Primary Site >> Stomach Cancer
Gene >> GNAS
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371100 |
| Start | 58855130:58855130(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1865G>A |
| AA Mutation | p.Arg622Gln(p.R622Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371100 |
| Start | 58855254:58855254(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1989G>C |
| AA Mutation | p.Lys663Asn(p.K663N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371100 |
| Start | 58854185:58854185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.920C>A |
| AA Mutation | p.Pro307His(p.P307H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371085 |
| Start | 58910369:58910369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1006C>T |
| AA Mutation | p.Arg336Trp(p.R336W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371100 |
| Start | 58855067:58855067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1802G>A |
| AA Mutation | p.Arg601Gln(p.R601Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371085 |
| Start | 58909366:58909366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121913495 |
| CDS Mutation | c.602G>A |
| AA Mutation | p.Arg201His(p.R201H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371085 |
| Start | 58909365:58909365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs11554273 |
| CDS Mutation | c.601C>T |
| AA Mutation | p.Arg201Cys(p.R201C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371100 |
| Start | 58853612:58853612(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.347C>A |
| AA Mutation | p.Pro116His(p.P116H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371100 |
| Start | 58854544:58854544(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1279G>T |
| AA Mutation | p.Ala427Ser(p.A427S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371100 |
| Start | 58854896:58854896(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1631G>A |
| AA Mutation | p.Arg544Gln(p.R544Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371100 |
| Start | 58853489:58853489(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.224G>T |
| AA Mutation | p.Arg75Ile(p.R75I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371100 |
| Start | 58854053:58854053(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.788C>T |
| AA Mutation | p.Ala263Val(p.A263V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371085 |
| Start | 58909758:58909758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.793C>T |
| AA Mutation | p.Arg265Cys(p.R265C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371085 |
| Start | 58903684:58903684(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.325G>A |
| AA Mutation | p.Ala109Thr(p.A109T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371100 |
| Start | 58855159:58855159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1894C>T |
| AA Mutation | p.Arg632Cys(p.R632C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371100 |
| Start | 58854016:58854016(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.751G>A |
| AA Mutation | p.Gly251Ser(p.G251S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371100 |
| Start | 58854109:58854109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.844G>A |
| AA Mutation | p.Gly282Ser(p.G282S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371085 |
| Start | 58909546:58909546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758829628 |
| CDS Mutation | c.685G>A |
| AA Mutation | p.Asp229Asn(p.D229N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371100 |
| Start | 58854541:58854541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1276G>A |
| AA Mutation | p.Ala426Thr(p.A426T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371100 |
| Start | 58855003:58855003(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1738G>A |
| AA Mutation | p.Glu580Lys(p.E580K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371085 |
| Start | 58905428:58905428(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.478C>T |
| AA Mutation | p.Arg160Cys(p.R160C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371085 |
| Start | 58910741:58910741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1097C>A |
| AA Mutation | p.Ala366Asp(p.A366D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371100 |
| Start | 58853526:58853526(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.261A>C |
| AA Mutation | p.Glu87Asp(p.E87D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371085 |
| Start | 58910710:58910710(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1066C>T |
| AA Mutation | p.Arg356Cys(p.R356C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371100 |
| Start | 58853625:58853625(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.360G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371085 |
| Start | 58891819:58891819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780295677 |
| CDS Mutation | c.93G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371100 |
| Start | 58853667:58853667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771418632 |
| CDS Mutation | c.402C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371085 |
| Start | 58905424:58905424(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.474A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371100 |
| Start | 58854030:58854030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772781318 |
| CDS Mutation | c.765C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371100 |
| Start | 58854435:58854435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1170C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371100 |
| Start | 58854111:58854111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.846C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371100 |
| Start | 58853448:58853448(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752813109 |
| CDS Mutation | c.183C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371085 |
| Start | 58910362:58910362(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777482454 |
| CDS Mutation | c.999C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |