n.929G>A n.67+195G>A c.555+1G>A (n.555+1G>A) c.195+1G>A (n.195+1G>A) c.639+1G>A (n.639+1G>A) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674859del | CA913190589 | TP53 | c.672+1del c.276+1del c.393+1del c.651+1del n.929del n.67+195del c.555+1del c.195+1del c.639+1del | ClinVar dbSNP |
17 | g.7674858_7674861del | CA645588707 | TP53 | c.670_672+1del c.274_276+1del c.391_393+1del c.649_651+1del n.926_929del n.67+192_67+195del c.553_555+1del c.193_195+1del c.637_639+1del | COSMIC |
17 | g.7674859C>A | CA397839776 | TP53 | c.672G>T (p.Glu224Asp) c.276G>T (p.Glu92Asp) c.393G>T (p.Glu131Asp) c.651G>T (p.Glu217Asp) n.928G>T n.67+194G>T c.555G>T (p.Glu185Asp) c.195G>T (p.Glu65Asp) c.639G>T (p.Glu213Asp) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674859C= | CA2245953877 | TP53 | c.672G= (p.Glu224=) c.276G= (p.Glu92=) c.393G= (p.Glu131=) c.651G= (p.Glu217=) n.928G= n.67+194G= c.555G= (p.Glu185=) c.195G= (p.Glu65=) c.639G= (p.Glu213=) | |
17 | g.7674859C>G | CA397839777 | TP53 | c.672G>C (p.Glu224Asp) c.276G>C (p.Glu92Asp) c.393G>C (p.Glu131Asp) c.651G>C (p.Glu217Asp) n.928G>C n.67+194G>C c.555G>C (p.Glu185Asp) c.195G>C (p.Glu65Asp) c.639G>C (p.Glu213Asp) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674859C>T | CA000328 | TP53 | c.672G>A (p.Glu224=) c.276G>A (p.Glu92=) c.393G>A (p.Glu131=) c.651G>A (p.Glu217=) n.928G>A n.67+194G>A c.555G>A (p.Glu185=) c.195G>A (p.Glu65=) c.639G>A (p.Glu213=) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674860_7674870del | CA645588709 | TP53 | c.662_672del (p.Glu221GlyfsTer4) c.266_276del (p.Glu89GlyfsTer4) c.383_393del (p.Glu128GlyfsTer4) c.641_651del (p.Glu214GlyfsTer4) n.918_928del n.67+184_67+194del c.545_555del (p.Glu182GlyfsTer4) c.185_195del (p.Glu62GlyfsTer4) c.629_639del (p.Glu210GlyfsTer4) | COSMIC |
17 | g.7674861_7676624dup | CA2573130640 | TP53 | c.-28_672dup c.-21-1386_276dup c.-28_393dup c.-28_651dup c.-25-3_672dup n.112_928dup c.-262_555dup c.-145_555dup c.-142-3_555dup | |
17 | g.7674860T>A | CA397839780 | TP53 | c.671A>T (p.Glu224Val) c.275A>T (p.Glu92Val) c.392A>T (p.Glu131Val) c.650A>T (p.Glu217Val) n.927A>T n.67+193A>T c.554A>T (p.Glu185Val) c.194A>T (p.Glu65Val) c.638A>T (p.Glu213Val) | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674860T>C | CA397839783 | TP53 | c.671A>G (p.Glu224Gly) c.275A>G (p.Glu92Gly) c.392A>G (p.Glu131Gly) c.650A>G (p.Glu217Gly) n.927A>G n.67+193A>G c.554A>G (p.Glu185Gly) c.194A>G (p.Glu65Gly) c.638A>G (p.Glu213Gly) | ClinVar dbSNP COSMIC |
17 | g.7674860T>G | CA397839786 | TP53 | c.671A>C (p.Glu224Ala) c.275A>C (p.Glu92Ala) c.392A>C (p.Glu131Ala) c.650A>C (p.Glu217Ala) n.927A>C n.67+193A>C c.554A>C (p.Glu185Ala) c.194A>C (p.Glu65Ala) c.638A>C (p.Glu213Ala) | ClinVar dbSNP |
17 | g.7674860T= | CA2245953891 | TP53 | c.671A= (p.Glu224=) c.275A= (p.Glu92=) c.392A= (p.Glu131=) c.650A= (p.Glu217=) n.927A= n.67+193A= c.554A= (p.Glu185=) c.194A= (p.Glu65=) c.638A= (p.Glu213=) | |
17 | g.7674860delinsAGA | CA645588710 | TP53 | c.671delinsTCT (p.Glu224ValfsTer24) c.275delinsTCT (p.Glu92ValfsTer24) c.392delinsTCT (p.Glu131ValfsTer24) c.650delinsTCT (p.Glu217ValfsTer24) n.927delinsTCT n.67+193delinsTCT c.554delinsTCT (p.Glu185ValfsTer24) c.194delinsTCT (p.Glu65ValfsTer24) c.638delinsTCT (p.Glu213ValfsTer24) | COSMIC |
17 | g.7674860_7674876delinsTCAGGCGGCTCATAGGG | CA2245953899 | TP53 | c.655_671delinsCCCTATGAGCCGCCTGA (p.Pro219=) c.259_275delinsCCCTATGAGCCGCCTGA (p.Pro87=) c.376_392delinsCCCTATGAGCCGCCTGA (p.Pro126=) c.634_650delinsCCCTATGAGCCGCCTGA (p.Pro212=) n.911_927delinsCCCTATGAGCCGCCTGA n.67+177_67+193delinsCCCTATGAGCCGCCTGA c.538_554delinsCCCTATGAGCCGCCTGA (p.Pro180=) c.178_194delinsCCCTATGAGCCGCCTGA (p.Pro60=) c.622_638delinsCCCTATGAGCCGCCTGA (p.Pro208=) | |
17 | g.7674861del | CA497925275 | TP53 | c.670del (p.Glu224ArgfsTer23) c.274del (p.Glu92ArgfsTer23) c.391del (p.Glu131ArgfsTer23) c.649del (p.Glu217ArgfsTer23) n.926del n.67+192del c.553del (p.Glu185ArgfsTer23) c.193del (p.Glu65ArgfsTer23) c.637del (p.Glu213ArgfsTer23) | COSMIC |
17 | g.7674861C>A | CA397839787 | TP53 | c.670G>T (p.Glu224Ter) c.274G>T (p.Glu92Ter) c.391G>T (p.Glu131Ter) c.649G>T (p.Glu217Ter) n.926G>T n.67+192G>T c.553G>T (p.Glu185Ter) c.193G>T (p.Glu65Ter) c.637G>T (p.Glu213Ter) | gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674861C= | CA2245953913 | TP53 | c.670G= (p.Glu224=) c.274G= (p.Glu92=) c.391G= (p.Glu131=) c.649G= (p.Glu217=) n.926G= n.67+192G= c.553G= (p.Glu185=) c.193G= (p.Glu65=) c.637G= (p.Glu213=) | |
17 | g.7674861C>G | CA397839788 | TP53 | c.670G>C (p.Glu224Gln) c.274G>C (p.Glu92Gln) c.391G>C (p.Glu131Gln) c.649G>C (p.Glu217Gln) n.926G>C n.67+192G>C c.553G>C (p.Glu185Gln) c.193G>C (p.Glu65Gln) c.637G>C (p.Glu213Gln) | dbSNP gnomAD v4 |
17 | g.7674861C>T | CA397839791 | TP53 | c.670G>A (p.Glu224Lys) c.274G>A (p.Glu92Lys) c.391G>A (p.Glu131Lys) c.649G>A (p.Glu217Lys) n.926G>A n.67+192G>A c.553G>A (p.Glu185Lys) c.193G>A (p.Glu65Lys) c.637G>A (p.Glu213Lys) | ClinVar dbSNP COSMIC |
17 | g.7674861_7674862del | CA645588712 | TP53 | c.669_670del (p.Glu224GlyfsTer4) c.273_274del (p.Glu92GlyfsTer4) c.390_391del (p.Glu131GlyfsTer4) c.648_649del (p.Glu217GlyfsTer4) n.925_926del n.67+191_67+192del c.552_553del (p.Glu185GlyfsTer4) c.192_193del (p.Glu65GlyfsTer4) c.636_637del (p.Glu213GlyfsTer4) | COSMIC |
17 | g.7674861_7674868del | CA645588711 | TP53 | c.663_670del (p.Pro222GlyfsTer4) c.267_274del (p.Pro90GlyfsTer4) c.384_391del (p.Pro129GlyfsTer4) c.642_649del (p.Pro215GlyfsTer4) n.919_926del n.67+185_67+192del c.546_553del (p.Pro183GlyfsTer4) c.186_193del (p.Pro63GlyfsTer4) c.630_637del (p.Pro211GlyfsTer4) | COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674863_7674878del | CA658656530 | TP53 | c.655_670del (p.Pro219ArgfsTer23) c.259_274del (p.Pro87ArgfsTer23) c.376_391del (p.Pro126ArgfsTer23) c.634_649del (p.Pro212ArgfsTer23) n.911_926del n.67+177_67+192del c.538_553del (p.Pro180ArgfsTer23) c.178_193del (p.Pro60ArgfsTer23) c.622_637del (p.Pro208ArgfsTer23) | ClinVar dbSNP |
17 | g.7674862A>C | CA497925276 | TP53 | c.669T>G (p.Pro223=) c.273T>G (p.Pro91=) c.390T>G (p.Pro130=) c.648T>G (p.Pro216=) n.925T>G n.67+191T>G c.552T>G (p.Pro184=) c.192T>G (p.Pro64=) c.636T>G (p.Pro212=) | dbSNP COSMIC |
17 | g.7674862A>G | CA497925277 | TP53 | c.669T>C (p.Pro223=) c.273T>C (p.Pro91=) c.390T>C (p.Pro130=) c.648T>C (p.Pro216=) n.925T>C n.67+191T>C c.552T>C (p.Pro184=) c.192T>C (p.Pro64=) c.636T>C (p.Pro212=) | dbSNP COSMIC |
17 | g.7674862A>T | CA497925278 | TP53 | c.669T>A (p.Pro223=) c.273T>A (p.Pro91=) c.390T>A (p.Pro130=) c.648T>A (p.Pro216=) n.925T>A n.67+191T>A c.552T>A (p.Pro184=) c.192T>A (p.Pro64=) c.636T>A (p.Pro212=) | dbSNP gnomAD v4 COSMIC |
17 | g.7674862_7674874delinsAGGCGGCTCATAG | CA2245953922 | TP53 | c.657_669delinsCTATGAGCCGCCT (p.Pro219=) c.261_273delinsCTATGAGCCGCCT (p.Pro87=) c.378_390delinsCTATGAGCCGCCT (p.Pro126=) c.636_648delinsCTATGAGCCGCCT (p.Pro212=) n.913_925delinsCTATGAGCCGCCT n.67+179_67+191delinsCTATGAGCCGCCT c.540_552delinsCTATGAGCCGCCT (p.Pro180=) c.180_192delinsCTATGAGCCGCCT (p.Pro60=) c.624_636delinsCTATGAGCCGCCT (p.Pro208=) | |
17 | g.7674863G>A | CA10580928 | TP53 | c.668C>T (p.Pro223Leu) c.272C>T (p.Pro91Leu) c.389C>T (p.Pro130Leu) c.647C>T (p.Pro216Leu) n.924C>T n.67+190C>T c.551C>T (p.Pro184Leu) c.191C>T (p.Pro64Leu) c.635C>T (p.Pro212Leu) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674863G>C | CA397839798 | TP53 | c.668C>G (p.Pro223Arg) c.272C>G (p.Pro91Arg) c.389C>G (p.Pro130Arg) c.647C>G (p.Pro216Arg) n.924C>G n.67+190C>G c.551C>G (p.Pro184Arg) c.191C>G (p.Pro64Arg) c.635C>G (p.Pro212Arg) | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674863G= | CA2245953936 | TP53 | c.668C= (p.Pro223=) c.272C= (p.Pro91=) c.389C= (p.Pro130=) c.647C= (p.Pro216=) n.924C= n.67+190C= c.551C= (p.Pro184=) c.191C= (p.Pro64=) c.635C= (p.Pro212=) | |
17 | g.7674863G>T | CA287488301 | TP53 | c.668C>A (p.Pro223His) c.272C>A (p.Pro91His) c.389C>A (p.Pro130His) c.647C>A (p.Pro216His) n.924C>A n.67+190C>A c.551C>A (p.Pro184His) c.191C>A (p.Pro64His) c.635C>A (p.Pro212His) | dbSNP COSMIC |
17 | g.7674864del | CA497925279 | TP53 | c.668del (p.Pro223LeufsTer24) c.272del (p.Pro91LeufsTer24) c.389del (p.Pro130LeufsTer24) c.647del (p.Pro216LeufsTer24) n.924del n.67+190del c.551del (p.Pro184LeufsTer24) c.191del (p.Pro64LeufsTer24) c.635del (p.Pro212LeufsTer24) | ClinVar COSMIC |
17 | g.7674864_7674867del | CA645588714 | TP53 | c.665_668del (p.Pro222LeufsTer24) c.269_272del (p.Pro90LeufsTer24) c.386_389del (p.Pro129LeufsTer24) c.644_647del (p.Pro215LeufsTer24) n.921_924del n.67+187_67+190del c.548_551del (p.Pro183LeufsTer24) c.188_191del (p.Pro63LeufsTer24) c.632_635del (p.Pro211LeufsTer24) | COSMIC |
17 | g.7674866_7674877del | CA10580929 | TP53 | c.657_668del (p.Tyr220_Pro223del) c.261_272del (p.Tyr88_Pro91del) c.378_389del (p.Tyr127_Pro130del) c.636_647del (p.Tyr213_Pro216del) n.913_924del n.67+179_67+190del c.540_551del (p.Tyr181_Pro184del) c.180_191del (p.Tyr61_Pro64del) c.624_635del (p.Tyr209_Pro212del) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674864G>A | CA397839806 | TP53 | c.667C>T (p.Pro223Ser) c.271C>T (p.Pro91Ser) c.388C>T (p.Pro130Ser) c.646C>T (p.Pro216Ser) n.923C>T n.67+189C>T c.550C>T (p.Pro184Ser) c.190C>T (p.Pro64Ser) c.634C>T (p.Pro212Ser) | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674864G>C | CA397839809 | TP53 | c.667C>G (p.Pro223Ala) c.271C>G (p.Pro91Ala) c.388C>G (p.Pro130Ala) c.646C>G (p.Pro216Ala) n.923C>G n.67+189C>G c.550C>G (p.Pro184Ala) c.190C>G (p.Pro64Ala) c.634C>G (p.Pro212Ala) | dbSNP COSMIC |
17 | g.7674864G>T | CA397839812 | TP53 | c.667C>A (p.Pro223Thr) c.271C>A (p.Pro91Thr) c.388C>A (p.Pro130Thr) c.646C>A (p.Pro216Thr) n.923C>A n.67+189C>A c.550C>A (p.Pro184Thr) c.190C>A (p.Pro64Thr) c.634C>A (p.Pro212Thr) | dbSNP gnomAD v4 |
17 | g.7674865_7674866del | CA645588716 | TP53 | c.666_667del (p.Pro223Ter) c.270_271del (p.Pro91Ter) c.387_388del (p.Pro130Ter) c.645_646del (p.Pro216Ter) n.922_923del n.67+188_67+189del c.549_550del (p.Pro184Ter) c.189_190del (p.Pro64Ter) c.633_634del (p.Pro212Ter) | COSMIC COSMIC COSMIC COSMIC |
17 | g.7674864_7674870dup | CA645588715 | TP53 | c.661_667dup (p.Pro223ArgfsTer4) c.265_271dup (p.Pro91ArgfsTer4) c.382_388dup (p.Pro130ArgfsTer4) c.640_646dup (p.Pro216ArgfsTer4) n.917_923dup n.67+183_67+189dup c.544_550dup (p.Pro184ArgfsTer4) c.184_190dup (p.Pro64ArgfsTer4) c.628_634dup (p.Pro212ArgfsTer4) | COSMIC COSMIC COSMIC COSMIC |
17 | g.7674864_7674880delinsGCGGCTCATAGGGCACC | CA2245953948 | TP53 | c.651_667delinsGGTGCCCTATGAGCCGC (p.Val217=) c.255_271delinsGGTGCCCTATGAGCCGC (p.Val85=) c.372_388delinsGGTGCCCTATGAGCCGC (p.Val124=) c.630_646delinsGGTGCCCTATGAGCCGC (p.Val210=) n.907_923delinsGGTGCCCTATGAGCCGC n.67+173_67+189delinsGGTGCCCTATGAGCCGC c.534_550delinsGGTGCCCTATGAGCCGC (p.Val178=) c.174_190delinsGGTGCCCTATGAGCCGC (p.Val58=) c.618_634delinsGGTGCCCTATGAGCCGC (p.Val206=) | |
17 | g.7674865C>A | CA000321 | TP53 | c.666G>T (p.Pro222=) c.270G>T (p.Pro90=) c.387G>T (p.Pro129=) c.645G>T (p.Pro215=) n.922G>T n.67+188G>T c.549G>T (p.Pro183=) c.189G>T (p.Pro63=) c.633G>T (p.Pro211=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
17 | g.7674865C= | CA2245953968 | TP53 | c.666G= (p.Pro222=) c.270G= (p.Pro90=) c.387G= (p.Pro129=) c.645G= (p.Pro215=) n.922G= n.67+188G= c.549G= (p.Pro183=) c.189G= (p.Pro63=) c.633G= (p.Pro211=) | |
17 | g.7674865C>G | CA497925280 | TP53 | c.666G>C (p.Pro222=) c.270G>C (p.Pro90=) c.387G>C (p.Pro129=) c.645G>C (p.Pro215=) n.922G>C n.67+188G>C c.549G>C (p.Pro183=) c.189G>C (p.Pro63=) c.633G>C (p.Pro211=) | dbSNP gnomAD v4 COSMIC |
17 | g.7674865C>T | CA000319 | TP53 | c.666G>A (p.Pro222=) c.270G>A (p.Pro90=) c.387G>A (p.Pro129=) c.645G>A (p.Pro215=) n.922G>A n.67+188G>A c.549G>A (p.Pro183=) c.189G>A (p.Pro63=) c.633G>A (p.Pro211=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
17 | g.7674865_7674866delinsCG | CA2245953962 | TP53 | c.665_666delinsCG (p.Pro222=) c.269_270delinsCG (p.Pro90=) c.386_387delinsCG (p.Pro129=) c.644_645delinsCG (p.Pro215=) n.921_922delinsCG n.67+187_67+188delinsCG c.548_549delinsCG (p.Pro183=) c.188_189delinsCG (p.Pro63=) c.632_633delinsCG (p.Pro211=) | |
17 | g.7674866_7674870del | CA645588717 | TP53 | c.662_666del (p.Glu221AlafsTer2) c.266_270del (p.Glu89AlafsTer2) c.383_387del (p.Glu128AlafsTer2) c.641_645del (p.Glu214AlafsTer2) n.918_922del n.67+184_67+188del c.545_549del (p.Glu182AlafsTer2) c.185_189del (p.Glu62AlafsTer2) c.629_633del (p.Glu210AlafsTer2) | ClinVar dbSNP COSMIC |
17 | g.7674865_7674874delinsCGGCTCATAG | CA2245953964 | TP53 | c.657_666delinsCTATGAGCCG (p.Pro219=) c.261_270delinsCTATGAGCCG (p.Pro87=) c.378_387delinsCTATGAGCCG (p.Pro126=) c.636_645delinsCTATGAGCCG (p.Pro212=) n.913_922delinsCTATGAGCCG n.67+179_67+188delinsCTATGAGCCG c.540_549delinsCTATGAGCCG (p.Pro180=) c.180_189delinsCTATGAGCCG (p.Pro60=) c.624_633delinsCTATGAGCCG (p.Pro208=) | |
17 | g.7674865_7674880del | CA000310 | TP53 | c.651_666del (p.Val218LeufsTer24) c.255_270del (p.Val86LeufsTer24) c.372_387del (p.Val125LeufsTer24) c.630_645del (p.Val211LeufsTer24) n.907_922del n.67+173_67+188del c.534_549del (p.Val179LeufsTer24) c.174_189del (p.Val59LeufsTer24) c.618_633del (p.Val207LeufsTer24) | ClinVar dbSNP |
17 | g.7674866G>A | CA000317 | TP53 | c.665C>T (p.Pro222Leu) c.269C>T (p.Pro90Leu) c.386C>T (p.Pro129Leu) c.644C>T (p.Pro215Leu) n.921C>T n.67+187C>T c.548C>T (p.Pro183Leu) c.188C>T (p.Pro63Leu) c.632C>T (p.Pro211Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
17 | g.7674866G>C | CA397839834 | TP53 | c.665C>G (p.Pro222Arg) c.269C>G (p.Pro90Arg) c.386C>G (p.Pro129Arg) c.644C>G (p.Pro215Arg) n.921C>G n.67+187C>G c.548C>G (p.Pro183Arg) c.188C>G (p.Pro63Arg) c.632C>G (p.Pro211Arg) | dbSNP |
17 | g.7674866G= | CA2245953991 | TP53 | c.665C= (p.Pro222=) c.269C= (p.Pro90=) c.386C= (p.Pro129=) c.644C= (p.Pro215=) n.921C= n.67+187C= c.548C= (p.Pro183=) c.188C= (p.Pro63=) c.632C= (p.Pro211=) | |
17 | g.7674866G>T | CA397839839 | TP53 | c.665C>A (p.Pro222Gln) c.269C>A (p.Pro90Gln) c.386C>A (p.Pro129Gln) c.644C>A (p.Pro215Gln) n.921C>A n.67+187C>A c.548C>A (p.Pro183Gln) c.188C>A (p.Pro63Gln) c.632C>A (p.Pro211Gln) | ClinVar dbSNP COSMIC |
17 | g.7674866_7674867delinsAA | CA645588718 | TP53 | c.664_665delinsTT (p.Pro222Leu) c.268_269delinsTT (p.Pro90Leu) c.385_386delinsTT (p.Pro129Leu) c.643_644delinsTT (p.Pro215Leu) n.920_921delinsTT n.67+186_67+187delinsTT c.547_548delinsTT (p.Pro183Leu) c.187_188delinsTT (p.Pro63Leu) c.631_632delinsTT (p.Pro211Leu) | COSMIC |
17 | g.7674867dup | CA2499224965 | TP53 | c.665dup (p.Pro223AlafsTer2) c.269dup (p.Pro91AlafsTer2) c.386dup (p.Pro130AlafsTer2) c.644dup (p.Pro216AlafsTer2) n.921dup n.67+187dup c.548dup (p.Pro184AlafsTer2) c.188dup (p.Pro64AlafsTer2) c.632dup (p.Pro212AlafsTer2) | ClinVar dbSNP |
17 | g.7674867del | CA497925281 | TP53 | c.665del (p.Pro222ArgfsTer25) c.269del (p.Pro90ArgfsTer25) c.386del (p.Pro129ArgfsTer25) c.644del (p.Pro215ArgfsTer25) n.921del n.67+187del c.548del (p.Pro183ArgfsTer25) c.188del (p.Pro63ArgfsTer25) c.632del (p.Pro211ArgfsTer25) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674869_7674877del | CA10580930 | TP53 | c.657_665del (p.Tyr220_Pro222del) c.261_269del (p.Tyr88_Pro90del) c.378_386del (p.Tyr127_Pro129del) c.636_644del (p.Tyr213_Pro215del) n.913_921del n.67+179_67+187del c.540_548del (p.Tyr181_Pro183del) c.180_188del (p.Tyr61_Pro63del) c.624_632del (p.Tyr209_Pro211del) | ClinVar dbSNP |
17 | g.7674867G>A | CA16615720 | TP53 | c.664C>T (p.Pro222Ser) c.268C>T (p.Pro90Ser) c.385C>T (p.Pro129Ser) c.643C>T (p.Pro215Ser) n.920C>T n.67+186C>T c.547C>T (p.Pro183Ser) c.187C>T (p.Pro63Ser) c.631C>T (p.Pro211Ser) | ClinVar dbSNP gnomAD v4 COSMIC |
17 | g.7674867G>C | CA397839848 | TP53 | c.664C>G (p.Pro222Ala) c.268C>G (p.Pro90Ala) c.385C>G (p.Pro129Ala) c.643C>G (p.Pro215Ala) n.920C>G n.67+186C>G c.547C>G (p.Pro183Ala) c.187C>G (p.Pro63Ala) c.631C>G (p.Pro211Ala) | dbSNP COSMIC |
17 | g.7674867G= | CA2245954000 | TP53 | c.664C= (p.Pro222=) c.268C= (p.Pro90=) c.385C= (p.Pro129=) c.643C= (p.Pro215=) n.920C= n.67+186C= c.547C= (p.Pro183=) c.187C= (p.Pro63=) c.631C= (p.Pro211=) | |
17 | g.7674867G>T | CA397839851 | TP53 | c.664C>A (p.Pro222Thr) c.268C>A (p.Pro90Thr) c.385C>A (p.Pro129Thr) c.643C>A (p.Pro215Thr) n.920C>A n.67+186C>A c.547C>A (p.Pro183Thr) c.187C>A (p.Pro63Thr) c.631C>A (p.Pro211Thr) | dbSNP COSMIC |
17 | g.7674868_7674874del | CA645588719 | TP53 | c.658_664del (p.Tyr220ArgfsTer25) c.262_268del (p.Tyr88ArgfsTer25) c.379_385del (p.Tyr127ArgfsTer25) c.637_643del (p.Tyr213ArgfsTer25) n.914_920del n.67+180_67+186del c.541_547del (p.Tyr181ArgfsTer25) c.181_187del (p.Tyr61ArgfsTer25) c.625_631del (p.Tyr209ArgfsTer25) | gnomAD v4 COSMIC |
17 | g.7674868C>A | CA397839856 | TP53 | c.663G>T (p.Glu221Asp) c.267G>T (p.Glu89Asp) c.384G>T (p.Glu128Asp) c.642G>T (p.Glu214Asp) n.919G>T n.67+185G>T c.546G>T (p.Glu182Asp) c.186G>T (p.Glu62Asp) c.630G>T (p.Glu210Asp) | dbSNP COSMIC |
17 | g.7674868C= | CA2245954006 | TP53 | c.663G= (p.Glu221=) c.267G= (p.Glu89=) c.384G= (p.Glu128=) c.642G= (p.Glu214=) n.919G= n.67+185G= c.546G= (p.Glu182=) c.186G= (p.Glu62=) c.630G= (p.Glu210=) | |
17 | g.7674868C>G | CA397839857 | TP53 | c.663G>C (p.Glu221Asp) c.267G>C (p.Glu89Asp) c.384G>C (p.Glu128Asp) c.642G>C (p.Glu214Asp) n.919G>C n.67+185G>C c.546G>C (p.Glu182Asp) c.186G>C (p.Glu62Asp) c.630G>C (p.Glu210Asp) | dbSNP COSMIC |
17 | g.7674868C>T | CA16615692 | TP53 | c.663G>A (p.Glu221=) c.267G>A (p.Glu89=) c.384G>A (p.Glu128=) c.642G>A (p.Glu214=) n.919G>A n.67+185G>A c.546G>A (p.Glu182=) c.186G>A (p.Glu62=) c.630G>A (p.Glu210=) | ClinVar dbSNP COSMIC |
17 | g.7674868_7674869delinsCT | CA2245954005 | TP53 | c.662_663delinsAG (p.Glu221=) c.266_267delinsAG (p.Glu89=) c.383_384delinsAG (p.Glu128=) c.641_642delinsAG (p.Glu214=) n.918_919delinsAG n.67+184_67+185delinsAG c.545_546delinsAG (p.Glu182=) c.185_186delinsAG (p.Glu62=) c.629_630delinsAG (p.Glu210=) | |
17 | g.7674869_7674880dup | CA2580094935 | TP53 | c.652_663dup (p.Glu221_Pro222insValProTyrGlu) c.256_267dup (p.Glu89_Pro90insValProTyrGlu) c.373_384dup (p.Glu128_Pro129insValProTyrGlu) c.631_642dup (p.Glu214_Pro215insValProTyrGlu) n.908_919dup n.67+174_67+185dup c.535_546dup (p.Glu182_Pro183insValProTyrGlu) c.175_186dup (p.Glu62_Pro63insValProTyrGlu) c.619_630dup (p.Glu210_Pro211insValProTyrGlu) | ClinVar |
17 | g.7674869_7674880del | CA645588720 | TP53 | c.652_663del (p.Val218_Glu221del) c.256_267del (p.Val86_Glu89del) c.373_384del (p.Val125_Glu128del) c.631_642del (p.Val211_Glu214del) n.908_919del n.67+174_67+185del c.535_546del (p.Val179_Glu182del) c.175_186del (p.Val59_Glu62del) c.619_630del (p.Val207_Glu210del) | ClinVar COSMIC |
17 | g.7674869del | CA10583678 | TP53 | c.662del (p.Glu221GlyfsTer26) c.266del (p.Glu89GlyfsTer26) c.383del (p.Glu128GlyfsTer26) c.641del (p.Glu214GlyfsTer26) n.918del n.67+184del c.545del (p.Glu182GlyfsTer26) c.185del (p.Glu62GlyfsTer26) c.629del (p.Glu210GlyfsTer26) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674869T>A | CA397839864 | TP53 | c.662A>T (p.Glu221Val) c.266A>T (p.Glu89Val) c.383A>T (p.Glu128Val) c.641A>T (p.Glu214Val) n.918A>T n.67+184A>T c.545A>T (p.Glu182Val) c.185A>T (p.Glu62Val) c.629A>T (p.Glu210Val) | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674869T>C | CA397839867 | TP53 | c.662A>G (p.Glu221Gly) c.266A>G (p.Glu89Gly) c.383A>G (p.Glu128Gly) c.641A>G (p.Glu214Gly) n.918A>G n.67+184A>G c.545A>G (p.Glu182Gly) c.185A>G (p.Glu62Gly) c.629A>G (p.Glu210Gly) | dbSNP COSMIC |
17 | g.7674869T>G | CA397839870 | TP53 | c.662A>C (p.Glu221Ala) c.266A>C (p.Glu89Ala) c.383A>C (p.Glu128Ala) c.641A>C (p.Glu214Ala) n.918A>C n.67+184A>C c.545A>C (p.Glu182Ala) c.185A>C (p.Glu62Ala) c.629A>C (p.Glu210Ala) | ClinVar dbSNP |
17 | g.7674869T= | CA2245954019 | TP53 | c.662A= (p.Glu221=) c.266A= (p.Glu89=) c.383A= (p.Glu128=) c.641A= (p.Glu214=) n.918A= n.67+184A= c.545A= (p.Glu182=) c.185A= (p.Glu62=) c.629A= (p.Glu210=) | |
17 | g.7674869_7674870delinsAT | CA2739265560 | TP53 | c.661_662delinsAT (p.Glu221Met) c.265_266delinsAT (p.Glu89Met) c.382_383delinsAT (p.Glu128Met) c.640_641delinsAT (p.Glu214Met) n.917_918delinsAT n.67+183_67+184delinsAT c.544_545delinsAT (p.Glu182Met) c.184_185delinsAT (p.Glu62Met) c.628_629delinsAT (p.Glu210Met) | ClinVar |
17 | g.7674869_7674886del | CA2580617666 | TP53 | c.645_662del (p.Ser215_Glu221delinsArg) c.249_266del (p.Ser83_Glu89delinsArg) c.366_383del (p.Ser122_Glu128delinsArg) c.624_641del (p.Ser208_Glu214delinsArg) n.901_918del n.67+167_67+184del c.528_545del (p.Ser176_Glu182delinsArg) c.168_185del (p.Ser56_Glu62delinsArg) c.612_629del (p.Ser204_Glu210delinsArg) | ClinVar |
17 | g.7674870del | CA497925282 | TP53 | c.661del (p.Glu221SerfsTer26) c.265del (p.Glu89SerfsTer26) c.382del (p.Glu128SerfsTer26) c.640del (p.Glu214SerfsTer26) n.917del n.67+183del c.544del (p.Glu182SerfsTer26) c.184del (p.Glu62SerfsTer26) c.628del (p.Glu210SerfsTer26) | COSMIC |
17 | g.7674870C>A | CA397839876 | TP53 | c.661G>T (p.Glu221Ter) c.265G>T (p.Glu89Ter) c.382G>T (p.Glu128Ter) c.640G>T (p.Glu214Ter) n.917G>T n.67+183G>T c.544G>T (p.Glu182Ter) c.184G>T (p.Glu62Ter) c.628G>T (p.Glu210Ter) | ClinVar dbSNP gnomAD v2 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674870C= | CA2245954040 | TP53 | c.661G= (p.Glu221=) c.265G= (p.Glu89=) c.382G= (p.Glu128=) c.640G= (p.Glu214=) n.917G= n.67+183G= c.544G= (p.Glu182=) c.184G= (p.Glu62=) c.628G= (p.Glu210=) | |
17 | g.7674870C>G | CA397839879 | TP53 | c.661G>C (p.Glu221Gln) c.265G>C (p.Glu89Gln) c.382G>C (p.Glu128Gln) c.640G>C (p.Glu214Gln) n.917G>C n.67+183G>C c.544G>C (p.Glu182Gln) c.184G>C (p.Glu62Gln) c.628G>C (p.Glu210Gln) | dbSNP |
17 | g.7674870C>T | CA000316 | TP53 | c.661G>A (p.Glu221Lys) c.265G>A (p.Glu89Lys) c.382G>A (p.Glu128Lys) c.640G>A (p.Glu214Lys) n.917G>A n.67+183G>A c.544G>A (p.Glu182Lys) c.184G>A (p.Glu62Lys) c.628G>A (p.Glu210Lys) | ClinVar dbSNP gnomAD v2 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674871_7674879del | CA645588724 | TP53 | c.653_661del (p.Val218_Tyr220del) c.257_265del (p.Val86_Tyr88del) c.374_382del (p.Val125_Tyr127del) c.632_640del (p.Val211_Tyr213del) n.909_917del n.67+175_67+183del c.536_544del (p.Val179_Tyr181del) c.176_184del (p.Val59_Tyr61del) c.620_628del (p.Val207_Tyr209del) | COSMIC |
17 | g.7674872_7674881del | CA645588722 | TP53 | c.652_661del (p.Val218SerfsTer26) c.256_265del (p.Val86SerfsTer26) c.373_382del (p.Val125SerfsTer26) c.631_640del (p.Val211SerfsTer26) n.908_917del n.67+174_67+183del c.535_544del (p.Val179SerfsTer26) c.175_184del (p.Val59SerfsTer26) c.619_628del (p.Val207SerfsTer26) | COSMIC |
17 | g.7674872_7674886del | CA645588723 | TP53 | c.647_661del (p.Val216_Tyr220del) c.251_265del (p.Val84_Tyr88del) c.368_382del (p.Val123_Tyr127del) c.626_640del (p.Val209_Tyr213del) n.903_917del n.67+169_67+183del c.530_544del (p.Val177_Tyr181del) c.170_184del (p.Val57_Tyr61del) c.614_628del (p.Val205_Tyr209del) | COSMIC |
17 | g.7674871del | CA497925283 | TP53 | c.660del (p.Tyr220Ter) c.264del (p.Tyr88Ter) c.381del (p.Tyr127Ter) c.639del (p.Tyr213Ter) n.916del n.67+182del c.543del (p.Tyr181Ter) c.183del (p.Tyr61Ter) c.627del (p.Tyr209Ter) | COSMIC |
17 | g.7674871A= | CA2245954045 | TP53 | c.660T= (p.Tyr220=) c.264T= (p.Tyr88=) c.381T= (p.Tyr127=) c.639T= (p.Tyr213=) n.916T= n.67+182T= c.543T= (p.Tyr181=) c.183T= (p.Tyr61=) c.627T= (p.Tyr209=) | |
17 | g.7674871A>C | CA397839882 | TP53 | c.660T>G (p.Tyr220Ter) c.264T>G (p.Tyr88Ter) c.381T>G (p.Tyr127Ter) c.639T>G (p.Tyr213Ter) n.916T>G n.67+182T>G c.543T>G (p.Tyr181Ter) c.183T>G (p.Tyr61Ter) c.627T>G (p.Tyr209Ter) | COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674871A>G | CA497925284 | TP53 | c.660T>C (p.Tyr220=) c.264T>C (p.Tyr88=) c.381T>C (p.Tyr127=) c.639T>C (p.Tyr213=) n.916T>C n.67+182T>C c.543T>C (p.Tyr181=) c.183T>C (p.Tyr61=) c.627T>C (p.Tyr209=) | ClinVar dbSNP |
17 | g.7674871A>T | CA397839886 | TP53 | c.660T>A (p.Tyr220Ter) c.264T>A (p.Tyr88Ter) c.381T>A (p.Tyr127Ter) c.639T>A (p.Tyr213Ter) n.916T>A n.67+182T>A c.543T>A (p.Tyr181Ter) c.183T>A (p.Tyr61Ter) c.627T>A (p.Tyr209Ter) | ClinVar dbSNP COSMIC |
17 | g.7674872_7674873del | CA2825002657 | TP53 | c.659_660del (p.Tyr220Ter) c.263_264del (p.Tyr88Ter) c.380_381del (p.Tyr127Ter) c.638_639del (p.Tyr213Ter) n.915_916del n.67+181_67+182del c.542_543del (p.Tyr181Ter) c.182_183del (p.Tyr61Ter) c.626_627del (p.Tyr209Ter) | ClinVar |
17 | g.7674873_7674890del | CA2695223076 | TP53 | c.643_660del (p.Ser215_Tyr220del) c.247_264del (p.Ser83_Tyr88del) c.364_381del (p.Ser122_Tyr127del) c.622_639del (p.Ser208_Tyr213del) n.899_916del n.67+165_67+182del c.526_543del (p.Ser176_Tyr181del) c.166_183del (p.Ser56_Tyr61del) c.610_627del (p.Ser204_Tyr209del) | |
17 | g.7674872_7674895del | CA2825002658 | TP53 | c.637_660del (p.Arg213_Tyr220del) c.241_264del (p.Arg81_Tyr88del) c.358_381del (p.Arg120_Tyr127del) c.616_639del (p.Arg206_Tyr213del) n.893_916del n.67+159_67+182del c.520_543del (p.Arg174_Tyr181del) c.160_183del (p.Arg54_Tyr61del) c.604_627del (p.Arg202_Tyr209del) | ClinVar |
17 | g.7674872T>A | CA397839889 | TP53 | c.659A>T (p.Tyr220Phe) c.263A>T (p.Tyr88Phe) c.380A>T (p.Tyr127Phe) c.638A>T (p.Tyr213Phe) n.915A>T n.67+181A>T c.542A>T (p.Tyr181Phe) c.182A>T (p.Tyr61Phe) c.626A>T (p.Tyr209Phe) | dbSNP |
17 | g.7674872T>C | CA000315 | TP53 | c.659A>G (p.Tyr220Cys) c.263A>G (p.Tyr88Cys) c.380A>G (p.Tyr127Cys) c.638A>G (p.Tyr213Cys) n.915A>G n.67+181A>G c.542A>G (p.Tyr181Cys) c.182A>G (p.Tyr61Cys) c.626A>G (p.Tyr209Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674872T>G | CA000314 | TP53 | c.659A>C (p.Tyr220Ser) c.263A>C (p.Tyr88Ser) c.380A>C (p.Tyr127Ser) c.638A>C (p.Tyr213Ser) n.915A>C n.67+181A>C c.542A>C (p.Tyr181Ser) c.182A>C (p.Tyr61Ser) c.626A>C (p.Tyr209Ser) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674872T= | CA2245954057 | TP53 | c.659A= (p.Tyr220=) c.263A= (p.Tyr88=) c.380A= (p.Tyr127=) c.638A= (p.Tyr213=) n.915A= n.67+181A= c.542A= (p.Tyr181=) c.182A= (p.Tyr61=) c.626A= (p.Tyr209=) | |
17 | g.7674874_7674889del | CA645588725 | TP53 | c.644_659del (p.Ser215MetfsTer27) c.248_263del (p.Ser83MetfsTer27) c.365_380del (p.Ser122MetfsTer27) c.623_638del (p.Ser208MetfsTer27) n.900_915del n.67+166_67+181del c.527_542del (p.Ser176MetfsTer27) c.167_182del (p.Ser56MetfsTer27) c.611_626del (p.Ser204MetfsTer27) | COSMIC |
17 | g.7674872_7674909del | CA645588726 | TP53 | c.622_659del (p.Asp208Ter) c.226_263del (p.Asp76Ter) c.343_380del (p.Asp115Ter) c.601_638del (p.Asp201Ter) n.878_915del n.67+144_67+181del c.505_542del (p.Asp169Ter) c.145_182del (p.Asp49Ter) c.589_626del (p.Asp197Ter) | COSMIC |
17 | g.7674873del | CA645588727 | TP53 | c.658del (p.Tyr220MetfsTer27) c.262del (p.Tyr88MetfsTer27) c.379del (p.Tyr127MetfsTer27) c.637del (p.Tyr213MetfsTer27) n.914del n.67+180del c.541del (p.Tyr181MetfsTer27) c.181del (p.Tyr61MetfsTer27) c.625del (p.Tyr209MetfsTer27) | gnomAD v4 COSMIC |
17 | g.7674873A= | CA2245954079 | TP53 | c.658T= (p.Tyr220=) c.262T= (p.Tyr88=) c.379T= (p.Tyr127=) c.637T= (p.Tyr213=) n.914T= n.67+180T= c.541T= (p.Tyr181=) c.181T= (p.Tyr61=) c.625T= (p.Tyr209=) | |
17 | g.7674873A>C | CA16603102 | TP53 | c.658T>G (p.Tyr220Asp) c.262T>G (p.Tyr88Asp) c.379T>G (p.Tyr127Asp) c.637T>G (p.Tyr213Asp) n.914T>G n.67+180T>G c.541T>G (p.Tyr181Asp) c.181T>G (p.Tyr61Asp) c.625T>G (p.Tyr209Asp) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674873A>G | CA002135 | TP53 | c.658T>C (p.Tyr220His) c.262T>C (p.Tyr88His) c.379T>C (p.Tyr127His) c.637T>C (p.Tyr213His) n.914T>C n.67+180T>C c.541T>C (p.Tyr181His) c.181T>C (p.Tyr61His) c.625T>C (p.Tyr209His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674873A>T | CA16603101 | TP53 | c.658T>A (p.Tyr220Asn) c.262T>A (p.Tyr88Asn) c.379T>A (p.Tyr127Asn) c.637T>A (p.Tyr213Asn) n.914T>A n.67+180T>A c.541T>A (p.Tyr181Asn) c.181T>A (p.Tyr61Asn) c.625T>A (p.Tyr209Asn) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674874_7674881del | CA2573154668 | TP53 | c.651_658del (p.Val218Ter) c.255_262del (p.Val86Ter) c.372_379del (p.Val125Ter) c.630_637del (p.Val211Ter) n.907_914del n.67+173_67+180del c.534_541del (p.Val179Ter) c.174_181del (p.Val59Ter) c.618_625del (p.Val207Ter) | ClinVar dbSNP |
17 | g.7674875_7674976dup | CA2580094939 | TP53 | c.560-3_658dup c.164-3_262dup c.281-3_379dup c.539-3_637dup n.816-3_914dup n.67+79_67+180dup c.443-3_541dup c.83-3_181dup c.527-3_625dup | ClinVar |
17 | g.7674874G>A | CA497925285 | TP53 | c.657C>T (p.Pro219=) c.261C>T (p.Pro87=) c.378C>T (p.Pro126=) c.636C>T (p.Pro212=) n.913C>T n.67+179C>T c.540C>T (p.Pro180=) c.180C>T (p.Pro60=) c.624C>T (p.Pro208=) | dbSNP COSMIC |
17 | g.7674874G>C | CA497925286 | TP53 | c.657C>G (p.Pro219=) c.261C>G (p.Pro87=) c.378C>G (p.Pro126=) c.636C>G (p.Pro212=) n.913C>G n.67+179C>G c.540C>G (p.Pro180=) c.180C>G (p.Pro60=) c.624C>G (p.Pro208=) | dbSNP COSMIC |
17 | g.7674874G= | CA2245954098 | TP53 | c.657C= (p.Pro219=) c.261C= (p.Pro87=) c.378C= (p.Pro126=) c.636C= (p.Pro212=) n.913C= n.67+179C= c.540C= (p.Pro180=) c.180C= (p.Pro60=) c.624C= (p.Pro208=) | |
17 | g.7674874G>T | CA000313 | TP53 | c.657C>A (p.Pro219=) c.261C>A (p.Pro87=) c.378C>A (p.Pro126=) c.636C>A (p.Pro212=) n.913C>A n.67+179C>A c.540C>A (p.Pro180=) c.180C>A (p.Pro60=) c.624C>A (p.Pro208=) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674874_7674875delinsAA | CA645588728 | TP53 | c.656_657delinsTT (p.Pro219Leu) c.260_261delinsTT (p.Pro87Leu) c.377_378delinsTT (p.Pro126Leu) c.635_636delinsTT (p.Pro212Leu) n.912_913delinsTT n.67+178_67+179delinsTT c.539_540delinsTT (p.Pro180Leu) c.179_180delinsTT (p.Pro60Leu) c.623_624delinsTT (p.Pro208Leu) | COSMIC |
17 | g.7674876dup | CA891842251 | TP53 | c.657dup (p.Tyr220LeufsTer2) c.261dup (p.Tyr88LeufsTer2) c.378dup (p.Tyr127LeufsTer2) c.636dup (p.Tyr213LeufsTer2) n.913dup n.67+179dup c.540dup (p.Tyr181LeufsTer2) c.180dup (p.Tyr61LeufsTer2) c.624dup (p.Tyr209LeufsTer2) | ClinVar |
17 | g.7674876del | CA497925287 | TP53 | c.657del (p.Tyr220MetfsTer27) c.261del (p.Tyr88MetfsTer27) c.378del (p.Tyr127MetfsTer27) c.636del (p.Tyr213MetfsTer27) n.913del n.67+179del c.540del (p.Tyr181MetfsTer27) c.180del (p.Tyr61MetfsTer27) c.624del (p.Tyr209MetfsTer27) | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674875G>A | CA397839907 | TP53 | c.656C>T (p.Pro219Leu) c.260C>T (p.Pro87Leu) c.377C>T (p.Pro126Leu) c.635C>T (p.Pro212Leu) n.912C>T n.67+178C>T c.539C>T (p.Pro180Leu) c.179C>T (p.Pro60Leu) c.623C>T (p.Pro208Leu) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
17 | g.7674875G>C | CA397839911 | TP53 | c.656C>G (p.Pro219Arg) c.260C>G (p.Pro87Arg) c.377C>G (p.Pro126Arg) c.635C>G (p.Pro212Arg) n.912C>G n.67+178C>G c.539C>G (p.Pro180Arg) c.179C>G (p.Pro60Arg) c.623C>G (p.Pro208Arg) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674875G= | CA2245954114 | TP53 | c.656C= (p.Pro219=) c.260C= (p.Pro87=) c.377C= (p.Pro126=) c.635C= (p.Pro212=) n.912C= n.67+178C= c.539C= (p.Pro180=) c.179C= (p.Pro60=) c.623C= (p.Pro208=) | |
17 | g.7674875G>T | CA397839913 | TP53 | c.656C>A (p.Pro219His) c.260C>A (p.Pro87His) c.377C>A (p.Pro126His) c.635C>A (p.Pro212His) n.912C>A n.67+178C>A c.539C>A (p.Pro180His) c.179C>A (p.Pro60His) c.623C>A (p.Pro208His) | dbSNP COSMIC |
17 | g.7674875_7674876delinsCA | CA645588729 | TP53 | c.655_656delinsTG (p.Pro219Cys) c.259_260delinsTG (p.Pro87Cys) c.376_377delinsTG (p.Pro126Cys) c.634_635delinsTG (p.Pro212Cys) n.911_912delinsTG n.67+177_67+178delinsTG c.538_539delinsTG (p.Pro180Cys) c.178_179delinsTG (p.Pro60Cys) c.622_623delinsTG (p.Pro208Cys) | COSMIC |
17 | g.7674875_7674878delinsGGCA | CA2245954109 | TP53 | c.653_656delinsTGCC (p.Val218=) c.257_260delinsTGCC (p.Val86=) c.374_377delinsTGCC (p.Val125=) c.632_635delinsTGCC (p.Val211=) n.909_912delinsTGCC n.67+175_67+178delinsTGCC c.536_539delinsTGCC (p.Val179=) c.176_179delinsTGCC (p.Val59=) c.620_623delinsTGCC (p.Val207=) | |
17 | g.7674875_7674884del | CA645588730 | TP53 | c.647_656del (p.Val216AlafsTer28) c.251_260del (p.Val84AlafsTer28) c.368_377del (p.Val123AlafsTer28) c.626_635del (p.Val209AlafsTer28) n.903_912del n.67+169_67+178del c.530_539del (p.Val177AlafsTer28) c.170_179del (p.Val57AlafsTer28) c.614_623del (p.Val205AlafsTer28) | COSMIC |
17 | g.7674876G>A | CA10584589 | TP53 | c.655C>T (p.Pro219Ser) c.259C>T (p.Pro87Ser) c.376C>T (p.Pro126Ser) c.634C>T (p.Pro212Ser) n.911C>T n.67+177C>T c.538C>T (p.Pro180Ser) c.178C>T (p.Pro60Ser) c.622C>T (p.Pro208Ser) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
17 | g.7674876G>C | CA397839917 | TP53 | c.655C>G (p.Pro219Ala) c.259C>G (p.Pro87Ala) c.376C>G (p.Pro126Ala) c.634C>G (p.Pro212Ala) n.911C>G n.67+177C>G c.538C>G (p.Pro180Ala) c.178C>G (p.Pro60Ala) c.622C>G (p.Pro208Ala) | ClinVar |
17 | g.7674876G= | CA2245954126 | TP53 | c.655C= (p.Pro219=) c.259C= (p.Pro87=) c.376C= (p.Pro126=) c.634C= (p.Pro212=) n.911C= n.67+177C= c.538C= (p.Pro180=) c.178C= (p.Pro60=) c.622C= (p.Pro208=) | |
17 | g.7674876G>T | CA397839922 | TP53 | c.655C>A (p.Pro219Thr) c.259C>A (p.Pro87Thr) c.376C>A (p.Pro126Thr) c.634C>A (p.Pro212Thr) n.911C>A n.67+177C>A c.538C>A (p.Pro180Thr) c.178C>A (p.Pro60Thr) c.622C>A (p.Pro208Thr) | ClinVar COSMIC |
17 | g.7674876_7674878del | CA2245954125 | TP53 | c.653_655del (p.Val218_Pro219delinsAla) c.257_259del (p.Val86_Pro87delinsAla) c.374_376del (p.Val125_Pro126delinsAla) c.632_634del (p.Val211_Pro212delinsAla) n.909_911del n.67+175_67+177del c.536_538del (p.Val179_Pro180delinsAla) c.176_178del (p.Val59_Pro60delinsAla) c.620_622del (p.Val207_Pro208delinsAla) | ClinVar dbSNP |
17 | g.7674876_7674879delinsGCAC | CA2245954129 | TP53 | c.652_655delinsGTGC (p.Val218=) c.256_259delinsGTGC (p.Val86=) c.373_376delinsGTGC (p.Val125=) c.631_634delinsGTGC (p.Val211=) n.908_911delinsGTGC n.67+174_67+177delinsGTGC c.535_538delinsGTGC (p.Val179=) c.175_178delinsGTGC (p.Val59=) c.619_622delinsGTGC (p.Val207=) | |
17 | g.7674877_7674901del | CA645588731 | TP53 | c.631_655del (p.Thr211ProfsTer28) c.235_259del (p.Thr79ProfsTer28) c.352_376del (p.Thr118ProfsTer28) c.610_634del (p.Thr204ProfsTer28) n.887_911del n.67+153_67+177del c.514_538del (p.Thr172ProfsTer28) c.154_178del (p.Thr52ProfsTer28) c.598_622del (p.Thr200ProfsTer28) | COSMIC |
17 | g.7674876_7674877insAAC | CA645588732 | TP53 | c.654_655insGTT (p.Val218_Pro219insVal) c.258_259insGTT (p.Val86_Pro87insVal) c.375_376insGTT (p.Val125_Pro126insVal) c.633_634insGTT (p.Val211_Pro212insVal) n.910_911insGTT n.67+176_67+177insGTT c.537_538insGTT (p.Val179_Pro180insVal) c.177_178insGTT (p.Val59_Pro60insVal) c.621_622insGTT (p.Val207_Pro208insVal) | COSMIC |
17 | g.7674877C>A | CA497925288 | TP53 | c.654G>T (p.Val218=) c.258G>T (p.Val86=) c.375G>T (p.Val125=) c.633G>T (p.Val211=) n.910G>T n.67+176G>T c.537G>T (p.Val179=) c.177G>T (p.Val59=) c.621G>T (p.Val207=) | ClinVar |
17 | g.7674877C= | CA2245954143 | TP53 | c.654G= (p.Val218=) c.258G= (p.Val86=) c.375G= (p.Val125=) c.633G= (p.Val211=) n.910G= n.67+176G= c.537G= (p.Val179=) c.177G= (p.Val59=) c.621G= (p.Val207=) | |
17 | g.7674877C>G | CA497925289 | TP53 | c.654G>C (p.Val218=) c.258G>C (p.Val86=) c.375G>C (p.Val125=) c.633G>C (p.Val211=) n.910G>C n.67+176G>C c.537G>C (p.Val179=) c.177G>C (p.Val59=) c.621G>C (p.Val207=) | dbSNP |
17 | g.7674877C>T | CA000311 | TP53 | c.654G>A (p.Val218=) c.258G>A (p.Val86=) c.375G>A (p.Val125=) c.633G>A (p.Val211=) n.910G>A n.67+176G>A c.537G>A (p.Val179=) c.177G>A (p.Val59=) c.621G>A (p.Val207=) | ClinVar dbSNP ExAC gnomAD v2 COSMIC |
17 | g.7674883_7674885dup | CA891842252 | TP53 | c.652_654dup (p.Val218_Pro219insVal) c.256_258dup (p.Val86_Pro87insVal) c.373_375dup (p.Val125_Pro126insVal) c.631_633dup (p.Val211_Pro212insVal) n.908_910dup n.67+174_67+176dup c.535_537dup (p.Val179_Pro180insVal) c.175_177dup (p.Val59_Pro60insVal) c.619_621dup (p.Val207_Pro208insVal) | |
17 | g.7674883_7674885del | CA16044100 | TP53 | c.652_654del (p.Val218del) c.256_258del (p.Val86del) c.373_375del (p.Val125del) c.631_633del (p.Val211del) n.908_910del n.67+174_67+176del c.535_537del (p.Val179del) c.175_177del (p.Val59del) c.619_621del (p.Val207del) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674877_7674878insG | CA497925290 | TP53 | c.653_654insC (p.Pro219AlafsTer3) c.257_258insC (p.Pro87AlafsTer3) c.374_375insC (p.Pro126AlafsTer3) c.632_633insC (p.Pro212AlafsTer3) n.909_910insC n.67+175_67+176insC c.536_537insC (p.Pro180AlafsTer3) c.176_177insC (p.Pro60AlafsTer3) c.620_621insC (p.Pro208AlafsTer3) | |
17 | g.7674878A= | CA2245954156 | TP53 | c.653T= (p.Val218=) c.257T= (p.Val86=) c.374T= (p.Val125=) c.632T= (p.Val211=) n.909T= n.67+175T= c.536T= (p.Val179=) c.176T= (p.Val59=) c.620T= (p.Val207=) | |
17 | g.7674878A>C | CA397839930 | TP53 | c.653T>G (p.Val218Gly) c.257T>G (p.Val86Gly) c.374T>G (p.Val125Gly) c.632T>G (p.Val211Gly) n.909T>G n.67+175T>G c.536T>G (p.Val179Gly) c.176T>G (p.Val59Gly) c.620T>G (p.Val207Gly) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674878A>G | CA397839935 | TP53 | c.653T>C (p.Val218Ala) c.257T>C (p.Val86Ala) c.374T>C (p.Val125Ala) c.632T>C (p.Val211Ala) n.909T>C n.67+175T>C c.536T>C (p.Val179Ala) c.176T>C (p.Val59Ala) c.620T>C (p.Val207Ala) | COSMIC |
17 | g.7674878A>T | CA397839938 | TP53 | c.653T>A (p.Val218Glu) c.257T>A (p.Val86Glu) c.374T>A (p.Val125Glu) c.632T>A (p.Val211Glu) n.909T>A n.67+175T>A c.536T>A (p.Val179Glu) c.176T>A (p.Val59Glu) c.620T>A (p.Val207Glu) | ClinVar COSMIC |
17 | g.7674878_7674886del | CA645588733 | TP53 | c.645_653del (p.Ser215_Val218delinsArg) c.249_257del (p.Ser83_Val86delinsArg) c.366_374del (p.Ser122_Val125delinsArg) c.624_632del (p.Ser208_Val211delinsArg) n.901_909del n.67+167_67+175del c.528_536del (p.Ser176_Val179delinsArg) c.168_176del (p.Ser56_Val59delinsArg) c.612_620del (p.Ser204_Val207delinsArg) | COSMIC |
17 | g.7674879C>A | CA397839943 | TP53 | c.652G>T (p.Val218Leu) c.256G>T (p.Val86Leu) c.373G>T (p.Val125Leu) c.631G>T (p.Val211Leu) n.908G>T n.67+174G>T c.535G>T (p.Val179Leu) c.175G>T (p.Val59Leu) c.619G>T (p.Val207Leu) | dbSNP COSMIC |
17 | g.7674879C= | CA2245954167 | TP53 | c.652G= (p.Val218=) c.256G= (p.Val86=) c.373G= (p.Val125=) c.631G= (p.Val211=) n.908G= n.67+174G= c.535G= (p.Val179=) c.175G= (p.Val59=) c.619G= (p.Val207=) | |
17 | g.7674879C>G | CA397839946 | TP53 | c.652G>C (p.Val218Leu) c.256G>C (p.Val86Leu) c.373G>C (p.Val125Leu) c.631G>C (p.Val211Leu) n.908G>C n.67+174G>C c.535G>C (p.Val179Leu) c.175G>C (p.Val59Leu) c.619G>C (p.Val207Leu) | dbSNP |
17 | g.7674879C>T | CA10583679 | TP53 | c.652G>A (p.Val218Met) c.256G>A (p.Val86Met) c.373G>A (p.Val125Met) c.631G>A (p.Val211Met) n.908G>A n.67+174G>A c.535G>A (p.Val179Met) c.175G>A (p.Val59Met) c.619G>A (p.Val207Met) | ClinVar dbSNP COSMIC |
17 | g.7674880dup | CA2695223077 | TP53 | c.652dup (p.Val218GlyfsTer4) c.256dup (p.Val86GlyfsTer4) c.373dup (p.Val125GlyfsTer4) c.631dup (p.Val211GlyfsTer4) n.908dup n.67+174dup c.535dup (p.Val179GlyfsTer4) c.175dup (p.Val59GlyfsTer4) c.619dup (p.Val207GlyfsTer4) | |
17 | g.7674880del | CA497925291 | TP53 | c.652del (p.Val218CysfsTer29) c.256del (p.Val86CysfsTer29) c.373del (p.Val125CysfsTer29) c.631del (p.Val211CysfsTer29) n.908del n.67+174del c.535del (p.Val179CysfsTer29) c.175del (p.Val59CysfsTer29) c.619del (p.Val207CysfsTer29) | ClinVar gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674879_7674887del | CA645588735 | TP53 | c.644_652del (p.Ser215_Val218delinsMet) c.248_256del (p.Ser83_Val86delinsMet) c.365_373del (p.Ser122_Val125delinsMet) c.623_631del (p.Ser208_Val211delinsMet) n.900_908del n.67+166_67+174del c.527_535del (p.Ser176_Val179delinsMet) c.167_175del (p.Ser56_Val59delinsMet) c.611_619del (p.Ser204_Val207delinsMet) | COSMIC |
17 | g.7674879_7674888del | CA645588734 | TP53 | c.643_652del (p.Ser215CysfsTer29) c.247_256del (p.Ser83CysfsTer29) c.364_373del (p.Ser122CysfsTer29) c.622_631del (p.Ser208CysfsTer29) n.899_908del n.67+165_67+174del c.526_535del (p.Ser176CysfsTer29) c.166_175del (p.Ser56CysfsTer29) c.610_619del (p.Ser204CysfsTer29) | COSMIC |
17 | g.7674880C>A | CA497925292 | TP53 | c.651G>T (p.Val217=) c.255G>T (p.Val85=) c.372G>T (p.Val124=) c.630G>T (p.Val210=) n.907G>T n.67+173G>T c.534G>T (p.Val178=) c.174G>T (p.Val58=) c.618G>T (p.Val206=) | ClinVar dbSNP |
17 | g.7674880C= | CA2245954177 | TP53 | c.651G= (p.Val217=) c.255G= (p.Val85=) c.372G= (p.Val124=) c.630G= (p.Val210=) n.907G= n.67+173G= c.534G= (p.Val178=) c.174G= (p.Val58=) c.618G= (p.Val206=) | |
17 | g.7674880C>G | CA497925294 | TP53 | c.651G>C (p.Val217=) c.255G>C (p.Val85=) c.372G>C (p.Val124=) c.630G>C (p.Val210=) n.907G>C n.67+173G>C c.534G>C (p.Val178=) c.174G>C (p.Val58=) c.618G>C (p.Val206=) | ClinVar dbSNP |
17 | g.7674880C>T | CA497925293 | TP53 | c.651G>A (p.Val217=) c.255G>A (p.Val85=) c.372G>A (p.Val124=) c.630G>A (p.Val210=) n.907G>A n.67+173G>A c.534G>A (p.Val178=) c.174G>A (p.Val58=) c.618G>A (p.Val206=) | dbSNP COSMIC |
17 | g.7674883_7674887dup | CA913190590 | TP53 | c.647_651dup (p.Val218TrpfsTer31) c.251_255dup (p.Val86TrpfsTer31) c.368_372dup (p.Val125TrpfsTer31) c.626_630dup (p.Val211TrpfsTer31) n.903_907dup n.67+169_67+173dup c.530_534dup (p.Val179TrpfsTer31) c.170_174dup (p.Val59TrpfsTer31) c.614_618dup (p.Val207TrpfsTer31) | ClinVar dbSNP |
17 | g.7674881A>C | CA397839953 | TP53 | c.650T>G (p.Val217Gly) c.254T>G (p.Val85Gly) c.371T>G (p.Val124Gly) c.629T>G (p.Val210Gly) n.906T>G n.67+172T>G c.533T>G (p.Val178Gly) c.173T>G (p.Val58Gly) c.617T>G (p.Val206Gly) | dbSNP gnomAD v4 |
17 | g.7674881A>G | CA397839955 | TP53 | c.650T>C (p.Val217Ala) c.254T>C (p.Val85Ala) c.371T>C (p.Val124Ala) c.629T>C (p.Val210Ala) n.906T>C n.67+172T>C c.533T>C (p.Val178Ala) c.173T>C (p.Val58Ala) c.617T>C (p.Val206Ala) | COSMIC |
17 | g.7674881A>T | CA397839961 | TP53 | c.650T>A (p.Val217Glu) c.254T>A (p.Val85Glu) c.371T>A (p.Val124Glu) c.629T>A (p.Val210Glu) n.906T>A n.67+172T>A c.533T>A (p.Val178Glu) c.173T>A (p.Val58Glu) c.617T>A (p.Val206Glu) | dbSNP COSMIC |
17 | g.7674881_7674889del | CA645588736 | TP53 | c.642_650del (p.His214_Val217delinsGln) c.246_254del (p.His82_Val85delinsGln) c.363_371del (p.His121_Val124delinsGln) c.621_629del (p.His207_Val210delinsGln) n.898_906del n.67+164_67+172del c.525_533del (p.His175_Val178delinsGln) c.165_173del (p.His55_Val58delinsGln) c.609_617del (p.His203_Val206delinsGln) | COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674882C>A | CA397839966 | TP53 | c.649G>T (p.Val217Leu) c.253G>T (p.Val85Leu) c.370G>T (p.Val124Leu) c.628G>T (p.Val210Leu) n.905G>T n.67+171G>T c.532G>T (p.Val178Leu) c.172G>T (p.Val58Leu) c.616G>T (p.Val206Leu) | ClinVar dbSNP gnomAD v4 COSMIC |
17 | g.7674882C= | CA2245954192 | TP53 | c.649G= (p.Val217=) c.253G= (p.Val85=) c.370G= (p.Val124=) c.628G= (p.Val210=) n.905G= n.67+171G= c.532G= (p.Val178=) c.172G= (p.Val58=) c.616G= (p.Val206=) | |
17 | g.7674882C>G | CA397839964 | TP53 | c.649G>C (p.Val217Leu) c.253G>C (p.Val85Leu) c.370G>C (p.Val124Leu) c.628G>C (p.Val210Leu) n.905G>C n.67+171G>C c.532G>C (p.Val178Leu) c.172G>C (p.Val58Leu) c.616G>C (p.Val206Leu) | |
17 | g.7674882C>T | CA000309 | TP53 | c.649G>A (p.Val217Met) c.253G>A (p.Val85Met) c.370G>A (p.Val124Met) c.628G>A (p.Val210Met) n.905G>A n.67+171G>A c.532G>A (p.Val178Met) c.172G>A (p.Val58Met) c.616G>A (p.Val206Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7674883del | CA2580094946 | TP53 | c.649del (p.Val217TrpfsTer30) c.253del (p.Val85TrpfsTer30) c.370del (p.Val124TrpfsTer30) c.628del (p.Val210TrpfsTer30) n.905del n.67+171del c.532del (p.Val178TrpfsTer30) c.172del (p.Val58TrpfsTer30) c.616del (p.Val206TrpfsTer30) | ClinVar |
17 | g.7674883_7674909del | CA645588738 | TP53 | c.623_649del (p.Asp208_Val216del) c.227_253del (p.Asp76_Val84del) c.344_370del (p.Asp115_Val123del) c.602_628del (p.Asp201_Val209del) n.879_905del n.67+145_67+171del c.506_532del (p.Asp169_Val177del) c.146_172del (p.Asp49_Val57del) c.590_616del (p.Asp197_Val205del) | COSMIC |
17 | g.7674885_7674914del | CA645588737 | TP53 | c.620_649del (p.Asp207_Val216del) c.224_253del (p.Asp75_Val84del) c.341_370del (p.Asp114_Val123del) c.599_628del (p.Asp200_Val209del) n.876_905del n.67+142_67+171del c.503_532del (p.Asp168_Val177del) c.143_172del (p.Asp48_Val57del) c.587_616del (p.Asp196_Val205del) | COSMIC |
17 | g.7674883C>A | CA497925295 | TP53 | c.648G>T (p.Val216=) c.252G>T (p.Val84=) c.369G>T (p.Val123=) c.627G>T (p.Val209=) n.904G>T n.67+170G>T c.531G>T (p.Val177=) c.171G>T (p.Val57=) c.615G>T (p.Val205=) | |
17 | g.7674883C= | CA2245954205 | TP53 | c.648G= (p.Val216=) c.252G= (p.Val84=) c.369G= (p.Val123=) c.627G= (p.Val209=) n.904G= n.67+170G= c.531G= (p.Val177=) c.171G= (p.Val57=) c.615G= (p.Val205=) | |
17 | g.7674883C>G | CA002159 | TP53 | c.648G>C (p.Val216=) c.252G>C (p.Val84=) c.369G>C (p.Val123=) c.627G>C (p.Val209=) n.904G>C n.67+170G>C c.531G>C (p.Val177=) c.171G>C (p.Val57=) c.615G>C (p.Val205=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7674883C>T | CA497925296 | TP53 | c.648G>A (p.Val216=) c.252G>A (p.Val84=) c.369G>A (p.Val123=) c.627G>A (p.Val209=) n.904G>A n.67+170G>A c.531G>A (p.Val177=) c.171G>A (p.Val57=) c.615G>A (p.Val205=) | ClinVar dbSNP |
17 | g.7674886_7674887del | CA645588739 | TP53 | c.647_648del (p.Val216GlyfsTer5) c.251_252del (p.Val84GlyfsTer5) c.368_369del (p.Val123GlyfsTer5) c.626_627del (p.Val209GlyfsTer5) n.903_904del n.67+169_67+170del c.530_531del (p.Val177GlyfsTer5) c.170_171del (p.Val57GlyfsTer5) c.614_615del (p.Val205GlyfsTer5) | COSMIC |
17 | g.7674884del | CA497925297 | TP53 | c.647del (p.Val216GlyfsTer?) c.251del (p.Val84GlyfsTer?) c.368del (p.Val123GlyfsTer?) c.626del (p.Val209GlyfsTer?) n.903del n.67+169del c.530del (p.Val177GlyfsTer?) c.170del (p.Val57GlyfsTer?) c.614del (p.Val205GlyfsTer?) | COSMIC |
17 | g.7674884A= | CA2245954219 | TP53 | c.647T= (p.Val216=) c.251T= (p.Val84=) c.368T= (p.Val123=) c.626T= (p.Val209=) n.903T= n.67+169T= c.530T= (p.Val177=) c.170T= (p.Val57=) c.614T= (p.Val205=) | |
17 | g.7674884A>C | CA16603085 | TP53 | c.647T>G (p.Val216Gly) c.251T>G (p.Val84Gly) c.368T>G (p.Val123Gly) c.626T>G (p.Val209Gly) n.903T>G n.67+169T>G c.530T>G (p.Val177Gly) c.170T>G (p.Val57Gly) c.614T>G (p.Val205Gly) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674884A>G | CA397839975 | TP53 | c.647T>C (p.Val216Ala) c.251T>C (p.Val84Ala) c.368T>C (p.Val123Ala) c.626T>C (p.Val209Ala) n.903T>C n.67+169T>C c.530T>C (p.Val177Ala) c.170T>C (p.Val57Ala) c.614T>C (p.Val205Ala) | dbSNP COSMIC |
17 | g.7674884A>T | CA16603086 | TP53 | c.647T>A (p.Val216Glu) c.251T>A (p.Val84Glu) c.368T>A (p.Val123Glu) c.626T>A (p.Val209Glu) n.903T>A n.67+169T>A c.530T>A (p.Val177Glu) c.170T>A (p.Val57Glu) c.614T>A (p.Val205Glu) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674884_7674886del | CA2573154669 | TP53 | c.645_647del (p.Ser215_Val216delinsArg) c.249_251del (p.Ser83_Val84delinsArg) c.366_368del (p.Ser122_Val123delinsArg) c.624_626del (p.Ser208_Val209delinsArg) n.901_903del n.67+167_67+169del c.528_530del (p.Ser176_Val177delinsArg) c.168_170del (p.Ser56_Val57delinsArg) c.612_614del (p.Ser204_Val205delinsArg) | ClinVar dbSNP |
17 | g.7674884_7674891del | CA645588741 | TP53 | c.640_647del (p.His214GlyfsTer5) c.244_251del (p.His82GlyfsTer5) c.361_368del (p.His121GlyfsTer5) c.619_626del (p.His207GlyfsTer5) n.896_903del n.67+162_67+169del c.523_530del (p.His175GlyfsTer5) c.163_170del (p.His55GlyfsTer5) c.607_614del (p.His203GlyfsTer5) | COSMIC |
17 | g.7674885C>A | CA16603084 | TP53 | c.646G>T (p.Val216Leu) c.250G>T (p.Val84Leu) c.367G>T (p.Val123Leu) c.625G>T (p.Val209Leu) n.902G>T n.67+168G>T c.529G>T (p.Val177Leu) c.169G>T (p.Val57Leu) c.613G>T (p.Val205Leu) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674885C= | CA2245954239 | TP53 | c.646G= (p.Val216=) c.250G= (p.Val84=) c.367G= (p.Val123=) c.625G= (p.Val209=) n.902G= n.67+168G= c.529G= (p.Val177=) c.169G= (p.Val57=) c.613G= (p.Val205=) | |
17 | g.7674885C>G | CA16615950 | TP53 | c.646G>C (p.Val216Leu) c.250G>C (p.Val84Leu) c.367G>C (p.Val123Leu) c.625G>C (p.Val209Leu) n.902G>C n.67+168G>C c.529G>C (p.Val177Leu) c.169G>C (p.Val57Leu) c.613G>C (p.Val205Leu) | ClinVar dbSNP |
17 | g.7674885C>T | CA000308 | TP53 | c.646G>A (p.Val216Met) c.250G>A (p.Val84Met) c.367G>A (p.Val123Met) c.625G>A (p.Val209Met) n.902G>A n.67+168G>A c.529G>A (p.Val177Met) c.169G>A (p.Val57Met) c.613G>A (p.Val205Met) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674885delinsACCA | CA2695223078 | TP53 | c.646delinsTGGT (p.Val216delinsTrpLeu) c.250delinsTGGT (p.Val84delinsTrpLeu) c.367delinsTGGT (p.Val123delinsTrpLeu) c.625delinsTGGT (p.Val209delinsTrpLeu) n.902delinsTGGT n.67+168delinsTGGT c.529delinsTGGT (p.Val177delinsTrpLeu) c.169delinsTGGT (p.Val57delinsTrpLeu) c.613delinsTGGT (p.Val205delinsTrpLeu) | |
17 | g.7674885_7674888del | CA645588742 | TP53 | c.643_646del (p.Ser215TrpfsTer?) c.247_250del (p.Ser83TrpfsTer?) c.364_367del (p.Ser122TrpfsTer?) c.622_625del (p.Ser208TrpfsTer?) n.899_902del n.67+165_67+168del c.526_529del (p.Ser176TrpfsTer?) c.166_169del (p.Ser56TrpfsTer?) c.610_613del (p.Ser204TrpfsTer?) | COSMIC |
17 | g.7674886del | CA2573154670 | TP53 | c.645del (p.Ser215ArgfsTer?) c.249del (p.Ser83ArgfsTer?) c.366del (p.Ser122ArgfsTer?) c.624del (p.Ser208ArgfsTer?) n.901del n.67+167del c.528del (p.Ser176ArgfsTer?) c.168del (p.Ser56ArgfsTer?) c.612del (p.Ser204ArgfsTer?) | ClinVar dbSNP |
17 | g.7674886A= | CA2245954258 | TP53 | c.645T= (p.Ser215=) c.249T= (p.Ser83=) c.366T= (p.Ser122=) c.624T= (p.Ser208=) n.901T= n.67+167T= c.528T= (p.Ser176=) c.168T= (p.Ser56=) c.612T= (p.Ser204=) | |
17 | g.7674886A>C | CA16603076 | TP53 | c.645T>G (p.Ser215Arg) c.249T>G (p.Ser83Arg) c.366T>G (p.Ser122Arg) c.624T>G (p.Ser208Arg) n.901T>G n.67+167T>G c.528T>G (p.Ser176Arg) c.168T>G (p.Ser56Arg) c.612T>G (p.Ser204Arg) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
17 | g.7674886A>G | CA497925298 | TP53 | c.645T>C (p.Ser215=) c.249T>C (p.Ser83=) c.366T>C (p.Ser122=) c.624T>C (p.Ser208=) n.901T>C n.67+167T>C c.528T>C (p.Ser176=) c.168T>C (p.Ser56=) c.612T>C (p.Ser204=) | ClinVar dbSNP COSMIC |
17 | g.7674886A>T | CA397839990 | TP53 | c.645T>A (p.Ser215Arg) c.249T>A (p.Ser83Arg) c.366T>A (p.Ser122Arg) c.624T>A (p.Ser208Arg) n.901T>A n.67+167T>A c.528T>A (p.Ser176Arg) c.168T>A (p.Ser56Arg) c.612T>A (p.Ser204Arg) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674886_7674887delinsAC | CA2245954257 | TP53 | c.644_645delinsGT (p.Ser215=) c.248_249delinsGT (p.Ser83=) c.365_366delinsGT (p.Ser122=) c.623_624delinsGT (p.Ser208=) n.900_901delinsGT n.67+166_67+167delinsGT c.527_528delinsGT (p.Ser176=) c.167_168delinsGT (p.Ser56=) c.611_612delinsGT (p.Ser204=) | |
17 | g.7674887_7674897del | CA2825002600 | TP53 | c.635_645del (p.Phe212CysfsTer6) c.239_249del (p.Phe80CysfsTer6) c.356_366del (p.Phe119CysfsTer6) c.614_624del (p.Phe205CysfsTer6) n.891_901del n.67+157_67+167del c.518_528del (p.Phe173CysfsTer6) c.158_168del (p.Phe53CysfsTer6) c.602_612del (p.Phe201CysfsTer6) | ClinVar |
17 | g.7674886_7674900del | CA645588743 | TP53 | c.631_645del (p.Thr211_Ser215del) c.235_249del (p.Thr79_Ser83del) c.352_366del (p.Thr118_Ser122del) c.610_624del (p.Thr204_Ser208del) n.887_901del n.67+153_67+167del c.514_528del (p.Thr172_Ser176del) c.154_168del (p.Thr52_Ser56del) c.598_612del (p.Thr200_Ser204del) | COSMIC |
17 | g.7674887del | CA497925299 | TP53 | c.644del (p.Ser215MetfsTer?) c.248del (p.Ser83MetfsTer?) c.365del (p.Ser122MetfsTer?) c.623del (p.Ser208MetfsTer?) n.900del n.67+166del c.527del (p.Ser176MetfsTer?) c.167del (p.Ser56MetfsTer?) c.611del (p.Ser204MetfsTer?) | ClinVar dbSNP COSMIC |
17 | g.7674887C>A | CA16603075 | TP53 | c.644G>T (p.Ser215Ile) c.248G>T (p.Ser83Ile) c.365G>T (p.Ser122Ile) c.623G>T (p.Ser208Ile) n.900G>T n.67+166G>T c.527G>T (p.Ser176Ile) c.167G>T (p.Ser56Ile) c.611G>T (p.Ser204Ile) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674887C= | CA2245954292 | TP53 | c.644G= (p.Ser215=) c.248G= (p.Ser83=) c.365G= (p.Ser122=) c.623G= (p.Ser208=) n.900G= n.67+166G= c.527G= (p.Ser176=) c.167G= (p.Ser56=) c.611G= (p.Ser204=) | |
17 | g.7674887C>G | CA000307 | TP53 | c.644G>C (p.Ser215Thr) c.248G>C (p.Ser83Thr) c.365G>C (p.Ser122Thr) c.623G>C (p.Ser208Thr) n.900G>C n.67+166G>C c.527G>C (p.Ser176Thr) c.167G>C (p.Ser56Thr) c.611G>C (p.Ser204Thr) | ClinVar dbSNP gnomAD v4 COSMIC |
17 | g.7674887C>T | CA16603077 | TP53 | c.644G>A (p.Ser215Asn) c.248G>A (p.Ser83Asn) c.365G>A (p.Ser122Asn) c.623G>A (p.Ser208Asn) n.900G>A n.67+166G>A c.527G>A (p.Ser176Asn) c.167G>A (p.Ser56Asn) c.611G>A (p.Ser204Asn) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674887_7674888del | CA645588745 | TP53 | c.643_644del (p.Ser215CysfsTer6) c.247_248del (p.Ser83CysfsTer6) c.364_365del (p.Ser122CysfsTer6) c.622_623del (p.Ser208CysfsTer6) n.899_900del n.67+165_67+166del c.526_527del (p.Ser176CysfsTer6) c.166_167del (p.Ser56CysfsTer6) c.610_611del (p.Ser204CysfsTer6) | COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674887_7674888dup | CA658683990 | TP53 | c.643_644dup (p.Ser215ArgfsTer?) c.247_248dup (p.Ser83ArgfsTer?) c.364_365dup (p.Ser122ArgfsTer?) c.622_623dup (p.Ser208ArgfsTer?) n.899_900dup n.67+165_67+166dup c.526_527dup (p.Ser176ArgfsTer?) c.166_167dup (p.Ser56ArgfsTer?) c.610_611dup (p.Ser204ArgfsTer?) | ClinVar dbSNP |
17 | g.7674887_7674889delinsCTA | CA2245954299 | TP53 | c.642_644delinsTAG (p.His214=) c.246_248delinsTAG (p.His82=) c.363_365delinsTAG (p.His121=) c.621_623delinsTAG (p.His207=) n.898_900delinsTAG n.67+164_67+166delinsTAG c.525_527delinsTAG (p.His175=) c.165_167delinsTAG (p.His55=) c.609_611delinsTAG (p.His203=) | |
17 | g.7674887_7674906del | CA645588744 | TP53 | c.625_644del (p.Arg209CysfsTer6) c.229_248del (p.Arg77CysfsTer6) c.346_365del (p.Arg116CysfsTer6) c.604_623del (p.Arg202CysfsTer6) n.881_900del n.67+147_67+166del c.508_527del (p.Arg170CysfsTer6) c.148_167del (p.Arg50CysfsTer6) c.592_611del (p.Arg198CysfsTer6) | COSMIC |
17 | g.7674888del | CA497925300 | TP53 | c.643del (p.Ser215ValfsTer?) c.247del (p.Ser83ValfsTer?) c.364del (p.Ser122ValfsTer?) c.622del (p.Ser208ValfsTer?) n.899del n.67+165del c.526del (p.Ser176ValfsTer?) c.166del (p.Ser56ValfsTer?) c.610del (p.Ser204ValfsTer?) | ClinVar COSMIC |
17 | g.7674888T>A | CA397840015 | TP53 | c.643A>T (p.Ser215Cys) c.247A>T (p.Ser83Cys) c.364A>T (p.Ser122Cys) c.622A>T (p.Ser208Cys) n.899A>T n.67+165A>T c.526A>T (p.Ser176Cys) c.166A>T (p.Ser56Cys) c.610A>T (p.Ser204Cys) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674888T>C | CA10588671 | TP53 | c.643A>G (p.Ser215Gly) c.247A>G (p.Ser83Gly) c.364A>G (p.Ser122Gly) c.622A>G (p.Ser208Gly) n.899A>G n.67+165A>G c.526A>G (p.Ser176Gly) c.166A>G (p.Ser56Gly) c.610A>G (p.Ser204Gly) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674888T>G | CA397840019 | TP53 | c.643A>C (p.Ser215Arg) c.247A>C (p.Ser83Arg) c.364A>C (p.Ser122Arg) c.622A>C (p.Ser208Arg) n.899A>C n.67+165A>C c.526A>C (p.Ser176Arg) c.166A>C (p.Ser56Arg) c.610A>C (p.Ser204Arg) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674888T= | CA2245954328 | TP53 | c.643A= (p.Ser215=) c.247A= (p.Ser83=) c.364A= (p.Ser122=) c.622A= (p.Ser208=) n.899A= n.67+165A= c.526A= (p.Ser176=) c.166A= (p.Ser56=) c.610A= (p.Ser204=) | |
17 | g.7674888dup | CA913190591 | TP53 | c.643dup (p.Ser215LysfsTer7) c.247dup (p.Ser83LysfsTer7) c.364dup (p.Ser122LysfsTer7) c.622dup (p.Ser208LysfsTer7) n.899dup n.67+165dup c.526dup (p.Ser176LysfsTer7) c.166dup (p.Ser56LysfsTer7) c.610dup (p.Ser204LysfsTer7) | ClinVar dbSNP |
17 | g.7674889_7674890del | CA645588746 | TP53 | c.642_643del (p.His214GlnfsTer7) c.246_247del (p.His82GlnfsTer7) c.363_364del (p.His121GlnfsTer7) c.621_622del (p.His207GlnfsTer7) n.898_899del n.67+164_67+165del c.525_526del (p.His175GlnfsTer7) c.165_166del (p.His55GlnfsTer7) c.609_610del (p.His203GlnfsTer7) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674888_7674894del | CA645588747 | TP53 | c.637_643del (p.Arg213ValfsTer?) c.241_247del (p.Arg81ValfsTer?) c.358_364del (p.Arg120ValfsTer?) c.616_622del (p.Arg206ValfsTer?) n.893_899del n.67+159_67+165del c.520_526del (p.Arg174ValfsTer?) c.160_166del (p.Arg54ValfsTer?) c.604_610del (p.Arg202ValfsTer?) | COSMIC |
17 | g.7674889del | CA2825002601 | TP53 | c.642del (p.His214GlnfsTer?) c.246del (p.His82GlnfsTer?) c.363del (p.His121GlnfsTer?) c.621del (p.His207GlnfsTer?) n.898del n.67+164del c.525del (p.His175GlnfsTer?) c.165del (p.His55GlnfsTer?) c.609del (p.His203GlnfsTer?) | ClinVar |
17 | g.7674889A= | CA2245954343 | TP53 | c.642T= (p.His214=) c.246T= (p.His82=) c.363T= (p.His121=) c.621T= (p.His207=) n.898T= n.67+164T= c.525T= (p.His175=) c.165T= (p.His55=) c.609T= (p.His203=) | |
17 | g.7674889A>C | CA000305 | TP53 | c.642T>G (p.His214Gln) c.246T>G (p.His82Gln) c.363T>G (p.His121Gln) c.621T>G (p.His207Gln) n.898T>G n.67+164T>G c.525T>G (p.His175Gln) c.165T>G (p.His55Gln) c.609T>G (p.His203Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
17 | g.7674889A>G | CA002168 | TP53 | c.642T>C (p.His214=) c.246T>C (p.His82=) c.363T>C (p.His121=) c.621T>C (p.His207=) n.898T>C n.67+164T>C c.525T>C (p.His175=) c.165T>C (p.His55=) c.609T>C (p.His203=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
17 | g.7674889A>T | CA397840030 | TP53 | c.642T>A (p.His214Gln) c.246T>A (p.His82Gln) c.363T>A (p.His121Gln) c.621T>A (p.His207Gln) n.898T>A n.67+164T>A c.525T>A (p.His175Gln) c.165T>A (p.His55Gln) c.609T>A (p.His203Gln) | dbSNP COSMIC |
17 | g.7674890_7674897del | CA2695195447 | TP53 | c.635_642del (p.Phe212Ter) c.239_246del (p.Phe80Ter) c.356_363del (p.Phe119Ter) c.614_621del (p.Phe205Ter) n.891_898del n.67+157_67+164del c.518_525del (p.Phe173Ter) c.158_165del (p.Phe53Ter) c.602_609del (p.Phe201Ter) | ClinVar |
17 | g.7674891_7674932del | CA645588748 | TP53 | c.601_642del (p.Leu201_His214del) c.205_246del (p.Leu69_His82del) c.322_363del (p.Leu108_His121del) c.580_621del (p.Leu194_His207del) n.857_898del n.67+123_67+164del c.484_525del (p.Leu162_His175del) c.124_165del (p.Leu42_His55del) c.568_609del (p.Leu190_His203del) | COSMIC |
17 | g.7674890del | CA497925301 | TP53 | c.641del (p.His214LeufsTer?) c.245del (p.His82LeufsTer?) c.362del (p.His121LeufsTer?) c.620del (p.His207LeufsTer?) n.897del n.67+163del c.524del (p.His175LeufsTer?) c.164del (p.His55LeufsTer?) c.608del (p.His203LeufsTer?) | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674890T>A | CA16603036 | TP53 | c.641A>T (p.His214Leu) c.245A>T (p.His82Leu) c.362A>T (p.His121Leu) c.620A>T (p.His207Leu) n.897A>T n.67+163A>T c.524A>T (p.His175Leu) c.164A>T (p.His55Leu) c.608A>T (p.His203Leu) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674890T>C | CA16040595 | TP53 | c.641A>G (p.His214Arg) c.245A>G (p.His82Arg) c.362A>G (p.His121Arg) c.620A>G (p.His207Arg) n.897A>G n.67+163A>G c.524A>G (p.His175Arg) c.164A>G (p.His55Arg) c.608A>G (p.His203Arg) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674890T>G | CA397840046 | TP53 | c.641A>C (p.His214Pro) c.245A>C (p.His82Pro) c.362A>C (p.His121Pro) c.620A>C (p.His207Pro) n.897A>C n.67+163A>C c.524A>C (p.His175Pro) c.164A>C (p.His55Pro) c.608A>C (p.His203Pro) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674890T= | CA2245954369 | TP53 | c.641A= (p.His214=) c.245A= (p.His82=) c.362A= (p.His121=) c.620A= (p.His207=) n.897A= n.67+163A= c.524A= (p.His175=) c.164A= (p.His55=) c.608A= (p.His203=) | |
17 | g.7674890dup | CA645588750 | TP53 | c.641dup (p.His214GlnfsTer2) c.245dup (p.His82GlnfsTer2) c.362dup (p.His121GlnfsTer2) c.620dup (p.His207GlnfsTer2) n.897dup n.67+163dup c.524dup (p.His175GlnfsTer2) c.164dup (p.His55GlnfsTer2) c.608dup (p.His203GlnfsTer2) | COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674893_7674902del | CA1139768487 | TP53 | c.632_641del (p.Thr211IlefsTer?) c.236_245del (p.Thr79IlefsTer?) c.353_362del (p.Thr118IlefsTer?) c.611_620del (p.Thr204IlefsTer?) n.888_897del n.67+154_67+163del c.515_524del (p.Thr172IlefsTer?) c.155_164del (p.Thr52IlefsTer?) c.599_608del (p.Thr200IlefsTer?) | |
17 | g.7674891del | CA497925302 | TP53 | c.640del (p.His214IlefsTer?) c.244del (p.His82IlefsTer?) c.361del (p.His121IlefsTer?) c.619del (p.His207IlefsTer?) n.896del n.67+162del c.523del (p.His175IlefsTer?) c.163del (p.His55IlefsTer?) c.607del (p.His203IlefsTer?) | COSMIC |
17 | g.7674891G>A | CA397840049 | TP53 | c.640C>T (p.His214Tyr) c.244C>T (p.His82Tyr) c.361C>T (p.His121Tyr) c.619C>T (p.His207Tyr) n.896C>T n.67+162C>T c.523C>T (p.His175Tyr) c.163C>T (p.His55Tyr) c.607C>T (p.His203Tyr) | ClinVar dbSNP COSMIC |
17 | g.7674891G>C | CA397840055 | TP53 | c.640C>G (p.His214Asp) c.244C>G (p.His82Asp) c.361C>G (p.His121Asp) c.619C>G (p.His207Asp) n.896C>G n.67+162C>G c.523C>G (p.His175Asp) c.163C>G (p.His55Asp) c.607C>G (p.His203Asp) | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674891G= | CA2245954387 | TP53 | c.640C= (p.His214=) c.244C= (p.His82=) c.361C= (p.His121=) c.619C= (p.His207=) n.896C= n.67+162C= c.523C= (p.His175=) c.163C= (p.His55=) c.607C= (p.His203=) | |
17 | g.7674891G>T | CA10580931 | TP53 | c.640C>A (p.His214Asn) c.244C>A (p.His82Asn) c.361C>A (p.His121Asn) c.619C>A (p.His207Asn) n.896C>A n.67+162C>A c.523C>A (p.His175Asn) c.163C>A (p.His55Asn) c.607C>A (p.His203Asn) | ClinVar dbSNP |
17 | g.7674893_7674900del | CA2695223080 | TP53 | c.633_640del (p.Phe212Ter) c.237_244del (p.Phe80Ter) c.354_361del (p.Phe119Ter) c.612_619del (p.Phe205Ter) n.889_896del n.67+155_67+162del c.516_523del (p.Phe173Ter) c.156_163del (p.Phe53Ter) c.600_607del (p.Phe201Ter) | |
17 | g.7674891_7674903delinsGTCGAAAAGTGTT | CA2245954391 | TP53 | c.628_640delinsAACACTTTTCGAC (p.Asn210=) c.232_244delinsAACACTTTTCGAC (p.Asn78=) c.349_361delinsAACACTTTTCGAC (p.Asn117=) c.607_619delinsAACACTTTTCGAC (p.Asn203=) n.884_896delinsAACACTTTTCGAC n.67+150_67+162delinsAACACTTTTCGAC c.511_523delinsAACACTTTTCGAC (p.Asn171=) c.151_163delinsAACACTTTTCGAC (p.Asn51=) c.595_607delinsAACACTTTTCGAC (p.Asn199=) | |
17 | g.7674892T>A | CA287488323 | TP53 | c.639A>T (p.Arg213=) c.243A>T (p.Arg81=) c.360A>T (p.Arg120=) c.618A>T (p.Arg206=) n.895A>T n.67+161A>T c.522A>T (p.Arg174=) c.162A>T (p.Arg54=) c.606A>T (p.Arg202=) | dbSNP |
17 | g.7674892T>C | CA000303 | TP53 | c.639A>G (p.Arg213=) c.243A>G (p.Arg81=) c.360A>G (p.Arg120=) c.618A>G (p.Arg206=) n.895A>G n.67+161A>G c.522A>G (p.Arg174=) c.162A>G (p.Arg54=) c.606A>G (p.Arg202=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7674892T>G | CA497925304 | TP53 | c.639A>C (p.Arg213=) c.243A>C (p.Arg81=) c.360A>C (p.Arg120=) c.618A>C (p.Arg206=) n.895A>C n.67+161A>C c.522A>C (p.Arg174=) c.162A>C (p.Arg54=) c.606A>C (p.Arg202=) | dbSNP |
17 | g.7674892T= | CA2245954403 | TP53 | c.639A= (p.Arg213=) c.243A= (p.Arg81=) c.360A= (p.Arg120=) c.618A= (p.Arg206=) n.895A= n.67+161A= c.522A= (p.Arg174=) c.162A= (p.Arg54=) c.606A= (p.Arg202=) | |
17 | g.7674892dup | CA645588751 | TP53 | c.639dup (p.His214ThrfsTer2) c.243dup (p.His82ThrfsTer2) c.360dup (p.His121ThrfsTer2) c.618dup (p.His207ThrfsTer2) n.895dup n.67+161dup c.522dup (p.His175ThrfsTer2) c.162dup (p.His55ThrfsTer2) c.606dup (p.His203ThrfsTer2) | COSMIC |
17 | g.7674892_7674894delinsCCA | CA10602177 | TP53 | c.637_639delinsTGG (p.Arg213Trp) c.241_243delinsTGG (p.Arg81Trp) c.358_360delinsTGG (p.Arg120Trp) c.616_618delinsTGG (p.Arg206Trp) n.893_895delinsTGG n.67+159_67+161delinsTGG c.520_522delinsTGG (p.Arg174Trp) c.160_162delinsTGG (p.Arg54Trp) c.604_606delinsTGG (p.Arg202Trp) | COSMIC |
17 | g.7674894_7674905del | CA1139665122 | TP53 | c.628_639del (p.Asn210_Arg213del) c.232_243del (p.Asn78_Arg81del) c.349_360del (p.Asn117_Arg120del) c.607_618del (p.Asn203_Arg206del) n.884_895del n.67+150_67+161del c.511_522del (p.Asn171_Arg174del) c.151_162del (p.Asn51_Arg54del) c.595_606del (p.Asn199_Arg202del) | ClinVar dbSNP |
17 | g.7674892_7674906del | CA645588753 | TP53 | c.625_639del (p.Arg209_Arg213del) c.229_243del (p.Arg77_Arg81del) c.346_360del (p.Arg116_Arg120del) c.604_618del (p.Arg202_Arg206del) n.881_895del n.67+147_67+161del c.508_522del (p.Arg170_Arg174del) c.148_162del (p.Arg50_Arg54del) c.592_606del (p.Arg198_Arg202del) | COSMIC |
17 | g.7674892_7674912del | CA645588752 | TP53 | c.619_639del (p.Asp207_Arg213del) c.223_243del (p.Asp75_Arg81del) c.340_360del (p.Asp114_Arg120del) c.598_618del (p.Asp200_Arg206del) n.875_895del n.67+141_67+161del c.502_522del (p.Asp168_Arg174del) c.142_162del (p.Asp48_Arg54del) c.586_606del (p.Asp196_Arg202del) | COSMIC |
17 | g.7674893del | CA645369128 | TP53 | c.638del (p.Arg213HisfsTer?) c.242del (p.Arg81HisfsTer?) c.359del (p.Arg120HisfsTer?) c.617del (p.Arg206HisfsTer?) n.894del n.67+160del c.521del (p.Arg174HisfsTer?) c.161del (p.Arg54HisfsTer?) c.605del (p.Arg202HisfsTer?) | |
17 | g.7674893C>A | CA16603067 | TP53 | c.638G>T (p.Arg213Leu) c.242G>T (p.Arg81Leu) c.359G>T (p.Arg120Leu) c.617G>T (p.Arg206Leu) n.894G>T n.67+160G>T c.521G>T (p.Arg174Leu) c.161G>T (p.Arg54Leu) c.605G>T (p.Arg202Leu) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674893C= | CA2245954428 | TP53 | c.638G= (p.Arg213=) c.242G= (p.Arg81=) c.359G= (p.Arg120=) c.617G= (p.Arg206=) n.894G= n.67+160G= c.521G= (p.Arg174=) c.161G= (p.Arg54=) c.605G= (p.Arg202=) | |
17 | g.7674893C>G | CA10580932 | TP53 | c.638G>C (p.Arg213Pro) c.242G>C (p.Arg81Pro) c.359G>C (p.Arg120Pro) c.617G>C (p.Arg206Pro) n.894G>C n.67+160G>C c.521G>C (p.Arg174Pro) c.161G>C (p.Arg54Pro) c.605G>C (p.Arg202Pro) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674893C>T | CA000302 | TP53 | c.638G>A (p.Arg213Gln) c.242G>A (p.Arg81Gln) c.359G>A (p.Arg120Gln) c.617G>A (p.Arg206Gln) n.894G>A n.67+160G>A c.521G>A (p.Arg174Gln) c.161G>A (p.Arg54Gln) c.605G>A (p.Arg202Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674893_7674894del | CA645588756 | TP53 | c.637_638del (p.Arg213ThrfsTer2) c.241_242del (p.Arg81ThrfsTer2) c.358_359del (p.Arg120ThrfsTer2) c.616_617del (p.Arg206ThrfsTer2) n.893_894del n.67+159_67+160del c.520_521del (p.Arg174ThrfsTer2) c.160_161del (p.Arg54ThrfsTer2) c.604_605del (p.Arg202ThrfsTer2) | COSMIC |
17 | g.7674894del | CA497925306 | TP53 | c.637del (p.Arg213AspfsTer?) c.241del (p.Arg81AspfsTer?) c.358del (p.Arg120AspfsTer?) c.616del (p.Arg206AspfsTer?) n.893del n.67+159del c.520del (p.Arg174AspfsTer?) c.160del (p.Arg54AspfsTer?) c.604del (p.Arg202AspfsTer?) | COSMIC |
17 | g.7674894G>A | CA000301 | TP53 | c.637C>T (p.Arg213Ter) c.241C>T (p.Arg81Ter) c.358C>T (p.Arg120Ter) c.616C>T (p.Arg206Ter) n.893C>T n.67+159C>T c.520C>T (p.Arg174Ter) c.160C>T (p.Arg54Ter) c.604C>T (p.Arg202Ter) | ClinVar dbSNP ExAC gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674894G>C | CA16603068 | TP53 | c.637C>G (p.Arg213Gly) c.241C>G (p.Arg81Gly) c.358C>G (p.Arg120Gly) c.616C>G (p.Arg206Gly) n.893C>G n.67+159C>G c.520C>G (p.Arg174Gly) c.160C>G (p.Arg54Gly) c.604C>G (p.Arg202Gly) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674894G= | CA2245954463 | TP53 | c.637C= (p.Arg213=) c.241C= (p.Arg81=) c.358C= (p.Arg120=) c.616C= (p.Arg206=) n.893C= n.67+159C= c.520C= (p.Arg174=) c.160C= (p.Arg54=) c.604C= (p.Arg202=) | |
17 | g.7674894G>T | CA497925305 | TP53 | c.637C>A (p.Arg213=) c.241C>A (p.Arg81=) c.358C>A (p.Arg120=) c.616C>A (p.Arg206=) n.893C>A n.67+159C>A c.520C>A (p.Arg174=) c.160C>A (p.Arg54=) c.604C>A (p.Arg202=) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674894_7674896delinsGAA | CA2245954464 | TP53 | c.635_637delinsTTC (p.Phe212=) c.239_241delinsTTC (p.Phe80=) c.356_358delinsTTC (p.Phe119=) c.614_616delinsTTC (p.Phe205=) n.891_893delinsTTC n.67+157_67+159delinsTTC c.518_520delinsTTC (p.Phe173=) c.158_160delinsTTC (p.Phe53=) c.602_604delinsTTC (p.Phe201=) | |
17 | g.7674895A>C | CA397840085 | TP53 | c.636T>G (p.Phe212Leu) c.240T>G (p.Phe80Leu) c.357T>G (p.Phe119Leu) c.615T>G (p.Phe205Leu) n.892T>G n.67+158T>G c.519T>G (p.Phe173Leu) c.159T>G (p.Phe53Leu) c.603T>G (p.Phe201Leu) | dbSNP |
17 | g.7674895A>G | CA497925307 | TP53 | c.636T>C (p.Phe212=) c.240T>C (p.Phe80=) c.357T>C (p.Phe119=) c.615T>C (p.Phe205=) n.892T>C n.67+158T>C c.519T>C (p.Phe173=) c.159T>C (p.Phe53=) c.603T>C (p.Phe201=) | gnomAD v4 |
17 | g.7674895A>T | CA397840105 | TP53 | c.636T>A (p.Phe212Leu) c.240T>A (p.Phe80Leu) c.357T>A (p.Phe119Leu) c.615T>A (p.Phe205Leu) n.892T>A n.67+158T>A c.519T>A (p.Phe173Leu) c.159T>A (p.Phe53Leu) c.603T>A (p.Phe201Leu) | dbSNP COSMIC |
17 | g.7674898dup | CA645588760 | TP53 | c.636dup (p.Arg213SerfsTer3) c.240dup (p.Arg81SerfsTer3) c.357dup (p.Arg120SerfsTer3) c.615dup (p.Arg206SerfsTer3) n.892dup n.67+158dup c.519dup (p.Arg174SerfsTer3) c.159dup (p.Arg54SerfsTer3) c.603dup (p.Arg202SerfsTer3) | COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674897_7674898dup | CA645588759 | TP53 | c.635_636dup (p.Arg213PhefsTer?) c.239_240dup (p.Arg81PhefsTer?) c.356_357dup (p.Arg120PhefsTer?) c.614_615dup (p.Arg206PhefsTer?) n.891_892dup n.67+157_67+158dup c.518_519dup (p.Arg174PhefsTer?) c.158_159dup (p.Arg54PhefsTer?) c.602_603dup (p.Arg202PhefsTer?) | COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674898del | CA248848 | TP53 | c.636del (p.Arg213AspfsTer?) c.240del (p.Arg81AspfsTer?) c.357del (p.Arg120AspfsTer?) c.615del (p.Arg206AspfsTer?) n.892del n.67+158del c.519del (p.Arg174AspfsTer?) c.159del (p.Arg54AspfsTer?) c.603del (p.Arg202AspfsTer?) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674897_7674898del | CA645369684 | TP53 | c.635_636del (p.Phe212SerfsTer3) c.239_240del (p.Phe80SerfsTer3) c.356_357del (p.Phe119SerfsTer3) c.614_615del (p.Phe205SerfsTer3) n.891_892del n.67+157_67+158del c.518_519del (p.Phe173SerfsTer3) c.158_159del (p.Phe53SerfsTer3) c.602_603del (p.Phe201SerfsTer3) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674895_7674933dup | CA2245954579 | TP53 | c.598_636dup (p.Phe212_Arg213insAsnLeuArgValGluTyrLeuAspAspArgAsnThrPhe) c.202_240dup (p.Phe80_Arg81insAsnLeuArgValGluTyrLeuAspAspArgAsnThrPhe) c.319_357dup (p.Phe119_Arg120insAsnLeuArgValGluTyrLeuAspAspArgAsnThrPhe) c.577_615dup (p.Phe205_Arg206insAsnLeuArgValGluTyrLeuAspAspArgAsnThrPhe) n.854_892dup n.67+120_67+158dup c.481_519dup (p.Phe173_Arg174insAsnLeuArgValGluTyrLeuAspAspArgAsnThrPhe) c.121_159dup (p.Phe53_Arg54insAsnLeuArgValGluTyrLeuAspAspArgAsnThrPhe) c.565_603dup (p.Phe201_Arg202insAsnLeuArgValGluTyrLeuAspAspArgAsnThrPhe) | ClinVar dbSNP |
17 | g.7674896A>C | CA397840106 | TP53 | c.635T>G (p.Phe212Cys) c.239T>G (p.Phe80Cys) c.356T>G (p.Phe119Cys) c.614T>G (p.Phe205Cys) n.891T>G n.67+157T>G c.518T>G (p.Phe173Cys) c.158T>G (p.Phe53Cys) c.602T>G (p.Phe201Cys) | |
17 | g.7674896A>G | CA397840108 | TP53 | c.635T>C (p.Phe212Ser) c.239T>C (p.Phe80Ser) c.356T>C (p.Phe119Ser) c.614T>C (p.Phe205Ser) n.891T>C n.67+157T>C c.518T>C (p.Phe173Ser) c.158T>C (p.Phe53Ser) c.602T>C (p.Phe201Ser) | COSMIC |
17 | g.7674896A>T | CA397840110 | TP53 | c.635T>A (p.Phe212Tyr) c.239T>A (p.Phe80Tyr) c.356T>A (p.Phe119Tyr) c.614T>A (p.Phe205Tyr) n.891T>A n.67+157T>A c.518T>A (p.Phe173Tyr) c.158T>A (p.Phe53Tyr) c.602T>A (p.Phe201Tyr) | dbSNP COSMIC |
17 | g.7674896_7674906del | CA891842253 | TP53 | c.625_635del (p.Arg209SerfsTer3) c.229_239del (p.Arg77SerfsTer3) c.346_356del (p.Arg116SerfsTer3) c.604_614del (p.Arg202SerfsTer3) n.881_891del n.67+147_67+157del c.508_518del (p.Arg170SerfsTer3) c.148_158del (p.Arg50SerfsTer3) c.592_602del (p.Arg198SerfsTer3) | |
17 | g.7674897A= | CA2245954585 | TP53 | c.634T= (p.Phe212=) c.238T= (p.Phe80=) c.355T= (p.Phe119=) c.613T= (p.Phe205=) n.890T= n.67+156T= c.517T= (p.Phe173=) c.157T= (p.Phe53=) c.601T= (p.Phe201=) | |
17 | g.7674897A>C | CA397840119 | TP53 | c.634T>G (p.Phe212Val) c.238T>G (p.Phe80Val) c.355T>G (p.Phe119Val) c.613T>G (p.Phe205Val) n.890T>G n.67+156T>G c.517T>G (p.Phe173Val) c.157T>G (p.Phe53Val) c.601T>G (p.Phe201Val) | COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674897A>G | CA397840122 | TP53 | c.634T>C (p.Phe212Leu) c.238T>C (p.Phe80Leu) c.355T>C (p.Phe119Leu) c.613T>C (p.Phe205Leu) n.890T>C n.67+156T>C c.517T>C (p.Phe173Leu) c.157T>C (p.Phe53Leu) c.601T>C (p.Phe201Leu) | dbSNP COSMIC |
17 | g.7674897A>T | CA16620624 | TP53 | c.634T>A (p.Phe212Ile) c.238T>A (p.Phe80Ile) c.355T>A (p.Phe119Ile) c.613T>A (p.Phe205Ile) n.890T>A n.67+156T>A c.517T>A (p.Phe173Ile) c.157T>A (p.Phe53Ile) c.601T>A (p.Phe201Ile) | ClinVar dbSNP COSMIC |
17 | g.7674897_7674901del | CA2825002602 | TP53 | c.630_634del (p.Thr211SerfsTer3) c.234_238del (p.Thr79SerfsTer3) c.351_355del (p.Thr118SerfsTer3) c.609_613del (p.Thr204SerfsTer3) n.886_890del n.67+152_67+156del c.513_517del (p.Thr172SerfsTer3) c.153_157del (p.Thr52SerfsTer3) c.597_601del (p.Thr200SerfsTer3) | ClinVar |
17 | g.7674897_7674903del | CA645588762 | TP53 | c.628_634del (p.Asn210PhefsTer?) c.232_238del (p.Asn78PhefsTer?) c.349_355del (p.Asn117PhefsTer?) c.607_613del (p.Asn203PhefsTer?) n.884_890del n.67+150_67+156del c.511_517del (p.Asn171PhefsTer?) c.151_157del (p.Asn51PhefsTer?) c.595_601del (p.Asn199PhefsTer?) | COSMIC |
17 | g.7674897_7674906del | CA645588761 | TP53 | c.625_634del (p.Arg209PhefsTer?) c.229_238del (p.Arg77PhefsTer?) c.346_355del (p.Arg116PhefsTer?) c.604_613del (p.Arg202PhefsTer?) n.881_890del n.67+147_67+156del c.508_517del (p.Arg170PhefsTer?) c.148_157del (p.Arg50PhefsTer?) c.592_601del (p.Arg198PhefsTer?) | COSMIC |
17 | g.7674898A= | CA2245954593 | TP53 | c.633T= (p.Thr211=) c.237T= (p.Thr79=) c.354T= (p.Thr118=) c.612T= (p.Thr204=) n.889T= n.67+155T= c.516T= (p.Thr172=) c.156T= (p.Thr52=) c.600T= (p.Thr200=) | |
17 | g.7674898A>C | CA287488329 | TP53 | c.633T>G (p.Thr211=) c.237T>G (p.Thr79=) c.354T>G (p.Thr118=) c.612T>G (p.Thr204=) n.889T>G n.67+155T>G c.516T>G (p.Thr172=) c.156T>G (p.Thr52=) c.600T>G (p.Thr200=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.7674898A>G | CA497925309 | TP53 | c.633T>C (p.Thr211=) c.237T>C (p.Thr79=) c.354T>C (p.Thr118=) c.612T>C (p.Thr204=) n.889T>C n.67+155T>C c.516T>C (p.Thr172=) c.156T>C (p.Thr52=) c.600T>C (p.Thr200=) | gnomAD v4 COSMIC |
17 | g.7674898A>T | CA497925308 | TP53 | c.633T>A (p.Thr211=) c.237T>A (p.Thr79=) c.354T>A (p.Thr118=) c.612T>A (p.Thr204=) n.889T>A n.67+155T>A c.516T>A (p.Thr172=) c.156T>A (p.Thr52=) c.600T>A (p.Thr200=) | dbSNP COSMIC |
17 | g.7674898_7674899del | CA645588764 | TP53 | c.632_633del (p.Thr211IlefsTer4) c.236_237del (p.Thr79IlefsTer4) c.353_354del (p.Thr118IlefsTer4) c.611_612del (p.Thr204IlefsTer4) n.888_889del n.67+154_67+155del c.515_516del (p.Thr172IlefsTer4) c.155_156del (p.Thr52IlefsTer4) c.599_600del (p.Thr200IlefsTer4) | COSMIC |
17 | g.7674899_7674947del | CA645588763 | TP53 | c.585_633del (p.Arg196PhefsTer?) c.189_237del (p.Arg64PhefsTer?) c.306_354del (p.Arg103PhefsTer?) c.564_612del (p.Arg189PhefsTer?) n.841_889del n.67+107_67+155del c.468_516del (p.Arg157PhefsTer?) c.108_156del (p.Arg37PhefsTer?) c.552_600del (p.Arg185PhefsTer?) | COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674899G>A | CA397840127 | TP53 | c.632C>T (p.Thr211Ile) c.236C>T (p.Thr79Ile) c.353C>T (p.Thr118Ile) c.611C>T (p.Thr204Ile) n.888C>T n.67+154C>T c.515C>T (p.Thr172Ile) c.155C>T (p.Thr52Ile) c.599C>T (p.Thr200Ile) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674899G>C | CA397840130 | TP53 | c.632C>G (p.Thr211Ser) c.236C>G (p.Thr79Ser) c.353C>G (p.Thr118Ser) c.611C>G (p.Thr204Ser) n.888C>G n.67+154C>G c.515C>G (p.Thr172Ser) c.155C>G (p.Thr52Ser) c.599C>G (p.Thr200Ser) | ClinVar dbSNP gnomAD v4 COSMIC |
17 | g.7674899G= | CA2245954604 | TP53 | c.632C= (p.Thr211=) c.236C= (p.Thr79=) c.353C= (p.Thr118=) c.611C= (p.Thr204=) n.888C= n.67+154C= c.515C= (p.Thr172=) c.155C= (p.Thr52=) c.599C= (p.Thr200=) | |
17 | g.7674899G>T | CA397840131 | TP53 | c.632C>A (p.Thr211Asn) c.236C>A (p.Thr79Asn) c.353C>A (p.Thr118Asn) c.611C>A (p.Thr204Asn) n.888C>A n.67+154C>A c.515C>A (p.Thr172Asn) c.155C>A (p.Thr52Asn) c.599C>A (p.Thr200Asn) | COSMIC |
17 | g.7674901_7674902del | CA645588765 | TP53 | c.631_632del (p.Thr211PhefsTer4) c.235_236del (p.Thr79PhefsTer4) c.352_353del (p.Thr118PhefsTer4) c.610_611del (p.Thr204PhefsTer4) n.887_888del n.67+153_67+154del c.514_515del (p.Thr172PhefsTer4) c.154_155del (p.Thr52PhefsTer4) c.598_599del (p.Thr200PhefsTer4) | ClinVar COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674899_7674924del | CA2733136428 | TP53 | c.607_632del (p.Val203PhefsTer4) c.211_236del (p.Val71PhefsTer4) c.328_353del (p.Val110PhefsTer4) c.586_611del (p.Val196PhefsTer4) n.863_888del n.67+129_67+154del c.490_515del (p.Val164PhefsTer4) c.130_155del (p.Val44PhefsTer4) c.574_599del (p.Val192PhefsTer4) | dbSNP |
17 | g.7674900del | CA497925310 | TP53 | c.631del (p.Thr211LeufsTer?) c.235del (p.Thr79LeufsTer?) c.352del (p.Thr118LeufsTer?) c.610del (p.Thr204LeufsTer?) n.887del n.67+153del c.514del (p.Thr172LeufsTer?) c.154del (p.Thr52LeufsTer?) c.598del (p.Thr200LeufsTer?) | COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674900T>A | CA397840132 | TP53 | c.631A>T (p.Thr211Ser) c.235A>T (p.Thr79Ser) c.352A>T (p.Thr118Ser) c.610A>T (p.Thr204Ser) n.887A>T n.67+153A>T c.514A>T (p.Thr172Ser) c.154A>T (p.Thr52Ser) c.598A>T (p.Thr200Ser) | dbSNP |
17 | g.7674900T>C | CA16615722 | TP53 | c.631A>G (p.Thr211Ala) c.235A>G (p.Thr79Ala) c.352A>G (p.Thr118Ala) c.610A>G (p.Thr204Ala) n.887A>G n.67+153A>G c.514A>G (p.Thr172Ala) c.154A>G (p.Thr52Ala) c.598A>G (p.Thr200Ala) | ClinVar dbSNP COSMIC |
17 | g.7674900T>G | CA397840134 | TP53 | c.631A>C (p.Thr211Pro) c.235A>C (p.Thr79Pro) c.352A>C (p.Thr118Pro) c.610A>C (p.Thr204Pro) n.887A>C n.67+153A>C c.514A>C (p.Thr172Pro) c.154A>C (p.Thr52Pro) c.598A>C (p.Thr200Pro) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674900T= | CA2245954610 | TP53 | c.631A= (p.Thr211=) c.235A= (p.Thr79=) c.352A= (p.Thr118=) c.610A= (p.Thr204=) n.887A= n.67+153A= c.514A= (p.Thr172=) c.154A= (p.Thr52=) c.598A= (p.Thr200=) | |
17 | g.7674900_7674906del | CA645588767 | TP53 | c.625_631del (p.Arg209LeufsTer?) c.229_235del (p.Arg77LeufsTer?) c.346_352del (p.Arg116LeufsTer?) c.604_610del (p.Arg202LeufsTer?) n.881_887del n.67+147_67+153del c.508_514del (p.Arg170LeufsTer?) c.148_154del (p.Arg50LeufsTer?) c.592_598del (p.Arg198LeufsTer?) | COSMIC |
17 | g.7674901del | CA497925311 | TP53 | c.630del (p.Asn210LysfsTer?) c.234del (p.Asn78LysfsTer?) c.351del (p.Asn117LysfsTer?) c.609del (p.Asn203LysfsTer?) n.886del n.67+152del c.513del (p.Asn171LysfsTer?) c.153del (p.Asn51LysfsTer?) c.597del (p.Asn199LysfsTer?) | COSMIC |
17 | g.7674901G>A | CA497925312 | TP53 | c.630C>T (p.Asn210=) c.234C>T (p.Asn78=) c.351C>T (p.Asn117=) c.609C>T (p.Asn203=) n.886C>T n.67+152C>T c.513C>T (p.Asn171=) c.153C>T (p.Asn51=) c.597C>T (p.Asn199=) | ClinVar dbSNP gnomAD v4 COSMIC |
17 | g.7674901G>C | CA397840138 | TP53 | c.630C>G (p.Asn210Lys) c.234C>G (p.Asn78Lys) c.351C>G (p.Asn117Lys) c.609C>G (p.Asn203Lys) n.886C>G n.67+152C>G c.513C>G (p.Asn171Lys) c.153C>G (p.Asn51Lys) c.597C>G (p.Asn199Lys) | COSMIC |
17 | g.7674901G= | CA2245954626 | TP53 | c.630C= (p.Asn210=) c.234C= (p.Asn78=) c.351C= (p.Asn117=) c.609C= (p.Asn203=) n.886C= n.67+152C= c.513C= (p.Asn171=) c.153C= (p.Asn51=) c.597C= (p.Asn199=) | |
17 | g.7674901G>T | CA397840136 | TP53 | c.630C>A (p.Asn210Lys) c.234C>A (p.Asn78Lys) c.351C>A (p.Asn117Lys) c.609C>A (p.Asn203Lys) n.886C>A n.67+152C>A c.513C>A (p.Asn171Lys) c.153C>A (p.Asn51Lys) c.597C>A (p.Asn199Lys) | |
17 | g.7674901_7674903delinsGTT | CA2245954623 | TP53 | c.628_630delinsAAC (p.Asn210=) c.232_234delinsAAC (p.Asn78=) c.349_351delinsAAC (p.Asn117=) c.607_609delinsAAC (p.Asn203=) n.884_886delinsAAC n.67+150_67+152delinsAAC c.511_513delinsAAC (p.Asn171=) c.151_153delinsAAC (p.Asn51=) c.595_597delinsAAC (p.Asn199=) | |
17 | g.7674901_7674921del | CA645588768 | TP53 | c.610_630del (p.Glu204_Asn210del) c.214_234del (p.Glu72_Asn78del) c.331_351del (p.Glu111_Asn117del) c.589_609del (p.Glu197_Asn203del) n.866_886del n.67+132_67+152del c.493_513del (p.Glu165_Asn171del) c.133_153del (p.Glu45_Asn51del) c.577_597del (p.Glu193_Asn199del) | COSMIC |
17 | g.7674902T>A | CA397840142 | TP53 | c.629A>T (p.Asn210Ile) c.233A>T (p.Asn78Ile) c.350A>T (p.Asn117Ile) c.608A>T (p.Asn203Ile) n.885A>T n.67+151A>T c.512A>T (p.Asn171Ile) c.152A>T (p.Asn51Ile) c.596A>T (p.Asn199Ile) | dbSNP |
17 | g.7674902T>C | CA397840145 | TP53 | c.629A>G (p.Asn210Ser) c.233A>G (p.Asn78Ser) c.350A>G (p.Asn117Ser) c.608A>G (p.Asn203Ser) n.885A>G n.67+151A>G c.512A>G (p.Asn171Ser) c.152A>G (p.Asn51Ser) c.596A>G (p.Asn199Ser) | ClinVar gnomAD v4 COSMIC |
17 | g.7674902T>G | CA397840151 | TP53 | c.629A>C (p.Asn210Thr) c.233A>C (p.Asn78Thr) c.350A>C (p.Asn117Thr) c.608A>C (p.Asn203Thr) n.885A>C n.67+151A>C c.512A>C (p.Asn171Thr) c.152A>C (p.Asn51Thr) c.596A>C (p.Asn199Thr) | dbSNP COSMIC |
17 | g.7674904del | CA497925313 | TP53 | c.629del (p.Asn210ThrfsTer?) c.233del (p.Asn78ThrfsTer?) c.350del (p.Asn117ThrfsTer?) c.608del (p.Asn203ThrfsTer?) n.885del n.67+151del c.512del (p.Asn171ThrfsTer?) c.152del (p.Asn51ThrfsTer?) c.596del (p.Asn199ThrfsTer?) | COSMIC |
17 | g.7674903_7674904del | CA000300 | TP53 | c.628_629del (p.Asn210HisfsTer5) c.232_233del (p.Asn78HisfsTer5) c.349_350del (p.Asn117HisfsTer5) c.607_608del (p.Asn203HisfsTer5) n.884_885del n.67+150_67+151del c.511_512del (p.Asn171HisfsTer5) c.151_152del (p.Asn51HisfsTer5) c.595_596del (p.Asn199HisfsTer5) | ClinVar dbSNP |
17 | g.7674902_7674906del | CA645588769 | TP53 | c.625_629del (p.Arg209HisfsTer5) c.229_233del (p.Arg77HisfsTer5) c.346_350del (p.Arg116HisfsTer5) c.604_608del (p.Arg202HisfsTer5) n.881_885del n.67+147_67+151del c.508_512del (p.Arg170HisfsTer5) c.148_152del (p.Arg50HisfsTer5) c.592_596del (p.Arg198HisfsTer5) | COSMIC |
17 | g.7674903T>A | CA16615726 | TP53 | c.628A>T (p.Asn210Tyr) c.232A>T (p.Asn78Tyr) c.349A>T (p.Asn117Tyr) c.607A>T (p.Asn203Tyr) n.884A>T n.67+150A>T c.511A>T (p.Asn171Tyr) c.151A>T (p.Asn51Tyr) c.595A>T (p.Asn199Tyr) | ClinVar dbSNP gnomAD v4 |
17 | g.7674903T>C | CA397840159 | TP53 | c.628A>G (p.Asn210Asp) c.232A>G (p.Asn78Asp) c.349A>G (p.Asn117Asp) c.607A>G (p.Asn203Asp) n.884A>G n.67+150A>G c.511A>G (p.Asn171Asp) c.151A>G (p.Asn51Asp) c.595A>G (p.Asn199Asp) | COSMIC |
17 | g.7674903T>G | CA397840162 | TP53 | c.628A>C (p.Asn210His) c.232A>C (p.Asn78His) c.349A>C (p.Asn117His) c.607A>C (p.Asn203His) n.884A>C n.67+150A>C c.511A>C (p.Asn171His) c.151A>C (p.Asn51His) c.595A>C (p.Asn199His) | dbSNP gnomAD v4 COSMIC |
17 | g.7674903T= | CA2245954645 | TP53 | c.628A= (p.Asn210=) c.232A= (p.Asn78=) c.349A= (p.Asn117=) c.607A= (p.Asn203=) n.884A= n.67+150A= c.511A= (p.Asn171=) c.151A= (p.Asn51=) c.595A= (p.Asn199=) | |
17 | g.7674903_7674905delinsTTC | CA2245954649 | TP53 | c.626_628delinsGAA (p.Arg209=) c.230_232delinsGAA (p.Arg77=) c.347_349delinsGAA (p.Arg116=) c.605_607delinsGAA (p.Arg202=) n.882_884delinsGAA n.67+148_67+150delinsGAA c.509_511delinsGAA (p.Arg170=) c.149_151delinsGAA (p.Arg50=) c.593_595delinsGAA (p.Arg198=) | |
17 | g.7674904_7674911del | CA645588770 | TP53 | c.621_628del (p.Asp207GlufsTer6) c.225_232del (p.Asp75GlufsTer6) c.342_349del (p.Asp114GlufsTer6) c.600_607del (p.Asp200GlufsTer6) n.877_884del n.67+143_67+150del c.504_511del (p.Asp168GlufsTer6) c.144_151del (p.Asp48GlufsTer6) c.588_595del (p.Asp196GlufsTer6) | COSMIC |
17 | g.7674904T>A | CA397840166 | TP53 | c.627A>T (p.Arg209Ser) c.231A>T (p.Arg77Ser) c.348A>T (p.Arg116Ser) c.606A>T (p.Arg202Ser) n.883A>T n.67+149A>T c.510A>T (p.Arg170Ser) c.150A>T (p.Arg50Ser) c.594A>T (p.Arg198Ser) | COSMIC |
17 | g.7674904T>C | CA497925314 | TP53 | c.627A>G (p.Arg209=) c.231A>G (p.Arg77=) c.348A>G (p.Arg116=) c.606A>G (p.Arg202=) n.883A>G n.67+149A>G c.510A>G (p.Arg170=) c.150A>G (p.Arg50=) c.594A>G (p.Arg198=) | |
17 | g.7674904T>G | CA397840167 | TP53 | c.627A>C (p.Arg209Ser) c.231A>C (p.Arg77Ser) c.348A>C (p.Arg116Ser) c.606A>C (p.Arg202Ser) n.883A>C n.67+149A>C c.510A>C (p.Arg170Ser) c.150A>C (p.Arg50Ser) c.594A>C (p.Arg198Ser) | ClinVar |
17 | g.7674904T= | CA2245954661 | TP53 | c.627A= (p.Arg209=) c.231A= (p.Arg77=) c.348A= (p.Arg116=) c.606A= (p.Arg202=) n.883A= n.67+149A= c.510A= (p.Arg170=) c.150A= (p.Arg50=) c.594A= (p.Arg198=) | |
17 | g.7674905_7674906dup | CA2695223084 | TP53 | c.626_627dup (p.Asn210GlufsTer?) c.230_231dup (p.Asn78GlufsTer?) c.347_348dup (p.Asn117GlufsTer?) c.605_606dup (p.Asn203GlufsTer?) n.882_883dup n.67+148_67+149dup c.509_510dup (p.Asn171GlufsTer?) c.149_150dup (p.Asn51GlufsTer?) c.593_594dup (p.Asn199GlufsTer?) | |
17 | g.7674905_7674906del | CA16043138 | TP53 | c.626_627del (p.Arg209LysfsTer6) c.230_231del (p.Arg77LysfsTer6) c.347_348del (p.Arg116LysfsTer6) c.605_606del (p.Arg202LysfsTer6) n.882_883del n.67+148_67+149del c.509_510del (p.Arg170LysfsTer6) c.149_150del (p.Arg50LysfsTer6) c.593_594del (p.Arg198LysfsTer6) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674906_7674909del | CA645588773 | TP53 | c.624_627del (p.Asp208GlufsTer?) c.228_231del (p.Asp76GlufsTer?) c.345_348del (p.Asp115GlufsTer?) c.603_606del (p.Asp201GlufsTer?) n.880_883del n.67+146_67+149del c.507_510del (p.Asp169GlufsTer?) c.147_150del (p.Asp49GlufsTer?) c.591_594del (p.Asp197GlufsTer?) | COSMIC |
17 | g.7674905_7674917del | CA2695201733 | TP53 | c.615_627del (p.Tyr205Ter) c.219_231del (p.Tyr73Ter) c.336_348del (p.Tyr112Ter) c.594_606del (p.Tyr198Ter) n.871_883del n.67+137_67+149del c.498_510del (p.Tyr166Ter) c.138_150del (p.Tyr46Ter) c.582_594del (p.Tyr194Ter) | |
17 | g.7674905del | CA497925315 | TP53 | c.626del (p.Arg209LysfsTer?) c.230del (p.Arg77LysfsTer?) c.347del (p.Arg116LysfsTer?) c.605del (p.Arg202LysfsTer?) n.882del n.67+148del c.509del (p.Arg170LysfsTer?) c.149del (p.Arg50LysfsTer?) c.593del (p.Arg198LysfsTer?) | COSMIC |
17 | g.7674905C>A | CA397840171 | TP53 | c.626G>T (p.Arg209Ile) c.230G>T (p.Arg77Ile) c.347G>T (p.Arg116Ile) c.605G>T (p.Arg202Ile) n.882G>T n.67+148G>T c.509G>T (p.Arg170Ile) c.149G>T (p.Arg50Ile) c.593G>T (p.Arg198Ile) | COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674905C= | CA2245954669 | TP53 | c.626G= (p.Arg209=) c.230G= (p.Arg77=) c.347G= (p.Arg116=) c.605G= (p.Arg202=) n.882G= n.67+148G= c.509G= (p.Arg170=) c.149G= (p.Arg50=) c.593G= (p.Arg198=) | |
17 | g.7674905C>G | CA397840174 | TP53 | c.626G>C (p.Arg209Thr) c.230G>C (p.Arg77Thr) c.347G>C (p.Arg116Thr) c.605G>C (p.Arg202Thr) n.882G>C n.67+148G>C c.509G>C (p.Arg170Thr) c.149G>C (p.Arg50Thr) c.593G>C (p.Arg198Thr) | dbSNP COSMIC |
17 | g.7674905C>T | CA397840177 | TP53 | c.626G>A (p.Arg209Lys) c.230G>A (p.Arg77Lys) c.347G>A (p.Arg116Lys) c.605G>A (p.Arg202Lys) n.882G>A n.67+148G>A c.509G>A (p.Arg170Lys) c.149G>A (p.Arg50Lys) c.593G>A (p.Arg198Lys) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674905dup | CA1139665123 | TP53 | c.626dup (p.Asn210LysfsTer6) c.230dup (p.Asn78LysfsTer6) c.347dup (p.Asn117LysfsTer6) c.605dup (p.Asn203LysfsTer6) n.882dup n.67+148dup c.509dup (p.Asn171LysfsTer6) c.149dup (p.Asn51LysfsTer6) c.593dup (p.Asn199LysfsTer6) | ClinVar dbSNP |
17 | g.7674906_7674913del | CA645588774 | TP53 | c.619_626del (p.Asp207LysfsTer6) c.223_230del (p.Asp75LysfsTer6) c.340_347del (p.Asp114LysfsTer6) c.598_605del (p.Asp200LysfsTer6) n.875_882del n.67+141_67+148del c.502_509del (p.Asp168LysfsTer6) c.142_149del (p.Asp48LysfsTer6) c.586_593del (p.Asp196LysfsTer6) | COSMIC |
17 | g.7674906T>A | CA397840186 | TP53 | c.625A>T (p.Arg209Ter) c.229A>T (p.Arg77Ter) c.346A>T (p.Arg116Ter) c.604A>T (p.Arg202Ter) n.881A>T n.67+147A>T c.508A>T (p.Arg170Ter) c.148A>T (p.Arg50Ter) c.592A>T (p.Arg198Ter) | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674906T>C | CA397840184 | TP53 | c.625A>G (p.Arg209Gly) c.229A>G (p.Arg77Gly) c.346A>G (p.Arg116Gly) c.604A>G (p.Arg202Gly) n.881A>G n.67+147A>G c.508A>G (p.Arg170Gly) c.148A>G (p.Arg50Gly) c.592A>G (p.Arg198Gly) | ClinVar dbSNP gnomAD v4 |
17 | g.7674906T>G | CA497925316 | TP53 | c.625A>C (p.Arg209=) c.229A>C (p.Arg77=) c.346A>C (p.Arg116=) c.604A>C (p.Arg202=) n.881A>C n.67+147A>C c.508A>C (p.Arg170=) c.148A>C (p.Arg50=) c.592A>C (p.Arg198=) | ClinVar COSMIC |
17 | g.7674906T= | CA2245954680 | TP53 | c.625A= (p.Arg209=) c.229A= (p.Arg77=) c.346A= (p.Arg116=) c.604A= (p.Arg202=) n.881A= n.67+147A= c.508A= (p.Arg170=) c.148A= (p.Arg50=) c.592A= (p.Arg198=) | |
17 | g.7674907G>A | CA497925317 | TP53 | c.624C>T (p.Asp208=) c.228C>T (p.Asp76=) c.345C>T (p.Asp115=) c.603C>T (p.Asp201=) n.880C>T n.67+146C>T c.507C>T (p.Asp169=) c.147C>T (p.Asp49=) c.591C>T (p.Asp197=) | ClinVar dbSNP |
17 | g.7674907G>C | CA397840189 | TP53 | c.624C>G (p.Asp208Glu) c.228C>G (p.Asp76Glu) c.345C>G (p.Asp115Glu) c.603C>G (p.Asp201Glu) n.880C>G n.67+146C>G c.507C>G (p.Asp169Glu) c.147C>G (p.Asp49Glu) c.591C>G (p.Asp197Glu) | dbSNP COSMIC |
17 | g.7674907G>T | CA397840194 | TP53 | c.624C>A (p.Asp208Glu) c.228C>A (p.Asp76Glu) c.345C>A (p.Asp115Glu) c.603C>A (p.Asp201Glu) n.880C>A n.67+146C>A c.507C>A (p.Asp169Glu) c.147C>A (p.Asp49Glu) c.591C>A (p.Asp197Glu) | COSMIC |
17 | g.7674907_7674908insGAG | CA2808380022 | TP53 | c.624_625insTCC (p.Asp208_Arg209insSer) c.228_229insTCC (p.Asp76_Arg77insSer) c.345_346insTCC (p.Asp115_Arg116insSer) c.603_604insTCC (p.Asp201_Arg202insSer) n.880_881insTCC n.67+146_67+147insTCC c.507_508insTCC (p.Asp169_Arg170insSer) c.147_148insTCC (p.Asp49_Arg50insSer) c.591_592insTCC (p.Asp197_Arg198insSer) | |
17 | g.7674908del | CA497925318 | TP53 | c.623del (p.Asp208AlafsTer?) c.227del (p.Asp76AlafsTer?) c.344del (p.Asp115AlafsTer?) c.602del (p.Asp201AlafsTer?) n.879del n.67+145del c.506del (p.Asp169AlafsTer?) c.146del (p.Asp49AlafsTer?) c.590del (p.Asp197AlafsTer?) | COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674908T>A | CA397840195 | TP53 | c.623A>T (p.Asp208Val) c.227A>T (p.Asp76Val) c.344A>T (p.Asp115Val) c.602A>T (p.Asp201Val) n.879A>T n.67+145A>T c.506A>T (p.Asp169Val) c.146A>T (p.Asp49Val) c.590A>T (p.Asp197Val) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674908T>C | CA397840196 | TP53 | c.623A>G (p.Asp208Gly) c.227A>G (p.Asp76Gly) c.344A>G (p.Asp115Gly) c.602A>G (p.Asp201Gly) n.879A>G n.67+145A>G c.506A>G (p.Asp169Gly) c.146A>G (p.Asp49Gly) c.590A>G (p.Asp197Gly) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674908T>G | CA397840197 | TP53 | c.623A>C (p.Asp208Ala) c.227A>C (p.Asp76Ala) c.344A>C (p.Asp115Ala) c.602A>C (p.Asp201Ala) n.879A>C n.67+145A>C c.506A>C (p.Asp169Ala) c.146A>C (p.Asp49Ala) c.590A>C (p.Asp197Ala) | ClinVar dbSNP |
17 | g.7674908T= | CA2245954690 | TP53 | c.623A= (p.Asp208=) c.227A= (p.Asp76=) c.344A= (p.Asp115=) c.602A= (p.Asp201=) n.879A= n.67+145A= c.506A= (p.Asp169=) c.146A= (p.Asp49=) c.590A= (p.Asp197=) | |
17 | g.7674908_7674909delinsAT | CA645588775 | TP53 | c.622_623delinsAT (p.Asp208Ile) c.226_227delinsAT (p.Asp76Ile) c.343_344delinsAT (p.Asp115Ile) c.601_602delinsAT (p.Asp201Ile) n.878_879delinsAT n.67+144_67+145delinsAT c.505_506delinsAT (p.Asp169Ile) c.145_146delinsAT (p.Asp49Ile) c.589_590delinsAT (p.Asp197Ile) | COSMIC |
17 | g.7674909del | CA2808380029 | TP53 | c.622del (p.Asp208ThrfsTer?) c.226del (p.Asp76ThrfsTer?) c.343del (p.Asp115ThrfsTer?) c.601del (p.Asp201ThrfsTer?) n.878del n.67+144del c.505del (p.Asp169ThrfsTer?) c.145del (p.Asp49ThrfsTer?) c.589del (p.Asp197ThrfsTer?) | |
17 | g.7674909C>A | CA397840200 | TP53 | c.622G>T (p.Asp208Tyr) c.226G>T (p.Asp76Tyr) c.343G>T (p.Asp115Tyr) c.601G>T (p.Asp201Tyr) n.878G>T n.67+144G>T c.505G>T (p.Asp169Tyr) c.145G>T (p.Asp49Tyr) c.589G>T (p.Asp197Tyr) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674909C= | CA2245954696 | TP53 | c.622G= (p.Asp208=) c.226G= (p.Asp76=) c.343G= (p.Asp115=) c.601G= (p.Asp201=) n.878G= n.67+144G= c.505G= (p.Asp169=) c.145G= (p.Asp49=) c.589G= (p.Asp197=) | |
17 | g.7674909C>G | CA397840203 | TP53 | c.622G>C (p.Asp208His) c.226G>C (p.Asp76His) c.343G>C (p.Asp115His) c.601G>C (p.Asp201His) n.878G>C n.67+144G>C c.505G>C (p.Asp169His) c.145G>C (p.Asp49His) c.589G>C (p.Asp197His) | ClinVar dbSNP COSMIC |
17 | g.7674909C>T | CA397840204 | TP53 | c.622G>A (p.Asp208Asn) c.226G>A (p.Asp76Asn) c.343G>A (p.Asp115Asn) c.601G>A (p.Asp201Asn) n.878G>A n.67+144G>A c.505G>A (p.Asp169Asn) c.145G>A (p.Asp49Asn) c.589G>A (p.Asp197Asn) | ClinVar dbSNP COSMIC |
17 | g.7674911_7674923del | CA645588776 | TP53 | c.610_622del (p.Glu204ThrfsTer?) c.214_226del (p.Glu72ThrfsTer?) c.331_343del (p.Glu111ThrfsTer?) c.589_601del (p.Glu197ThrfsTer?) n.866_878del n.67+132_67+144del c.493_505del (p.Glu165ThrfsTer?) c.133_145del (p.Glu45ThrfsTer?) c.577_589del (p.Glu193ThrfsTer?) | COSMIC |
17 | g.7674910A>C | CA397840205 | TP53 | c.621T>G (p.Asp207Glu) c.225T>G (p.Asp75Glu) c.342T>G (p.Asp114Glu) c.600T>G (p.Asp200Glu) n.877T>G n.67+143T>G c.504T>G (p.Asp168Glu) c.144T>G (p.Asp48Glu) c.588T>G (p.Asp196Glu) | dbSNP gnomAD v4 |
17 | g.7674910A>G | CA497925319 | TP53 | c.621T>C (p.Asp207=) c.225T>C (p.Asp75=) c.342T>C (p.Asp114=) c.600T>C (p.Asp200=) n.877T>C n.67+143T>C c.504T>C (p.Asp168=) c.144T>C (p.Asp48=) c.588T>C (p.Asp196=) | COSMIC |
17 | g.7674910A>T | CA397840208 | TP53 | c.621T>A (p.Asp207Glu) c.225T>A (p.Asp75Glu) c.342T>A (p.Asp114Glu) c.600T>A (p.Asp200Glu) n.877T>A n.67+143T>A c.504T>A (p.Asp168Glu) c.144T>A (p.Asp48Glu) c.588T>A (p.Asp196Glu) | dbSNP COSMIC |