Primary Site >> Stomach Cancer
Gene >> SON
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356577 |
| Start | 33552250:33552250(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3019C>T |
| AA Mutation | p.Arg1007Cys(p.R1007C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356577 |
| Start | 33559294:33559294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6386C>T |
| AA Mutation | p.Ser2129Leu(p.S2129L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356577 |
| Start | 33550859:33550859(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755601747 |
| CDS Mutation | c.1628C>T |
| AA Mutation | p.Thr543Met(p.T543M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356577 |
| Start | 33549779:33549779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.548C>A |
| AA Mutation | p.Pro183His(p.P183H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356577 |
| Start | 33550078:33550078(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.847T>A |
| AA Mutation | p.Ser283Thr(p.S283T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356577 |
| Start | 33559260:33559260(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6352G>T |
| AA Mutation | p.Asp2118Tyr(p.D2118Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356577 |
| Start | 33553780:33553780(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4549G>A |
| AA Mutation | p.Glu1517Lys(p.E1517K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356577 |
| Start | 33553367:33553367(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4136C>T |
| AA Mutation | p.Ser1379Leu(p.S1379L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356577 |
| Start | 33552143:33552143(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2912G>A |
| AA Mutation | p.Arg971Lys(p.R971K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356577 |
| Start | 33550744:33550744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376838017 |
| CDS Mutation | c.1513G>A |
| AA Mutation | p.Glu505Lys(p.E505K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356577 |
| Start | 33552650:33552650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3419A>C |
| AA Mutation | p.Tyr1140Ser(p.Y1140S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356577 |
| Start | 33553843:33553843(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4612A>G |
| AA Mutation | p.Asn1538Asp(p.N1538D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356577 |
| Start | 33554804:33554804(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5573G>A |
| AA Mutation | p.Arg1858His(p.R1858H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356577 |
| Start | 33549884:33549884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.653C>A |
| AA Mutation | p.Ser218Tyr(p.S218Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356577 |
| Start | 33555322:33555322(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6091T>C |
| AA Mutation | p.Ser2031Pro(p.S2031P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356577 |
| Start | 33552909:33552909(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752226746 |
| CDS Mutation | c.3678G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356577 |
| Start | 33552709:33552709(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3478T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356577 |
| Start | 33554196:33554196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746428275 |
| CDS Mutation | c.4965T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356577 |
| Start | 33550518:33550518(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1287G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356577 |
| Start | 33550305:33550305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370296512 |
| CDS Mutation | c.1074G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356577 |
| Start | 33551145:33551145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775353389 |
| CDS Mutation | c.1914G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356577 |
| Start | 33552858:33552858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs137934017 |
| CDS Mutation | c.3627G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356577 |
| Start | 33550836:33550836(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1605G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356577 |
| Start | 33549822:33549822(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.591A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356577 |
| Start | 33546273:33546273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs536267719 |
| CDS Mutation | c.138G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356577 |
| Start | 33551964:33551964(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2733T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356577 |
| Start | 33549651:33549651(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763843570 |
| CDS Mutation | c.420G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356577 |
| Start | 33552270:33552270(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150871748 |
| CDS Mutation | c.3039C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356577 |
| Start | 33559685:33559685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747011396 |
| CDS Mutation | c.6567T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356577 |
| Start | 33550581:33550581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200678788 |
| CDS Mutation | c.1350G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000356577 |
| Start | 33551241:33551268(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2012_2039delAGTCCCTGGAGGTGCCCTCGACGACAGC |
| AA Mutation | p.Gln671ArgfsTer8(p.Q671Rfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |