| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.7674213_7674962del | CA645588534 | TP53 | c.564_745del c.168_349del c.447_628del c.87_268del n.564_745del n.531_712del | COSMIC COSMIC COSMIC |
| 17 | g.7674748T>C | CA981210253 | TP53 | c.672+111A>G (p.=) c.276+111A>G (p.=) c.555+111A>G (p.=) c.195+111A>G (p.=) n.672+111A>G (p.=) n.1039A>G c.393+111A>G (p.=) n.67+305A>G n.639+111A>G (p.=) | |
| 17 | g.7674749A>T | CA775171375 | TP53 | c.672+110T>A (p.=) c.276+110T>A (p.=) c.555+110T>A (p.=) c.195+110T>A (p.=) n.672+110T>A (p.=) n.1038T>A c.393+110T>A (p.=) n.67+304T>A n.639+110T>A (p.=) | |
| 17 | g.7674751A>G | CA287488245 | TP53 | c.672+108T>C (p.=) c.276+108T>C (p.=) c.555+108T>C (p.=) c.195+108T>C (p.=) n.672+108T>C (p.=) n.1036T>C c.393+108T>C (p.=) n.67+302T>C n.639+108T>C (p.=) | dbSNP |
| 17 | g.7674753G>A | CA981210274 | TP53 | c.672+106C>T (p.=) c.276+106C>T (p.=) c.555+106C>T (p.=) c.195+106C>T (p.=) n.672+106C>T (p.=) n.1034C>T c.393+106C>T (p.=) n.67+300C>T n.639+106C>T (p.=) | |
| 17 | g.7674754G>A | CA287488247 | TP53 | c.672+105C>T (p.=) c.276+105C>T (p.=) c.555+105C>T (p.=) c.195+105C>T (p.=) n.672+105C>T (p.=) n.1033C>T c.393+105C>T (p.=) n.67+299C>T n.639+105C>T (p.=) | dbSNP gnomAD |
| 17 | g.7674759C>T | CA775171376 | TP53 | c.672+100G>A (p.=) c.276+100G>A (p.=) c.555+100G>A (p.=) c.195+100G>A (p.=) n.672+100G>A (p.=) n.1028G>A c.393+100G>A (p.=) n.67+294G>A n.639+100G>A (p.=) | |
| 17 | g.7674766G>A | CA775171381 | TP53 | c.672+93C>T (p.=) c.276+93C>T (p.=) c.555+93C>T (p.=) c.195+93C>T (p.=) n.672+93C>T (p.=) n.1021C>T c.393+93C>T (p.=) n.67+287C>T n.639+93C>T (p.=) | |
| 17 | g.7674772G>A | CA287488249 | TP53 | c.672+87C>T (p.=) c.276+87C>T (p.=) c.555+87C>T (p.=) c.195+87C>T (p.=) n.672+87C>T (p.=) n.1015C>T c.393+87C>T (p.=) n.67+281C>T n.639+87C>T (p.=) | dbSNP gnomAD |
| 17 | g.7674779G>A | CA8354862 | TP53 | c.672+80C>T (p.=) c.276+80C>T (p.=) c.555+80C>T (p.=) c.195+80C>T (p.=) n.672+80C>T (p.=) n.1008C>T c.393+80C>T (p.=) n.67+274C>T n.639+80C>T (p.=) | ExAC gnomAD |
| 17 | g.7674780C>T | CA775171405 | TP53 | c.672+79G>A (p.=) c.276+79G>A (p.=) c.555+79G>A (p.=) c.195+79G>A (p.=) n.672+79G>A (p.=) n.1007G>A c.393+79G>A (p.=) n.67+273G>A n.639+79G>A (p.=) | |
| 17 | g.7674785dup | CA624865030 | TP53 | c.672+79dup (p.=) c.276+79dup (p.=) c.555+79dup (p.=) c.195+79dup (p.=) n.672+79dup (p.=) n.1007dup c.393+79dup (p.=) n.67+273dup n.639+79dup (p.=) | gnomAD |
| 17 | g.7674780del | CA8354863 | TP53 | c.672+74del (p.=) c.276+74del (p.=) c.555+74del (p.=) c.195+74del (p.=) n.672+74del (p.=) n.1002del c.393+74del (p.=) n.67+268del n.639+74del (p.=) | dbSNP ExAC gnomAD |
| 17 | g.7674781C>T | CA001919 | TP53 | c.672+78G>A (p.=) c.276+78G>A (p.=) c.555+78G>A (p.=) c.195+78G>A (p.=) n.672+78G>A (p.=) n.1006G>A c.393+78G>A (p.=) n.67+272G>A n.639+78G>A (p.=) | dbSNP ExAC gnomAD |
| 17 | g.7674783C>A | CA287488257 | TP53 | c.672+76G>T (p.=) c.276+76G>T (p.=) c.555+76G>T (p.=) c.195+76G>T (p.=) n.672+76G>T (p.=) n.1004G>T c.393+76G>T (p.=) n.67+270G>T n.639+76G>T (p.=) | dbSNP |
| 17 | g.7674783C>T | CA001926 | TP53 | c.672+76G>A (p.=) c.276+76G>A (p.=) c.555+76G>A (p.=) c.195+76G>A (p.=) n.672+76G>A (p.=) n.1004G>A c.393+76G>A (p.=) n.67+270G>A n.639+76G>A (p.=) | dbSNP ExAC gnomAD |
| 17 | g.7674784C>G | CA624865031 | TP53 | c.672+75G>C (p.=) c.276+75G>C (p.=) c.555+75G>C (p.=) c.195+75G>C (p.=) n.672+75G>C (p.=) n.1003G>C c.393+75G>C (p.=) n.67+269G>C n.639+75G>C (p.=) | gnomAD |
| 17 | g.7674784C>T | CA624865032 | TP53 | c.672+75G>A (p.=) c.276+75G>A (p.=) c.555+75G>A (p.=) c.195+75G>A (p.=) n.672+75G>A (p.=) n.1003G>A c.393+75G>A (p.=) n.67+269G>A n.639+75G>A (p.=) | gnomAD |
| 17 | g.7674785C>T | CA001933 | TP53 | c.672+74G>A (p.=) c.276+74G>A (p.=) c.555+74G>A (p.=) c.195+74G>A (p.=) n.672+74G>A (p.=) n.1002G>A c.393+74G>A (p.=) n.67+268G>A n.639+74G>A (p.=) | dbSNP ExAC gnomAD |
| 17 | g.7674787A>G | CA624865033 | TP53 | c.672+72T>C (p.=) c.276+72T>C (p.=) c.555+72T>C (p.=) c.195+72T>C (p.=) n.672+72T>C (p.=) n.1000T>C c.393+72T>C (p.=) n.67+266T>C n.639+72T>C (p.=) | gnomAD |
| 17 | g.7674788C>T | CA624865034 | TP53 | c.672+71G>A (p.=) c.276+71G>A (p.=) c.555+71G>A (p.=) c.195+71G>A (p.=) n.672+71G>A (p.=) n.999G>A c.393+71G>A (p.=) n.67+265G>A n.639+71G>A (p.=) | gnomAD |
| 17 | g.7674789T>C | CA624865035 | TP53 | c.672+70A>G (p.=) c.276+70A>G (p.=) c.555+70A>G (p.=) c.195+70A>G (p.=) n.672+70A>G (p.=) n.998A>G c.393+70A>G (p.=) n.67+264A>G n.639+70A>G (p.=) | gnomAD |
| 17 | g.7674790G>A | CA624865036 | TP53 | c.672+69C>T (p.=) c.276+69C>T (p.=) c.555+69C>T (p.=) c.195+69C>T (p.=) n.672+69C>T (p.=) n.997C>T c.393+69C>T (p.=) n.67+263C>T n.639+69C>T (p.=) | gnomAD |
| 17 | g.7674790G>T | CA001941 | TP53 | c.672+69C>A (p.=) c.276+69C>A (p.=) c.555+69C>A (p.=) c.195+69C>A (p.=) n.672+69C>A (p.=) n.997C>A c.393+69C>A (p.=) n.67+263C>A n.639+69C>A (p.=) | dbSNP ExAC |
| 17 | g.7674797T>A | CA624865037 | TP53 | c.672+62A>T (p.=) c.276+62A>T (p.=) c.555+62A>T (p.=) c.195+62A>T (p.=) n.672+62A>T (p.=) n.990A>T c.393+62A>T (p.=) n.67+256A>T n.639+62A>T (p.=) | gnomAD |
| 17 | g.7674797T>C | CA001948 | TP53 | c.672+62A>G (p.=) c.276+62A>G (p.=) c.555+62A>G (p.=) c.195+62A>G (p.=) n.672+62A>G (p.=) n.990A>G c.393+62A>G (p.=) n.67+256A>G n.639+62A>G (p.=) | ClinVar dbSNP ExAC gnomAD |
| 17 | g.7674797T>G | CA001950 | TP53 | c.672+62A>C (p.=) c.276+62A>C (p.=) c.555+62A>C (p.=) c.195+62A>C (p.=) n.672+62A>C (p.=) n.990A>C c.393+62A>C (p.=) n.67+256A>C n.639+62A>C (p.=) | dbSNP ExAC gnomAD |
| 17 | g.7674797_7674852del | CA891842248 | TP53 | c.672+7_672+62del (p.=) c.276+7_276+62del (p.=) c.555+7_555+62del (p.=) c.195+7_195+62del (p.=) n.672+7_672+62del (p.=) n.935_990del c.393+7_393+62del (p.=) n.67+201_67+256del n.639+7_639+62del (p.=) | |
| 17 | g.7674798G>A | CA287488267 | TP53 | c.672+61C>T (p.=) c.276+61C>T (p.=) c.555+61C>T (p.=) c.195+61C>T (p.=) n.672+61C>T (p.=) n.989C>T c.393+61C>T (p.=) n.67+255C>T n.639+61C>T (p.=) | dbSNP gnomAD |
| 17 | g.7674801G>A | CA624865038 | TP53 | c.672+58C>T (p.=) c.276+58C>T (p.=) c.555+58C>T (p.=) c.195+58C>T (p.=) n.672+58C>T (p.=) n.986C>T c.393+58C>T (p.=) n.67+252C>T n.639+58C>T (p.=) | gnomAD COSMIC |
| 17 | g.7674802G>A | CA624865039 | TP53 | c.672+57C>T (p.=) c.276+57C>T (p.=) c.555+57C>T (p.=) c.195+57C>T (p.=) n.672+57C>T (p.=) n.985C>T c.393+57C>T (p.=) n.67+251C>T n.639+57C>T (p.=) | gnomAD |
| 17 | g.7674804C>T | CA001962 | TP53 | c.672+55G>A (p.=) c.276+55G>A (p.=) c.555+55G>A (p.=) c.195+55G>A (p.=) n.672+55G>A (p.=) n.983G>A c.393+55G>A (p.=) n.67+249G>A n.639+55G>A (p.=) | dbSNP ExAC gnomAD |
| 17 | g.7674805C>T | CA001970 | TP53 | c.672+54G>A (p.=) c.276+54G>A (p.=) c.555+54G>A (p.=) c.195+54G>A (p.=) n.672+54G>A (p.=) n.982G>A c.393+54G>A (p.=) n.67+248G>A n.639+54G>A (p.=) | dbSNP ExAC gnomAD |
| 17 | g.7674807C>T | CA001977 | TP53 | c.672+52G>A (p.=) c.276+52G>A (p.=) c.555+52G>A (p.=) c.195+52G>A (p.=) n.672+52G>A (p.=) n.980G>A c.393+52G>A (p.=) n.67+246G>A n.639+52G>A (p.=) | dbSNP ExAC gnomAD |
| 17 | g.7674809G>A | CA287488273 | TP53 | c.672+50C>T (p.=) c.276+50C>T (p.=) c.555+50C>T (p.=) c.195+50C>T (p.=) n.672+50C>T (p.=) n.978C>T c.393+50C>T (p.=) n.67+244C>T n.639+50C>T (p.=) | dbSNP gnomAD |
| 17 | g.7674810A>G | CA001985 | TP53 | c.672+49T>C (p.=) c.276+49T>C (p.=) c.555+49T>C (p.=) c.195+49T>C (p.=) n.672+49T>C (p.=) n.977T>C c.393+49T>C (p.=) n.67+243T>C n.639+49T>C (p.=) | dbSNP ExAC gnomAD |
| 17 | g.7674811C>A | CA001992 | TP53 | c.672+48G>T (p.=) c.276+48G>T (p.=) c.555+48G>T (p.=) c.195+48G>T (p.=) n.672+48G>T (p.=) n.976G>T c.393+48G>T (p.=) n.67+242G>T n.639+48G>T (p.=) | dbSNP ExAC gnomAD |
| 17 | g.7674811C>T | CA001993 | TP53 | c.672+48G>A (p.=) c.276+48G>A (p.=) c.555+48G>A (p.=) c.195+48G>A (p.=) n.672+48G>A (p.=) n.976G>A c.393+48G>A (p.=) n.67+242G>A n.639+48G>A (p.=) | dbSNP ExAC gnomAD |
| 17 | g.7674814C>T | CA624865040 | TP53 | c.672+45G>A (p.=) c.276+45G>A (p.=) c.555+45G>A (p.=) c.195+45G>A (p.=) n.672+45G>A (p.=) n.973G>A c.393+45G>A (p.=) n.67+239G>A n.639+45G>A (p.=) | gnomAD |
| 17 | g.7674818C>A | CA002005 | TP53 | c.672+41G>T (p.=) c.276+41G>T (p.=) c.555+41G>T (p.=) c.195+41G>T (p.=) n.672+41G>T (p.=) n.969G>T c.393+41G>T (p.=) n.67+235G>T n.639+41G>T (p.=) | dbSNP ExAC gnomAD |
| 17 | g.7674818C>G | CA624865041 | TP53 | c.672+41G>C (p.=) c.276+41G>C (p.=) c.555+41G>C (p.=) c.195+41G>C (p.=) n.672+41G>C (p.=) n.969G>C c.393+41G>C (p.=) n.67+235G>C n.639+41G>C (p.=) | gnomAD |
| 17 | g.7674819C>A | CA645588690 | TP53 | c.672+40G>T (p.=) c.276+40G>T (p.=) c.555+40G>T (p.=) c.195+40G>T (p.=) n.672+40G>T (p.=) n.968G>T c.393+40G>T (p.=) n.67+234G>T n.639+40G>T (p.=) | COSMIC |
| 17 | g.7674821T>A | CA002012 | TP53 | c.672+38A>T (p.=) c.276+38A>T (p.=) c.555+38A>T (p.=) c.195+38A>T (p.=) n.672+38A>T (p.=) n.966A>T c.393+38A>T (p.=) n.67+232A>T n.639+38A>T (p.=) | dbSNP ExAC gnomAD |
| 17 | g.7674822A>G | CA624865042 | TP53 | c.672+37T>C (p.=) c.276+37T>C (p.=) c.555+37T>C (p.=) c.195+37T>C (p.=) n.672+37T>C (p.=) n.965T>C c.393+37T>C (p.=) n.67+231T>C n.639+37T>C (p.=) | gnomAD |
| 17 | g.7674822A>T | CA002020 | TP53 | c.672+37T>A (p.=) c.276+37T>A (p.=) c.555+37T>A (p.=) c.195+37T>A (p.=) n.672+37T>A (p.=) n.965T>A c.393+37T>A (p.=) n.67+231T>A n.639+37T>A (p.=) | dbSNP ExAC gnomAD |
| 17 | g.7674822_7674861del | CA645588691 | TP53 | c.669_672+36del c.273_276+36del c.552_555+36del c.192_195+36del n.669_672+36del n.925_964del c.390_393+36del n.67+191_67+230del n.636_639+36del | COSMIC |
| 17 | g.7674823A>C | CA981210304 | TP53 | c.672+36T>G (p.=) c.276+36T>G (p.=) c.555+36T>G (p.=) c.195+36T>G (p.=) n.672+36T>G (p.=) n.964T>G c.393+36T>G (p.=) n.67+230T>G n.639+36T>G (p.=) | |
| 17 | g.7674823A>G | CA002027 | TP53 | c.672+36T>C (p.=) c.276+36T>C (p.=) c.555+36T>C (p.=) c.195+36T>C (p.=) n.672+36T>C (p.=) n.964T>C c.393+36T>C (p.=) n.67+230T>C n.639+36T>C (p.=) | dbSNP ExAC gnomAD |
| 17 | g.7674824C>A | CA000327 | TP53 | c.672+35G>T (p.=) c.276+35G>T (p.=) c.555+35G>T (p.=) c.195+35G>T (p.=) n.672+35G>T (p.=) n.963G>T c.393+35G>T (p.=) n.67+229G>T n.639+35G>T (p.=) | ClinVar dbSNP ExAC gnomAD |
| 17 | g.7674824C>T | CA624865043 | TP53 | c.672+35G>A (p.=) c.276+35G>A (p.=) c.555+35G>A (p.=) c.195+35G>A (p.=) n.672+35G>A (p.=) n.963G>A c.393+35G>A (p.=) n.67+229G>A n.639+35G>A (p.=) | gnomAD |