Primary Site >> Stomach Cancer
Gene >> KCNMA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286628 |
| Start | 76914986:76914986(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369646039 |
| CDS Mutation | c.2966G>A |
| AA Mutation | p.Arg989His(p.R989H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286628 |
| Start | 77184849:77184849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.670T>G |
| AA Mutation | p.Phe224Val(p.F224V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286628 |
| Start | 77251205:77251205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.592G>T |
| AA Mutation | p.Asp198Tyr(p.D198Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286628 |
| Start | 76949278:76949278(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773879015 |
| CDS Mutation | c.2573G>A |
| AA Mutation | p.Arg858Gln(p.R858Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286628 |
| Start | 76891646:76891646(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3221C>T |
| AA Mutation | p.Ala1074Val(p.A1074V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286628 |
| Start | 77637356:77637356(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.287T>C |
| AA Mutation | p.Val96Ala(p.V96A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286628 |
| Start | 76891571:76891571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768399208 |
| CDS Mutation | c.3296G>A |
| AA Mutation | p.Arg1099His(p.R1099H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286628 |
| Start | 77637285:77637285(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.358C>A |
| AA Mutation | p.His120Asn(p.H120N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286628 |
| Start | 77403905:77403905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.497C>T |
| AA Mutation | p.Ala166Val(p.A166V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286628 |
| Start | 76891566:76891566(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3301G>T |
| AA Mutation | p.Ala1101Ser(p.A1101S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286628 |
| Start | 76891577:76891577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3290G>A |
| AA Mutation | p.Arg1097His(p.R1097H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286628 |
| Start | 77183439:77183439(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.790T>G |
| AA Mutation | p.Leu264Val(p.L264V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000286628 |
| Start | 77019013:77019013(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2015G>A |
| AA Mutation | p.Arg672Lys(p.R672K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286628 |
| Start | 77112374:77112374(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.953T>C |
| AA Mutation | p.Ile318Thr(p.I318T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286628 |
| Start | 76949189:76949189(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2662C>T |
| AA Mutation | p.Arg888Trp(p.R888W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286628 |
| Start | 77183468:77183468(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.761C>T |
| AA Mutation | p.Thr254Met(p.T254M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286628 |
| Start | 77110276:77110276(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1028T>C |
| AA Mutation | p.Val343Ala(p.V343A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286628 |
| Start | 77183425:77183425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.804G>T |
| AA Mutation | p.Trp268Cys(p.W268C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286628 |
| Start | 77084658:77084658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1502A>T |
| AA Mutation | p.Glu501Val(p.E501V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286628 |
| Start | 77086528:77086528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754219838 |
| CDS Mutation | c.1400A>T |
| AA Mutation | p.Gln467Leu(p.Q467L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286628 |
| Start | 76891695:76891695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3172A>G |
| AA Mutation | p.Thr1058Ala(p.T1058A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286628 |
| Start | 77637440:77637440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.203C>T |
| AA Mutation | p.Ala68Val(p.A68V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286628 |
| Start | 76887378:76887378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3599G>A |
| AA Mutation | p.Ser1200Asn(p.S1200N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286628 |
| Start | 76891534:76891534(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200045097 |
| CDS Mutation | c.3333G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286628 |
| Start | 77012013:77012013(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2046T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286628 |
| Start | 76891657:76891657(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752923387 |
| CDS Mutation | c.3210G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286628 |
| Start | 76953858:76953858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202085429 |
| CDS Mutation | c.2427C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286628 |
| Start | 76891600:76891600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs189703190 |
| CDS Mutation | c.3267G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286628 |
| Start | 77084648:77084648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773511314 |
| CDS Mutation | c.1512G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286628 |
| Start | 77637280:77637280(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141758134 |
| CDS Mutation | c.363C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286628 |
| Start | 76887473:76887473(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200945011 |
| CDS Mutation | c.3504G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286628 |
| Start | 77084660:77084660(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201400928 |
| CDS Mutation | c.1500G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286628 |
| Start | 77403934:77403934(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140636629 |
| CDS Mutation | c.468C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286628 |
| Start | 76910059:76910059(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3054T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286628 |
| Start | 76887389:76887389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs75138661 |
| CDS Mutation | c.3588G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286628 |
| Start | 76949307:76949307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139475681 |
| CDS Mutation | c.2544C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000286628 |
| Start | 77183458:77183458(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.771delC |
| AA Mutation | p.Val258CysfsTer7(p.V258Cfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000286628 |
| Start | 77012033:77012033(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs762705295 |
| CDS Mutation | c.2026delT |
| AA Mutation | p.Tyr676ThrfsTer15(p.Y676Tfs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000286628 |
| Start | 77011983:77011983(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2076delA |
| AA Mutation | p.Lys692AsnfsTer15(p.K692Nfs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000286628 |
| Start | 76970028:76970028(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs771351714 |
| CDS Mutation | c.2306delA |
| AA Mutation | p.Lys769SerfsTer17(p.K769Sfs*17) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |