Primary Site >> Stomach Cancer
Gene >> CLCA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234701 |
| Start | 86499956:86499956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748700845 |
| CDS Mutation | c.2656A>G |
| AA Mutation | p.Asn886Asp(p.N886D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234701 |
| Start | 86482241:86482241(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.594G>T |
| AA Mutation | p.Lys198Asn(p.K198N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234701 |
| Start | 86486536:86486536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146483639 |
| CDS Mutation | c.965G>A |
| AA Mutation | p.Arg322His(p.R322H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234701 |
| Start | 86491270:86491270(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1363T>G |
| AA Mutation | p.Leu455Val(p.L455V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000234701 |
| Start | 86499654:86499654(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2354C>A |
| AA Mutation | p.Ala785Asp(p.A785D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234701 |
| Start | 86495619:86495619(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199729425 |
| CDS Mutation | c.2057G>A |
| AA Mutation | p.Arg686Gln(p.R686Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234701 |
| Start | 86498772:86498772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2314A>T |
| AA Mutation | p.Thr772Ser(p.T772S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234701 |
| Start | 86482221:86482221(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.574A>G |
| AA Mutation | p.Thr192Ala(p.T192A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234701 |
| Start | 86498656:86498656(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs570837989 |
| CDS Mutation | c.2198C>T |
| AA Mutation | p.Ser733Leu(p.S733L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000234701 |
| Start | 86494255:86494255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763299806 |
| CDS Mutation | c.1749G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |