Primary Site >> Stomach Cancer
Gene >> POLQ
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264233 |
| Start | 121533130:121533130(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767741010 |
| CDS Mutation | c.820G>A |
| AA Mutation | p.Val274Met(p.V274M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264233 |
| Start | 121468366:121468366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6784A>G |
| AA Mutation | p.Thr2262Ala(p.T2262A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264233 |
| Start | 121537180:121537180(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.660G>A |
| AA Mutation | p.Met220Ile(p.M220I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264233 |
| Start | 121533033:121533033(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.917C>T |
| AA Mutation | p.Ser306Leu(p.S306L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264233 |
| Start | 121487763:121487763(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748483271 |
| CDS Mutation | c.5168G>A |
| AA Mutation | p.Arg1723His(p.R1723H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264233 |
| Start | 121487538:121487538(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5393C>A |
| AA Mutation | p.Pro1798His(p.P1798H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264233 |
| Start | 121488703:121488703(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4228C>A |
| AA Mutation | p.Leu1410Met(p.L1410M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264233 |
| Start | 121496853:121496853(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373455498 |
| CDS Mutation | c.2233C>T |
| AA Mutation | p.Arg745Cys(p.R745C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264233 |
| Start | 121519960:121519960(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763394640 |
| CDS Mutation | c.1379G>A |
| AA Mutation | p.Arg460Gln(p.R460Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264233 |
| Start | 121433024:121433024(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200303341 |
| CDS Mutation | c.7553G>A |
| AA Mutation | p.Arg2518Gln(p.R2518Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264233 |
| Start | 121522071:121522071(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1187G>A |
| AA Mutation | p.Arg396His(p.R396H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264233 |
| Start | 121539502:121539502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.562G>A |
| AA Mutation | p.Val188Ile(p.V188I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264233 |
| Start | 121544825:121544825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.245A>T |
| AA Mutation | p.Glu82Val(p.E82V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264233 |
| Start | 121490223:121490223(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2708T>G |
| AA Mutation | p.Leu903Arg(p.L903R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264233 |
| Start | 121519915:121519915(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1424A>T |
| AA Mutation | p.Lys475Met(p.K475M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264233 |
| Start | 121509600:121509600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1920G>T |
| AA Mutation | p.Lys640Asn(p.K640N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264233 |
| Start | 121541429:121541429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201454367 |
| CDS Mutation | c.394C>T |
| AA Mutation | p.Arg132Trp(p.R132W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264233 |
| Start | 121440030:121440030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7351C>T |
| AA Mutation | p.Pro2451Ser(p.P2451S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264233 |
| Start | 121460069:121460069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7133T>C |
| AA Mutation | p.Leu2378Pro(p.L2378P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264233 |
| Start | 121487440:121487440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772328819 |
| CDS Mutation | c.5491G>A |
| AA Mutation | p.Ala1831Thr(p.A1831T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264233 |
| Start | 121520048:121520048(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1291G>C |
| AA Mutation | p.Ala431Pro(p.A431P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264233 |
| Start | 121468312:121468312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6838A>G |
| AA Mutation | p.Met2280Val(p.M2280V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264233 |
| Start | 121510056:121510056(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1799C>T |
| AA Mutation | p.Ala600Val(p.A600V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264233 |
| Start | 121539547:121539547(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.517G>A |
| AA Mutation | p.Gly173Ser(p.G173S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264233 |
| Start | 121490030:121490030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2901T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264233 |
| Start | 121460170:121460170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7032T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264233 |
| Start | 121489088:121489088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3843G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264233 |
| Start | 121541388:121541388(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.435C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264233 |
| Start | 121539563:121539563(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.501A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264233 |
| Start | 121539470:121539470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.594C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264233 |
| Start | 121440007:121440007(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7374T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264233 |
| Start | 121510220:121510220(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1635T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264233 |
| Start | 121432921:121432921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7656T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264233 |
| Start | 121509645:121509645(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1875A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264233 |
| Start | 121488281:121488281(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4650T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000264233 |
| Start | 121520075:121520078(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1261_1264delACTT |
| AA Mutation | p.Thr421LeufsTer29(p.T421Lfs*29) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000264233 |
| Start | 121488642:121488642(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.4289delT |
| AA Mutation | p.Leu1430Ter(p.L1430*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000264233 |
| Start | 121473459:121473459(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.6434delC |
| AA Mutation | p.Pro2145GlnfsTer5(p.P2145Qfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000264233 |
| Start | 121493687:121493687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2313G>A |
| AA Mutation | p.Trp771Ter(p.W771*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000264233 |
| Start | 121529678:121529678(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779818079 |
| CDS Mutation | c.1075C>T |
| AA Mutation | p.Arg359Ter(p.R359*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000264233 |
| Start | 121481590:121481590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6193C>T |
| AA Mutation | p.Gln2065Ter(p.Q2065*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000264233 |
| Start | 121488641:121488642(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs755281591 |
| CDS Mutation | c.4289dupT |
| AA Mutation | p.Leu1430PhefsTer5(p.L1430Ffs*5) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |