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.7673473_7673539dup | CA2535386204 | TP53 | c.991_993+64dup c.595_597+64dup c.712_714+64dup c.970_972+64dup c.782+644_782+710dup (n.782+644_782+710dup) c.51_53+64dup c.874_876+64dup c.514_516+64dup c.958_960+64dup | gnomAD v4 |
17 | g.7673491G>A | CA2733124653 | TP53 | c.993+44C>T (n.993+44C>T) c.597+44C>T (n.597+44C>T) c.714+44C>T (n.714+44C>T) c.972+44C>T (n.972+44C>T) c.782+690C>T (n.782+690C>T) c.53+44C>T c.876+44C>T (n.876+44C>T) c.516+44C>T (n.516+44C>T) c.960+44C>T (n.960+44C>T) | dbSNP |
17 | g.7673491G>C | CA2733124679 | TP53 | c.993+44C>G (n.993+44C>G) c.597+44C>G (n.597+44C>G) c.714+44C>G (n.714+44C>G) c.972+44C>G (n.972+44C>G) c.782+690C>G (n.782+690C>G) c.53+44C>G c.876+44C>G (n.876+44C>G) c.516+44C>G (n.516+44C>G) c.960+44C>G (n.960+44C>G) | dbSNP |
17 | g.7673491G>T | CA2580612863 | TP53 | c.993+44C>A (n.993+44C>A) c.597+44C>A (n.597+44C>A) c.714+44C>A (n.714+44C>A) c.972+44C>A (n.972+44C>A) c.782+690C>A (n.782+690C>A) c.53+44C>A c.876+44C>A (n.876+44C>A) c.516+44C>A (n.516+44C>A) c.960+44C>A (n.960+44C>A) | ClinVar dbSNP gnomAD v4 |
17 | g.7673492A>G | CA2635873997 | TP53 | c.993+43T>C (n.993+43T>C) c.597+43T>C (n.597+43T>C) c.714+43T>C (n.714+43T>C) c.972+43T>C (n.972+43T>C) c.782+689T>C (n.782+689T>C) c.53+43T>C c.876+43T>C (n.876+43T>C) c.516+43T>C (n.516+43T>C) c.960+43T>C (n.960+43T>C) | dbSNP gnomAD v4 |
17 | g.7673492A>T | CA2733124801 | TP53 | c.993+43T>A (n.993+43T>A) c.597+43T>A (n.597+43T>A) c.714+43T>A (n.714+43T>A) c.972+43T>A (n.972+43T>A) c.782+689T>A (n.782+689T>A) c.53+43T>A c.876+43T>A (n.876+43T>A) c.516+43T>A (n.516+43T>A) c.960+43T>A (n.960+43T>A) | dbSNP |
17 | g.7673493C>A | CA2733124807 | TP53 | c.993+42G>T (n.993+42G>T) c.597+42G>T (n.597+42G>T) c.714+42G>T (n.714+42G>T) c.972+42G>T (n.972+42G>T) c.782+688G>T (n.782+688G>T) c.53+42G>T c.876+42G>T (n.876+42G>T) c.516+42G>T (n.516+42G>T) c.960+42G>T (n.960+42G>T) | dbSNP |
17 | g.7673493C>G | CA2733125050 | TP53 | c.993+42G>C (n.993+42G>C) c.597+42G>C (n.597+42G>C) c.714+42G>C (n.714+42G>C) c.972+42G>C (n.972+42G>C) c.782+688G>C (n.782+688G>C) c.53+42G>C c.876+42G>C (n.876+42G>C) c.516+42G>C (n.516+42G>C) c.960+42G>C (n.960+42G>C) | dbSNP |
17 | g.7673493C>T | CA2733125003 | TP53 | c.993+42G>A (n.993+42G>A) c.597+42G>A (n.597+42G>A) c.714+42G>A (n.714+42G>A) c.972+42G>A (n.972+42G>A) c.782+688G>A (n.782+688G>A) c.53+42G>A c.876+42G>A (n.876+42G>A) c.516+42G>A (n.516+42G>A) c.960+42G>A (n.960+42G>A) | dbSNP |
17 | g.7673494T>A | CA001147 | TP53 | c.993+41A>T (n.993+41A>T) c.597+41A>T (n.597+41A>T) c.714+41A>T (n.714+41A>T) c.972+41A>T (n.972+41A>T) c.782+687A>T (n.782+687A>T) c.53+41A>T c.876+41A>T (n.876+41A>T) c.516+41A>T (n.516+41A>T) c.960+41A>T (n.960+41A>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.7673494T>C | CA624865098 | TP53 | c.993+41A>G (n.993+41A>G) c.597+41A>G (n.597+41A>G) c.714+41A>G (n.714+41A>G) c.972+41A>G (n.972+41A>G) c.782+687A>G (n.782+687A>G) c.53+41A>G c.876+41A>G (n.876+41A>G) c.516+41A>G (n.516+41A>G) c.960+41A>G (n.960+41A>G) | dbSNP gnomAD v2 |
17 | g.7673494T= | CA2245947232 | TP53 | c.993+41A= (n.993+41A=) c.597+41A= (n.597+41A=) c.714+41A= (n.714+41A=) c.972+41A= (n.972+41A=) c.782+687A= (n.782+687A=) c.53+41A= c.876+41A= (n.876+41A=) c.516+41A= (n.516+41A=) c.960+41A= (n.960+41A=) | |
17 | g.7673496G>A | CA2733125096 | TP53 | c.993+39C>T (n.993+39C>T) c.597+39C>T (n.597+39C>T) c.714+39C>T (n.714+39C>T) c.972+39C>T (n.972+39C>T) c.782+685C>T (n.782+685C>T) c.53+39C>T c.876+39C>T (n.876+39C>T) c.516+39C>T (n.516+39C>T) c.960+39C>T (n.960+39C>T) | dbSNP |
17 | g.7673496G>T | CA2733125060 | TP53 | c.993+39C>A (n.993+39C>A) c.597+39C>A (n.597+39C>A) c.714+39C>A (n.714+39C>A) c.972+39C>A (n.972+39C>A) c.782+685C>A (n.782+685C>A) c.53+39C>A c.876+39C>A (n.876+39C>A) c.516+39C>A (n.516+39C>A) c.960+39C>A (n.960+39C>A) | dbSNP |
17 | g.7673497A>C | CA2733125155 | TP53 | c.993+38T>G (n.993+38T>G) c.597+38T>G (n.597+38T>G) c.714+38T>G (n.714+38T>G) c.972+38T>G (n.972+38T>G) c.782+684T>G (n.782+684T>G) c.53+38T>G c.876+38T>G (n.876+38T>G) c.516+38T>G (n.516+38T>G) c.960+38T>G (n.960+38T>G) | dbSNP |
17 | g.7673497A>G | CA2733125186 | TP53 | c.993+38T>C (n.993+38T>C) c.597+38T>C (n.597+38T>C) c.714+38T>C (n.714+38T>C) c.972+38T>C (n.972+38T>C) c.782+684T>C (n.782+684T>C) c.53+38T>C c.876+38T>C (n.876+38T>C) c.516+38T>C (n.516+38T>C) c.960+38T>C (n.960+38T>C) | dbSNP |
17 | g.7673497A>T | CA2733125133 | TP53 | c.993+38T>A (n.993+38T>A) c.597+38T>A (n.597+38T>A) c.714+38T>A (n.714+38T>A) c.972+38T>A (n.972+38T>A) c.782+684T>A (n.782+684T>A) c.53+38T>A c.876+38T>A (n.876+38T>A) c.516+38T>A (n.516+38T>A) c.960+38T>A (n.960+38T>A) | dbSNP |
17 | g.7673498A>G | CA2635874014 | TP53 | c.993+37T>C (n.993+37T>C) c.597+37T>C (n.597+37T>C) c.714+37T>C (n.714+37T>C) c.972+37T>C (n.972+37T>C) c.782+683T>C (n.782+683T>C) c.53+37T>C c.876+37T>C (n.876+37T>C) c.516+37T>C (n.516+37T>C) c.960+37T>C (n.960+37T>C) | dbSNP gnomAD v4 |
17 | g.7673498A>T | CA2733125270 | TP53 | c.993+37T>A (n.993+37T>A) c.597+37T>A (n.597+37T>A) c.714+37T>A (n.714+37T>A) c.972+37T>A (n.972+37T>A) c.782+683T>A (n.782+683T>A) c.53+37T>A c.876+37T>A (n.876+37T>A) c.516+37T>A (n.516+37T>A) c.960+37T>A (n.960+37T>A) | dbSNP |
17 | g.7673499A= | CA2245947234 | TP53 | c.993+36T= (n.993+36T=) c.597+36T= (n.597+36T=) c.714+36T= (n.714+36T=) c.972+36T= (n.972+36T=) c.782+682T= (n.782+682T=) c.53+36T= c.876+36T= (n.876+36T=) c.516+36T= (n.516+36T=) c.960+36T= (n.960+36T=) | |
17 | g.7673499A>C | CA624865099 | TP53 | c.993+36T>G (n.993+36T>G) c.597+36T>G (n.597+36T>G) c.714+36T>G (n.714+36T>G) c.972+36T>G (n.972+36T>G) c.782+682T>G (n.782+682T>G) c.53+36T>G c.876+36T>G (n.876+36T>G) c.516+36T>G (n.516+36T>G) c.960+36T>G (n.960+36T>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7673499A>G | CA656753436 | TP53 | c.993+36T>C (n.993+36T>C) c.597+36T>C (n.597+36T>C) c.714+36T>C (n.714+36T>C) c.972+36T>C (n.972+36T>C) c.782+682T>C (n.782+682T>C) c.53+36T>C c.876+36T>C (n.876+36T>C) c.516+36T>C (n.516+36T>C) c.960+36T>C (n.960+36T>C) | dbSNP COSMIC |
17 | g.7673499A>T | CA2732945373 | TP53 | c.993+36T>A (n.993+36T>A) c.597+36T>A (n.597+36T>A) c.714+36T>A (n.714+36T>A) c.972+36T>A (n.972+36T>A) c.782+682T>A (n.782+682T>A) c.53+36T>A c.876+36T>A (n.876+36T>A) c.516+36T>A (n.516+36T>A) c.960+36T>A (n.960+36T>A) | dbSNP |
17 | g.7673500C>A | CA2732925028 | TP53 | c.993+35G>T (n.993+35G>T) c.597+35G>T (n.597+35G>T) c.714+35G>T (n.714+35G>T) c.972+35G>T (n.972+35G>T) c.782+681G>T (n.782+681G>T) c.53+35G>T c.876+35G>T (n.876+35G>T) c.516+35G>T (n.516+35G>T) c.960+35G>T (n.960+35G>T) | dbSNP |
17 | g.7673500C= | CA2245947238 | TP53 | c.993+35G= (n.993+35G=) c.597+35G= (n.597+35G=) c.714+35G= (n.714+35G=) c.972+35G= (n.972+35G=) c.782+681G= (n.782+681G=) c.53+35G= c.876+35G= (n.876+35G=) c.516+35G= (n.516+35G=) c.960+35G= (n.960+35G=) | |
17 | g.7673500C>G | CA001155 | TP53 | c.993+35G>C (n.993+35G>C) c.597+35G>C (n.597+35G>C) c.714+35G>C (n.714+35G>C) c.972+35G>C (n.972+35G>C) c.782+681G>C (n.782+681G>C) c.53+35G>C c.876+35G>C (n.876+35G>C) c.516+35G>C (n.516+35G>C) c.960+35G>C (n.960+35G>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7673500C>T | CA001153 | TP53 | c.993+35G>A (n.993+35G>A) c.597+35G>A (n.597+35G>A) c.714+35G>A (n.714+35G>A) c.972+35G>A (n.972+35G>A) c.782+681G>A (n.782+681G>A) c.53+35G>A c.876+35G>A (n.876+35G>A) c.516+35G>A (n.516+35G>A) c.960+35G>A (n.960+35G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.7673501T>A | CA2733125382 | TP53 | c.993+34A>T (n.993+34A>T) c.597+34A>T (n.597+34A>T) c.714+34A>T (n.714+34A>T) c.972+34A>T (n.972+34A>T) c.782+680A>T (n.782+680A>T) c.53+34A>T c.876+34A>T (n.876+34A>T) c.516+34A>T (n.516+34A>T) c.960+34A>T (n.960+34A>T) | dbSNP |
17 | g.7673501T>C | CA2733125417 | TP53 | c.993+34A>G (n.993+34A>G) c.597+34A>G (n.597+34A>G) c.714+34A>G (n.714+34A>G) c.972+34A>G (n.972+34A>G) c.782+680A>G (n.782+680A>G) c.53+34A>G c.876+34A>G (n.876+34A>G) c.516+34A>G (n.516+34A>G) c.960+34A>G (n.960+34A>G) | dbSNP |
17 | g.7673502T>A | CA2733125446 | TP53 | c.993+33A>T (n.993+33A>T) c.597+33A>T (n.597+33A>T) c.714+33A>T (n.714+33A>T) c.972+33A>T (n.972+33A>T) c.782+679A>T (n.782+679A>T) c.53+33A>T c.876+33A>T (n.876+33A>T) c.516+33A>T (n.516+33A>T) c.960+33A>T (n.960+33A>T) | dbSNP |
17 | g.7673502T>C | CA2733125421 | TP53 | c.993+33A>G (n.993+33A>G) c.597+33A>G (n.597+33A>G) c.714+33A>G (n.714+33A>G) c.972+33A>G (n.972+33A>G) c.782+679A>G (n.782+679A>G) c.53+33A>G c.876+33A>G (n.876+33A>G) c.516+33A>G (n.516+33A>G) c.960+33A>G (n.960+33A>G) | dbSNP |
17 | g.7673502T>G | CA2733125445 | TP53 | c.993+33A>C (n.993+33A>C) c.597+33A>C (n.597+33A>C) c.714+33A>C (n.714+33A>C) c.972+33A>C (n.972+33A>C) c.782+679A>C (n.782+679A>C) c.53+33A>C c.876+33A>C (n.876+33A>C) c.516+33A>C (n.516+33A>C) c.960+33A>C (n.960+33A>C) | dbSNP |
17 | g.7673503T>A | CA2635874022 | TP53 | c.993+32A>T (n.993+32A>T) c.597+32A>T (n.597+32A>T) c.714+32A>T (n.714+32A>T) c.972+32A>T (n.972+32A>T) c.782+678A>T (n.782+678A>T) c.53+32A>T c.876+32A>T (n.876+32A>T) c.516+32A>T (n.516+32A>T) c.960+32A>T (n.960+32A>T) | gnomAD v4 |
17 | g.7673503T>C | CA775168442 | TP53 | c.993+32A>G (n.993+32A>G) c.597+32A>G (n.597+32A>G) c.714+32A>G (n.714+32A>G) c.972+32A>G (n.972+32A>G) c.782+678A>G (n.782+678A>G) c.53+32A>G c.876+32A>G (n.876+32A>G) c.516+32A>G (n.516+32A>G) c.960+32A>G (n.960+32A>G) | dbSNP |
17 | g.7673503T= | CA2245947244 | TP53 | c.993+32A= (n.993+32A=) c.597+32A= (n.597+32A=) c.714+32A= (n.714+32A=) c.972+32A= (n.972+32A=) c.782+678A= (n.782+678A=) c.53+32A= c.876+32A= (n.876+32A=) c.516+32A= (n.516+32A=) c.960+32A= (n.960+32A=) | |
17 | g.7673504C>A | CA2733125473 | TP53 | c.993+31G>T (n.993+31G>T) c.597+31G>T (n.597+31G>T) c.714+31G>T (n.714+31G>T) c.972+31G>T (n.972+31G>T) c.782+677G>T (n.782+677G>T) c.53+31G>T c.876+31G>T (n.876+31G>T) c.516+31G>T (n.516+31G>T) c.960+31G>T (n.960+31G>T) | dbSNP |
17 | g.7673504C>T | CA2733125471 | TP53 | c.993+31G>A (n.993+31G>A) c.597+31G>A (n.597+31G>A) c.714+31G>A (n.714+31G>A) c.972+31G>A (n.972+31G>A) c.782+677G>A (n.782+677G>A) c.53+31G>A c.876+31G>A (n.876+31G>A) c.516+31G>A (n.516+31G>A) c.960+31G>A (n.960+31G>A) | dbSNP |
17 | g.7673505C>A | CA2732985595 | TP53 | c.993+30G>T (n.993+30G>T) c.597+30G>T (n.597+30G>T) c.714+30G>T (n.714+30G>T) c.972+30G>T (n.972+30G>T) c.782+676G>T (n.782+676G>T) c.53+30G>T c.876+30G>T (n.876+30G>T) c.516+30G>T (n.516+30G>T) c.960+30G>T (n.960+30G>T) | dbSNP |
17 | g.7673505C= | CA2245947248 | TP53 | c.993+30G= (n.993+30G=) c.597+30G= (n.597+30G=) c.714+30G= (n.714+30G=) c.972+30G= (n.972+30G=) c.782+676G= (n.782+676G=) c.53+30G= c.876+30G= (n.876+30G=) c.516+30G= (n.516+30G=) c.960+30G= (n.960+30G=) | |
17 | g.7673505C>G | CA2732985596 | TP53 | c.993+30G>C (n.993+30G>C) c.597+30G>C (n.597+30G>C) c.714+30G>C (n.714+30G>C) c.972+30G>C (n.972+30G>C) c.782+676G>C (n.782+676G>C) c.53+30G>C c.876+30G>C (n.876+30G>C) c.516+30G>C (n.516+30G>C) c.960+30G>C (n.960+30G>C) | dbSNP |
17 | g.7673505C>T | CA981209202 | TP53 | c.993+30G>A (n.993+30G>A) c.597+30G>A (n.597+30G>A) c.714+30G>A (n.714+30G>A) c.972+30G>A (n.972+30G>A) c.782+676G>A (n.782+676G>A) c.53+30G>A c.876+30G>A (n.876+30G>A) c.516+30G>A (n.516+30G>A) c.960+30G>A (n.960+30G>A) | dbSNP gnomAD v3 gnomAD v4 |
17 | g.7673506A>C | CA2733125477 | TP53 | c.993+29T>G (n.993+29T>G) c.597+29T>G (n.597+29T>G) c.714+29T>G (n.714+29T>G) c.972+29T>G (n.972+29T>G) c.782+675T>G (n.782+675T>G) c.53+29T>G c.876+29T>G (n.876+29T>G) c.516+29T>G (n.516+29T>G) c.960+29T>G (n.960+29T>G) | dbSNP |
17 | g.7673506A>G | CA2733125478 | TP53 | c.993+29T>C (n.993+29T>C) c.597+29T>C (n.597+29T>C) c.714+29T>C (n.714+29T>C) c.972+29T>C (n.972+29T>C) c.782+675T>C (n.782+675T>C) c.53+29T>C c.876+29T>C (n.876+29T>C) c.516+29T>C (n.516+29T>C) c.960+29T>C (n.960+29T>C) | dbSNP |
17 | g.7673506A>T | CA2733125479 | TP53 | c.993+29T>A (n.993+29T>A) c.597+29T>A (n.597+29T>A) c.714+29T>A (n.714+29T>A) c.972+29T>A (n.972+29T>A) c.782+675T>A (n.782+675T>A) c.53+29T>A c.876+29T>A (n.876+29T>A) c.516+29T>A (n.516+29T>A) c.960+29T>A (n.960+29T>A) | dbSNP |
17 | g.7673507C>A | CA2732954355 | TP53 | c.993+28G>T (n.993+28G>T) c.597+28G>T (n.597+28G>T) c.714+28G>T (n.714+28G>T) c.972+28G>T (n.972+28G>T) c.782+674G>T (n.782+674G>T) c.53+28G>T c.876+28G>T (n.876+28G>T) c.516+28G>T (n.516+28G>T) c.960+28G>T (n.960+28G>T) | dbSNP |
17 | g.7673507C= | CA2245947251 | TP53 | c.993+28G= (n.993+28G=) c.597+28G= (n.597+28G=) c.714+28G= (n.714+28G=) c.972+28G= (n.972+28G=) c.782+674G= (n.782+674G=) c.53+28G= c.876+28G= (n.876+28G=) c.516+28G= (n.516+28G=) c.960+28G= (n.960+28G=) | |
17 | g.7673507C>G | CA624865100 | TP53 | c.993+28G>C (n.993+28G>C) c.597+28G>C (n.597+28G>C) c.714+28G>C (n.714+28G>C) c.972+28G>C (n.972+28G>C) c.782+674G>C (n.782+674G>C) c.53+28G>C c.876+28G>C (n.876+28G>C) c.516+28G>C (n.516+28G>C) c.960+28G>C (n.960+28G>C) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.7673507C>T | CA2732954353 | TP53 | c.993+28G>A (n.993+28G>A) c.597+28G>A (n.597+28G>A) c.714+28G>A (n.714+28G>A) c.972+28G>A (n.972+28G>A) c.782+674G>A (n.782+674G>A) c.53+28G>A c.876+28G>A (n.876+28G>A) c.516+28G>A (n.516+28G>A) c.960+28G>A (n.960+28G>A) | dbSNP |
17 | g.7673508T>A | CA2732985603 | TP53 | c.993+27A>T (n.993+27A>T) c.597+27A>T (n.597+27A>T) c.714+27A>T (n.714+27A>T) c.972+27A>T (n.972+27A>T) c.782+673A>T (n.782+673A>T) c.53+27A>T c.876+27A>T (n.876+27A>T) c.516+27A>T (n.516+27A>T) c.960+27A>T (n.960+27A>T) | dbSNP |
17 | g.7673508T>C | CA981209208 | TP53 | c.993+27A>G (n.993+27A>G) c.597+27A>G (n.597+27A>G) c.714+27A>G (n.714+27A>G) c.972+27A>G (n.972+27A>G) c.782+673A>G (n.782+673A>G) c.53+27A>G c.876+27A>G (n.876+27A>G) c.516+27A>G (n.516+27A>G) c.960+27A>G (n.960+27A>G) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.7673508T= | CA2245947256 | TP53 | c.993+27A= (n.993+27A=) c.597+27A= (n.597+27A=) c.714+27A= (n.714+27A=) c.972+27A= (n.972+27A=) c.782+673A= (n.782+673A=) c.53+27A= c.876+27A= (n.876+27A=) c.516+27A= (n.516+27A=) c.960+27A= (n.960+27A=) | |
17 | g.7673509T>A | CA2732985604 | TP53 | c.993+26A>T (n.993+26A>T) c.597+26A>T (n.597+26A>T) c.714+26A>T (n.714+26A>T) c.972+26A>T (n.972+26A>T) c.782+672A>T (n.782+672A>T) c.53+26A>T c.876+26A>T (n.876+26A>T) c.516+26A>T (n.516+26A>T) c.960+26A>T (n.960+26A>T) | dbSNP |
17 | g.7673509T>C | CA981209211 | TP53 | c.993+26A>G (n.993+26A>G) c.597+26A>G (n.597+26A>G) c.714+26A>G (n.714+26A>G) c.972+26A>G (n.972+26A>G) c.782+672A>G (n.782+672A>G) c.53+26A>G c.876+26A>G (n.876+26A>G) c.516+26A>G (n.516+26A>G) c.960+26A>G (n.960+26A>G) | dbSNP gnomAD v3 gnomAD v4 |
17 | g.7673509T>G | CA2566747584 | TP53 | c.993+26A>C (n.993+26A>C) c.597+26A>C (n.597+26A>C) c.714+26A>C (n.714+26A>C) c.972+26A>C (n.972+26A>C) c.782+672A>C (n.782+672A>C) c.53+26A>C c.876+26A>C (n.876+26A>C) c.516+26A>C (n.516+26A>C) c.960+26A>C (n.960+26A>C) | |
17 | g.7673509T= | CA2245947259 | TP53 | c.993+26A= (n.993+26A=) c.597+26A= (n.597+26A=) c.714+26A= (n.714+26A=) c.972+26A= (n.972+26A=) c.782+672A= (n.782+672A=) c.53+26A= c.876+26A= (n.876+26A=) c.516+26A= (n.516+26A=) c.960+26A= (n.960+26A=) | |
17 | g.7673510G>A | CA2733125482 | TP53 | c.993+25C>T (n.993+25C>T) c.597+25C>T (n.597+25C>T) c.714+25C>T (n.714+25C>T) c.972+25C>T (n.972+25C>T) c.782+671C>T (n.782+671C>T) c.53+25C>T c.876+25C>T (n.876+25C>T) c.516+25C>T (n.516+25C>T) c.960+25C>T (n.960+25C>T) | dbSNP |
17 | g.7673510G>C | CA2733125502 | TP53 | c.993+25C>G (n.993+25C>G) c.597+25C>G (n.597+25C>G) c.714+25C>G (n.714+25C>G) c.972+25C>G (n.972+25C>G) c.782+671C>G (n.782+671C>G) c.53+25C>G c.876+25C>G (n.876+25C>G) c.516+25C>G (n.516+25C>G) c.960+25C>G (n.960+25C>G) | dbSNP |
17 | g.7673510G>T | CA2733125584 | TP53 | c.993+25C>A (n.993+25C>A) c.597+25C>A (n.597+25C>A) c.714+25C>A (n.714+25C>A) c.972+25C>A (n.972+25C>A) c.782+671C>A (n.782+671C>A) c.53+25C>A c.876+25C>A (n.876+25C>A) c.516+25C>A (n.516+25C>A) c.960+25C>A (n.960+25C>A) | dbSNP |
17 | g.7673510_7673534del | CA645587336 | TP53 | c.993+1_993+25del (n.993+1_993+25del) c.597+1_597+25del (n.597+1_597+25del) c.714+1_714+25del (n.714+1_714+25del) c.972+1_972+25del (n.972+1_972+25del) c.782+647_782+671del (n.782+647_782+671del) c.53+1_53+25del c.876+1_876+25del (n.876+1_876+25del) c.516+1_516+25del (n.516+1_516+25del) c.960+1_960+25del (n.960+1_960+25del) | COSMIC COSMIC COSMIC COSMIC |
17 | g.7673511A= | CA2245947261 | TP53 | c.993+24T= (n.993+24T=) c.597+24T= (n.597+24T=) c.714+24T= (n.714+24T=) c.972+24T= (n.972+24T=) c.782+670T= (n.782+670T=) c.53+24T= c.876+24T= (n.876+24T=) c.516+24T= (n.516+24T=) c.960+24T= (n.960+24T=) | |
17 | g.7673511A>G | CA287486485 | TP53 | c.993+24T>C (n.993+24T>C) c.597+24T>C (n.597+24T>C) c.714+24T>C (n.714+24T>C) c.972+24T>C (n.972+24T>C) c.782+670T>C (n.782+670T>C) c.53+24T>C c.876+24T>C (n.876+24T>C) c.516+24T>C (n.516+24T>C) c.960+24T>C (n.960+24T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7673511A>T | CA2732942237 | TP53 | c.993+24T>A (n.993+24T>A) c.597+24T>A (n.597+24T>A) c.714+24T>A (n.714+24T>A) c.972+24T>A (n.972+24T>A) c.782+670T>A (n.782+670T>A) c.53+24T>A c.876+24T>A (n.876+24T>A) c.516+24T>A (n.516+24T>A) c.960+24T>A (n.960+24T>A) | dbSNP |
17 | g.7673512_7673515dup | CA2635874035 | TP53 | c.993+20_993+23dup (n.993+20_993+23dup) c.597+20_597+23dup (n.597+20_597+23dup) c.714+20_714+23dup (n.714+20_714+23dup) c.972+20_972+23dup (n.972+20_972+23dup) c.782+666_782+669dup (n.782+666_782+669dup) c.53+20_53+23dup c.876+20_876+23dup (n.876+20_876+23dup) c.516+20_516+23dup (n.516+20_516+23dup) c.960+20_960+23dup (n.960+20_960+23dup) | gnomAD v4 |
17 | g.7673513A>G | CA2544471111 | TP53 | c.993+22T>C (n.993+22T>C) c.597+22T>C (n.597+22T>C) c.714+22T>C (n.714+22T>C) c.972+22T>C (n.972+22T>C) c.782+668T>C (n.782+668T>C) c.53+22T>C c.876+22T>C (n.876+22T>C) c.516+22T>C (n.516+22T>C) c.960+22T>C (n.960+22T>C) | dbSNP |
17 | g.7673513A>T | CA2733125597 | TP53 | c.993+22T>A (n.993+22T>A) c.597+22T>A (n.597+22T>A) c.714+22T>A (n.714+22T>A) c.972+22T>A (n.972+22T>A) c.782+668T>A (n.782+668T>A) c.53+22T>A c.876+22T>A (n.876+22T>A) c.516+22T>A (n.516+22T>A) c.960+22T>A (n.960+22T>A) | dbSNP |
17 | g.7673514A>G | CA2576230608 | TP53 | c.993+21T>C (n.993+21T>C) c.597+21T>C (n.597+21T>C) c.714+21T>C (n.714+21T>C) c.972+21T>C (n.972+21T>C) c.782+667T>C (n.782+667T>C) c.53+21T>C c.876+21T>C (n.876+21T>C) c.516+21T>C (n.516+21T>C) c.960+21T>C (n.960+21T>C) | dbSNP |
17 | g.7673514A>T | CA2733125743 | TP53 | c.993+21T>A (n.993+21T>A) c.597+21T>A (n.597+21T>A) c.714+21T>A (n.714+21T>A) c.972+21T>A (n.972+21T>A) c.782+667T>A (n.782+667T>A) c.53+21T>A c.876+21T>A (n.876+21T>A) c.516+21T>A (n.516+21T>A) c.960+21T>A (n.960+21T>A) | dbSNP |
17 | g.7673515G>A | CA2580094890 | TP53 | c.993+20C>T (n.993+20C>T) c.597+20C>T (n.597+20C>T) c.714+20C>T (n.714+20C>T) c.972+20C>T (n.972+20C>T) c.782+666C>T (n.782+666C>T) c.53+20C>T c.876+20C>T (n.876+20C>T) c.516+20C>T (n.516+20C>T) c.960+20C>T (n.960+20C>T) | ClinVar dbSNP |
17 | g.7673515G>C | CA2245947265 | TP53 | c.993+20C>G (n.993+20C>G) c.597+20C>G (n.597+20C>G) c.714+20C>G (n.714+20C>G) c.972+20C>G (n.972+20C>G) c.782+666C>G (n.782+666C>G) c.53+20C>G c.876+20C>G (n.876+20C>G) c.516+20C>G (n.516+20C>G) c.960+20C>G (n.960+20C>G) | dbSNP |
17 | g.7673515G= | CA2245947264 | TP53 | c.993+20C= (n.993+20C=) c.597+20C= (n.597+20C=) c.714+20C= (n.714+20C=) c.972+20C= (n.972+20C=) c.782+666C= (n.782+666C=) c.53+20C= c.876+20C= (n.876+20C=) c.516+20C= (n.516+20C=) c.960+20C= (n.960+20C=) | |
17 | g.7673515G>T | CA2732985607 | TP53 | c.993+20C>A (n.993+20C>A) c.597+20C>A (n.597+20C>A) c.714+20C>A (n.714+20C>A) c.972+20C>A (n.972+20C>A) c.782+666C>A (n.782+666C>A) c.53+20C>A c.876+20C>A (n.876+20C>A) c.516+20C>A (n.516+20C>A) c.960+20C>A (n.960+20C>A) | dbSNP |
17 | g.7673516A= | CA2245947269 | TP53 | c.993+19T= (n.993+19T=) c.597+19T= (n.597+19T=) c.714+19T= (n.714+19T=) c.972+19T= (n.972+19T=) c.782+665T= (n.782+665T=) c.53+19T= c.876+19T= (n.876+19T=) c.516+19T= (n.516+19T=) c.960+19T= (n.960+19T=) | |
17 | g.7673516A>G | CA2732925963 | TP53 | c.993+19T>C (n.993+19T>C) c.597+19T>C (n.597+19T>C) c.714+19T>C (n.714+19T>C) c.972+19T>C (n.972+19T>C) c.782+665T>C (n.782+665T>C) c.53+19T>C c.876+19T>C (n.876+19T>C) c.516+19T>C (n.516+19T>C) c.960+19T>C (n.960+19T>C) | dbSNP |
17 | g.7673516A>T | CA001165 | TP53 | c.993+19T>A (n.993+19T>A) c.597+19T>A (n.597+19T>A) c.714+19T>A (n.714+19T>A) c.972+19T>A (n.972+19T>A) c.782+665T>A (n.782+665T>A) c.53+19T>A c.876+19T>A (n.876+19T>A) c.516+19T>A (n.516+19T>A) c.960+19T>A (n.960+19T>A) | ClinVar dbSNP ExAC gnomAD v2 |
17 | g.7673517G>A | CA001171 | TP53 | c.993+18C>T (n.993+18C>T) c.597+18C>T (n.597+18C>T) c.714+18C>T (n.714+18C>T) c.972+18C>T (n.972+18C>T) c.782+664C>T (n.782+664C>T) c.53+18C>T c.876+18C>T (n.876+18C>T) c.516+18C>T (n.516+18C>T) c.960+18C>T (n.960+18C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7673517G>C | CA2732926315 | TP53 | c.993+18C>G (n.993+18C>G) c.597+18C>G (n.597+18C>G) c.714+18C>G (n.714+18C>G) c.972+18C>G (n.972+18C>G) c.782+664C>G (n.782+664C>G) c.53+18C>G c.876+18C>G (n.876+18C>G) c.516+18C>G (n.516+18C>G) c.960+18C>G (n.960+18C>G) | dbSNP |
17 | g.7673517G= | CA2245947274 | TP53 | c.993+18C= (n.993+18C=) c.597+18C= (n.597+18C=) c.714+18C= (n.714+18C=) c.972+18C= (n.972+18C=) c.782+664C= (n.782+664C=) c.53+18C= c.876+18C= (n.876+18C=) c.516+18C= (n.516+18C=) c.960+18C= (n.960+18C=) | |
17 | g.7673517G>T | CA2695202234 | TP53 | c.993+18C>A (n.993+18C>A) c.597+18C>A (n.597+18C>A) c.714+18C>A (n.714+18C>A) c.972+18C>A (n.972+18C>A) c.782+664C>A (n.782+664C>A) c.53+18C>A c.876+18C>A (n.876+18C>A) c.516+18C>A (n.516+18C>A) c.960+18C>A (n.960+18C>A) | dbSNP |
17 | g.7673518G>A | CA2580094892 | TP53 | c.993+17C>T (n.993+17C>T) c.597+17C>T (n.597+17C>T) c.714+17C>T (n.714+17C>T) c.972+17C>T (n.972+17C>T) c.782+663C>T (n.782+663C>T) c.53+17C>T c.876+17C>T (n.876+17C>T) c.516+17C>T (n.516+17C>T) c.960+17C>T (n.960+17C>T) | ClinVar dbSNP |
17 | g.7673518G>C | CA2732931740 | TP53 | c.993+17C>G (n.993+17C>G) c.597+17C>G (n.597+17C>G) c.714+17C>G (n.714+17C>G) c.972+17C>G (n.972+17C>G) c.782+663C>G (n.782+663C>G) c.53+17C>G c.876+17C>G (n.876+17C>G) c.516+17C>G (n.516+17C>G) c.960+17C>G (n.960+17C>G) | dbSNP |
17 | g.7673518G= | CA2245947277 | TP53 | c.993+17C= (n.993+17C=) c.597+17C= (n.597+17C=) c.714+17C= (n.714+17C=) c.972+17C= (n.972+17C=) c.782+663C= (n.782+663C=) c.53+17C= c.876+17C= (n.876+17C=) c.516+17C= (n.516+17C=) c.960+17C= (n.960+17C=) | |
17 | g.7673518G>T | CA287486489 | TP53 | c.993+17C>A (n.993+17C>A) c.597+17C>A (n.597+17C>A) c.714+17C>A (n.714+17C>A) c.972+17C>A (n.972+17C>A) c.782+663C>A (n.782+663C>A) c.53+17C>A c.876+17C>A (n.876+17C>A) c.516+17C>A (n.516+17C>A) c.960+17C>A (n.960+17C>A) | dbSNP |
17 | g.7673519T>A | CA2733125754 | TP53 | c.993+16A>T (n.993+16A>T) c.597+16A>T (n.597+16A>T) c.714+16A>T (n.714+16A>T) c.972+16A>T (n.972+16A>T) c.782+662A>T (n.782+662A>T) c.53+16A>T c.876+16A>T (n.876+16A>T) c.516+16A>T (n.516+16A>T) c.960+16A>T (n.960+16A>T) | dbSNP |
17 | g.7673519T>C | CA2733125771 | TP53 | c.993+16A>G (n.993+16A>G) c.597+16A>G (n.597+16A>G) c.714+16A>G (n.714+16A>G) c.972+16A>G (n.972+16A>G) c.782+662A>G (n.782+662A>G) c.53+16A>G c.876+16A>G (n.876+16A>G) c.516+16A>G (n.516+16A>G) c.960+16A>G (n.960+16A>G) | dbSNP |
17 | g.7673519T>G | CA2733125788 | TP53 | c.993+16A>C (n.993+16A>C) c.597+16A>C (n.597+16A>C) c.714+16A>C (n.714+16A>C) c.972+16A>C (n.972+16A>C) c.782+662A>C (n.782+662A>C) c.53+16A>C c.876+16A>C (n.876+16A>C) c.516+16A>C (n.516+16A>C) c.960+16A>C (n.960+16A>C) | dbSNP |
17 | g.7673520C>A | CA658683979 | TP53 | c.993+15G>T (n.993+15G>T) c.597+15G>T (n.597+15G>T) c.714+15G>T (n.714+15G>T) c.972+15G>T (n.972+15G>T) c.782+661G>T (n.782+661G>T) c.53+15G>T c.876+15G>T (n.876+15G>T) c.516+15G>T (n.516+15G>T) c.960+15G>T (n.960+15G>T) | ClinVar dbSNP |
17 | g.7673520C= | CA2245947284 | TP53 | c.993+15G= (n.993+15G=) c.597+15G= (n.597+15G=) c.714+15G= (n.714+15G=) c.972+15G= (n.972+15G=) c.782+661G= (n.782+661G=) c.53+15G= c.876+15G= (n.876+15G=) c.516+15G= (n.516+15G=) c.960+15G= (n.960+15G=) | |
17 | g.7673520C>G | CA2635874040 | TP53 | c.993+15G>C (n.993+15G>C) c.597+15G>C (n.597+15G>C) c.714+15G>C (n.714+15G>C) c.972+15G>C (n.972+15G>C) c.782+661G>C (n.782+661G>C) c.53+15G>C c.876+15G>C (n.876+15G>C) c.516+15G>C (n.516+15G>C) c.960+15G>C (n.960+15G>C) | ClinVar dbSNP gnomAD v4 |
17 | g.7673520C>T | CA2732963321 | TP53 | c.993+15G>A (n.993+15G>A) c.597+15G>A (n.597+15G>A) c.714+15G>A (n.714+15G>A) c.972+15G>A (n.972+15G>A) c.782+661G>A (n.782+661G>A) c.53+15G>A c.876+15G>A (n.876+15G>A) c.516+15G>A (n.516+15G>A) c.960+15G>A (n.960+15G>A) | ClinVar dbSNP |
17 | g.7673521C>A | CA2733125832 | TP53 | c.993+14G>T (n.993+14G>T) c.597+14G>T (n.597+14G>T) c.714+14G>T (n.714+14G>T) c.972+14G>T (n.972+14G>T) c.782+660G>T (n.782+660G>T) c.53+14G>T c.876+14G>T (n.876+14G>T) c.516+14G>T (n.516+14G>T) c.960+14G>T (n.960+14G>T) | dbSNP |
17 | g.7673521C>G | CA2573154621 | TP53 | c.993+14G>C (n.993+14G>C) c.597+14G>C (n.597+14G>C) c.714+14G>C (n.714+14G>C) c.972+14G>C (n.972+14G>C) c.782+660G>C (n.782+660G>C) c.53+14G>C c.876+14G>C (n.876+14G>C) c.516+14G>C (n.516+14G>C) c.960+14G>C (n.960+14G>C) | ClinVar dbSNP gnomAD v4 |
17 | g.7673521C>T | CA2733125800 | TP53 | c.993+14G>A (n.993+14G>A) c.597+14G>A (n.597+14G>A) c.714+14G>A (n.714+14G>A) c.972+14G>A (n.972+14G>A) c.782+660G>A (n.782+660G>A) c.53+14G>A c.876+14G>A (n.876+14G>A) c.516+14G>A (n.516+14G>A) c.960+14G>A (n.960+14G>A) | dbSNP |
17 | g.7673522C>A | CA2732925964 | TP53 | c.993+13G>T (n.993+13G>T) c.597+13G>T (n.597+13G>T) c.714+13G>T (n.714+13G>T) c.972+13G>T (n.972+13G>T) c.782+659G>T (n.782+659G>T) c.53+13G>T c.876+13G>T (n.876+13G>T) c.516+13G>T (n.516+13G>T) c.960+13G>T (n.960+13G>T) | dbSNP |
17 | g.7673522C= | CA2245947294 | TP53 | c.993+13G= (n.993+13G=) c.597+13G= (n.597+13G=) c.714+13G= (n.714+13G=) c.972+13G= (n.972+13G=) c.782+659G= (n.782+659G=) c.53+13G= c.876+13G= (n.876+13G=) c.516+13G= (n.516+13G=) c.960+13G= (n.960+13G=) | |
17 | g.7673522C>G | CA000522 | TP53 | c.993+13G>C (n.993+13G>C) c.597+13G>C (n.597+13G>C) c.714+13G>C (n.714+13G>C) c.972+13G>C (n.972+13G>C) c.782+659G>C (n.782+659G>C) c.53+13G>C c.876+13G>C (n.876+13G>C) c.516+13G>C (n.516+13G>C) c.960+13G>C (n.960+13G>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7673522C>T | CA2573154623 | TP53 | c.993+13G>A (n.993+13G>A) c.597+13G>A (n.597+13G>A) c.714+13G>A (n.714+13G>A) c.972+13G>A (n.972+13G>A) c.782+659G>A (n.782+659G>A) c.53+13G>A c.876+13G>A (n.876+13G>A) c.516+13G>A (n.516+13G>A) c.960+13G>A (n.960+13G>A) | ClinVar dbSNP gnomAD v4 |
17 | g.7673522_7673523delinsTG | CA2573154622 | TP53 | c.993+12_993+13delinsCA (n.993+12_993+13delinsCA) c.597+12_597+13delinsCA (n.597+12_597+13delinsCA) c.714+12_714+13delinsCA (n.714+12_714+13delinsCA) c.972+12_972+13delinsCA (n.972+12_972+13delinsCA) c.782+658_782+659delinsCA (n.782+658_782+659delinsCA) c.53+12_53+13delinsCA c.876+12_876+13delinsCA (n.876+12_876+13delinsCA) c.516+12_516+13delinsCA (n.516+12_516+13delinsCA) c.960+12_960+13delinsCA (n.960+12_960+13delinsCA) | ClinVar |
17 | g.7673523A= | CA2245947305 | TP53 | c.993+12T= (n.993+12T=) c.597+12T= (n.597+12T=) c.714+12T= (n.714+12T=) c.972+12T= (n.972+12T=) c.782+658T= (n.782+658T=) c.53+12T= c.876+12T= (n.876+12T=) c.516+12T= (n.516+12T=) c.960+12T= (n.960+12T=) | |
17 | g.7673523A>C | CA2580574841 | TP53 | c.993+12T>G (n.993+12T>G) c.597+12T>G (n.597+12T>G) c.714+12T>G (n.714+12T>G) c.972+12T>G (n.972+12T>G) c.782+658T>G (n.782+658T>G) c.53+12T>G c.876+12T>G (n.876+12T>G) c.516+12T>G (n.516+12T>G) c.960+12T>G (n.960+12T>G) | |
17 | g.7673523A>G | CA000520 | TP53 | c.993+12T>C (n.993+12T>C) c.597+12T>C (n.597+12T>C) c.714+12T>C (n.714+12T>C) c.972+12T>C (n.972+12T>C) c.782+658T>C (n.782+658T>C) c.53+12T>C c.876+12T>C (n.876+12T>C) c.516+12T>C (n.516+12T>C) c.960+12T>C (n.960+12T>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7673523A>T | CA2580574842 | TP53 | c.993+12T>A (n.993+12T>A) c.597+12T>A (n.597+12T>A) c.714+12T>A (n.714+12T>A) c.972+12T>A (n.972+12T>A) c.782+658T>A (n.782+658T>A) c.53+12T>A c.876+12T>A (n.876+12T>A) c.516+12T>A (n.516+12T>A) c.960+12T>A (n.960+12T>A) | dbSNP |
17 | g.7673524A= | CA2245947313 | TP53 | c.993+11T= (n.993+11T=) c.597+11T= (n.597+11T=) c.714+11T= (n.714+11T=) c.972+11T= (n.972+11T=) c.782+657T= (n.782+657T=) c.53+11T= c.876+11T= (n.876+11T=) c.516+11T= (n.516+11T=) c.960+11T= (n.960+11T=) | |
17 | g.7673524A>G | CA001188 | TP53 | c.993+11T>C (n.993+11T>C) c.597+11T>C (n.597+11T>C) c.714+11T>C (n.714+11T>C) c.972+11T>C (n.972+11T>C) c.782+657T>C (n.782+657T>C) c.53+11T>C c.876+11T>C (n.876+11T>C) c.516+11T>C (n.516+11T>C) c.960+11T>C (n.960+11T>C) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
17 | g.7673524A>T | CA2732930950 | TP53 | c.993+11T>A (n.993+11T>A) c.597+11T>A (n.597+11T>A) c.714+11T>A (n.714+11T>A) c.972+11T>A (n.972+11T>A) c.782+657T>A (n.782+657T>A) c.53+11T>A c.876+11T>A (n.876+11T>A) c.516+11T>A (n.516+11T>A) c.960+11T>A (n.960+11T>A) | dbSNP |
17 | g.7673525G>A | CA2733125845 | TP53 | c.993+10C>T (n.993+10C>T) c.597+10C>T (n.597+10C>T) c.714+10C>T (n.714+10C>T) c.972+10C>T (n.972+10C>T) c.782+656C>T (n.782+656C>T) c.53+10C>T c.876+10C>T (n.876+10C>T) c.516+10C>T (n.516+10C>T) c.960+10C>T (n.960+10C>T) | dbSNP |
17 | g.7673525G>C | CA2635874081 | TP53 | c.993+10C>G (n.993+10C>G) c.597+10C>G (n.597+10C>G) c.714+10C>G (n.714+10C>G) c.972+10C>G (n.972+10C>G) c.782+656C>G (n.782+656C>G) c.53+10C>G c.876+10C>G (n.876+10C>G) c.516+10C>G (n.516+10C>G) c.960+10C>G (n.960+10C>G) | dbSNP gnomAD v4 |
17 | g.7673525G>T | CA2733125848 | TP53 | c.993+10C>A (n.993+10C>A) c.597+10C>A (n.597+10C>A) c.714+10C>A (n.714+10C>A) c.972+10C>A (n.972+10C>A) c.782+656C>A (n.782+656C>A) c.53+10C>A c.876+10C>A (n.876+10C>A) c.516+10C>A (n.516+10C>A) c.960+10C>A (n.960+10C>A) | dbSNP |
17 | g.7673525_7673526insGGTG | CA2635874080 | TP53 | c.993+10_993+11insACCC (n.993+10_993+11insACCC) c.597+10_597+11insACCC (n.597+10_597+11insACCC) c.714+10_714+11insACCC (n.714+10_714+11insACCC) c.972+10_972+11insACCC (n.972+10_972+11insACCC) c.782+656_782+657insACCC (n.782+656_782+657insACCC) c.53+10_53+11insACCC c.876+10_876+11insACCC (n.876+10_876+11insACCC) c.516+10_516+11insACCC (n.516+10_516+11insACCC) c.960+10_960+11insACCC (n.960+10_960+11insACCC) | gnomAD v4 |
17 | g.7673526A>G | CA2576230614 | TP53 | c.993+9T>C (n.993+9T>C) c.597+9T>C (n.597+9T>C) c.714+9T>C (n.714+9T>C) c.972+9T>C (n.972+9T>C) c.782+655T>C (n.782+655T>C) c.53+9T>C c.876+9T>C (n.876+9T>C) c.516+9T>C (n.516+9T>C) c.960+9T>C (n.960+9T>C) | ClinVar dbSNP |
17 | g.7673526A>T | CA2733125877 | TP53 | c.993+9T>A (n.993+9T>A) c.597+9T>A (n.597+9T>A) c.714+9T>A (n.714+9T>A) c.972+9T>A (n.972+9T>A) c.782+655T>A (n.782+655T>A) c.53+9T>A c.876+9T>A (n.876+9T>A) c.516+9T>A (n.516+9T>A) c.960+9T>A (n.960+9T>A) | dbSNP |
17 | g.7673526_7673531delinsGGTGAAA | CA2825002629 | TP53 | c.993+4_993+9delinsTTTCACC (n.993+4_993+9delinsTTTCACC) c.597+4_597+9delinsTTTCACC (n.597+4_597+9delinsTTTCACC) c.714+4_714+9delinsTTTCACC (n.714+4_714+9delinsTTTCACC) c.972+4_972+9delinsTTTCACC (n.972+4_972+9delinsTTTCACC) c.782+650_782+655delinsTTTCACC (n.782+650_782+655delinsTTTCACC) c.53+4_53+9delinsTTTCACC c.876+4_876+9delinsTTTCACC (n.876+4_876+9delinsTTTCACC) c.516+4_516+9delinsTTTCACC (n.516+4_516+9delinsTTTCACC) c.960+4_960+9delinsTTTCACC (n.960+4_960+9delinsTTTCACC) | ClinVar |
17 | g.7673527C>A | CA2732943608 | TP53 | c.993+8G>T (n.993+8G>T) c.597+8G>T (n.597+8G>T) c.714+8G>T (n.714+8G>T) c.972+8G>T (n.972+8G>T) c.782+654G>T (n.782+654G>T) c.53+8G>T c.876+8G>T (n.876+8G>T) c.516+8G>T (n.516+8G>T) c.960+8G>T (n.960+8G>T) | dbSNP |
17 | g.7673527C= | CA2245947326 | TP53 | c.993+8G= (n.993+8G=) c.597+8G= (n.597+8G=) c.714+8G= (n.714+8G=) c.972+8G= (n.972+8G=) c.782+654G= (n.782+654G=) c.53+8G= c.876+8G= (n.876+8G=) c.516+8G= (n.516+8G=) c.960+8G= (n.960+8G=) | |
17 | g.7673527C>G | CA2576230615 | TP53 | c.993+8G>C (n.993+8G>C) c.597+8G>C (n.597+8G>C) c.714+8G>C (n.714+8G>C) c.972+8G>C (n.972+8G>C) c.782+654G>C (n.782+654G>C) c.53+8G>C c.876+8G>C (n.876+8G>C) c.516+8G>C (n.516+8G>C) c.960+8G>C (n.960+8G>C) | ClinVar gnomAD v4 |
17 | g.7673527C>T | CA16615685 | TP53 | c.993+8G>A (n.993+8G>A) c.597+8G>A (n.597+8G>A) c.714+8G>A (n.714+8G>A) c.972+8G>A (n.972+8G>A) c.782+654G>A (n.782+654G>A) c.53+8G>A c.876+8G>A (n.876+8G>A) c.516+8G>A (n.516+8G>A) c.960+8G>A (n.960+8G>A) | ClinVar dbSNP |
17 | g.7673527_7673529del | CA2635874085 | TP53 | c.993+6_993+8del (n.993+6_993+8del) c.597+6_597+8del (n.597+6_597+8del) c.714+6_714+8del (n.714+6_714+8del) c.972+6_972+8del (n.972+6_972+8del) c.782+652_782+654del (n.782+652_782+654del) c.53+6_53+8del c.876+6_876+8del (n.876+6_876+8del) c.516+6_516+8del (n.516+6_516+8del) c.960+6_960+8del (n.960+6_960+8del) | gnomAD v4 |
17 | g.7673528T>A | CA2732941348 | TP53 | c.993+7A>T (n.993+7A>T) c.597+7A>T (n.597+7A>T) c.714+7A>T (n.714+7A>T) c.972+7A>T (n.972+7A>T) c.782+653A>T (n.782+653A>T) c.53+7A>T c.876+7A>T (n.876+7A>T) c.516+7A>T (n.516+7A>T) c.960+7A>T (n.960+7A>T) | dbSNP |
17 | g.7673528T>C | CA287486495 | TP53 | c.993+7A>G (n.993+7A>G) c.597+7A>G (n.597+7A>G) c.714+7A>G (n.714+7A>G) c.972+7A>G (n.972+7A>G) c.782+653A>G (n.782+653A>G) c.53+7A>G c.876+7A>G (n.876+7A>G) c.516+7A>G (n.516+7A>G) c.960+7A>G (n.960+7A>G) | ClinVar dbSNP gnomAD v4 |
17 | g.7673528T>G | CA2732941347 | TP53 | c.993+7A>C (n.993+7A>C) c.597+7A>C (n.597+7A>C) c.714+7A>C (n.714+7A>C) c.972+7A>C (n.972+7A>C) c.782+653A>C (n.782+653A>C) c.53+7A>C c.876+7A>C (n.876+7A>C) c.516+7A>C (n.516+7A>C) c.960+7A>C (n.960+7A>C) | dbSNP |
17 | g.7673528T= | CA2245947329 | TP53 | c.993+7A= (n.993+7A=) c.597+7A= (n.597+7A=) c.714+7A= (n.714+7A=) c.972+7A= (n.972+7A=) c.782+653A= (n.782+653A=) c.53+7A= c.876+7A= (n.876+7A=) c.516+7A= (n.516+7A=) c.960+7A= (n.960+7A=) | |
17 | g.7673529_7673532dup | CA2573154625 | TP53 | c.993+4_993+7dup (n.993+4_993+7dup) c.597+4_597+7dup (n.597+4_597+7dup) c.714+4_714+7dup (n.714+4_714+7dup) c.972+4_972+7dup (n.972+4_972+7dup) c.782+650_782+653dup (n.782+650_782+653dup) c.53+4_53+7dup c.876+4_876+7dup (n.876+4_876+7dup) c.516+4_516+7dup (n.516+4_516+7dup) c.960+4_960+7dup (n.960+4_960+7dup) | ClinVar dbSNP |
17 | g.7673528_7673536del | CA2573154624 | TP53 | c.992_993+7del c.596_597+7del c.713_714+7del c.971_972+7del c.782+645_782+653del (n.782+645_782+653del) c.52_53+7del c.875_876+7del c.515_516+7del c.959_960+7del | dbSNP |
17 | g.7673528_7673529insG | CA2576230616 | TP53 | c.993+6_993+7insC (n.993+6_993+7insC) c.597+6_597+7insC (n.597+6_597+7insC) c.714+6_714+7insC (n.714+6_714+7insC) c.972+6_972+7insC (n.972+6_972+7insC) c.782+652_782+653insC (n.782+652_782+653insC) c.53+6_53+7insC c.876+6_876+7insC (n.876+6_876+7insC) c.516+6_516+7insC (n.516+6_516+7insC) c.960+6_960+7insC (n.960+6_960+7insC) | |
17 | g.7673529T>A | CA2576230617 | TP53 | c.993+6A>T (n.993+6A>T) c.597+6A>T (n.597+6A>T) c.714+6A>T (n.714+6A>T) c.972+6A>T (n.972+6A>T) c.782+652A>T (n.782+652A>T) c.53+6A>T c.876+6A>T (n.876+6A>T) c.516+6A>T (n.516+6A>T) c.960+6A>T (n.960+6A>T) | |
17 | g.7673529T>C | CA2573154626 | TP53 | c.993+6A>G (n.993+6A>G) c.597+6A>G (n.597+6A>G) c.714+6A>G (n.714+6A>G) c.972+6A>G (n.972+6A>G) c.782+652A>G (n.782+652A>G) c.53+6A>G c.876+6A>G (n.876+6A>G) c.516+6A>G (n.516+6A>G) c.960+6A>G (n.960+6A>G) | ClinVar dbSNP gnomAD v4 |
17 | g.7673529T>G | CA2733125928 | TP53 | c.993+6A>C (n.993+6A>C) c.597+6A>C (n.597+6A>C) c.714+6A>C (n.714+6A>C) c.972+6A>C (n.972+6A>C) c.782+652A>C (n.782+652A>C) c.53+6A>C c.876+6A>C (n.876+6A>C) c.516+6A>C (n.516+6A>C) c.960+6A>C (n.960+6A>C) | dbSNP |
17 | g.7673529_7673541del | CA645587337 | TP53 | c.987_993+6del c.591_597+6del c.708_714+6del c.966_972+6del c.782+640_782+652del (n.782+640_782+652del) c.47_53+6del c.870_876+6del c.510_516+6del c.954_960+6del | COSMIC COSMIC COSMIC COSMIC |
17 | g.7673530A= | CA2245947338 | TP53 | c.993+5T= (n.993+5T=) c.597+5T= (n.597+5T=) c.714+5T= (n.714+5T=) c.972+5T= (n.972+5T=) c.782+651T= (n.782+651T=) c.53+5T= c.876+5T= (n.876+5T=) c.516+5T= (n.516+5T=) c.960+5T= (n.960+5T=) | |
17 | g.7673530A>C | CA915949513 | TP53 | c.993+5T>G (n.993+5T>G) c.597+5T>G (n.597+5T>G) c.714+5T>G (n.714+5T>G) c.972+5T>G (n.972+5T>G) c.782+651T>G (n.782+651T>G) c.53+5T>G c.876+5T>G (n.876+5T>G) c.516+5T>G (n.516+5T>G) c.960+5T>G (n.960+5T>G) | ClinVar dbSNP gnomAD v4 |
17 | g.7673530A>G | CA658656522 | TP53 | c.993+5T>C (n.993+5T>C) c.597+5T>C (n.597+5T>C) c.714+5T>C (n.714+5T>C) c.972+5T>C (n.972+5T>C) c.782+651T>C (n.782+651T>C) c.53+5T>C c.876+5T>C (n.876+5T>C) c.516+5T>C (n.516+5T>C) c.960+5T>C (n.960+5T>C) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.7673530A>T | CA2732953019 | TP53 | c.993+5T>A (n.993+5T>A) c.597+5T>A (n.597+5T>A) c.714+5T>A (n.714+5T>A) c.972+5T>A (n.972+5T>A) c.782+651T>A (n.782+651T>A) c.53+5T>A c.876+5T>A (n.876+5T>A) c.516+5T>A (n.516+5T>A) c.960+5T>A (n.960+5T>A) | dbSNP |
17 | g.7673530_7673531delinsAG | CA2245947337 | TP53 | c.993+4_993+5delinsCT (n.993+4_993+5delinsCT) c.597+4_597+5delinsCT (n.597+4_597+5delinsCT) c.714+4_714+5delinsCT (n.714+4_714+5delinsCT) c.972+4_972+5delinsCT (n.972+4_972+5delinsCT) c.782+650_782+651delinsCT (n.782+650_782+651delinsCT) c.53+4_53+5delinsCT c.876+4_876+5delinsCT (n.876+4_876+5delinsCT) c.516+4_516+5delinsCT (n.516+4_516+5delinsCT) c.960+4_960+5delinsCT (n.960+4_960+5delinsCT) | |
17 | g.7673531del | CA10580907 | TP53 | c.993+4del (n.993+4del) c.597+4del (n.597+4del) c.714+4del (n.714+4del) c.972+4del (n.972+4del) c.782+650del (n.782+650del) c.53+4del c.876+4del (n.876+4del) c.516+4del (n.516+4del) c.960+4del (n.960+4del) | ClinVar dbSNP |
17 | g.7673531G>A | CA658798695 | TP53 | c.993+4C>T (n.993+4C>T) c.597+4C>T (n.597+4C>T) c.714+4C>T (n.714+4C>T) c.972+4C>T (n.972+4C>T) c.782+650C>T (n.782+650C>T) c.53+4C>T c.876+4C>T (n.876+4C>T) c.516+4C>T (n.516+4C>T) c.960+4C>T (n.960+4C>T) | ClinVar dbSNP gnomAD v4 |
17 | g.7673531G>C | CA913188777 | TP53 | c.993+4C>G (n.993+4C>G) c.597+4C>G (n.597+4C>G) c.714+4C>G (n.714+4C>G) c.972+4C>G (n.972+4C>G) c.782+650C>G (n.782+650C>G) c.53+4C>G c.876+4C>G (n.876+4C>G) c.516+4C>G (n.516+4C>G) c.960+4C>G (n.960+4C>G) | ClinVar dbSNP |
17 | g.7673531G= | CA2245947358 | TP53 | c.993+4C= (n.993+4C=) c.597+4C= (n.597+4C=) c.714+4C= (n.714+4C=) c.972+4C= (n.972+4C=) c.782+650C= (n.782+650C=) c.53+4C= c.876+4C= (n.876+4C=) c.516+4C= (n.516+4C=) c.960+4C= (n.960+4C=) | |
17 | g.7673531G>T | CA2732963322 | TP53 | c.993+4C>A (n.993+4C>A) c.597+4C>A (n.597+4C>A) c.714+4C>A (n.714+4C>A) c.972+4C>A (n.972+4C>A) c.782+650C>A (n.782+650C>A) c.53+4C>A c.876+4C>A (n.876+4C>A) c.516+4C>A (n.516+4C>A) c.960+4C>A (n.960+4C>A) | dbSNP |
17 | g.7673532_7673541del | CA645587338 | TP53 | c.988_993+4del c.592_597+4del c.709_714+4del c.967_972+4del c.782+641_782+650del (n.782+641_782+650del) c.48_53+4del c.871_876+4del c.511_516+4del c.955_960+4del | COSMIC COSMIC COSMIC COSMIC |
17 | g.7673532T>A | CA2573154627 | TP53 | c.993+3A>T (n.993+3A>T) c.597+3A>T (n.597+3A>T) c.714+3A>T (n.714+3A>T) c.972+3A>T (n.972+3A>T) c.782+649A>T (n.782+649A>T) c.53+3A>T c.876+3A>T (n.876+3A>T) c.516+3A>T (n.516+3A>T) c.960+3A>T (n.960+3A>T) | ClinVar dbSNP gnomAD v4 |
17 | g.7673532T>C | CA2733126018 | TP53 | c.993+3A>G (n.993+3A>G) c.597+3A>G (n.597+3A>G) c.714+3A>G (n.714+3A>G) c.972+3A>G (n.972+3A>G) c.782+649A>G (n.782+649A>G) c.53+3A>G c.876+3A>G (n.876+3A>G) c.516+3A>G (n.516+3A>G) c.960+3A>G (n.960+3A>G) | dbSNP |
17 | g.7673532T>G | CA2733126009 | TP53 | c.993+3A>C (n.993+3A>C) c.597+3A>C (n.597+3A>C) c.714+3A>C (n.714+3A>C) c.972+3A>C (n.972+3A>C) c.782+649A>C (n.782+649A>C) c.53+3A>C c.876+3A>C (n.876+3A>C) c.516+3A>C (n.516+3A>C) c.960+3A>C (n.960+3A>C) | dbSNP |
17 | g.7673532_7673534delinsG | CA645587339 | TP53 | c.993+1_993+3delinsC (n.993+1_993+3delinsC) c.597+1_597+3delinsC (n.597+1_597+3delinsC) c.714+1_714+3delinsC (n.714+1_714+3delinsC) c.972+1_972+3delinsC (n.972+1_972+3delinsC) c.782+647_782+649delinsC (n.782+647_782+649delinsC) c.53+1_53+3delinsC c.876+1_876+3delinsC (n.876+1_876+3delinsC) c.516+1_516+3delinsC (n.516+1_516+3delinsC) c.960+1_960+3delinsC (n.960+1_960+3delinsC) | COSMIC |
17 | g.7673533del | CA2832533698 | TP53 | c.993+2del (n.993+2del) c.597+2del (n.597+2del) c.714+2del (n.714+2del) c.972+2del (n.972+2del) c.782+648del (n.782+648del) c.53+2del c.876+2del (n.876+2del) c.516+2del (n.516+2del) c.960+2del (n.960+2del) | |
17 | g.7673533A= | CA2245947371 | TP53 | c.993+2T= (n.993+2T=) c.597+2T= (n.597+2T=) c.714+2T= (n.714+2T=) c.972+2T= (n.972+2T=) c.782+648T= (n.782+648T=) c.53+2T= c.876+2T= (n.876+2T=) c.516+2T= (n.516+2T=) c.960+2T= (n.960+2T=) | |
17 | g.7673533A>C | CA397835626 | TP53 | c.993+2T>G (n.993+2T>G) c.597+2T>G (n.597+2T>G) c.714+2T>G (n.714+2T>G) c.972+2T>G (n.972+2T>G) c.782+648T>G (n.782+648T>G) c.53+2T>G c.876+2T>G (n.876+2T>G) c.516+2T>G (n.516+2T>G) c.960+2T>G (n.960+2T>G) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673533A>G | CA397835629 | TP53 | c.993+2T>C (n.993+2T>C) c.597+2T>C (n.597+2T>C) c.714+2T>C (n.714+2T>C) c.972+2T>C (n.972+2T>C) c.782+648T>C (n.782+648T>C) c.53+2T>C c.876+2T>C (n.876+2T>C) c.516+2T>C (n.516+2T>C) c.960+2T>C (n.960+2T>C) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
17 | g.7673533A>T | CA397835635 | TP53 | c.993+2T>A (n.993+2T>A) c.597+2T>A (n.597+2T>A) c.714+2T>A (n.714+2T>A) c.972+2T>A (n.972+2T>A) c.782+648T>A (n.782+648T>A) c.53+2T>A c.876+2T>A (n.876+2T>A) c.516+2T>A (n.516+2T>A) c.960+2T>A (n.960+2T>A) | dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673533_7673534delinsAC | CA2245947369 | TP53 | c.993+1_993+2delinsGT (n.993+1_993+2delinsGT) c.597+1_597+2delinsGT (n.597+1_597+2delinsGT) c.714+1_714+2delinsGT (n.714+1_714+2delinsGT) c.972+1_972+2delinsGT (n.972+1_972+2delinsGT) c.782+647_782+648delinsGT (n.782+647_782+648delinsGT) c.53+1_53+2delinsGT c.876+1_876+2delinsGT (n.876+1_876+2delinsGT) c.516+1_516+2delinsGT (n.516+1_516+2delinsGT) c.960+1_960+2delinsGT (n.960+1_960+2delinsGT) | |
17 | g.7673533_7673541delinsTA | CA2580094895 | TP53 | c.987_993+2delinsTA c.591_597+2delinsTA c.708_714+2delinsTA c.966_972+2delinsTA c.782+640_782+648delinsTA (n.782+640_782+648delinsTA) c.47_53+2delinsTA c.870_876+2delinsTA c.510_516+2delinsTA c.954_960+2delinsTA | ClinVar |
17 | g.7673534C>A | CA287486498 | TP53 | c.993+1G>T (n.993+1G>T) c.597+1G>T (n.597+1G>T) c.714+1G>T (n.714+1G>T) c.972+1G>T (n.972+1G>T) c.782+647G>T (n.782+647G>T) c.53+1G>T c.876+1G>T (n.876+1G>T) c.516+1G>T (n.516+1G>T) c.960+1G>T (n.960+1G>T) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673534C= | CA2245947398 | TP53 | c.993+1G= (n.993+1G=) c.597+1G= (n.597+1G=) c.714+1G= (n.714+1G=) c.972+1G= (n.972+1G=) c.782+647G= (n.782+647G=) c.53+1G= c.876+1G= (n.876+1G=) c.516+1G= (n.516+1G=) c.960+1G= (n.960+1G=) | |
17 | g.7673534C>G | CA16607519 | TP53 | c.993+1G>C (n.993+1G>C) c.597+1G>C (n.597+1G>C) c.714+1G>C (n.714+1G>C) c.972+1G>C (n.972+1G>C) c.782+647G>C (n.782+647G>C) c.53+1G>C c.876+1G>C (n.876+1G>C) c.516+1G>C (n.516+1G>C) c.960+1G>C (n.960+1G>C) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673534C>T | CA397835645 | TP53 | c.993+1G>A (n.993+1G>A) c.597+1G>A (n.597+1G>A) c.714+1G>A (n.714+1G>A) c.972+1G>A (n.972+1G>A) c.782+647G>A (n.782+647G>A) c.53+1G>A c.876+1G>A (n.876+1G>A) c.516+1G>A (n.516+1G>A) c.960+1G>A (n.960+1G>A) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
17 | g.7673535del | CA645369685 | TP53 | c.993+1del c.597+1del c.714+1del c.972+1del c.782+647del (n.782+647del) c.53+1del c.876+1del c.516+1del c.960+1del | ClinVar dbSNP |
17 | g.7673534_7673538delinsCCTGA | CA2245947390 | TP53 | c.990_993+1delinsTCAGG c.594_597+1delinsTCAGG c.711_714+1delinsTCAGG c.969_972+1delinsTCAGG c.782+643_782+647delinsTCAGG (n.782+643_782+647delinsTCAGG) c.50_53+1delinsTCAGG c.873_876+1delinsTCAGG c.513_516+1delinsTCAGG c.957_960+1delinsTCAGG | |
17 | g.7673535C>A | CA287486501 | TP53 | c.993G>T (p.Gln331His) c.597G>T (p.Gln199His) c.714G>T (p.Gln238His) c.972G>T (p.Gln324His) c.782+646G>T (n.782+646G>T) c.53G>T c.876G>T (p.Gln292His) c.516G>T (p.Gln172His) c.960G>T (p.Gln320His) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673535C= | CA2245947419 | TP53 | c.993G= (p.Gln331=) c.597G= (p.Gln199=) c.714G= (p.Gln238=) c.972G= (p.Gln324=) c.782+646G= (n.782+646G=) c.53G= c.876G= (p.Gln292=) c.516G= (p.Gln172=) c.960G= (p.Gln320=) | |
17 | g.7673535C>G | CA397835662 | TP53 | c.993G>C (p.Gln331His) c.597G>C (p.Gln199His) c.714G>C (p.Gln238His) c.972G>C (p.Gln324His) c.782+646G>C (n.782+646G>C) c.53G>C c.876G>C (p.Gln292His) c.516G>C (p.Gln172His) c.960G>C (p.Gln320His) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673535C>T | CA10590137 | TP53 | c.993G>A (p.Gln331=) c.597G>A (p.Gln199=) c.714G>A (p.Gln238=) c.972G>A (p.Gln324=) c.782+646G>A (n.782+646G>A) c.53G>A c.876G>A (p.Gln292=) c.516G>A (p.Gln172=) c.960G>A (p.Gln320=) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673535_7673536del | CA645587344 | TP53 | c.992_993del (p.Gln331HisfsTer5) c.596_597del (p.Gln199HisfsTer5) c.713_714del (p.Gln238HisfsTer5) c.971_972del (p.Gln324HisfsTer5) c.992_993del (p.Lys332AsnfsTer?) c.782+645_782+646del (n.782+645_782+646del) c.992_993del (p.Gln331ArgfsTer15) c.992_993del (p.Gln331HisfsTer4) c.596_597del (p.Gln199HisfsTer4) c.596_597del (p.Gln199=) c.596_597del (p.Gln199ArgfsTer15) c.52_53del c.875_876del (p.Gln292HisfsTer5) c.875_876del (p.Gln292HisfsTer4) c.515_516del (p.Gln172HisfsTer4) c.959_960del (p.Gln320HisfsTer5) c.515_516del (p.Gln172ArgfsTer15) c.515_516del (p.Gln172HisfsTer5) c.875_876del (p.Gln292ArgfsTer15) | COSMIC |
17 | g.7673535_7673536delinsTG | CA645587342 | TP53 | c.992_993delinsCA (p.Gln331Pro) c.596_597delinsCA (p.Gln199Pro) c.713_714delinsCA (p.Gln238Pro) c.971_972delinsCA (p.Gln324Pro) c.782+645_782+646delinsCA (n.782+645_782+646delinsCA) c.52_53delinsCA c.875_876delinsCA (p.Gln292Pro) c.515_516delinsCA (p.Gln172Pro) c.959_960delinsCA (p.Gln320Pro) | COSMIC |
17 | g.7673535_7673538del | CA658656523 | TP53 | c.990_993del (p.Gln331SerfsTer13) c.594_597del (p.Gln199SerfsTer13) c.711_714del (p.Gln238SerfsTer13) c.969_972del (p.Gln324SerfsTer13) c.990_993del (p.Gln331LysfsTer20) c.782+643_782+646del (n.782+643_782+646del) c.990_993del (p.Gln331ThrfsTer19) c.990_993del (p.Gln331CysfsTer11) c.594_597del (p.Gln199CysfsTer11) c.594_597del (p.Leu198=) c.594_597del (p.Gln199ThrfsTer19) c.50_53del c.873_876del (p.Gln292SerfsTer13) c.873_876del (p.Gln292CysfsTer11) c.513_516del (p.Gln172CysfsTer11) c.957_960del (p.Gln320SerfsTer13) c.513_516del (p.Gln172ThrfsTer19) c.513_516del (p.Gln172SerfsTer13) c.873_876del (p.Gln292ThrfsTer19) | ClinVar dbSNP |
17 | g.7673536T>A | CA397835673 | TP53 | c.992A>T (p.Gln331Leu) c.596A>T (p.Gln199Leu) c.713A>T (p.Gln238Leu) c.971A>T (p.Gln324Leu) c.782+645A>T (n.782+645A>T) c.52A>T c.875A>T (p.Gln292Leu) c.515A>T (p.Gln172Leu) c.959A>T (p.Gln320Leu) | |
17 | g.7673536T>C | CA16620611 | TP53 | c.992A>G (p.Gln331Arg) c.596A>G (p.Gln199Arg) c.713A>G (p.Gln238Arg) c.971A>G (p.Gln324Arg) c.782+645A>G (n.782+645A>G) c.52A>G c.875A>G (p.Gln292Arg) c.515A>G (p.Gln172Arg) c.959A>G (p.Gln320Arg) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
17 | g.7673536T>G | CA397835672 | TP53 | c.992A>C (p.Gln331Pro) c.596A>C (p.Gln199Pro) c.713A>C (p.Gln238Pro) c.971A>C (p.Gln324Pro) c.782+645A>C (n.782+645A>C) c.52A>C c.875A>C (p.Gln292Pro) c.515A>C (p.Gln172Pro) c.959A>C (p.Gln320Pro) | COSMIC |
17 | g.7673536T= | CA2245947430 | TP53 | c.992A= (p.Gln331=) c.596A= (p.Gln199=) c.713A= (p.Gln238=) c.971A= (p.Gln324=) c.782+645A= (n.782+645A=) c.52A= c.875A= (p.Gln292=) c.515A= (p.Gln172=) c.959A= (p.Gln320=) | |
17 | g.7673536_7673594dup | CA2499224956 | TP53 | c.934_992dup (p.Ile332ProfsTer33) c.538_596dup (p.Ile200ProfsTer33) c.655_713dup (p.Ile239ProfsTer33) c.913_971dup (p.Ile325ProfsTer33) c.934_992dup (p.Lys332ProfsTer40) c.782+587_782+645dup (n.782+587_782+645dup) c.934_992dup (p.Asp332ProfsTer39) c.934_992dup (p.Met332ProfsTer31) c.538_596dup (p.Met200ProfsTer31) c.538_596dup (p.Gln199=) c.538_596dup (p.Asp200ProfsTer39) c.817_875dup (p.Ile293ProfsTer33) c.817_875dup (p.Met293ProfsTer31) c.457_515dup (p.Met173ProfsTer31) c.901_959dup (p.Ile321ProfsTer33) c.457_515dup (p.Asp173ProfsTer39) c.457_515dup (p.Ile173ProfsTer33) c.817_875dup (p.Asp293ProfsTer39) | ClinVar dbSNP |
17 | g.7673537G>A | CA397835674 | TP53 | c.991C>T (p.Gln331Ter) c.595C>T (p.Gln199Ter) c.712C>T (p.Gln238Ter) c.970C>T (p.Gln324Ter) c.782+644C>T (n.782+644C>T) c.51C>T c.874C>T (p.Gln292Ter) c.514C>T (p.Gln172Ter) c.958C>T (p.Gln320Ter) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673537G>C | CA397835677 | TP53 | c.991C>G (p.Gln331Glu) c.595C>G (p.Gln199Glu) c.712C>G (p.Gln238Glu) c.970C>G (p.Gln324Glu) c.782+644C>G (n.782+644C>G) c.51C>G c.874C>G (p.Gln292Glu) c.514C>G (p.Gln172Glu) c.958C>G (p.Gln320Glu) | ClinVar |
17 | g.7673537G= | CA2245947449 | TP53 | c.991C= (p.Gln331=) c.595C= (p.Gln199=) c.712C= (p.Gln238=) c.970C= (p.Gln324=) c.782+644C= (n.782+644C=) c.51C= c.874C= (p.Gln292=) c.514C= (p.Gln172=) c.958C= (p.Gln320=) | |
17 | g.7673537G>T | CA397835679 | TP53 | c.991C>A (p.Gln331Lys) c.595C>A (p.Gln199Lys) c.712C>A (p.Gln238Lys) c.970C>A (p.Gln324Lys) c.782+644C>A (n.782+644C>A) c.51C>A c.874C>A (p.Gln292Lys) c.514C>A (p.Gln172Lys) c.958C>A (p.Gln320Lys) | ClinVar dbSNP |
17 | g.7673538A>C | CA497713725 | TP53 | c.990T>G (p.Leu330=) c.594T>G (p.Leu198=) c.711T>G (p.Leu237=) c.969T>G (p.Leu323=) c.782+643T>G (n.782+643T>G) c.50T>G c.873T>G (p.Leu291=) c.513T>G (p.Leu171=) c.957T>G (p.Leu319=) | dbSNP |
17 | g.7673538A>G | CA497713729 | TP53 | c.990T>C (p.Leu330=) c.594T>C (p.Leu198=) c.711T>C (p.Leu237=) c.969T>C (p.Leu323=) c.782+643T>C (n.782+643T>C) c.50T>C c.873T>C (p.Leu291=) c.513T>C (p.Leu171=) c.957T>C (p.Leu319=) | dbSNP |
17 | g.7673538A>T | CA497713734 | TP53 | c.990T>A (p.Leu330=) c.594T>A (p.Leu198=) c.711T>A (p.Leu237=) c.969T>A (p.Leu323=) c.782+643T>A (n.782+643T>A) c.50T>A c.873T>A (p.Leu291=) c.513T>A (p.Leu171=) c.957T>A (p.Leu319=) | dbSNP |
17 | g.7673539dup | CA645587345 | TP53 | c.990dup (p.Gln331SerfsTer6) c.594dup (p.Gln199SerfsTer6) c.711dup (p.Gln238SerfsTer6) c.969dup (p.Gln324SerfsTer6) c.990dup (p.Gln331SerfsTer?) c.782+643dup (n.782+643dup) c.990dup (p.Gln331SerfsTer16) c.990dup (p.Gln331SerfsTer5) c.594dup (p.Gln199SerfsTer5) c.594dup (p.Gln199SerfsTer?) c.594dup (p.Gln199SerfsTer16) c.50dup c.873dup (p.Gln292SerfsTer6) c.873dup (p.Gln292SerfsTer5) c.513dup (p.Gln172SerfsTer5) c.957dup (p.Gln320SerfsTer6) c.513dup (p.Gln172SerfsTer16) c.513dup (p.Gln172SerfsTer6) c.873dup (p.Gln292SerfsTer16) | COSMIC COSMIC |
17 | g.7673539del | CA497713744 | TP53 | c.990del (p.Gln331ArgfsTer14) c.594del (p.Gln199ArgfsTer14) c.711del (p.Gln238ArgfsTer14) c.969del (p.Gln324ArgfsTer14) c.990del (p.Gln331ArgfsTer21) c.782+643del (n.782+643del) c.990del (p.Gln331ArgfsTer20) c.990del (p.Gln331ArgfsTer12) c.594del (p.Gln199ArgfsTer12) c.594del (p.Leu198=) c.594del (p.Gln199ArgfsTer20) c.50del c.873del (p.Gln292ArgfsTer14) c.873del (p.Gln292ArgfsTer12) c.513del (p.Gln172ArgfsTer12) c.957del (p.Gln320ArgfsTer14) c.513del (p.Gln172ArgfsTer20) c.513del (p.Gln172ArgfsTer14) c.873del (p.Gln292ArgfsTer20) | ClinVar dbSNP COSMIC |
17 | g.7673538_7673539insT | CA497713747 | TP53 | c.989_990insA (p.Gln331SerfsTer6) c.593_594insA (p.Gln199SerfsTer6) c.710_711insA (p.Gln238SerfsTer6) c.968_969insA (p.Gln324SerfsTer6) c.989_990insA (p.Gln331SerfsTer?) c.782+642_782+643insA (n.782+642_782+643insA) c.989_990insA (p.Gln331SerfsTer16) c.989_990insA (p.Gln331SerfsTer5) c.593_594insA (p.Gln199SerfsTer5) c.593_594insA (p.Gln199SerfsTer?) c.593_594insA (p.Gln199SerfsTer16) c.49_50insA c.872_873insA (p.Gln292SerfsTer6) c.872_873insA (p.Gln292SerfsTer5) c.512_513insA (p.Gln172SerfsTer5) c.956_957insA (p.Gln320SerfsTer6) c.512_513insA (p.Gln172SerfsTer16) c.512_513insA (p.Gln172SerfsTer6) c.872_873insA (p.Gln292SerfsTer16) | |
17 | g.7673539A= | CA2245947462 | TP53 | c.989T= (p.Leu330=) c.593T= (p.Leu198=) c.710T= (p.Leu237=) c.968T= (p.Leu323=) c.782+642T= (n.782+642T=) c.49T= c.872T= (p.Leu291=) c.512T= (p.Leu171=) c.956T= (p.Leu319=) | |
17 | g.7673539A>C | CA397835702 | TP53 | c.989T>G (p.Leu330Arg) c.593T>G (p.Leu198Arg) c.710T>G (p.Leu237Arg) c.968T>G (p.Leu323Arg) c.782+642T>G (n.782+642T>G) c.49T>G c.872T>G (p.Leu291Arg) c.512T>G (p.Leu171Arg) c.956T>G (p.Leu319Arg) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
17 | g.7673539A>G | CA397835704 | TP53 | c.989T>C (p.Leu330Pro) c.593T>C (p.Leu198Pro) c.710T>C (p.Leu237Pro) c.968T>C (p.Leu323Pro) c.782+642T>C (n.782+642T>C) c.49T>C c.872T>C (p.Leu291Pro) c.512T>C (p.Leu171Pro) c.956T>C (p.Leu319Pro) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673539A>T | CA397835707 | TP53 | c.989T>A (p.Leu330His) c.593T>A (p.Leu198His) c.710T>A (p.Leu237His) c.968T>A (p.Leu323His) c.782+642T>A (n.782+642T>A) c.49T>A c.872T>A (p.Leu291His) c.512T>A (p.Leu171His) c.956T>A (p.Leu319His) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673539_7673540delinsAG | CA2245947468 | TP53 | c.988_989delinsCT (p.Leu330=) c.592_593delinsCT (p.Leu198=) c.709_710delinsCT (p.Leu237=) c.967_968delinsCT (p.Leu323=) c.782+641_782+642delinsCT (n.782+641_782+642delinsCT) c.48_49delinsCT c.871_872delinsCT (p.Leu291=) c.511_512delinsCT (p.Leu171=) c.955_956delinsCT (p.Leu319=) | |
17 | g.7673540G>A | CA397835712 | TP53 | c.988C>T (p.Leu330Phe) c.592C>T (p.Leu198Phe) c.709C>T (p.Leu237Phe) c.967C>T (p.Leu323Phe) c.782+641C>T (n.782+641C>T) c.48C>T c.871C>T (p.Leu291Phe) c.511C>T (p.Leu171Phe) c.955C>T (p.Leu319Phe) | ClinVar dbSNP |
17 | g.7673540G>C | CA397835714 | TP53 | c.988C>G (p.Leu330Val) c.592C>G (p.Leu198Val) c.709C>G (p.Leu237Val) c.967C>G (p.Leu323Val) c.782+641C>G (n.782+641C>G) c.48C>G c.871C>G (p.Leu291Val) c.511C>G (p.Leu171Val) c.955C>G (p.Leu319Val) | dbSNP |
17 | g.7673540G= | CA2245947485 | TP53 | c.988C= (p.Leu330=) c.592C= (p.Leu198=) c.709C= (p.Leu237=) c.967C= (p.Leu323=) c.782+641C= (n.782+641C=) c.48C= c.871C= (p.Leu291=) c.511C= (p.Leu171=) c.955C= (p.Leu319=) | |
17 | g.7673540G>T | CA397835718 | TP53 | c.988C>A (p.Leu330Ile) c.592C>A (p.Leu198Ile) c.709C>A (p.Leu237Ile) c.967C>A (p.Leu323Ile) c.782+641C>A (n.782+641C>A) c.48C>A c.871C>A (p.Leu291Ile) c.511C>A (p.Leu171Ile) c.955C>A (p.Leu319Ile) | dbSNP |
17 | g.7673542del | CA497713751 | TP53 | c.988del (p.Leu330PhefsTer15) c.592del (p.Leu198PhefsTer15) c.709del (p.Leu237PhefsTer15) c.967del (p.Leu323PhefsTer15) c.988del (p.Leu330PhefsTer22) c.782+641del (n.782+641del) c.988del (p.Leu330PhefsTer21) c.988del (p.Leu330PhefsTer13) c.592del (p.Leu198PhefsTer13) c.592del (p.Leu198PhefsTer?) c.592del (p.Leu198PhefsTer21) c.48del c.871del (p.Leu291PhefsTer15) c.871del (p.Leu291PhefsTer13) c.511del (p.Leu171PhefsTer13) c.955del (p.Leu319PhefsTer15) c.511del (p.Leu171PhefsTer21) c.511del (p.Leu171PhefsTer15) c.871del (p.Leu291PhefsTer21) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7673541G>A | CA497713763 | TP53 | c.987C>T (p.Thr329=) c.591C>T (p.Thr197=) c.708C>T (p.Thr236=) c.966C>T (p.Thr322=) c.782+640C>T (n.782+640C>T) c.47C>T c.870C>T (p.Thr290=) c.510C>T (p.Thr170=) c.954C>T (p.Thr318=) | ClinVar dbSNP gnomAD v4 COSMIC |
17 | g.7673541G>C | CA497713766 | TP53 | c.987C>G (p.Thr329=) c.591C>G (p.Thr197=) c.708C>G (p.Thr236=) c.966C>G (p.Thr322=) c.782+640C>G (n.782+640C>G) c.47C>G c.870C>G (p.Thr290=) c.510C>G (p.Thr170=) c.954C>G (p.Thr318=) | dbSNP |
17 | g.7673541G>T | CA497713769 | TP53 | c.987C>A (p.Thr329=) c.591C>A (p.Thr197=) c.708C>A (p.Thr236=) c.966C>A (p.Thr322=) c.782+640C>A (n.782+640C>A) c.47C>A c.870C>A (p.Thr290=) c.510C>A (p.Thr170=) c.954C>A (p.Thr318=) | ClinVar dbSNP COSMIC |
17 | g.7673541_7673542delinsAA | CA645587346 | TP53 | c.986_987delinsTT (p.Thr329Ile) c.590_591delinsTT (p.Thr197Ile) c.707_708delinsTT (p.Thr236Ile) c.965_966delinsTT (p.Thr322Ile) c.782+639_782+640delinsTT (n.782+639_782+640delinsTT) c.46_47delinsTT c.869_870delinsTT (p.Thr290Ile) c.509_510delinsTT (p.Thr170Ile) c.953_954delinsTT (p.Thr318Ile) | COSMIC COSMIC |
17 | g.7673541_7673560delinsGGTGAAATATTCTCCATCCA | CA2245947495 | TP53 | c.968_987delinsTGGATGGAGAATATTTCACC (p.Leu323=) c.572_591delinsTGGATGGAGAATATTTCACC (p.Leu191=) c.689_708delinsTGGATGGAGAATATTTCACC (p.Leu230=) c.947_966delinsTGGATGGAGAATATTTCACC (p.Leu316=) c.782+621_782+640delinsTGGATGGAGAATATTTCACC (n.782+621_782+640delinsTGGATGGAGAATATTTCACC) c.28_47delinsTGGATGGAGAATATTTCACC c.851_870delinsTGGATGGAGAATATTTCACC (p.Leu284=) c.491_510delinsTGGATGGAGAATATTTCACC (p.Leu164=) c.935_954delinsTGGATGGAGAATATTTCACC (p.Leu312=) | |
17 | g.7673542G>A | CA287486504 | TP53 | c.986C>T (p.Thr329Ile) c.590C>T (p.Thr197Ile) c.707C>T (p.Thr236Ile) c.965C>T (p.Thr322Ile) c.782+639C>T (n.782+639C>T) c.46C>T c.869C>T (p.Thr290Ile) c.509C>T (p.Thr170Ile) c.953C>T (p.Thr318Ile) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
17 | g.7673542G>C | CA397835725 | TP53 | c.986C>G (p.Thr329Ser) c.590C>G (p.Thr197Ser) c.707C>G (p.Thr236Ser) c.965C>G (p.Thr322Ser) c.782+639C>G (n.782+639C>G) c.46C>G c.869C>G (p.Thr290Ser) c.509C>G (p.Thr170Ser) c.953C>G (p.Thr318Ser) | dbSNP |
17 | g.7673542G= | CA2245947503 | TP53 | c.986C= (p.Thr329=) c.590C= (p.Thr197=) c.707C= (p.Thr236=) c.965C= (p.Thr322=) c.782+639C= (n.782+639C=) c.46C= c.869C= (p.Thr290=) c.509C= (p.Thr170=) c.953C= (p.Thr318=) | |
17 | g.7673542G>T | CA397835730 | TP53 | c.986C>A (p.Thr329Asn) c.590C>A (p.Thr197Asn) c.707C>A (p.Thr236Asn) c.965C>A (p.Thr322Asn) c.782+639C>A (n.782+639C>A) c.46C>A c.869C>A (p.Thr290Asn) c.509C>A (p.Thr170Asn) c.953C>A (p.Thr318Asn) | dbSNP |
17 | g.7673545_7673563del | CA913188778 | TP53 | c.968_986del (p.Leu323ProfsTer16) c.572_590del (p.Leu191ProfsTer16) c.689_707del (p.Leu230ProfsTer16) c.947_965del (p.Leu316ProfsTer16) c.968_986del (p.Leu323ProfsTer23) c.782+621_782+639del (n.782+621_782+639del) c.968_986del (p.Leu323ProfsTer22) c.968_986del (p.Leu323ProfsTer14) c.572_590del (p.Leu191ProfsTer14) c.572_590del (p.Leu191ProfsTer?) c.572_590del (p.Leu191ProfsTer22) c.28_46del c.851_869del (p.Leu284ProfsTer16) c.851_869del (p.Leu284ProfsTer14) c.491_509del (p.Leu164ProfsTer14) c.935_953del (p.Leu312ProfsTer16) c.491_509del (p.Leu164ProfsTer22) c.491_509del (p.Leu164ProfsTer16) c.851_869del (p.Leu284ProfsTer22) | ClinVar dbSNP |
17 | g.7673543T>A | CA397835737 | TP53 | c.985A>T (p.Thr329Ser) c.589A>T (p.Thr197Ser) c.706A>T (p.Thr236Ser) c.964A>T (p.Thr322Ser) c.782+638A>T (n.782+638A>T) c.45A>T c.868A>T (p.Thr290Ser) c.508A>T (p.Thr170Ser) c.952A>T (p.Thr318Ser) | dbSNP |
17 | g.7673543T>C | CA397835735 | TP53 | c.985A>G (p.Thr329Ala) c.589A>G (p.Thr197Ala) c.706A>G (p.Thr236Ala) c.964A>G (p.Thr322Ala) c.782+638A>G (n.782+638A>G) c.45A>G c.868A>G (p.Thr290Ala) c.508A>G (p.Thr170Ala) c.952A>G (p.Thr318Ala) | ClinVar dbSNP gnomAD v4 |
17 | g.7673543T>G | CA397835733 | TP53 | c.985A>C (p.Thr329Pro) c.589A>C (p.Thr197Pro) c.706A>C (p.Thr236Pro) c.964A>C (p.Thr322Pro) c.782+638A>C (n.782+638A>C) c.45A>C c.868A>C (p.Thr290Pro) c.508A>C (p.Thr170Pro) c.952A>C (p.Thr318Pro) | dbSNP |
17 | g.7673543T= | CA2245947510 | TP53 | c.985A= (p.Thr329=) c.589A= (p.Thr197=) c.706A= (p.Thr236=) c.964A= (p.Thr322=) c.782+638A= (n.782+638A=) c.45A= c.868A= (p.Thr290=) c.508A= (p.Thr170=) c.952A= (p.Thr318=) | |
17 | g.7673543_7673546dup | CA2825002630 | TP53 | c.982_985dup (p.Thr329IlefsTer9) c.586_589dup (p.Thr197IlefsTer9) c.703_706dup (p.Thr236IlefsTer9) c.961_964dup (p.Thr322IlefsTer9) c.982_985dup (p.Thr329IlefsTer?) c.782+635_782+638dup (n.782+635_782+638dup) c.982_985dup (p.Thr329IlefsTer19) c.982_985dup (p.Thr329IlefsTer8) c.586_589dup (p.Thr197IlefsTer8) c.586_589dup (p.Thr197IlefsTer?) c.586_589dup (p.Thr197IlefsTer19) c.42_45dup c.865_868dup (p.Thr290IlefsTer9) c.865_868dup (p.Thr290IlefsTer8) c.505_508dup (p.Thr170IlefsTer8) c.949_952dup (p.Thr318IlefsTer9) c.505_508dup (p.Thr170IlefsTer19) c.505_508dup (p.Thr170IlefsTer9) c.865_868dup (p.Thr290IlefsTer19) | ClinVar |
17 | g.7673544G>A | CA16608656 | TP53 | c.984C>T (p.Phe328=) c.588C>T (p.Phe196=) c.705C>T (p.Phe235=) c.963C>T (p.Phe321=) c.782+637C>T (n.782+637C>T) c.44C>T c.867C>T (p.Phe289=) c.507C>T (p.Phe169=) c.951C>T (p.Phe317=) | ClinVar dbSNP COSMIC |
17 | g.7673544G>C | CA397835743 | TP53 | c.984C>G (p.Phe328Leu) c.588C>G (p.Phe196Leu) c.705C>G (p.Phe235Leu) c.963C>G (p.Phe321Leu) c.782+637C>G (n.782+637C>G) c.44C>G c.867C>G (p.Phe289Leu) c.507C>G (p.Phe169Leu) c.951C>G (p.Phe317Leu) | dbSNP |
17 | g.7673544G= | CA2245947520 | TP53 | c.984C= (p.Phe328=) c.588C= (p.Phe196=) c.705C= (p.Phe235=) c.963C= (p.Phe321=) c.782+637C= (n.782+637C=) c.44C= c.867C= (p.Phe289=) c.507C= (p.Phe169=) c.951C= (p.Phe317=) | |
17 | g.7673544G>T | CA397835745 | TP53 | c.984C>A (p.Phe328Leu) c.588C>A (p.Phe196Leu) c.705C>A (p.Phe235Leu) c.963C>A (p.Phe321Leu) c.782+637C>A (n.782+637C>A) c.44C>A c.867C>A (p.Phe289Leu) c.507C>A (p.Phe169Leu) c.951C>A (p.Phe317Leu) | dbSNP |
17 | g.7673544_7673545insT | CA645587347 | TP53 | c.983_984insA (p.Phe328LeufsTer9) c.587_588insA (p.Phe196LeufsTer9) c.704_705insA (p.Phe235LeufsTer9) c.962_963insA (p.Phe321LeufsTer9) c.983_984insA (p.Phe328LeufsTer?) c.782+636_782+637insA (n.782+636_782+637insA) c.983_984insA (p.Phe328LeufsTer19) c.983_984insA (p.Phe328LeufsTer8) c.587_588insA (p.Phe196LeufsTer8) c.587_588insA (p.Phe196LeufsTer?) c.587_588insA (p.Phe196LeufsTer19) c.43_44insA c.866_867insA (p.Phe289LeufsTer9) c.866_867insA (p.Phe289LeufsTer8) c.506_507insA (p.Phe169LeufsTer8) c.950_951insA (p.Phe317LeufsTer9) c.506_507insA (p.Phe169LeufsTer19) c.506_507insA (p.Phe169LeufsTer9) c.866_867insA (p.Phe289LeufsTer19) | COSMIC |
17 | g.7673545A= | CA2245947539 | TP53 | c.983T= (p.Phe328=) c.587T= (p.Phe196=) c.704T= (p.Phe235=) c.962T= (p.Phe321=) c.782+636T= (n.782+636T=) c.43T= c.866T= (p.Phe289=) c.506T= (p.Phe169=) c.950T= (p.Phe317=) | |
17 | g.7673545A>C | CA397835749 | TP53 | c.983T>G (p.Phe328Cys) c.587T>G (p.Phe196Cys) c.704T>G (p.Phe235Cys) c.962T>G (p.Phe321Cys) c.782+636T>G (n.782+636T>G) c.43T>G c.866T>G (p.Phe289Cys) c.506T>G (p.Phe169Cys) c.950T>G (p.Phe317Cys) | |
17 | g.7673545A>G | CA397835751 | TP53 | c.983T>C (p.Phe328Ser) c.587T>C (p.Phe196Ser) c.704T>C (p.Phe235Ser) c.962T>C (p.Phe321Ser) c.782+636T>C (n.782+636T>C) c.43T>C c.866T>C (p.Phe289Ser) c.506T>C (p.Phe169Ser) c.950T>C (p.Phe317Ser) | ClinVar dbSNP COSMIC |
17 | g.7673545A>T | CA397835754 | TP53 | c.983T>A (p.Phe328Tyr) c.587T>A (p.Phe196Tyr) c.704T>A (p.Phe235Tyr) c.962T>A (p.Phe321Tyr) c.782+636T>A (n.782+636T>A) c.43T>A c.866T>A (p.Phe289Tyr) c.506T>A (p.Phe169Tyr) c.950T>A (p.Phe317Tyr) | dbSNP |
17 | g.7673547dup | CA10603410 | TP53 | c.983dup (p.Thr329HisfsTer8) c.587dup (p.Thr197HisfsTer8) c.704dup (p.Thr236HisfsTer8) c.962dup (p.Thr322HisfsTer8) c.983dup (p.Thr329HisfsTer?) c.782+636dup (n.782+636dup) c.983dup (p.Thr329HisfsTer18) c.983dup (p.Thr329HisfsTer7) c.587dup (p.Thr197HisfsTer7) c.587dup (p.Thr197HisfsTer?) c.587dup (p.Thr197HisfsTer18) c.43dup c.866dup (p.Thr290HisfsTer8) c.866dup (p.Thr290HisfsTer7) c.506dup (p.Thr170HisfsTer7) c.950dup (p.Thr318HisfsTer8) c.506dup (p.Thr170HisfsTer18) c.506dup (p.Thr170HisfsTer8) c.866dup (p.Thr290HisfsTer18) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673546_7673547dup | CA2573154629 | TP53 | c.982_983dup (p.Thr329SerfsTer17) c.586_587dup (p.Thr197SerfsTer17) c.703_704dup (p.Thr236SerfsTer17) c.961_962dup (p.Thr322SerfsTer17) c.982_983dup (p.Thr329SerfsTer24) c.782+635_782+636dup (n.782+635_782+636dup) c.982_983dup (p.Thr329SerfsTer23) c.982_983dup (p.Thr329SerfsTer15) c.586_587dup (p.Thr197SerfsTer15) c.586_587dup (p.Thr197SerfsTer?) c.586_587dup (p.Thr197SerfsTer23) c.42_43dup c.865_866dup (p.Thr290SerfsTer17) c.865_866dup (p.Thr290SerfsTer15) c.505_506dup (p.Thr170SerfsTer15) c.949_950dup (p.Thr318SerfsTer17) c.505_506dup (p.Thr170SerfsTer23) c.505_506dup (p.Thr170SerfsTer17) c.865_866dup (p.Thr290SerfsTer23) | ClinVar dbSNP |
17 | g.7673547del | CA497713799 | TP53 | c.983del (p.Phe328SerfsTer17) c.587del (p.Phe196SerfsTer17) c.704del (p.Phe235SerfsTer17) c.962del (p.Phe321SerfsTer17) c.983del (p.Phe328SerfsTer24) c.782+636del (n.782+636del) c.983del (p.Phe328SerfsTer23) c.983del (p.Phe328SerfsTer15) c.587del (p.Phe196SerfsTer15) c.587del (p.Phe196SerfsTer?) c.587del (p.Phe196SerfsTer23) c.43del c.866del (p.Phe289SerfsTer17) c.866del (p.Phe289SerfsTer15) c.506del (p.Phe169SerfsTer15) c.950del (p.Phe317SerfsTer17) c.506del (p.Phe169SerfsTer23) c.506del (p.Phe169SerfsTer17) c.866del (p.Phe289SerfsTer23) | COSMIC COSMIC COSMIC COSMIC |
17 | g.7673545_7673546insT | CA497713806 | TP53 | c.982_983insA (p.Phe328TyrfsTer9) c.586_587insA (p.Phe196TyrfsTer9) c.703_704insA (p.Phe235TyrfsTer9) c.961_962insA (p.Phe321TyrfsTer9) c.982_983insA (p.Phe328TyrfsTer?) c.782+635_782+636insA (n.782+635_782+636insA) c.982_983insA (p.Phe328TyrfsTer19) c.982_983insA (p.Phe328TyrfsTer8) c.586_587insA (p.Phe196TyrfsTer8) c.586_587insA (p.Phe196TyrfsTer?) c.586_587insA (p.Phe196TyrfsTer19) c.42_43insA c.865_866insA (p.Phe289TyrfsTer9) c.865_866insA (p.Phe289TyrfsTer8) c.505_506insA (p.Phe169TyrfsTer8) c.949_950insA (p.Phe317TyrfsTer9) c.505_506insA (p.Phe169TyrfsTer19) c.505_506insA (p.Phe169TyrfsTer9) c.865_866insA (p.Phe289TyrfsTer19) | |
17 | g.7673546A>C | CA397835758 | TP53 | c.982T>G (p.Phe328Val) c.586T>G (p.Phe196Val) c.703T>G (p.Phe235Val) c.961T>G (p.Phe321Val) c.782+635T>G (n.782+635T>G) c.42T>G c.865T>G (p.Phe289Val) c.505T>G (p.Phe169Val) c.949T>G (p.Phe317Val) | COSMIC |
17 | g.7673546A>G | CA397835759 | TP53 | c.982T>C (p.Phe328Leu) c.586T>C (p.Phe196Leu) c.703T>C (p.Phe235Leu) c.961T>C (p.Phe321Leu) c.782+635T>C (n.782+635T>C) c.42T>C c.865T>C (p.Phe289Leu) c.505T>C (p.Phe169Leu) c.949T>C (p.Phe317Leu) | |
17 | g.7673546A>T | CA397835761 | TP53 | c.982T>A (p.Phe328Ile) c.586T>A (p.Phe196Ile) c.703T>A (p.Phe235Ile) c.961T>A (p.Phe321Ile) c.782+635T>A (n.782+635T>A) c.42T>A c.865T>A (p.Phe289Ile) c.505T>A (p.Phe169Ile) c.949T>A (p.Phe317Ile) | dbSNP |
17 | g.7673546_7673548delinsAAT | CA2245947548 | TP53 | c.980_982delinsATT (p.Tyr327=) c.584_586delinsATT (p.Tyr195=) c.701_703delinsATT (p.Tyr234=) c.959_961delinsATT (p.Tyr320=) c.782+633_782+635delinsATT (n.782+633_782+635delinsATT) c.40_42delinsATT c.863_865delinsATT (p.Tyr288=) c.503_505delinsATT (p.Tyr168=) c.947_949delinsATT (p.Tyr316=) | |
17 | g.7673547A= | CA2245947559 | TP53 | c.981T= (p.Tyr327=) c.585T= (p.Tyr195=) c.702T= (p.Tyr234=) c.960T= (p.Tyr320=) c.782+634T= (n.782+634T=) c.41T= c.864T= (p.Tyr288=) c.504T= (p.Tyr168=) c.948T= (p.Tyr316=) | |
17 | g.7673547A>C | CA10584585 | TP53 | c.981T>G (p.Tyr327Ter) c.585T>G (p.Tyr195Ter) c.702T>G (p.Tyr234Ter) c.960T>G (p.Tyr320Ter) c.782+634T>G (n.782+634T>G) c.41T>G c.864T>G (p.Tyr288Ter) c.504T>G (p.Tyr168Ter) c.948T>G (p.Tyr316Ter) | ClinVar dbSNP COSMIC COSMIC |
17 | g.7673547A>G | CA497713821 | TP53 | c.981T>C (p.Tyr327=) c.585T>C (p.Tyr195=) c.702T>C (p.Tyr234=) c.960T>C (p.Tyr320=) c.782+634T>C (n.782+634T>C) c.41T>C c.864T>C (p.Tyr288=) c.504T>C (p.Tyr168=) c.948T>C (p.Tyr316=) | dbSNP |
17 | g.7673547A>T | CA397835766 | TP53 | c.981T>A (p.Tyr327Ter) c.585T>A (p.Tyr195Ter) c.702T>A (p.Tyr234Ter) c.960T>A (p.Tyr320Ter) c.782+634T>A (n.782+634T>A) c.41T>A c.864T>A (p.Tyr288Ter) c.504T>A (p.Tyr168Ter) c.948T>A (p.Tyr316Ter) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673549_7673550del | CA645587348 | TP53 | c.980_981del (p.Tyr327PhefsTer9) c.584_585del (p.Tyr195PhefsTer9) c.701_702del (p.Tyr234PhefsTer9) c.959_960del (p.Tyr320PhefsTer9) c.980_981del (p.Tyr327PhefsTer?) c.782+633_782+634del (n.782+633_782+634del) c.980_981del (p.Tyr327PhefsTer19) c.980_981del (p.Tyr327PhefsTer8) c.584_585del (p.Tyr195PhefsTer8) c.584_585del (p.Tyr195PhefsTer?) c.584_585del (p.Tyr195PhefsTer19) c.40_41del c.863_864del (p.Tyr288PhefsTer9) c.863_864del (p.Tyr288PhefsTer8) c.503_504del (p.Tyr168PhefsTer8) c.947_948del (p.Tyr316PhefsTer9) c.503_504del (p.Tyr168PhefsTer19) c.503_504del (p.Tyr168PhefsTer9) c.863_864del (p.Tyr288PhefsTer19) | ClinVar dbSNP COSMIC |
17 | g.7673548T>A | CA397835768 | TP53 | c.980A>T (p.Tyr327Phe) c.584A>T (p.Tyr195Phe) c.701A>T (p.Tyr234Phe) c.959A>T (p.Tyr320Phe) c.782+633A>T (n.782+633A>T) c.40A>T c.863A>T (p.Tyr288Phe) c.503A>T (p.Tyr168Phe) c.947A>T (p.Tyr316Phe) | dbSNP |
17 | g.7673548T>C | CA397835771 | TP53 | c.980A>G (p.Tyr327Cys) c.584A>G (p.Tyr195Cys) c.701A>G (p.Tyr234Cys) c.959A>G (p.Tyr320Cys) c.782+633A>G (n.782+633A>G) c.40A>G c.863A>G (p.Tyr288Cys) c.503A>G (p.Tyr168Cys) c.947A>G (p.Tyr316Cys) | ClinVar dbSNP |
17 | g.7673548T>G | CA397835778 | TP53 | c.980A>C (p.Tyr327Ser) c.584A>C (p.Tyr195Ser) c.701A>C (p.Tyr234Ser) c.959A>C (p.Tyr320Ser) c.782+633A>C (n.782+633A>C) c.40A>C c.863A>C (p.Tyr288Ser) c.503A>C (p.Tyr168Ser) c.947A>C (p.Tyr316Ser) | dbSNP |
17 | g.7673548_7673549insTT | CA645587349 | TP53 | c.980_981insAA (p.Tyr327Ter) c.584_585insAA (p.Tyr195Ter) c.701_702insAA (p.Tyr234Ter) c.959_960insAA (p.Tyr320Ter) c.782+633_782+634insAA (n.782+633_782+634insAA) c.40_41insAA c.863_864insAA (p.Tyr288Ter) c.503_504insAA (p.Tyr168Ter) c.947_948insAA (p.Tyr316Ter) | COSMIC |
17 | g.7673549A>C | CA397835781 | TP53 | c.979T>G (p.Tyr327Asp) c.583T>G (p.Tyr195Asp) c.700T>G (p.Tyr234Asp) c.958T>G (p.Tyr320Asp) c.782+632T>G (n.782+632T>G) c.39T>G c.862T>G (p.Tyr288Asp) c.502T>G (p.Tyr168Asp) c.946T>G (p.Tyr316Asp) | dbSNP COSMIC |
17 | g.7673549A>G | CA397835786 | TP53 | c.979T>C (p.Tyr327His) c.583T>C (p.Tyr195His) c.700T>C (p.Tyr234His) c.958T>C (p.Tyr320His) c.782+632T>C (n.782+632T>C) c.39T>C c.862T>C (p.Tyr288His) c.502T>C (p.Tyr168His) c.946T>C (p.Tyr316His) | |
17 | g.7673549A>T | CA397835783 | TP53 | c.979T>A (p.Tyr327Asn) c.583T>A (p.Tyr195Asn) c.700T>A (p.Tyr234Asn) c.958T>A (p.Tyr320Asn) c.782+632T>A (n.782+632T>A) c.39T>A c.862T>A (p.Tyr288Asn) c.502T>A (p.Tyr168Asn) c.946T>A (p.Tyr316Asn) | dbSNP |
17 | g.7673550T>A | CA287486513 | TP53 | c.978A>T (p.Glu326Asp) c.582A>T (p.Glu194Asp) c.699A>T (p.Glu233Asp) c.957A>T (p.Glu319Asp) c.782+631A>T (n.782+631A>T) c.38A>T c.861A>T (p.Glu287Asp) c.501A>T (p.Glu167Asp) c.945A>T (p.Glu315Asp) | ClinVar dbSNP gnomAD v4 |
17 | g.7673550T>C | CA497713840 | TP53 | c.978A>G (p.Glu326=) c.582A>G (p.Glu194=) c.699A>G (p.Glu233=) c.957A>G (p.Glu319=) c.782+631A>G (n.782+631A>G) c.38A>G c.861A>G (p.Glu287=) c.501A>G (p.Glu167=) c.945A>G (p.Glu315=) | ClinVar dbSNP |
17 | g.7673550T>G | CA397835791 | TP53 | c.978A>C (p.Glu326Asp) c.582A>C (p.Glu194Asp) c.699A>C (p.Glu233Asp) c.957A>C (p.Glu319Asp) c.782+631A>C (n.782+631A>C) c.38A>C c.861A>C (p.Glu287Asp) c.501A>C (p.Glu167Asp) c.945A>C (p.Glu315Asp) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.7673550T= | CA2245947569 | TP53 | c.978A= (p.Glu326=) c.582A= (p.Glu194=) c.699A= (p.Glu233=) c.957A= (p.Glu319=) c.782+631A= (n.782+631A=) c.38A= c.861A= (p.Glu287=) c.501A= (p.Glu167=) c.945A= (p.Glu315=) | |
17 | g.7673551_7673553del | CA2635874179 | TP53 | c.976_978del (p.Glu326del) c.580_582del (p.Glu194del) c.697_699del (p.Glu233del) c.955_957del (p.Glu319del) c.782+629_782+631del (n.782+629_782+631del) c.36_38del c.859_861del (p.Glu287del) c.499_501del (p.Glu167del) c.943_945del (p.Glu315del) | gnomAD v4 |
17 | g.7673551T>A | CA397835794 | TP53 | c.977A>T (p.Glu326Val) c.581A>T (p.Glu194Val) c.698A>T (p.Glu233Val) c.956A>T (p.Glu319Val) c.782+630A>T (n.782+630A>T) c.37A>T c.860A>T (p.Glu287Val) c.500A>T (p.Glu167Val) c.944A>T (p.Glu315Val) | ClinVar dbSNP |
17 | g.7673551T>C | CA397835798 | TP53 | c.977A>G (p.Glu326Gly) c.581A>G (p.Glu194Gly) c.698A>G (p.Glu233Gly) c.956A>G (p.Glu319Gly) c.782+630A>G (n.782+630A>G) c.37A>G c.860A>G (p.Glu287Gly) c.500A>G (p.Glu167Gly) c.944A>G (p.Glu315Gly) | dbSNP |
17 | g.7673551T>G | CA397835801 | TP53 | c.977A>C (p.Glu326Ala) c.581A>C (p.Glu194Ala) c.698A>C (p.Glu233Ala) c.956A>C (p.Glu319Ala) c.782+630A>C (n.782+630A>C) c.37A>C c.860A>C (p.Glu287Ala) c.500A>C (p.Glu167Ala) c.944A>C (p.Glu315Ala) | dbSNP |
17 | g.7673553_7673554dup | CA915949514 | TP53 | c.976_977dup (p.Tyr327AsnfsTer19) c.580_581dup (p.Tyr195AsnfsTer19) c.697_698dup (p.Tyr234AsnfsTer19) c.955_956dup (p.Tyr320AsnfsTer19) c.976_977dup (p.Tyr327AsnfsTer26) c.782+629_782+630dup (n.782+629_782+630dup) c.976_977dup (p.Tyr327AsnfsTer25) c.976_977dup (p.Tyr327AsnfsTer17) c.580_581dup (p.Tyr195AsnfsTer17) c.580_581dup (p.Tyr195AsnfsTer?) c.580_581dup (p.Tyr195AsnfsTer25) c.36_37dup c.859_860dup (p.Tyr288AsnfsTer19) c.859_860dup (p.Tyr288AsnfsTer17) c.499_500dup (p.Tyr168AsnfsTer17) c.943_944dup (p.Tyr316AsnfsTer19) c.499_500dup (p.Tyr168AsnfsTer25) c.499_500dup (p.Tyr168AsnfsTer19) c.859_860dup (p.Tyr288AsnfsTer25) | ClinVar dbSNP |
17 | g.7673552C>A | CA10580908 | TP53 | c.976G>T (p.Glu326Ter) c.580G>T (p.Glu194Ter) c.697G>T (p.Glu233Ter) c.955G>T (p.Glu319Ter) c.782+629G>T (n.782+629G>T) c.36G>T c.859G>T (p.Glu287Ter) c.499G>T (p.Glu167Ter) c.943G>T (p.Glu315Ter) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673552C= | CA2245947579 | TP53 | c.976G= (p.Glu326=) c.580G= (p.Glu194=) c.697G= (p.Glu233=) c.955G= (p.Glu319=) c.782+629G= (n.782+629G=) c.36G= c.859G= (p.Glu287=) c.499G= (p.Glu167=) c.943G= (p.Glu315=) | |
17 | g.7673552C>G | CA397835806 | TP53 | c.976G>C (p.Glu326Gln) c.580G>C (p.Glu194Gln) c.697G>C (p.Glu233Gln) c.955G>C (p.Glu319Gln) c.782+629G>C (n.782+629G>C) c.36G>C c.859G>C (p.Glu287Gln) c.499G>C (p.Glu167Gln) c.943G>C (p.Glu315Gln) | dbSNP |
17 | g.7673552C>T | CA397835809 | TP53 | c.976G>A (p.Glu326Lys) c.580G>A (p.Glu194Lys) c.697G>A (p.Glu233Lys) c.955G>A (p.Glu319Lys) c.782+629G>A (n.782+629G>A) c.36G>A c.859G>A (p.Glu287Lys) c.499G>A (p.Glu167Lys) c.943G>A (p.Glu315Lys) | dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673553T>A | CA497713884 | TP53 | c.975A>T (p.Gly325=) c.579A>T (p.Gly193=) c.696A>T (p.Gly232=) c.954A>T (p.Gly318=) c.782+628A>T (n.782+628A>T) c.35A>T c.858A>T (p.Gly286=) c.498A>T (p.Gly166=) c.942A>T (p.Gly314=) | |
17 | g.7673553T>C | CA497713893 | TP53 | c.975A>G (p.Gly325=) c.579A>G (p.Gly193=) c.696A>G (p.Gly232=) c.954A>G (p.Gly318=) c.782+628A>G (n.782+628A>G) c.35A>G c.858A>G (p.Gly286=) c.498A>G (p.Gly166=) c.942A>G (p.Gly314=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
17 | g.7673553T>G | CA497713894 | TP53 | c.975A>C (p.Gly325=) c.579A>C (p.Gly193=) c.696A>C (p.Gly232=) c.954A>C (p.Gly318=) c.782+628A>C (n.782+628A>C) c.35A>C c.858A>C (p.Gly286=) c.498A>C (p.Gly166=) c.942A>C (p.Gly314=) | |
17 | g.7673553T= | CA2245947582 | TP53 | c.975A= (p.Gly325=) c.579A= (p.Gly193=) c.696A= (p.Gly232=) c.954A= (p.Gly318=) c.782+628A= (n.782+628A=) c.35A= c.858A= (p.Gly286=) c.498A= (p.Gly166=) c.942A= (p.Gly314=) | |
17 | g.7673554C>A | CA000516 | TP53 | c.974G>T (p.Gly325Val) c.578G>T (p.Gly193Val) c.695G>T (p.Gly232Val) c.953G>T (p.Gly318Val) c.782+627G>T (n.782+627G>T) c.34G>T c.857G>T (p.Gly286Val) c.497G>T (p.Gly166Val) c.941G>T (p.Gly314Val) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
17 | g.7673554C= | CA2245947593 | TP53 | c.974G= (p.Gly325=) c.578G= (p.Gly193=) c.695G= (p.Gly232=) c.953G= (p.Gly318=) c.782+627G= (n.782+627G=) c.34G= c.857G= (p.Gly286=) c.497G= (p.Gly166=) c.941G= (p.Gly314=) | |
17 | g.7673554C>G | CA397835813 | TP53 | c.974G>C (p.Gly325Ala) c.578G>C (p.Gly193Ala) c.695G>C (p.Gly232Ala) c.953G>C (p.Gly318Ala) c.782+627G>C (n.782+627G>C) c.34G>C c.857G>C (p.Gly286Ala) c.497G>C (p.Gly166Ala) c.941G>C (p.Gly314Ala) | dbSNP COSMIC |
17 | g.7673554C>T | CA397835817 | TP53 | c.974G>A (p.Gly325Glu) c.578G>A (p.Gly193Glu) c.695G>A (p.Gly232Glu) c.953G>A (p.Gly318Glu) c.782+627G>A (n.782+627G>A) c.34G>A c.857G>A (p.Gly286Glu) c.497G>A (p.Gly166Glu) c.941G>A (p.Gly314Glu) | ClinVar dbSNP COSMIC |
17 | g.7673555C>A | CA335679 | TP53 | c.973G>T (p.Gly325Ter) c.577G>T (p.Gly193Ter) c.694G>T (p.Gly232Ter) c.952G>T (p.Gly318Ter) c.782+626G>T (n.782+626G>T) c.33G>T c.856G>T (p.Gly286Ter) c.496G>T (p.Gly166Ter) c.940G>T (p.Gly314Ter) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673555C= | CA2245947602 | TP53 | c.973G= (p.Gly325=) c.577G= (p.Gly193=) c.694G= (p.Gly232=) c.952G= (p.Gly318=) c.782+626G= (n.782+626G=) c.33G= c.856G= (p.Gly286=) c.496G= (p.Gly166=) c.940G= (p.Gly314=) | |
17 | g.7673555C>G | CA397835825 | TP53 | c.973G>C (p.Gly325Arg) c.577G>C (p.Gly193Arg) c.694G>C (p.Gly232Arg) c.952G>C (p.Gly318Arg) c.782+626G>C (n.782+626G>C) c.33G>C c.856G>C (p.Gly286Arg) c.496G>C (p.Gly166Arg) c.940G>C (p.Gly314Arg) | dbSNP |
17 | g.7673555C>T | CA397835820 | TP53 | c.973G>A (p.Gly325Arg) c.577G>A (p.Gly193Arg) c.694G>A (p.Gly232Arg) c.952G>A (p.Gly318Arg) c.782+626G>A (n.782+626G>A) c.33G>A c.856G>A (p.Gly286Arg) c.496G>A (p.Gly166Arg) c.940G>A (p.Gly314Arg) | ClinVar dbSNP |
17 | g.7673556A>C | CA397835833 | TP53 | c.972T>G (p.Asp324Glu) c.576T>G (p.Asp192Glu) c.693T>G (p.Asp231Glu) c.951T>G (p.Asp317Glu) c.782+625T>G (n.782+625T>G) c.32T>G c.855T>G (p.Asp285Glu) c.495T>G (p.Asp165Glu) c.939T>G (p.Asp313Glu) | dbSNP COSMIC |
17 | g.7673556A>G | CA497713910 | TP53 | c.972T>C (p.Asp324=) c.576T>C (p.Asp192=) c.693T>C (p.Asp231=) c.951T>C (p.Asp317=) c.782+625T>C (n.782+625T>C) c.32T>C c.855T>C (p.Asp285=) c.495T>C (p.Asp165=) c.939T>C (p.Asp313=) | dbSNP COSMIC |
17 | g.7673556A>T | CA397835829 | TP53 | c.972T>A (p.Asp324Glu) c.576T>A (p.Asp192Glu) c.693T>A (p.Asp231Glu) c.951T>A (p.Asp317Glu) c.782+625T>A (n.782+625T>A) c.32T>A c.855T>A (p.Asp285Glu) c.495T>A (p.Asp165Glu) c.939T>A (p.Asp313Glu) | ClinVar dbSNP COSMIC |
17 | g.7673557del | CA497713915 | TP53 | c.971del (p.Asp324ValfsTer21) c.575del (p.Asp192ValfsTer21) c.692del (p.Asp231ValfsTer21) c.950del (p.Asp317ValfsTer21) c.971del (p.Asp324ValfsTer28) c.782+624del (n.782+624del) c.971del (p.Asp324ValfsTer27) c.971del (p.Asp324ValfsTer19) c.575del (p.Asp192ValfsTer19) c.575del (p.Asp192ValfsTer?) c.575del (p.Asp192ValfsTer27) c.31del c.854del (p.Asp285ValfsTer21) c.854del (p.Asp285ValfsTer19) c.494del (p.Asp165ValfsTer19) c.938del (p.Asp313ValfsTer21) c.494del (p.Asp165ValfsTer27) c.494del (p.Asp165ValfsTer21) c.854del (p.Asp285ValfsTer27) | COSMIC |
17 | g.7673557T>A | CA397835834 | TP53 | c.971A>T (p.Asp324Val) c.575A>T (p.Asp192Val) c.692A>T (p.Asp231Val) c.950A>T (p.Asp317Val) c.782+624A>T (n.782+624A>T) c.31A>T c.854A>T (p.Asp285Val) c.494A>T (p.Asp165Val) c.938A>T (p.Asp313Val) | |
17 | g.7673557T>C | CA397835837 | TP53 | c.971A>G (p.Asp324Gly) c.575A>G (p.Asp192Gly) c.692A>G (p.Asp231Gly) c.950A>G (p.Asp317Gly) c.782+624A>G (n.782+624A>G) c.31A>G c.854A>G (p.Asp285Gly) c.494A>G (p.Asp165Gly) c.938A>G (p.Asp313Gly) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.7673557T>G | CA397835840 | TP53 | c.971A>C (p.Asp324Ala) c.575A>C (p.Asp192Ala) c.692A>C (p.Asp231Ala) c.950A>C (p.Asp317Ala) c.782+624A>C (n.782+624A>C) c.31A>C c.854A>C (p.Asp285Ala) c.494A>C (p.Asp165Ala) c.938A>C (p.Asp313Ala) | dbSNP |
17 | g.7673557T= | CA2245947614 | TP53 | c.971A= (p.Asp324=) c.575A= (p.Asp192=) c.692A= (p.Asp231=) c.950A= (p.Asp317=) c.782+624A= (n.782+624A=) c.31A= c.854A= (p.Asp285=) c.494A= (p.Asp165=) c.938A= (p.Asp313=) | |
17 | g.7673557_7673558delinsCT | CA645587350 | TP53 | c.970_971delinsAG (p.Asp324Ser) c.574_575delinsAG (p.Asp192Ser) c.691_692delinsAG (p.Asp231Ser) c.949_950delinsAG (p.Asp317Ser) c.782+623_782+624delinsAG (n.782+623_782+624delinsAG) c.30_31delinsAG c.853_854delinsAG (p.Asp285Ser) c.493_494delinsAG (p.Asp165Ser) c.937_938delinsAG (p.Asp313Ser) | COSMIC |
17 | g.7673557_7673558delinsTC | CA2245947611 | TP53 | c.970_971delinsGA (p.Asp324=) c.574_575delinsGA (p.Asp192=) c.691_692delinsGA (p.Asp231=) c.949_950delinsGA (p.Asp317=) c.782+623_782+624delinsGA (n.782+623_782+624delinsGA) c.30_31delinsGA c.853_854delinsGA (p.Asp285=) c.493_494delinsGA (p.Asp165=) c.937_938delinsGA (p.Asp313=) | |
17 | g.7673558C>A | CA397835843 | TP53 | c.970G>T (p.Asp324Tyr) c.574G>T (p.Asp192Tyr) c.691G>T (p.Asp231Tyr) c.949G>T (p.Asp317Tyr) c.782+623G>T (n.782+623G>T) c.30G>T c.853G>T (p.Asp285Tyr) c.493G>T (p.Asp165Tyr) c.937G>T (p.Asp313Tyr) | ClinVar dbSNP |
17 | g.7673558C= | CA2245947625 | TP53 | c.970G= (p.Asp324=) c.574G= (p.Asp192=) c.691G= (p.Asp231=) c.949G= (p.Asp317=) c.782+623G= (n.782+623G=) c.30G= c.853G= (p.Asp285=) c.493G= (p.Asp165=) c.937G= (p.Asp313=) | |
17 | g.7673558C>G | CA16620612 | TP53 | c.970G>C (p.Asp324His) c.574G>C (p.Asp192His) c.691G>C (p.Asp231His) c.949G>C (p.Asp317His) c.782+623G>C (n.782+623G>C) c.30G>C c.853G>C (p.Asp285His) c.493G>C (p.Asp165His) c.937G>C (p.Asp313His) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7673558C>T | CA397835847 | TP53 | c.970G>A (p.Asp324Asn) c.574G>A (p.Asp192Asn) c.691G>A (p.Asp231Asn) c.949G>A (p.Asp317Asn) c.782+623G>A (n.782+623G>A) c.30G>A c.853G>A (p.Asp285Asn) c.493G>A (p.Asp165Asn) c.937G>A (p.Asp313Asn) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
17 | g.7673559del | CA658683980 | TP53 | c.970del (p.Asp324MetfsTer21) c.574del (p.Asp192MetfsTer21) c.691del (p.Asp231MetfsTer21) c.949del (p.Asp317MetfsTer21) c.970del (p.Asp324MetfsTer28) c.782+623del (n.782+623del) c.970del (p.Asp324MetfsTer27) c.970del (p.Asp324MetfsTer19) c.574del (p.Asp192MetfsTer19) c.574del (p.Asp192MetfsTer?) c.574del (p.Asp192MetfsTer27) c.30del c.853del (p.Asp285MetfsTer21) c.853del (p.Asp285MetfsTer19) c.493del (p.Asp165MetfsTer19) c.937del (p.Asp313MetfsTer21) c.493del (p.Asp165MetfsTer27) c.493del (p.Asp165MetfsTer21) c.853del (p.Asp285MetfsTer27) | ClinVar dbSNP |
17 | g.7673558_7673580dup | CA645587351 | TP53 | c.948_970dup (p.Asp324AlafsTer29) c.552_574dup (p.Asp192AlafsTer29) c.669_691dup (p.Asp231AlafsTer29) c.927_949dup (p.Asp317AlafsTer29) c.948_970dup (p.Asp324AlafsTer36) c.782+601_782+623dup (n.782+601_782+623dup) c.948_970dup (p.Asp324AlafsTer35) c.948_970dup (p.Asp324AlafsTer27) c.552_574dup (p.Asp192AlafsTer27) c.552_574dup (p.Asp192AlafsTer?) c.552_574dup (p.Asp192AlafsTer35) c.8_30dup c.831_853dup (p.Asp285AlafsTer29) c.831_853dup (p.Asp285AlafsTer27) c.471_493dup (p.Asp165AlafsTer27) c.915_937dup (p.Asp313AlafsTer29) c.471_493dup (p.Asp165AlafsTer35) c.471_493dup (p.Asp165AlafsTer29) c.831_853dup (p.Asp285AlafsTer35) | COSMIC |
17 | g.7673559C>A | CA497713919 | TP53 | c.969G>T (p.Leu323=) c.573G>T (p.Leu191=) c.690G>T (p.Leu230=) c.948G>T (p.Leu316=) c.782+622G>T (n.782+622G>T) c.29G>T c.852G>T (p.Leu284=) c.492G>T (p.Leu164=) c.936G>T (p.Leu312=) | dbSNP |
17 | g.7673559C= | CA2245947634 | TP53 | c.969G= (p.Leu323=) c.573G= (p.Leu191=) c.690G= (p.Leu230=) c.948G= (p.Leu316=) c.782+622G= (n.782+622G=) c.29G= c.852G= (p.Leu284=) c.492G= (p.Leu164=) c.936G= (p.Leu312=) | |
17 | g.7673559C>G | CA497713923 | TP53 | c.969G>C (p.Leu323=) c.573G>C (p.Leu191=) c.690G>C (p.Leu230=) c.948G>C (p.Leu316=) c.782+622G>C (n.782+622G>C) c.29G>C c.852G>C (p.Leu284=) c.492G>C (p.Leu164=) c.936G>C (p.Leu312=) | ClinVar dbSNP |
17 | g.7673559C>T | CA000512 | TP53 | c.969G>A (p.Leu323=) c.573G>A (p.Leu191=) c.690G>A (p.Leu230=) c.948G>A (p.Leu316=) c.782+622G>A (n.782+622G>A) c.29G>A c.852G>A (p.Leu284=) c.492G>A (p.Leu164=) c.936G>A (p.Leu312=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.7673560A= | CA2245947643 | TP53 | c.968T= (p.Leu323=) c.572T= (p.Leu191=) c.689T= (p.Leu230=) c.947T= (p.Leu316=) c.782+621T= (n.782+621T=) c.28T= c.851T= (p.Leu284=) c.491T= (p.Leu164=) c.935T= (p.Leu312=) | |
17 | g.7673560A>C | CA397835852 | TP53 | c.968T>G (p.Leu323Arg) c.572T>G (p.Leu191Arg) c.689T>G (p.Leu230Arg) c.947T>G (p.Leu316Arg) c.782+621T>G (n.782+621T>G) c.28T>G c.851T>G (p.Leu284Arg) c.491T>G (p.Leu164Arg) c.935T>G (p.Leu312Arg) | COSMIC |
17 | g.7673560A>G | CA397835853 | TP53 | c.968T>C (p.Leu323Pro) c.572T>C (p.Leu191Pro) c.689T>C (p.Leu230Pro) c.947T>C (p.Leu316Pro) c.782+621T>C (n.782+621T>C) c.28T>C c.851T>C (p.Leu284Pro) c.491T>C (p.Leu164Pro) c.935T>C (p.Leu312Pro) | ClinVar dbSNP COSMIC |
17 | g.7673560A>T | CA397835857 | TP53 | c.968T>A (p.Leu323Gln) c.572T>A (p.Leu191Gln) c.689T>A (p.Leu230Gln) c.947T>A (p.Leu316Gln) c.782+621T>A (n.782+621T>A) c.28T>A c.851T>A (p.Leu284Gln) c.491T>A (p.Leu164Gln) c.935T>A (p.Leu312Gln) | dbSNP |
17 | g.7673560_7673561delinsCC | CA645587352 | TP53 | c.967_968delinsGG (p.Leu323Gly) c.571_572delinsGG (p.Leu191Gly) c.688_689delinsGG (p.Leu230Gly) c.946_947delinsGG (p.Leu316Gly) c.782+620_782+621delinsGG (n.782+620_782+621delinsGG) c.27_28delinsGG c.850_851delinsGG (p.Leu284Gly) c.490_491delinsGG (p.Leu164Gly) c.934_935delinsGG (p.Leu312Gly) | COSMIC |
17 | g.7673562_7673586del | CA645587353 | TP53 | c.944_968del (p.Ser315TrpfsTer22) c.548_572del (p.Ser183TrpfsTer22) c.665_689del (p.Ser222TrpfsTer22) c.923_947del (p.Ser308TrpfsTer22) c.944_968del (p.Ser315TrpfsTer29) c.782+597_782+621del (n.782+597_782+621del) c.944_968del (p.Ser315TrpfsTer28) c.944_968del (p.Ser315TrpfsTer20) c.548_572del (p.Ser183TrpfsTer20) c.548_572del (p.Ser183TrpfsTer?) c.548_572del (p.Ser183TrpfsTer28) c.4_28del c.827_851del (p.Ser276TrpfsTer22) c.827_851del (p.Ser276TrpfsTer20) c.467_491del (p.Ser156TrpfsTer20) c.911_935del (p.Ser304TrpfsTer22) c.467_491del (p.Ser156TrpfsTer28) c.467_491del (p.Ser156TrpfsTer22) c.827_851del (p.Ser276TrpfsTer28) | COSMIC |
17 | g.7673561del | CA497713940 | TP53 | c.967del (p.Leu323TrpfsTer22) c.571del (p.Leu191TrpfsTer22) c.688del (p.Leu230TrpfsTer22) c.946del (p.Leu316TrpfsTer22) c.967del (p.Leu323TrpfsTer29) c.782+620del (n.782+620del) c.967del (p.Leu323TrpfsTer28) c.967del (p.Leu323TrpfsTer20) c.571del (p.Leu191TrpfsTer20) c.571del (p.Leu191TrpfsTer?) c.571del (p.Leu191TrpfsTer28) c.27del c.850del (p.Leu284TrpfsTer22) c.850del (p.Leu284TrpfsTer20) c.490del (p.Leu164TrpfsTer20) c.934del (p.Leu312TrpfsTer22) c.490del (p.Leu164TrpfsTer28) c.490del (p.Leu164TrpfsTer22) c.850del (p.Leu284TrpfsTer28) | COSMIC |
17 | g.7673561G>A | CA497713934 | TP53 | c.967C>T (p.Leu323=) c.571C>T (p.Leu191=) c.688C>T (p.Leu230=) c.946C>T (p.Leu316=) c.782+620C>T (n.782+620C>T) c.27C>T c.850C>T (p.Leu284=) c.490C>T (p.Leu164=) c.934C>T (p.Leu312=) | dbSNP |
17 | g.7673561G>C | CA397835860 | TP53 | c.967C>G (p.Leu323Val) c.571C>G (p.Leu191Val) c.688C>G (p.Leu230Val) c.946C>G (p.Leu316Val) c.782+620C>G (n.782+620C>G) c.27C>G c.850C>G (p.Leu284Val) c.490C>G (p.Leu164Val) c.934C>G (p.Leu312Val) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
17 | g.7673561G= | CA2245947652 | TP53 | c.967C= (p.Leu323=) c.571C= (p.Leu191=) c.688C= (p.Leu230=) c.946C= (p.Leu316=) c.782+620C= (n.782+620C=) c.27C= c.850C= (p.Leu284=) c.490C= (p.Leu164=) c.934C= (p.Leu312=) | |
17 | g.7673561G>T | CA397835867 | TP53 | c.967C>A (p.Leu323Met) c.571C>A (p.Leu191Met) c.688C>A (p.Leu230Met) c.946C>A (p.Leu316Met) c.782+620C>A (n.782+620C>A) c.27C>A c.850C>A (p.Leu284Met) c.490C>A (p.Leu164Met) c.934C>A (p.Leu312Met) | dbSNP COSMIC |
17 | g.7673562T>A | CA497713943 | TP53 | c.966A>T (p.Pro322=) c.570A>T (p.Pro190=) c.687A>T (p.Pro229=) c.945A>T (p.Pro315=) c.782+619A>T (n.782+619A>T) c.26A>T c.849A>T (p.Pro283=) c.489A>T (p.Pro163=) c.933A>T (p.Pro311=) | |
17 | g.7673562T>C | CA497713945 | TP53 | c.966A>G (p.Pro322=) c.570A>G (p.Pro190=) c.687A>G (p.Pro229=) c.945A>G (p.Pro315=) c.782+619A>G (n.782+619A>G) c.26A>G c.849A>G (p.Pro283=) c.489A>G (p.Pro163=) c.933A>G (p.Pro311=) | ClinVar |
17 | g.7673562T>G | CA497713950 | TP53 | c.966A>C (p.Pro322=) c.570A>C (p.Pro190=) c.687A>C (p.Pro229=) c.945A>C (p.Pro315=) c.782+619A>C (n.782+619A>C) c.26A>C c.849A>C (p.Pro283=) c.489A>C (p.Pro163=) c.933A>C (p.Pro311=) | ClinVar |
17 | g.7673562dup | CA2245947657 | TP53 | c.966dup (p.Leu323ThrfsTer14) c.570dup (p.Leu191ThrfsTer14) c.687dup (p.Leu230ThrfsTer14) c.945dup (p.Leu316ThrfsTer14) c.966dup (p.Leu323ThrfsTer?) c.782+619dup (n.782+619dup) c.966dup (p.Leu323ThrfsTer24) c.966dup (p.Leu323ThrfsTer13) c.570dup (p.Leu191ThrfsTer13) c.570dup (p.Leu191ThrfsTer?) c.570dup (p.Leu191ThrfsTer24) c.26dup c.849dup (p.Leu284ThrfsTer14) c.849dup (p.Leu284ThrfsTer13) c.489dup (p.Leu164ThrfsTer13) c.933dup (p.Leu312ThrfsTer14) c.489dup (p.Leu164ThrfsTer24) c.489dup (p.Leu164ThrfsTer14) c.849dup (p.Leu284ThrfsTer24) | dbSNP |
17 | g.7673563G>A | CA397835873 | TP53 | c.965C>T (p.Pro322Leu) c.569C>T (p.Pro190Leu) c.686C>T (p.Pro229Leu) c.944C>T (p.Pro315Leu) c.782+618C>T (n.782+618C>T) c.25C>T c.848C>T (p.Pro283Leu) c.488C>T (p.Pro163Leu) c.932C>T (p.Pro311Leu) | dbSNP COSMIC |
17 | g.7673563G>C | CA397835872 | TP53 | c.965C>G (p.Pro322Arg) c.569C>G (p.Pro190Arg) c.686C>G (p.Pro229Arg) c.944C>G (p.Pro315Arg) c.782+618C>G (n.782+618C>G) c.25C>G c.848C>G (p.Pro283Arg) c.488C>G (p.Pro163Arg) c.932C>G (p.Pro311Arg) | ClinVar dbSNP COSMIC |
17 | g.7673563G>T | CA397835870 | TP53 | c.965C>A (p.Pro322Gln) c.569C>A (p.Pro190Gln) c.686C>A (p.Pro229Gln) c.944C>A (p.Pro315Gln) c.782+618C>A (n.782+618C>A) c.25C>A c.848C>A (p.Pro283Gln) c.488C>A (p.Pro163Gln) c.932C>A (p.Pro311Gln) | dbSNP |
17 | g.7673564del | CA497713957 | TP53 | c.965del (p.Pro322HisfsTer23) c.569del (p.Pro190HisfsTer23) c.686del (p.Pro229HisfsTer23) c.944del (p.Pro315HisfsTer23) c.965del (p.Pro322HisfsTer30) c.782+618del (n.782+618del) c.965del (p.Pro322HisfsTer29) c.965del (p.Pro322HisfsTer21) c.569del (p.Pro190HisfsTer21) c.569del (p.Pro190HisfsTer?) c.569del (p.Pro190HisfsTer29) c.25del c.848del (p.Pro283HisfsTer23) c.848del (p.Pro283HisfsTer21) c.488del (p.Pro163HisfsTer21) c.932del (p.Pro311HisfsTer23) c.488del (p.Pro163HisfsTer29) c.488del (p.Pro163HisfsTer23) c.848del (p.Pro283HisfsTer29) | ClinVar COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7673564G>A | CA336073 | TP53 | c.964C>T (p.Pro322Ser) c.568C>T (p.Pro190Ser) c.685C>T (p.Pro229Ser) c.943C>T (p.Pro315Ser) c.782+617C>T (n.782+617C>T) c.24C>T c.847C>T (p.Pro283Ser) c.487C>T (p.Pro163Ser) c.931C>T (p.Pro311Ser) | ClinVar dbSNP gnomAD v4 |
17 | g.7673564G>C | CA397835876 | TP53 | c.964C>G (p.Pro322Ala) c.568C>G (p.Pro190Ala) c.685C>G (p.Pro229Ala) c.943C>G (p.Pro315Ala) c.782+617C>G (n.782+617C>G) c.24C>G c.847C>G (p.Pro283Ala) c.487C>G (p.Pro163Ala) c.931C>G (p.Pro311Ala) | ClinVar dbSNP |
17 | g.7673564G= | CA2245947670 | TP53 | c.964C= (p.Pro322=) c.568C= (p.Pro190=) c.685C= (p.Pro229=) c.943C= (p.Pro315=) c.782+617C= (n.782+617C=) c.24C= c.847C= (p.Pro283=) c.487C= (p.Pro163=) c.931C= (p.Pro311=) | |
17 | g.7673564G>T | CA10580909 | TP53 | c.964C>A (p.Pro322Thr) c.568C>A (p.Pro190Thr) c.685C>A (p.Pro229Thr) c.943C>A (p.Pro315Thr) c.782+617C>A (n.782+617C>A) c.24C>A c.847C>A (p.Pro283Thr) c.487C>A (p.Pro163Thr) c.931C>A (p.Pro311Thr) | ClinVar dbSNP |
17 | g.7673565T>A | CA397835878 | TP53 | c.963A>T (p.Lys321Asn) c.567A>T (p.Lys189Asn) c.684A>T (p.Lys228Asn) c.942A>T (p.Lys314Asn) c.782+616A>T (n.782+616A>T) c.23A>T c.846A>T (p.Lys282Asn) c.486A>T (p.Lys162Asn) c.930A>T (p.Lys310Asn) | dbSNP |
17 | g.7673565T>C | CA497713967 | TP53 | c.963A>G (p.Lys321=) c.567A>G (p.Lys189=) c.684A>G (p.Lys228=) c.942A>G (p.Lys314=) c.782+616A>G (n.782+616A>G) c.23A>G c.846A>G (p.Lys282=) c.486A>G (p.Lys162=) c.930A>G (p.Lys310=) | ClinVar dbSNP COSMIC |
17 | g.7673565T>G | CA397835879 | TP53 | c.963A>C (p.Lys321Asn) c.567A>C (p.Lys189Asn) c.684A>C (p.Lys228Asn) c.942A>C (p.Lys314Asn) c.782+616A>C (n.782+616A>C) c.23A>C c.846A>C (p.Lys282Asn) c.486A>C (p.Lys162Asn) c.930A>C (p.Lys310Asn) | dbSNP |
17 | g.7673567dup | CA645587355 | TP53 | c.963dup (p.Pro322ThrfsTer15) c.567dup (p.Pro190ThrfsTer15) c.684dup (p.Pro229ThrfsTer15) c.942dup (p.Pro315ThrfsTer15) c.963dup (p.Pro322ThrfsTer?) c.782+616dup (n.782+616dup) c.963dup (p.Pro322ThrfsTer25) c.963dup (p.Pro322ThrfsTer14) c.567dup (p.Pro190ThrfsTer14) c.567dup (p.Pro190ThrfsTer?) c.567dup (p.Pro190ThrfsTer25) c.23dup c.846dup (p.Pro283ThrfsTer15) c.846dup (p.Pro283ThrfsTer14) c.486dup (p.Pro163ThrfsTer14) c.930dup (p.Pro311ThrfsTer15) c.486dup (p.Pro163ThrfsTer25) c.486dup (p.Pro163ThrfsTer15) c.846dup (p.Pro283ThrfsTer25) | COSMIC COSMIC COSMIC COSMIC |
17 | g.7673567del | CA497713971 | TP53 | c.963del (p.Lys321AsnfsTer24) c.567del (p.Lys189AsnfsTer24) c.684del (p.Lys228AsnfsTer24) c.942del (p.Lys314AsnfsTer24) c.963del (p.Lys321AsnfsTer?) c.782+616del (n.782+616del) c.963del (p.Lys321AsnfsTer30) c.963del (p.Lys321AsnfsTer22) c.567del (p.Lys189AsnfsTer22) c.567del (p.Lys189AsnfsTer?) c.567del (p.Lys189AsnfsTer30) c.23del c.846del (p.Lys282AsnfsTer24) c.846del (p.Lys282AsnfsTer22) c.486del (p.Lys162AsnfsTer22) c.930del (p.Lys310AsnfsTer24) c.486del (p.Lys162AsnfsTer30) c.486del (p.Lys162AsnfsTer24) c.846del (p.Lys282AsnfsTer30) | COSMIC |
17 | g.7673565_7673568delinsTTTC | CA2245947676 | TP53 | c.960_963delinsGAAA (p.Lys320=) c.564_567delinsGAAA (p.Lys188=) c.681_684delinsGAAA (p.Lys227=) c.939_942delinsGAAA (p.Lys313=) c.782+613_782+616delinsGAAA (n.782+613_782+616delinsGAAA) c.20_23delinsGAAA c.843_846delinsGAAA (p.Lys281=) c.483_486delinsGAAA (p.Lys161=) c.927_930delinsGAAA (p.Lys309=) | |
17 | g.7673565_7673605del | CA645587356 | TP53 | c.923_963del (p.Leu308ProfsTer15) c.527_567del (p.Leu176ProfsTer15) c.644_684del (p.Leu215ProfsTer15) c.902_942del (p.Leu301ProfsTer15) c.923_963del (p.Leu308ProfsTer?) c.782+576_782+616del (n.782+576_782+616del) c.923_963del (p.Leu308ProfsTer25) c.923_963del (p.Leu308ProfsTer14) c.527_567del (p.Leu176ProfsTer14) c.527_567del (p.Leu176ProfsTer?) c.527_567del (p.Leu176ProfsTer25) c.806_846del (p.Leu269ProfsTer15) c.806_846del (p.Leu269ProfsTer14) c.446_486del (p.Leu149ProfsTer14) c.890_930del (p.Leu297ProfsTer15) c.446_486del (p.Leu149ProfsTer25) c.446_486del (p.Leu149ProfsTer15) c.806_846del (p.Leu269ProfsTer25) | COSMIC |
17 | g.7673566T>A | CA397835881 | TP53 | c.962A>T (p.Lys321Ile) c.566A>T (p.Lys189Ile) c.683A>T (p.Lys228Ile) c.941A>T (p.Lys314Ile) c.782+615A>T (n.782+615A>T) c.22A>T c.845A>T (p.Lys282Ile) c.485A>T (p.Lys162Ile) c.929A>T (p.Lys310Ile) | dbSNP |
17 | g.7673566T>C | CA397835882 | TP53 | c.962A>G (p.Lys321Arg) c.566A>G (p.Lys189Arg) c.683A>G (p.Lys228Arg) c.941A>G (p.Lys314Arg) c.782+615A>G (n.782+615A>G) c.22A>G c.845A>G (p.Lys282Arg) c.485A>G (p.Lys162Arg) c.929A>G (p.Lys310Arg) | dbSNP |
17 | g.7673566T>G | CA397835886 | TP53 | c.962A>C (p.Lys321Thr) c.566A>C (p.Lys189Thr) c.683A>C (p.Lys228Thr) c.941A>C (p.Lys314Thr) c.782+615A>C (n.782+615A>C) c.22A>C c.845A>C (p.Lys282Thr) c.485A>C (p.Lys162Thr) c.929A>C (p.Lys310Thr) | dbSNP |
17 | g.7673571_7673573dup | CA645587357 | TP53 | c.960_962dup (p.Lys321_Pro322insLys) c.564_566dup (p.Lys189_Pro190insLys) c.681_683dup (p.Lys228_Pro229insLys) c.939_941dup (p.Lys314_Pro315insLys) c.782+613_782+615dup (n.782+613_782+615dup) c.20_22dup c.843_845dup (p.Lys282_Pro283insLys) c.483_485dup (p.Lys162_Pro163insLys) c.927_929dup (p.Lys310_Pro311insLys) | COSMIC COSMIC |
17 | g.7673571_7673573del | CA891844039 | TP53 | c.960_962del (p.Lys321del) c.564_566del (p.Lys189del) c.681_683del (p.Lys228del) c.939_941del (p.Lys314del) c.782+613_782+615del (n.782+613_782+615del) c.20_22del c.843_845del (p.Lys282del) c.483_485del (p.Lys162del) c.927_929del (p.Lys310del) | ClinVar dbSNP |
17 | g.7673567T>A | CA397835889 | TP53 | c.961A>T (p.Lys321Ter) c.565A>T (p.Lys189Ter) c.682A>T (p.Lys228Ter) c.940A>T (p.Lys314Ter) c.782+614A>T (n.782+614A>T) c.21A>T c.844A>T (p.Lys282Ter) c.484A>T (p.Lys162Ter) c.928A>T (p.Lys310Ter) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
17 | g.7673567T>C | CA397835893 | TP53 | c.961A>G (p.Lys321Glu) c.565A>G (p.Lys189Glu) c.682A>G (p.Lys228Glu) c.940A>G (p.Lys314Glu) c.782+614A>G (n.782+614A>G) c.21A>G c.844A>G (p.Lys282Glu) c.484A>G (p.Lys162Glu) c.928A>G (p.Lys310Glu) | |
17 | g.7673567T>G | CA397835894 | TP53 | c.961A>C (p.Lys321Gln) c.565A>C (p.Lys189Gln) c.682A>C (p.Lys228Gln) c.940A>C (p.Lys314Gln) c.782+614A>C (n.782+614A>C) c.21A>C c.844A>C (p.Lys282Gln) c.484A>C (p.Lys162Gln) c.928A>C (p.Lys310Gln) | |
17 | g.7673567T= | CA2245947687 | TP53 | c.961A= (p.Lys321=) c.565A= (p.Lys189=) c.682A= (p.Lys228=) c.940A= (p.Lys314=) c.782+614A= (n.782+614A=) c.21A= c.844A= (p.Lys282=) c.484A= (p.Lys162=) c.928A= (p.Lys310=) | |
17 | g.7673568del | CA645587358 | TP53 | c.960del (p.Lys321AsnfsTer24) c.564del (p.Lys189AsnfsTer24) c.681del (p.Lys228AsnfsTer24) c.939del (p.Lys314AsnfsTer24) c.960del (p.Lys321AsnfsTer?) c.782+613del (n.782+613del) c.960del (p.Lys321AsnfsTer22) c.564del (p.Lys189AsnfsTer22) c.564del (p.Lys189AsnfsTer?) c.20del c.843del (p.Lys282AsnfsTer24) c.843del (p.Lys282AsnfsTer22) c.483del (p.Lys162AsnfsTer22) c.927del (p.Lys310AsnfsTer24) c.483del (p.Lys162AsnfsTer?) c.483del (p.Lys162AsnfsTer24) c.843del (p.Lys282AsnfsTer?) | ClinVar COSMIC COSMIC COSMIC COSMIC |
17 | g.7673568C>A | CA397835895 | TP53 | c.960G>T (p.Lys320Asn) c.564G>T (p.Lys188Asn) c.681G>T (p.Lys227Asn) c.939G>T (p.Lys313Asn) c.782+613G>T (n.782+613G>T) c.20G>T c.843G>T (p.Lys281Asn) c.483G>T (p.Lys161Asn) c.927G>T (p.Lys309Asn) | dbSNP |
17 | g.7673568C>G | CA397835897 | TP53 | c.960G>C (p.Lys320Asn) c.564G>C (p.Lys188Asn) c.681G>C (p.Lys227Asn) c.939G>C (p.Lys313Asn) c.782+613G>C (n.782+613G>C) c.20G>C c.843G>C (p.Lys281Asn) c.483G>C (p.Lys161Asn) c.927G>C (p.Lys309Asn) | dbSNP COSMIC |
17 | g.7673568C>T | CA497713987 | TP53 | c.960G>A (p.Lys320=) c.564G>A (p.Lys188=) c.681G>A (p.Lys227=) c.939G>A (p.Lys313=) c.782+613G>A (n.782+613G>A) c.20G>A c.843G>A (p.Lys281=) c.483G>A (p.Lys161=) c.927G>A (p.Lys309=) | dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673569T>A | CA397835903 | TP53 | c.959A>T (p.Lys320Met) c.563A>T (p.Lys188Met) c.680A>T (p.Lys227Met) c.938A>T (p.Lys313Met) c.782+612A>T (n.782+612A>T) c.19A>T c.842A>T (p.Lys281Met) c.482A>T (p.Lys161Met) c.926A>T (p.Lys309Met) | dbSNP |
17 | g.7673569T>C | CA397835905 | TP53 | c.959A>G (p.Lys320Arg) c.563A>G (p.Lys188Arg) c.680A>G (p.Lys227Arg) c.938A>G (p.Lys313Arg) c.782+612A>G (n.782+612A>G) c.19A>G c.842A>G (p.Lys281Arg) c.482A>G (p.Lys161Arg) c.926A>G (p.Lys309Arg) | dbSNP |
17 | g.7673569T>G | CA397835900 | TP53 | c.959A>C (p.Lys320Thr) c.563A>C (p.Lys188Thr) c.680A>C (p.Lys227Thr) c.938A>C (p.Lys313Thr) c.782+612A>C (n.782+612A>C) c.19A>C c.842A>C (p.Lys281Thr) c.482A>C (p.Lys161Thr) c.926A>C (p.Lys309Thr) | ClinVar |
17 | g.7673570del | CA497714003 | TP53 | c.959del (p.Lys320ArgfsTer25) c.563del (p.Lys188ArgfsTer25) c.680del (p.Lys227ArgfsTer25) c.938del (p.Lys313ArgfsTer25) c.959del (p.Lys320ArgfsTer?) c.782+612del (n.782+612del) c.959del (p.Lys320ArgfsTer23) c.563del (p.Lys188ArgfsTer23) c.563del (p.Lys188ArgfsTer?) c.19del c.842del (p.Lys281ArgfsTer25) c.842del (p.Lys281ArgfsTer23) c.482del (p.Lys161ArgfsTer23) c.926del (p.Lys309ArgfsTer25) c.482del (p.Lys161ArgfsTer?) c.482del (p.Lys161ArgfsTer25) c.842del (p.Lys281ArgfsTer?) | COSMIC |
17 | g.7673570T>A | CA397835908 | TP53 | c.958A>T (p.Lys320Ter) c.562A>T (p.Lys188Ter) c.679A>T (p.Lys227Ter) c.937A>T (p.Lys313Ter) c.782+611A>T (n.782+611A>T) c.18A>T c.841A>T (p.Lys281Ter) c.481A>T (p.Lys161Ter) c.925A>T (p.Lys309Ter) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673570T>C | CA397835912 | TP53 | c.958A>G (p.Lys320Glu) c.562A>G (p.Lys188Glu) c.679A>G (p.Lys227Glu) c.937A>G (p.Lys313Glu) c.782+611A>G (n.782+611A>G) c.18A>G c.841A>G (p.Lys281Glu) c.481A>G (p.Lys161Glu) c.925A>G (p.Lys309Glu) | dbSNP |
17 | g.7673570T>G | CA397835915 | TP53 | c.958A>C (p.Lys320Gln) c.562A>C (p.Lys188Gln) c.679A>C (p.Lys227Gln) c.937A>C (p.Lys313Gln) c.782+611A>C (n.782+611A>C) c.18A>C c.841A>C (p.Lys281Gln) c.481A>C (p.Lys161Gln) c.925A>C (p.Lys309Gln) | |
17 | g.7673570_7673587del | CA645587360 | TP53 | c.941_958del (p.Ser314Ter) c.545_562del (p.Ser182Ter) c.662_679del (p.Ser221Ter) c.920_937del (p.Ser307Ter) c.782+594_782+611del (n.782+594_782+611del) c.1_18del c.824_841del (p.Ser275Ter) c.464_481del (p.Ser155Ter) c.908_925del (p.Ser303Ter) | COSMIC COSMIC COSMIC COSMIC |
17 | g.7673570_7673588del | CA645587363 | TP53 | c.940_958del (p.Ser314ArgfsTer25) c.544_562del (p.Ser182ArgfsTer25) c.661_679del (p.Ser221ArgfsTer25) c.919_937del (p.Ser307ArgfsTer25) c.940_958del (p.Ser314ArgfsTer?) c.782+593_782+611del (n.782+593_782+611del) c.940_958del (p.Ser314ArgfsTer23) c.544_562del (p.Ser182ArgfsTer23) c.544_562del (p.Ser182ArgfsTer?) c.823_841del (p.Ser275ArgfsTer25) c.823_841del (p.Ser275ArgfsTer23) c.463_481del (p.Ser155ArgfsTer23) c.907_925del (p.Ser303ArgfsTer25) c.463_481del (p.Ser155ArgfsTer?) c.463_481del (p.Ser155ArgfsTer25) c.823_841del (p.Ser275ArgfsTer?) | COSMIC |
17 | g.7673571del | CA645587364 | TP53 | c.957del (p.Lys320ArgfsTer25) c.561del (p.Lys188ArgfsTer25) c.678del (p.Lys227ArgfsTer25) c.936del (p.Lys313ArgfsTer25) c.957del (p.Lys320ArgfsTer?) c.782+610del (n.782+610del) c.957del (p.Lys320ArgfsTer23) c.561del (p.Lys188ArgfsTer23) c.561del (p.Lys188ArgfsTer?) c.17del c.840del (p.Lys281ArgfsTer25) c.840del (p.Lys281ArgfsTer23) c.480del (p.Lys161ArgfsTer23) c.924del (p.Lys309ArgfsTer25) c.480del (p.Lys161ArgfsTer?) c.480del (p.Lys161ArgfsTer25) c.840del (p.Lys281ArgfsTer?) | COSMIC COSMIC COSMIC COSMIC |
17 | g.7673571C>A | CA397835919 | TP53 | c.957G>T (p.Lys319Asn) c.561G>T (p.Lys187Asn) c.678G>T (p.Lys226Asn) c.936G>T (p.Lys312Asn) c.782+610G>T (n.782+610G>T) c.17G>T c.840G>T (p.Lys280Asn) c.480G>T (p.Lys160Asn) c.924G>T (p.Lys308Asn) | dbSNP COSMIC |
17 | g.7673571C>G | CA397835921 | TP53 | c.957G>C (p.Lys319Asn) c.561G>C (p.Lys187Asn) c.678G>C (p.Lys226Asn) c.936G>C (p.Lys312Asn) c.782+610G>C (n.782+610G>C) c.17G>C c.840G>C (p.Lys280Asn) c.480G>C (p.Lys160Asn) c.924G>C (p.Lys308Asn) | dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673571C>T | CA497714016 | TP53 | c.957G>A (p.Lys319=) c.561G>A (p.Lys187=) c.678G>A (p.Lys226=) c.936G>A (p.Lys312=) c.782+610G>A (n.782+610G>A) c.17G>A c.840G>A (p.Lys280=) c.480G>A (p.Lys160=) c.924G>A (p.Lys308=) | dbSNP COSMIC |
17 | g.7673572T>A | CA397835924 | TP53 | c.956A>T (p.Lys319Met) c.560A>T (p.Lys187Met) c.677A>T (p.Lys226Met) c.935A>T (p.Lys312Met) c.782+609A>T (n.782+609A>T) c.16A>T c.839A>T (p.Lys280Met) c.479A>T (p.Lys160Met) c.923A>T (p.Lys308Met) | dbSNP |
17 | g.7673572T>C | CA397835927 | TP53 | c.956A>G (p.Lys319Arg) c.560A>G (p.Lys187Arg) c.677A>G (p.Lys226Arg) c.935A>G (p.Lys312Arg) c.782+609A>G (n.782+609A>G) c.16A>G c.839A>G (p.Lys280Arg) c.479A>G (p.Lys160Arg) c.923A>G (p.Lys308Arg) | dbSNP COSMIC |
17 | g.7673572T>G | CA397835930 | TP53 | c.956A>C (p.Lys319Thr) c.560A>C (p.Lys187Thr) c.677A>C (p.Lys226Thr) c.935A>C (p.Lys312Thr) c.782+609A>C (n.782+609A>C) c.16A>C c.839A>C (p.Lys280Thr) c.479A>C (p.Lys160Thr) c.923A>C (p.Lys308Thr) | |
17 | g.7673573T>A | CA397835934 | TP53 | c.955A>T (p.Lys319Ter) c.559A>T (p.Lys187Ter) c.676A>T (p.Lys226Ter) c.934A>T (p.Lys312Ter) c.782+608A>T (n.782+608A>T) c.15A>T c.838A>T (p.Lys280Ter) c.478A>T (p.Lys160Ter) c.922A>T (p.Lys308Ter) | dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673573T>C | CA397835937 | TP53 | c.955A>G (p.Lys319Glu) c.559A>G (p.Lys187Glu) c.676A>G (p.Lys226Glu) c.934A>G (p.Lys312Glu) c.782+608A>G (n.782+608A>G) c.15A>G c.838A>G (p.Lys280Glu) c.478A>G (p.Lys160Glu) c.922A>G (p.Lys308Glu) | COSMIC |
17 | g.7673573T>G | CA397835940 | TP53 | c.955A>C (p.Lys319Gln) c.559A>C (p.Lys187Gln) c.676A>C (p.Lys226Gln) c.934A>C (p.Lys312Gln) c.782+608A>C (n.782+608A>C) c.15A>C c.838A>C (p.Lys280Gln) c.478A>C (p.Lys160Gln) c.922A>C (p.Lys308Gln) | |
17 | g.7673573_7673577delinsTTGGC | CA2245947690 | TP53 | c.951_955delinsGCCAA (p.Gln317=) c.555_559delinsGCCAA (p.Gln185=) c.672_676delinsGCCAA (p.Gln224=) c.930_934delinsGCCAA (p.Gln310=) c.782+604_782+608delinsGCCAA (n.782+604_782+608delinsGCCAA) c.11_15delinsGCCAA c.834_838delinsGCCAA (p.Gln278=) c.474_478delinsGCCAA (p.Gln158=) c.918_922delinsGCCAA (p.Gln306=) | |
17 | g.7673574T>A | CA497714040 | TP53 | c.954A>T (p.Pro318=) c.558A>T (p.Pro186=) c.675A>T (p.Pro225=) c.933A>T (p.Pro311=) c.782+607A>T (n.782+607A>T) c.14A>T c.837A>T (p.Pro279=) c.477A>T (p.Pro159=) c.921A>T (p.Pro307=) | ClinVar |
17 | g.7673574T>C | CA497714031 | TP53 | c.954A>G (p.Pro318=) c.558A>G (p.Pro186=) c.675A>G (p.Pro225=) c.933A>G (p.Pro311=) c.782+607A>G (n.782+607A>G) c.14A>G c.837A>G (p.Pro279=) c.477A>G (p.Pro159=) c.921A>G (p.Pro307=) | ClinVar dbSNP |
17 | g.7673574T>G | CA001195 | TP53 | c.954A>C (p.Pro318=) c.558A>C (p.Pro186=) c.675A>C (p.Pro225=) c.933A>C (p.Pro311=) c.782+607A>C (n.782+607A>C) c.14A>C c.837A>C (p.Pro279=) c.477A>C (p.Pro159=) c.921A>C (p.Pro307=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.7673574T= | CA2245947701 | TP53 | c.954A= (p.Pro318=) c.558A= (p.Pro186=) c.675A= (p.Pro225=) c.933A= (p.Pro311=) c.782+607A= (n.782+607A=) c.14A= c.837A= (p.Pro279=) c.477A= (p.Pro159=) c.921A= (p.Pro307=) | |
17 | g.7673577_7673580dup | CA645587367 | TP53 | c.951_954dup (p.Lys319AlafsTer19) c.555_558dup (p.Lys187AlafsTer19) c.672_675dup (p.Lys226AlafsTer19) c.930_933dup (p.Lys312AlafsTer19) c.951_954dup (p.Lys319AlafsTer?) c.782+604_782+607dup (n.782+604_782+607dup) c.951_954dup (p.Lys319AlafsTer29) c.951_954dup (p.Lys319AlafsTer18) c.555_558dup (p.Lys187AlafsTer18) c.555_558dup (p.Lys187AlafsTer?) c.555_558dup (p.Lys187AlafsTer29) c.11_14dup c.834_837dup (p.Lys280AlafsTer19) c.834_837dup (p.Lys280AlafsTer18) c.474_477dup (p.Lys160AlafsTer18) c.918_921dup (p.Lys308AlafsTer19) c.474_477dup (p.Lys160AlafsTer29) c.474_477dup (p.Lys160AlafsTer19) c.834_837dup (p.Lys280AlafsTer29) | COSMIC COSMIC |
17 | g.7673577_7673580del | CA915949515 | TP53 | c.951_954del (p.Pro318ArgfsTer26) c.555_558del (p.Pro186ArgfsTer26) c.672_675del (p.Pro225ArgfsTer26) c.930_933del (p.Pro311ArgfsTer26) c.951_954del (p.Pro318ArgfsTer?) c.782+604_782+607del (n.782+604_782+607del) c.951_954del (p.Pro318ArgfsTer24) c.555_558del (p.Pro186ArgfsTer24) c.555_558del (p.Pro186ArgfsTer?) c.11_14del c.834_837del (p.Pro279ArgfsTer26) c.834_837del (p.Pro279ArgfsTer24) c.474_477del (p.Pro159ArgfsTer24) c.918_921del (p.Pro307ArgfsTer26) c.474_477del (p.Pro159ArgfsTer?) c.474_477del (p.Pro159ArgfsTer26) c.834_837del (p.Pro279ArgfsTer?) | ClinVar dbSNP |
17 | g.7673575G>A | CA397835952 | TP53 | c.953C>T (p.Pro318Leu) c.557C>T (p.Pro186Leu) c.674C>T (p.Pro225Leu) c.932C>T (p.Pro311Leu) c.782+606C>T (n.782+606C>T) c.13C>T c.836C>T (p.Pro279Leu) c.476C>T (p.Pro159Leu) c.920C>T (p.Pro307Leu) | ClinVar dbSNP gnomAD v4 |
17 | g.7673575G>C | CA397835946 | TP53 | c.953C>G (p.Pro318Arg) c.557C>G (p.Pro186Arg) c.674C>G (p.Pro225Arg) c.932C>G (p.Pro311Arg) c.782+606C>G (n.782+606C>G) c.13C>G c.836C>G (p.Pro279Arg) c.476C>G (p.Pro159Arg) c.920C>G (p.Pro307Arg) | ClinVar dbSNP |
17 | g.7673575G= | CA2245947708 | TP53 | c.953C= (p.Pro318=) c.557C= (p.Pro186=) c.674C= (p.Pro225=) c.932C= (p.Pro311=) c.782+606C= (n.782+606C=) c.13C= c.836C= (p.Pro279=) c.476C= (p.Pro159=) c.920C= (p.Pro307=) | |
17 | g.7673575G>T | CA397835949 | TP53 | c.953C>A (p.Pro318Gln) c.557C>A (p.Pro186Gln) c.674C>A (p.Pro225Gln) c.932C>A (p.Pro311Gln) c.782+606C>A (n.782+606C>A) c.13C>A c.836C>A (p.Pro279Gln) c.476C>A (p.Pro159Gln) c.920C>A (p.Pro307Gln) | dbSNP |
17 | g.7673576G>A | CA397835955 | TP53 | c.952C>T (p.Pro318Ser) c.556C>T (p.Pro186Ser) c.673C>T (p.Pro225Ser) c.931C>T (p.Pro311Ser) c.782+605C>T (n.782+605C>T) c.12C>T c.835C>T (p.Pro279Ser) c.475C>T (p.Pro159Ser) c.919C>T (p.Pro307Ser) | ClinVar dbSNP |
17 | g.7673576G>C | CA397835958 | TP53 | c.952C>G (p.Pro318Ala) c.556C>G (p.Pro186Ala) c.673C>G (p.Pro225Ala) c.931C>G (p.Pro311Ala) c.782+605C>G (n.782+605C>G) c.12C>G c.835C>G (p.Pro279Ala) c.475C>G (p.Pro159Ala) c.919C>G (p.Pro307Ala) | dbSNP COSMIC |
17 | g.7673576G>T | CA397835961 | TP53 | c.952C>A (p.Pro318Thr) c.556C>A (p.Pro186Thr) c.673C>A (p.Pro225Thr) c.931C>A (p.Pro311Thr) c.782+605C>A (n.782+605C>A) c.12C>A c.835C>A (p.Pro279Thr) c.475C>A (p.Pro159Thr) c.919C>A (p.Pro307Thr) | dbSNP |
17 | g.7673577del | CA645587368 | TP53 | c.951del (p.Gln317HisfsTer28) c.555del (p.Gln185HisfsTer28) c.672del (p.Gln224HisfsTer28) c.930del (p.Gln310HisfsTer28) c.951del (p.Gln317HisfsTer?) c.782+604del (n.782+604del) c.951del (p.Gln317HisfsTer26) c.555del (p.Gln185HisfsTer26) c.555del (p.Gln185HisfsTer?) c.11del c.834del (p.Gln278HisfsTer28) c.834del (p.Gln278HisfsTer26) c.474del (p.Gln158HisfsTer26) c.918del (p.Gln306HisfsTer28) c.474del (p.Gln158HisfsTer?) c.474del (p.Gln158HisfsTer28) c.834del (p.Gln278HisfsTer?) | COSMIC COSMIC COSMIC COSMIC |
17 | g.7673577C>A | CA16615689 | TP53 | c.951G>T (p.Gln317His) c.555G>T (p.Gln185His) c.672G>T (p.Gln224His) c.930G>T (p.Gln310His) c.782+604G>T (n.782+604G>T) c.11G>T c.834G>T (p.Gln278His) c.474G>T (p.Gln158His) c.918G>T (p.Gln306His) | ClinVar dbSNP |
17 | g.7673577C= | CA2245947719 | TP53 | c.951G= (p.Gln317=) c.555G= (p.Gln185=) c.672G= (p.Gln224=) c.930G= (p.Gln310=) c.782+604G= (n.782+604G=) c.11G= c.834G= (p.Gln278=) c.474G= (p.Gln158=) c.918G= (p.Gln306=) | |
17 | g.7673577C>G | CA397835964 | TP53 | c.951G>C (p.Gln317His) c.555G>C (p.Gln185His) c.672G>C (p.Gln224His) c.930G>C (p.Gln310His) c.782+604G>C (n.782+604G>C) c.11G>C c.834G>C (p.Gln278His) c.474G>C (p.Gln158His) c.918G>C (p.Gln306His) | dbSNP |
17 | g.7673577C>T | CA497714069 | TP53 | c.951G>A (p.Gln317=) c.555G>A (p.Gln185=) c.672G>A (p.Gln224=) c.930G>A (p.Gln310=) c.782+604G>A (n.782+604G>A) c.11G>A c.834G>A (p.Gln278=) c.474G>A (p.Gln158=) c.918G>A (p.Gln306=) | ClinVar dbSNP |
17 | g.7673577_7673578delinsCT | CA2245947725 | TP53 | c.950_951delinsAG (p.Gln317=) c.554_555delinsAG (p.Gln185=) c.671_672delinsAG (p.Gln224=) c.929_930delinsAG (p.Gln310=) c.782+603_782+604delinsAG (n.782+603_782+604delinsAG) c.10_11delinsAG c.833_834delinsAG (p.Gln278=) c.473_474delinsAG (p.Gln158=) c.917_918delinsAG (p.Gln306=) | |
17 | g.7673578del | CA645587369 | TP53 | c.950del (p.Gln317ArgfsTer28) c.554del (p.Gln185ArgfsTer28) c.671del (p.Gln224ArgfsTer28) c.929del (p.Gln310ArgfsTer28) c.950del (p.Gln317ArgfsTer?) c.782+603del (n.782+603del) c.950del (p.Gln317ArgfsTer26) c.554del (p.Gln185ArgfsTer26) c.554del (p.Gln185ArgfsTer?) c.10del c.833del (p.Gln278ArgfsTer28) c.833del (p.Gln278ArgfsTer26) c.473del (p.Gln158ArgfsTer26) c.917del (p.Gln306ArgfsTer28) c.473del (p.Gln158ArgfsTer?) c.473del (p.Gln158ArgfsTer28) c.833del (p.Gln278ArgfsTer?) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673578T>A | CA397835969 | TP53 | c.950A>T (p.Gln317Leu) c.554A>T (p.Gln185Leu) c.671A>T (p.Gln224Leu) c.929A>T (p.Gln310Leu) c.782+603A>T (n.782+603A>T) c.10A>T c.833A>T (p.Gln278Leu) c.473A>T (p.Gln158Leu) c.917A>T (p.Gln306Leu) | ClinVar dbSNP |
17 | g.7673578T>C | CA397835971 | TP53 | c.950A>G (p.Gln317Arg) c.554A>G (p.Gln185Arg) c.671A>G (p.Gln224Arg) c.929A>G (p.Gln310Arg) c.782+603A>G (n.782+603A>G) c.10A>G c.833A>G (p.Gln278Arg) c.473A>G (p.Gln158Arg) c.917A>G (p.Gln306Arg) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
17 | g.7673578T>G | CA397835972 | TP53 | c.950A>C (p.Gln317Pro) c.554A>C (p.Gln185Pro) c.671A>C (p.Gln224Pro) c.929A>C (p.Gln310Pro) c.782+603A>C (n.782+603A>C) c.10A>C c.833A>C (p.Gln278Pro) c.473A>C (p.Gln158Pro) c.917A>C (p.Gln306Pro) | COSMIC |
17 | g.7673578T= | CA2245947747 | TP53 | c.950A= (p.Gln317=) c.554A= (p.Gln185=) c.671A= (p.Gln224=) c.929A= (p.Gln310=) c.782+603A= (n.782+603A=) c.10A= c.833A= (p.Gln278=) c.473A= (p.Gln158=) c.917A= (p.Gln306=) | |
17 | g.7673578_7673579delinsTG | CA2245947741 | TP53 | c.949_950delinsCA (p.Gln317=) c.553_554delinsCA (p.Gln185=) c.670_671delinsCA (p.Gln224=) c.928_929delinsCA (p.Gln310=) c.782+602_782+603delinsCA (n.782+602_782+603delinsCA) c.9_10delinsCA c.832_833delinsCA (p.Gln278=) c.472_473delinsCA (p.Gln158=) c.916_917delinsCA (p.Gln306=) | |
17 | g.7673578_7673582del | CA645587370 | TP53 | c.946_950del (p.Pro316AlafsTer19) c.550_554del (p.Pro184AlafsTer19) c.667_671del (p.Pro223AlafsTer19) c.925_929del (p.Pro309AlafsTer19) c.946_950del (p.Pro316AlafsTer?) c.782+599_782+603del (n.782+599_782+603del) c.946_950del (p.Pro316AlafsTer29) c.946_950del (p.Pro316AlafsTer18) c.550_554del (p.Pro184AlafsTer18) c.550_554del (p.Pro184AlafsTer?) c.550_554del (p.Pro184AlafsTer29) c.6_10del c.829_833del (p.Pro277AlafsTer19) c.829_833del (p.Pro277AlafsTer18) c.469_473del (p.Pro157AlafsTer18) c.913_917del (p.Pro305AlafsTer19) c.469_473del (p.Pro157AlafsTer29) c.469_473del (p.Pro157AlafsTer19) c.829_833del (p.Pro277AlafsTer29) | COSMIC |
17 | g.7673579G>A | CA397835973 | TP53 | c.949C>T (p.Gln317Ter) c.553C>T (p.Gln185Ter) c.670C>T (p.Gln224Ter) c.928C>T (p.Gln310Ter) c.782+602C>T (n.782+602C>T) c.9C>T c.832C>T (p.Gln278Ter) c.472C>T (p.Gln158Ter) c.916C>T (p.Gln306Ter) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673579G>C | CA397835975 | TP53 | c.949C>G (p.Gln317Glu) c.553C>G (p.Gln185Glu) c.670C>G (p.Gln224Glu) c.928C>G (p.Gln310Glu) c.782+602C>G (n.782+602C>G) c.9C>G c.832C>G (p.Gln278Glu) c.472C>G (p.Gln158Glu) c.916C>G (p.Gln306Glu) | dbSNP |
17 | g.7673579G= | CA2245947768 | TP53 | c.949C= (p.Gln317=) c.553C= (p.Gln185=) c.670C= (p.Gln224=) c.928C= (p.Gln310=) c.782+602C= (n.782+602C=) c.9C= c.832C= (p.Gln278=) c.472C= (p.Gln158=) c.916C= (p.Gln306=) | |
17 | g.7673579G>T | CA001204 | TP53 | c.949C>A (p.Gln317Lys) c.553C>A (p.Gln185Lys) c.670C>A (p.Gln224Lys) c.928C>A (p.Gln310Lys) c.782+602C>A (n.782+602C>A) c.9C>A c.832C>A (p.Gln278Lys) c.472C>A (p.Gln158Lys) c.916C>A (p.Gln306Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
17 | g.7673579_7673580delinsAA | CA645587373 | TP53 | c.948_949delinsTT (p.Pro317Ter) c.552_553delinsTT (p.Pro185Ter) c.669_670delinsTT (p.Pro224Ter) c.927_928delinsTT (p.Pro310Ter) c.782+601_782+602delinsTT (n.782+601_782+602delinsTT) c.8_9delinsTT c.831_832delinsTT (p.Pro278Ter) c.471_472delinsTT (p.Pro158Ter) c.915_916delinsTT (p.Pro306Ter) | COSMIC |
17 | g.7673582dup | CA645587372 | TP53 | c.949dup (p.Gln317ProfsTer20) c.553dup (p.Gln185ProfsTer20) c.670dup (p.Gln224ProfsTer20) c.928dup (p.Gln310ProfsTer20) c.949dup (p.Gln317ProfsTer?) c.782+602dup (n.782+602dup) c.949dup (p.Gln317ProfsTer30) c.949dup (p.Gln317ProfsTer19) c.553dup (p.Gln185ProfsTer19) c.553dup (p.Gln185ProfsTer?) c.553dup (p.Gln185ProfsTer30) c.9dup c.832dup (p.Gln278ProfsTer20) c.832dup (p.Gln278ProfsTer19) c.472dup (p.Gln158ProfsTer19) c.916dup (p.Gln306ProfsTer20) c.472dup (p.Gln158ProfsTer30) c.472dup (p.Gln158ProfsTer20) c.832dup (p.Gln278ProfsTer30) | COSMIC COSMIC COSMIC COSMIC |
17 | g.7673582del | CA497714083 | TP53 | c.949del (p.Gln317SerfsTer28) c.553del (p.Gln185SerfsTer28) c.670del (p.Gln224SerfsTer28) c.928del (p.Gln310SerfsTer28) c.949del (p.Gln317SerfsTer?) c.782+602del (n.782+602del) c.949del (p.Gln317SerfsTer26) c.553del (p.Gln185SerfsTer26) c.553del (p.Gln185SerfsTer?) c.9del c.832del (p.Gln278SerfsTer28) c.832del (p.Gln278SerfsTer26) c.472del (p.Gln158SerfsTer26) c.916del (p.Gln306SerfsTer28) c.472del (p.Gln158SerfsTer?) c.472del (p.Gln158SerfsTer28) c.832del (p.Gln278SerfsTer?) | ClinVar dbSNP COSMIC COSMIC COSMIC |
17 | g.7673581_7673582del | CA645587371 | TP53 | c.948_949del (p.Gln317AlafsTer19) c.552_553del (p.Gln185AlafsTer19) c.669_670del (p.Gln224AlafsTer19) c.927_928del (p.Gln310AlafsTer19) c.948_949del (p.Gln317AlafsTer?) c.782+601_782+602del (n.782+601_782+602del) c.948_949del (p.Gln317AlafsTer29) c.948_949del (p.Gln317AlafsTer18) c.552_553del (p.Gln185AlafsTer18) c.552_553del (p.Gln185AlafsTer?) c.552_553del (p.Gln185AlafsTer29) c.8_9del c.831_832del (p.Gln278AlafsTer19) c.831_832del (p.Gln278AlafsTer18) c.471_472del (p.Gln158AlafsTer18) c.915_916del (p.Gln306AlafsTer19) c.471_472del (p.Gln158AlafsTer29) c.471_472del (p.Gln158AlafsTer19) c.831_832del (p.Gln278AlafsTer29) | COSMIC |
17 | g.7673580G>A | CA497714095 | TP53 | c.948C>T (p.Pro316=) c.552C>T (p.Pro184=) c.669C>T (p.Pro223=) c.927C>T (p.Pro309=) c.782+601C>T (n.782+601C>T) c.8C>T c.831C>T (p.Pro277=) c.471C>T (p.Pro157=) c.915C>T (p.Pro305=) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673580G>C | CA497714109 | TP53 | c.948C>G (p.Pro316=) c.552C>G (p.Pro184=) c.669C>G (p.Pro223=) c.927C>G (p.Pro309=) c.782+601C>G (n.782+601C>G) c.8C>G c.831C>G (p.Pro277=) c.471C>G (p.Pro157=) c.915C>G (p.Pro305=) | ClinVar dbSNP |
17 | g.7673580G= | CA2245947794 | TP53 | c.948C= (p.Pro316=) c.552C= (p.Pro184=) c.669C= (p.Pro223=) c.927C= (p.Pro309=) c.782+601C= (n.782+601C=) c.8C= c.831C= (p.Pro277=) c.471C= (p.Pro157=) c.915C= (p.Pro305=) | |
17 | g.7673580G>T | CA497714113 | TP53 | c.948C>A (p.Pro316=) c.552C>A (p.Pro184=) c.669C>A (p.Pro223=) c.927C>A (p.Pro309=) c.782+601C>A (n.782+601C>A) c.8C>A c.831C>A (p.Pro277=) c.471C>A (p.Pro157=) c.915C>A (p.Pro305=) | |
17 | g.7673581G>A | CA397835981 | TP53 | c.947C>T (p.Pro316Leu) c.551C>T (p.Pro184Leu) c.668C>T (p.Pro223Leu) c.926C>T (p.Pro309Leu) c.782+600C>T (n.782+600C>T) c.7C>T c.830C>T (p.Pro277Leu) c.470C>T (p.Pro157Leu) c.914C>T (p.Pro305Leu) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
17 | g.7673581G>C | CA397835984 | TP53 | c.947C>G (p.Pro316Arg) c.551C>G (p.Pro184Arg) c.668C>G (p.Pro223Arg) c.926C>G (p.Pro309Arg) c.782+600C>G (n.782+600C>G) c.7C>G c.830C>G (p.Pro277Arg) c.470C>G (p.Pro157Arg) c.914C>G (p.Pro305Arg) | |
17 | g.7673581G= | CA2245947801 | TP53 | c.947C= (p.Pro316=) c.551C= (p.Pro184=) c.668C= (p.Pro223=) c.926C= (p.Pro309=) c.782+600C= (n.782+600C=) c.7C= c.830C= (p.Pro277=) c.470C= (p.Pro157=) c.914C= (p.Pro305=) | |
17 | g.7673581G>T | CA397835980 | TP53 | c.947C>A (p.Pro316His) c.551C>A (p.Pro184His) c.668C>A (p.Pro223His) c.926C>A (p.Pro309His) c.782+600C>A (n.782+600C>A) c.7C>A c.830C>A (p.Pro277His) c.470C>A (p.Pro157His) c.914C>A (p.Pro305His) | dbSNP |
17 | g.7673585_7673589del | CA2838032359 | TP53 | c.943_947del (p.Ser315ProfsTer20) c.547_551del (p.Ser183ProfsTer20) c.664_668del (p.Ser222ProfsTer20) c.922_926del (p.Ser308ProfsTer20) c.943_947del (p.Ser315ProfsTer?) c.782+596_782+600del (n.782+596_782+600del) c.943_947del (p.Ser315ProfsTer30) c.943_947del (p.Ser315ProfsTer19) c.547_551del (p.Ser183ProfsTer19) c.547_551del (p.Ser183ProfsTer?) c.547_551del (p.Ser183ProfsTer30) c.826_830del (p.Ser276ProfsTer20) c.826_830del (p.Ser276ProfsTer19) c.466_470del (p.Ser156ProfsTer19) c.910_914del (p.Ser304ProfsTer20) c.466_470del (p.Ser156ProfsTer30) c.466_470del (p.Ser156ProfsTer20) c.826_830del (p.Ser276ProfsTer30) | |
17 | g.7673581_7673591delinsGGAGAGGAGCT | CA2245947806 | TP53 | c.937_947delinsAGCTCCTCTCC (p.Ser313=) c.541_551delinsAGCTCCTCTCC (p.Ser181=) c.658_668delinsAGCTCCTCTCC (p.Ser220=) c.916_926delinsAGCTCCTCTCC (p.Ser306=) c.782+590_782+600delinsAGCTCCTCTCC (n.782+590_782+600delinsAGCTCCTCTCC) c.820_830delinsAGCTCCTCTCC (p.Ser274=) c.460_470delinsAGCTCCTCTCC (p.Ser154=) c.904_914delinsAGCTCCTCTCC (p.Ser302=) | |
17 | g.7673582G>A | CA397835996 | TP53 | c.946C>T (p.Pro316Ser) c.550C>T (p.Pro184Ser) c.667C>T (p.Pro223Ser) c.925C>T (p.Pro309Ser) c.782+599C>T (n.782+599C>T) c.6C>T c.829C>T (p.Pro277Ser) c.469C>T (p.Pro157Ser) c.913C>T (p.Pro305Ser) | ClinVar dbSNP |
17 | g.7673582G>C | CA397835999 | TP53 | c.946C>G (p.Pro316Ala) c.550C>G (p.Pro184Ala) c.667C>G (p.Pro223Ala) c.925C>G (p.Pro309Ala) c.782+599C>G (n.782+599C>G) c.6C>G c.829C>G (p.Pro277Ala) c.469C>G (p.Pro157Ala) c.913C>G (p.Pro305Ala) | dbSNP |
17 | g.7673582G= | CA2245947821 | TP53 | c.946C= (p.Pro316=) c.550C= (p.Pro184=) c.667C= (p.Pro223=) c.925C= (p.Pro309=) c.782+599C= (n.782+599C=) c.6C= c.829C= (p.Pro277=) c.469C= (p.Pro157=) c.913C= (p.Pro305=) | |
17 | g.7673582G>T | CA001212 | TP53 | c.946C>A (p.Pro316Thr) c.550C>A (p.Pro184Thr) c.667C>A (p.Pro223Thr) c.925C>A (p.Pro309Thr) c.782+599C>A (n.782+599C>A) c.6C>A c.829C>A (p.Pro277Thr) c.469C>A (p.Pro157Thr) c.913C>A (p.Pro305Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.7673582_7673583delinsGA | CA2245947828 | TP53 | c.945_946delinsTC (p.Ser315=) c.549_550delinsTC (p.Ser183=) c.666_667delinsTC (p.Ser222=) c.924_925delinsTC (p.Ser308=) c.782+598_782+599delinsTC (n.782+598_782+599delinsTC) c.5_6delinsTC c.828_829delinsTC (p.Ser276=) c.468_469delinsTC (p.Ser156=) c.912_913delinsTC (p.Ser304=) | |
17 | g.7673585_7673586dup | CA2573102338 | TP53 | c.945_946dup (p.Pro316LeufsTer30) c.549_550dup (p.Pro184LeufsTer30) c.666_667dup (p.Pro223LeufsTer30) c.924_925dup (p.Pro309LeufsTer30) c.945_946dup (p.Pro316LeufsTer?) c.782+598_782+599dup (n.782+598_782+599dup) c.945_946dup (p.Pro316LeufsTer28) c.549_550dup (p.Pro184LeufsTer28) c.549_550dup (p.Pro184LeufsTer?) c.5_6dup c.828_829dup (p.Pro277LeufsTer30) c.828_829dup (p.Pro277LeufsTer28) c.468_469dup (p.Pro157LeufsTer28) c.912_913dup (p.Pro305LeufsTer30) c.468_469dup (p.Pro157LeufsTer?) c.468_469dup (p.Pro157LeufsTer30) c.828_829dup (p.Pro277LeufsTer?) | |
17 | g.7673585_7673586del | CA645587374 | TP53 | c.945_946del (p.Gln317AlafsTer19) c.549_550del (p.Gln185AlafsTer19) c.666_667del (p.Gln224AlafsTer19) c.924_925del (p.Gln310AlafsTer19) c.945_946del (p.Gln317AlafsTer?) c.782+598_782+599del (n.782+598_782+599del) c.945_946del (p.Gln317AlafsTer18) c.549_550del (p.Gln185AlafsTer18) c.549_550del (p.Gln185AlafsTer?) c.5_6del c.828_829del (p.Gln278AlafsTer19) c.828_829del (p.Gln278AlafsTer18) c.468_469del (p.Gln158AlafsTer18) c.912_913del (p.Gln306AlafsTer19) c.468_469del (p.Gln158AlafsTer?) c.468_469del (p.Gln158AlafsTer19) c.828_829del (p.Gln278AlafsTer?) | ClinVar dbSNP COSMIC COSMIC |
17 | g.7673583_7673592del | CA913190577 | TP53 | c.937_946del (p.Ser313ProfsTer29) c.541_550del (p.Ser181ProfsTer29) c.658_667del (p.Ser220ProfsTer29) c.916_925del (p.Ser306ProfsTer29) c.937_946del (p.Ser313ProfsTer?) c.782+590_782+599del (n.782+590_782+599del) c.937_946del (p.Ser313ProfsTer27) c.541_550del (p.Ser181ProfsTer27) c.541_550del (p.Ser181ProfsTer?) c.820_829del (p.Ser274ProfsTer29) c.820_829del (p.Ser274ProfsTer27) c.460_469del (p.Ser154ProfsTer27) c.904_913del (p.Ser302ProfsTer29) c.460_469del (p.Ser154ProfsTer?) c.460_469del (p.Ser154ProfsTer29) c.820_829del (p.Ser274ProfsTer?) | ClinVar dbSNP |
17 | g.7673583del | CA915949516 | TP53 | c.945del (p.Gln317SerfsTer28) c.549del (p.Gln185SerfsTer28) c.666del (p.Gln224SerfsTer28) c.924del (p.Gln310SerfsTer28) c.945del (p.Gln317SerfsTer?) c.782+598del (n.782+598del) c.945del (p.Gln317SerfsTer26) c.549del (p.Gln185SerfsTer26) c.549del (p.Gln185SerfsTer?) c.5del c.828del (p.Gln278SerfsTer28) c.828del (p.Gln278SerfsTer26) c.468del (p.Gln158SerfsTer26) c.912del (p.Gln306SerfsTer28) c.468del (p.Gln158SerfsTer?) c.468del (p.Gln158SerfsTer28) c.828del (p.Gln278SerfsTer?) | ClinVar dbSNP |
17 | g.7673583A>C | CA497714137 | TP53 | c.945T>G (p.Ser315=) c.549T>G (p.Ser183=) c.666T>G (p.Ser222=) c.924T>G (p.Ser308=) c.782+598T>G (n.782+598T>G) c.5T>G c.828T>G (p.Ser276=) c.468T>G (p.Ser156=) c.912T>G (p.Ser304=) | COSMIC |
17 | g.7673583A>G | CA497714150 | TP53 | c.945T>C (p.Ser315=) c.549T>C (p.Ser183=) c.666T>C (p.Ser222=) c.924T>C (p.Ser308=) c.782+598T>C (n.782+598T>C) c.5T>C c.828T>C (p.Ser276=) c.468T>C (p.Ser156=) c.912T>C (p.Ser304=) | dbSNP |
17 | g.7673583A>T | CA497714154 | TP53 | c.945T>A (p.Ser315=) c.549T>A (p.Ser183=) c.666T>A (p.Ser222=) c.924T>A (p.Ser308=) c.782+598T>A (n.782+598T>A) c.5T>A c.828T>A (p.Ser276=) c.468T>A (p.Ser156=) c.912T>A (p.Ser304=) | dbSNP |
17 | g.7673583dup | CA645587375 | TP53 | c.945dup (p.Pro316SerfsTer21) c.549dup (p.Pro184SerfsTer21) c.666dup (p.Pro223SerfsTer21) c.924dup (p.Pro309SerfsTer21) c.945dup (p.Pro316SerfsTer?) c.782+598dup (n.782+598dup) c.945dup (p.Pro316SerfsTer20) c.549dup (p.Pro184SerfsTer20) c.549dup (p.Pro184SerfsTer?) c.5dup c.828dup (p.Pro277SerfsTer21) c.828dup (p.Pro277SerfsTer20) c.468dup (p.Pro157SerfsTer20) c.912dup (p.Pro305SerfsTer21) c.468dup (p.Pro157SerfsTer?) c.468dup (p.Pro157SerfsTer21) c.828dup (p.Pro277SerfsTer?) | ClinVar dbSNP COSMIC |
17 | g.7673583_7673584insT | CA497714157 | TP53 | c.944_945insA (p.Pro316SerfsTer21) c.548_549insA (p.Pro184SerfsTer21) c.665_666insA (p.Pro223SerfsTer21) c.923_924insA (p.Pro309SerfsTer21) c.944_945insA (p.Pro316SerfsTer?) c.782+597_782+598insA (n.782+597_782+598insA) c.944_945insA (p.Pro316SerfsTer20) c.548_549insA (p.Pro184SerfsTer20) c.548_549insA (p.Pro184SerfsTer?) c.4_5insA c.827_828insA (p.Pro277SerfsTer21) c.827_828insA (p.Pro277SerfsTer20) c.467_468insA (p.Pro157SerfsTer20) c.911_912insA (p.Pro305SerfsTer21) c.467_468insA (p.Pro157SerfsTer?) c.467_468insA (p.Pro157SerfsTer21) c.827_828insA (p.Pro277SerfsTer?) | |
17 | g.7673584G>A | CA397836004 | TP53 | c.944C>T (p.Ser315Phe) c.548C>T (p.Ser183Phe) c.665C>T (p.Ser222Phe) c.923C>T (p.Ser308Phe) c.782+597C>T (n.782+597C>T) c.4C>T c.827C>T (p.Ser276Phe) c.467C>T (p.Ser156Phe) c.911C>T (p.Ser304Phe) | ClinVar dbSNP |
17 | g.7673584G>C | CA397836006 | TP53 | c.944C>G (p.Ser315Cys) c.548C>G (p.Ser183Cys) c.665C>G (p.Ser222Cys) c.923C>G (p.Ser308Cys) c.782+597C>G (n.782+597C>G) c.4C>G c.827C>G (p.Ser276Cys) c.467C>G (p.Ser156Cys) c.911C>G (p.Ser304Cys) | ClinVar dbSNP gnomAD v4 COSMIC |
17 | g.7673584G= | CA2245947848 | TP53 | c.944C= (p.Ser315=) c.548C= (p.Ser183=) c.665C= (p.Ser222=) c.923C= (p.Ser308=) c.782+597C= (n.782+597C=) c.4C= c.827C= (p.Ser276=) c.467C= (p.Ser156=) c.911C= (p.Ser304=) | |
17 | g.7673584G>T | CA397836013 | TP53 | c.944C>A (p.Ser315Tyr) c.548C>A (p.Ser183Tyr) c.665C>A (p.Ser222Tyr) c.923C>A (p.Ser308Tyr) c.782+597C>A (n.782+597C>A) c.4C>A c.827C>A (p.Ser276Tyr) c.467C>A (p.Ser156Tyr) c.911C>A (p.Ser304Tyr) | dbSNP |
17 | g.7673585A= | CA2245947858 | TP53 | c.943T= (p.Ser315=) c.547T= (p.Ser183=) c.664T= (p.Ser222=) c.922T= (p.Ser308=) c.782+596T= (n.782+596T=) c.3T= c.826T= (p.Ser276=) c.466T= (p.Ser156=) c.910T= (p.Ser304=) | |
17 | g.7673585A>C | CA397836018 | TP53 | c.943T>G (p.Ser315Ala) c.547T>G (p.Ser183Ala) c.664T>G (p.Ser222Ala) c.922T>G (p.Ser308Ala) c.782+596T>G (n.782+596T>G) c.3T>G c.826T>G (p.Ser276Ala) c.466T>G (p.Ser156Ala) c.910T>G (p.Ser304Ala) | |
17 | g.7673585A>G | CA397836023 | TP53 | c.943T>C (p.Ser315Pro) c.547T>C (p.Ser183Pro) c.664T>C (p.Ser222Pro) c.922T>C (p.Ser308Pro) c.782+596T>C (n.782+596T>C) c.3T>C c.826T>C (p.Ser276Pro) c.466T>C (p.Ser156Pro) c.910T>C (p.Ser304Pro) | ClinVar dbSNP COSMIC |
17 | g.7673585A>T | CA000506 | TP53 | c.943T>A (p.Ser315Thr) c.547T>A (p.Ser183Thr) c.664T>A (p.Ser222Thr) c.922T>A (p.Ser308Thr) c.782+596T>A (n.782+596T>A) c.3T>A c.826T>A (p.Ser276Thr) c.466T>A (p.Ser156Thr) c.910T>A (p.Ser304Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.7673586G>A | CA497714190 | TP53 | c.942C>T (p.Ser314=) c.546C>T (p.Ser182=) c.663C>T (p.Ser221=) c.921C>T (p.Ser307=) c.782+595C>T (n.782+595C>T) c.2C>T c.825C>T (p.Ser275=) c.465C>T (p.Ser155=) c.909C>T (p.Ser303=) | dbSNP |
17 | g.7673586G>C | CA497714198 | TP53 | c.942C>G (p.Ser314=) c.546C>G (p.Ser182=) c.663C>G (p.Ser221=) c.921C>G (p.Ser307=) c.782+595C>G (n.782+595C>G) c.2C>G c.825C>G (p.Ser275=) c.465C>G (p.Ser155=) c.909C>G (p.Ser303=) | ClinVar dbSNP |
17 | g.7673586G= | CA2245947870 | TP53 | c.942C= (p.Ser314=) c.546C= (p.Ser182=) c.663C= (p.Ser221=) c.921C= (p.Ser307=) c.782+595C= (n.782+595C=) c.2C= c.825C= (p.Ser275=) c.465C= (p.Ser155=) c.909C= (p.Ser303=) | |
17 | g.7673586G>T | CA001225 | TP53 | c.942C>A (p.Ser314=) c.546C>A (p.Ser182=) c.663C>A (p.Ser221=) c.921C>A (p.Ser307=) c.782+595C>A (n.782+595C>A) c.2C>A c.825C>A (p.Ser275=) c.465C>A (p.Ser155=) c.909C>A (p.Ser303=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.7673587G>A | CA001234 | TP53 | c.941C>T (p.Ser314Phe) c.545C>T (p.Ser182Phe) c.662C>T (p.Ser221Phe) c.920C>T (p.Ser307Phe) c.782+594C>T (n.782+594C>T) c.1C>T c.824C>T (p.Ser275Phe) c.464C>T (p.Ser155Phe) c.908C>T (p.Ser303Phe) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
17 | g.7673587G>C | CA397836031 | TP53 | c.941C>G (p.Ser314Cys) c.545C>G (p.Ser182Cys) c.662C>G (p.Ser221Cys) c.920C>G (p.Ser307Cys) c.782+594C>G (n.782+594C>G) c.1C>G c.824C>G (p.Ser275Cys) c.464C>G (p.Ser155Cys) c.908C>G (p.Ser303Cys) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673587G= | CA2245947882 | TP53 | c.941C= (p.Ser314=) c.545C= (p.Ser182=) c.662C= (p.Ser221=) c.920C= (p.Ser307=) c.782+594C= (n.782+594C=) c.1C= c.824C= (p.Ser275=) c.464C= (p.Ser155=) c.908C= (p.Ser303=) | |
17 | g.7673587G>T | CA397836036 | TP53 | c.941C>A (p.Ser314Tyr) c.545C>A (p.Ser182Tyr) c.662C>A (p.Ser221Tyr) c.920C>A (p.Ser307Tyr) c.782+594C>A (n.782+594C>A) c.1C>A c.824C>A (p.Ser275Tyr) c.464C>A (p.Ser155Tyr) c.908C>A (p.Ser303Tyr) | dbSNP |
17 | g.7673588A>C | CA397836044 | TP53 | c.940T>G (p.Ser314Ala) c.544T>G (p.Ser182Ala) c.661T>G (p.Ser221Ala) c.919T>G (p.Ser307Ala) c.782+593T>G (n.782+593T>G) c.823T>G (p.Ser275Ala) c.463T>G (p.Ser155Ala) c.907T>G (p.Ser303Ala) | |
17 | g.7673588A>G | CA397836042 | TP53 | c.940T>C (p.Ser314Pro) c.544T>C (p.Ser182Pro) c.661T>C (p.Ser221Pro) c.919T>C (p.Ser307Pro) c.782+593T>C (n.782+593T>C) c.823T>C (p.Ser275Pro) c.463T>C (p.Ser155Pro) c.907T>C (p.Ser303Pro) | |
17 | g.7673588A>T | CA397836039 | TP53 | c.940T>A (p.Ser314Thr) c.544T>A (p.Ser182Thr) c.661T>A (p.Ser221Thr) c.919T>A (p.Ser307Thr) c.782+593T>A (n.782+593T>A) c.823T>A (p.Ser275Thr) c.463T>A (p.Ser155Thr) c.907T>A (p.Ser303Thr) | dbSNP |
17 | g.7673589G>A | CA497714209 | TP53 | c.939C>T (p.Ser313=) c.543C>T (p.Ser181=) c.660C>T (p.Ser220=) c.918C>T (p.Ser306=) c.782+592C>T (n.782+592C>T) c.822C>T (p.Ser274=) c.462C>T (p.Ser154=) c.906C>T (p.Ser302=) | dbSNP |
17 | g.7673589G>C | CA397836048 | TP53 | c.939C>G (p.Ser313Arg) c.543C>G (p.Ser181Arg) c.660C>G (p.Ser220Arg) c.918C>G (p.Ser306Arg) c.782+592C>G (n.782+592C>G) c.822C>G (p.Ser274Arg) c.462C>G (p.Ser154Arg) c.906C>G (p.Ser302Arg) | dbSNP |
17 | g.7673589G= | CA2245947895 | TP53 | c.939C= (p.Ser313=) c.543C= (p.Ser181=) c.660C= (p.Ser220=) c.918C= (p.Ser306=) c.782+592C= (n.782+592C=) c.822C= (p.Ser274=) c.462C= (p.Ser154=) c.906C= (p.Ser302=) | |
17 | g.7673589G>T | CA397836050 | TP53 | c.939C>A (p.Ser313Arg) c.543C>A (p.Ser181Arg) c.660C>A (p.Ser220Arg) c.918C>A (p.Ser306Arg) c.782+592C>A (n.782+592C>A) c.822C>A (p.Ser274Arg) c.462C>A (p.Ser154Arg) c.906C>A (p.Ser302Arg) | dbSNP |
17 | g.7673592_7673610del | CA645587376 | TP53 | c.921_939del c.525_543del c.642_660del c.900_918del c.782+574_782+592del (n.782+574_782+592del) c.804_822del c.444_462del c.888_906del | COSMIC |
17 | g.7673590del | CA891842223 | TP53 | c.938del (p.Ser313ThrfsTer?) c.542del (p.Ser181ThrfsTer?) c.659del (p.Ser220ThrfsTer?) c.917del (p.Ser306ThrfsTer?) c.782+591del (n.782+591del) c.938del (p.Ser313ThrfsTer30) c.542del (p.Ser181ThrfsTer30) c.821del (p.Ser274ThrfsTer?) c.821del (p.Ser274ThrfsTer30) c.461del (p.Ser154ThrfsTer30) c.905del (p.Ser302ThrfsTer?) c.461del (p.Ser154ThrfsTer?) | |
17 | g.7673590C>A | CA397836053 | TP53 | c.938G>T (p.Ser313Ile) c.542G>T (p.Ser181Ile) c.659G>T (p.Ser220Ile) c.917G>T (p.Ser306Ile) c.782+591G>T (n.782+591G>T) c.821G>T (p.Ser274Ile) c.461G>T (p.Ser154Ile) c.905G>T (p.Ser302Ile) | dbSNP |
17 | g.7673590C>G | CA397836056 | TP53 | c.938G>C (p.Ser313Thr) c.542G>C (p.Ser181Thr) c.659G>C (p.Ser220Thr) c.917G>C (p.Ser306Thr) c.782+591G>C (n.782+591G>C) c.821G>C (p.Ser274Thr) c.461G>C (p.Ser154Thr) c.905G>C (p.Ser302Thr) | dbSNP |
17 | g.7673590C>T | CA397836058 | TP53 | c.938G>A (p.Ser313Asn) c.542G>A (p.Ser181Asn) c.659G>A (p.Ser220Asn) c.917G>A (p.Ser306Asn) c.782+591G>A (n.782+591G>A) c.821G>A (p.Ser274Asn) c.461G>A (p.Ser154Asn) c.905G>A (p.Ser302Asn) | ClinVar dbSNP COSMIC |
17 | g.7673592_7673702del | CA645587377 | TP53 | c.919+1_938del c.523+1_542del c.640+1_659del c.898+1_917del c.782+481_782+591del (n.782+481_782+591del) c.802+1_821del c.442+1_461del c.886+1_905del | COSMIC |
17 | g.7673591T>A | CA397836061 | TP53 | c.937A>T (p.Ser313Cys) c.541A>T (p.Ser181Cys) c.658A>T (p.Ser220Cys) c.916A>T (p.Ser306Cys) c.782+590A>T (n.782+590A>T) c.820A>T (p.Ser274Cys) c.460A>T (p.Ser154Cys) c.904A>T (p.Ser302Cys) | COSMIC |
17 | g.7673591T>C | CA397836063 | TP53 | c.937A>G (p.Ser313Gly) c.541A>G (p.Ser181Gly) c.658A>G (p.Ser220Gly) c.916A>G (p.Ser306Gly) c.782+590A>G (n.782+590A>G) c.820A>G (p.Ser274Gly) c.460A>G (p.Ser154Gly) c.904A>G (p.Ser302Gly) | |
17 | g.7673591T>G | CA397836065 | TP53 | c.937A>C (p.Ser313Arg) c.541A>C (p.Ser181Arg) c.658A>C (p.Ser220Arg) c.916A>C (p.Ser306Arg) c.782+590A>C (n.782+590A>C) c.820A>C (p.Ser274Arg) c.460A>C (p.Ser154Arg) c.904A>C (p.Ser302Arg) |