Primary Site >> Stomach Cancer
Gene >> SLC4A3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317151 |
| Start | 219635362:219635362(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs577704484 |
| CDS Mutation | c.1838C>T |
| AA Mutation | p.Pro613Leu(p.P613L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317151 |
| Start | 219637669:219637669(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2624G>A |
| AA Mutation | p.Ser875Asn(p.S875N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317151 |
| Start | 219640840:219640840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776868780 |
| CDS Mutation | c.3499G>A |
| AA Mutation | p.Ala1167Thr(p.A1167T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317151 |
| Start | 219633312:219633312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1316G>C |
| AA Mutation | p.Arg439Pro(p.R439P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000317151 |
| Start | 219640598:219640598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3446A>C |
| AA Mutation | p.Lys1149Thr(p.K1149T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317151 |
| Start | 219632012:219632012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.856A>G |
| AA Mutation | p.Lys286Glu(p.K286E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000317151 |
| Start | 219634422:219634422(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1564T>C |
| AA Mutation | p.Cys522Arg(p.C522R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317151 |
| Start | 219632352:219632352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753981363 |
| CDS Mutation | c.1051G>A |
| AA Mutation | p.Val351Met(p.V351M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317151 |
| Start | 219628544:219628544(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.191G>A |
| AA Mutation | p.Arg64His(p.R64H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317151 |
| Start | 219638168:219638168(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2771G>A |
| AA Mutation | p.Arg924His(p.R924H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317151 |
| Start | 219637720:219637720(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2675C>T |
| AA Mutation | p.Thr892Met(p.T892M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317151 |
| Start | 219635830:219635830(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779177986 |
| CDS Mutation | c.2130C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317151 |
| Start | 219630345:219630345(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.804C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317151 |
| Start | 219630195:219630195(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.654G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317151 |
| Start | 219635456:219635456(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140228124 |
| CDS Mutation | c.1932C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317151 |
| Start | 219632908:219632908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1176G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317151 |
| Start | 219639635:219639635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138004203 |
| CDS Mutation | c.3177G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317151 |
| Start | 219639548:219639548(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3090C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317151 |
| Start | 219641683:219641683(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3654T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317151 |
| Start | 219630219:219630219(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764787712 |
| CDS Mutation | c.678G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317151 |
| Start | 219635363:219635363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747034568 |
| CDS Mutation | c.1839G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317151 |
| Start | 219635396:219635396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764475960 |
| CDS Mutation | c.1872C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317151 |
| Start | 219638783:219638783(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2937T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000317151 |
| Start | 219628020:219628020(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.32delG |
| AA Mutation | p.Gly11AlafsTer17(p.G11Afs*17) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000317151 |
| Start | 219640566:219640566(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3417delA |
| AA Mutation | p.Lys1139AsnfsTer9(p.K1139Nfs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000317151 |
| Start | 219637622:219637622(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2581delG |
| AA Mutation | p.Ala861ProfsTer46(p.A861Pfs*46) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000317151 |
| Start | 219633007:219633007(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1275delC |
| AA Mutation | p.His425GlnfsTer22(p.H425Qfs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000317151 |
| Start | 219639560:219639560(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs765884021 |
| CDS Mutation | c.3108delG |
| AA Mutation | p.Leu1037SerfsTer24(p.L1037Sfs*24) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000317151 |
| Start | 219637613:219637613(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2573delC |
| AA Mutation | p.Pro858LeufsTer49(p.P858Lfs*49) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000317151 |
| Start | 219636686:219636686(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150010736 |
| CDS Mutation | c.2347C>T |
| AA Mutation | p.Arg783Ter(p.R783*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000317151 |
| Start | 219635433:219635433(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1909C>T |
| AA Mutation | p.Arg637Ter(p.R637*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |