Primary Site >> Stomach Cancer
Gene >> TMC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297784 |
| Start | 72792287:72792287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1501C>T |
| AA Mutation | p.Pro501Ser(p.P501S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297784 |
| Start | 72772431:72772431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs111033497 |
| CDS Mutation | c.760G>A |
| AA Mutation | p.Val254Ile(p.V254I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297784 |
| Start | 72805386:72805386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1571T>G |
| AA Mutation | p.Phe524Cys(p.F524C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000297784 |
| Start | 72740208:72740208(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.452A>C |
| AA Mutation | p.Lys151Thr(p.K151T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297784 |
| Start | 72688738:72688738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140437301 |
| CDS Mutation | c.46G>A |
| AA Mutation | p.Glu16Lys(p.E16K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297784 |
| Start | 72789307:72789307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1214A>G |
| AA Mutation | p.Glu405Gly(p.E405G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297784 |
| Start | 72805420:72805420(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1605C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297784 |
| Start | 72791972:72791972(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs537381495 |
| CDS Mutation | c.1311C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |