Primary Site >> Stomach Cancer
Gene >> RNH1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354420 |
| Start | 500634:500634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746459533 |
| CDS Mutation | c.122C>T |
| AA Mutation | p.Thr41Met(p.T41M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354420 |
| Start | 502099:502099(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs557604333 |
| CDS Mutation | c.64G>A |
| AA Mutation | p.Glu22Lys(p.E22K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354420 |
| Start | 498463:498463(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150334174 |
| CDS Mutation | c.950C>T |
| AA Mutation | p.Ser317Leu(p.S317L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354420 |
| Start | 499100:499100(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs543262307 |
| CDS Mutation | c.529G>A |
| AA Mutation | p.Val177Ile(p.V177I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354420 |
| Start | 499088:499088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145250161 |
| CDS Mutation | c.541G>A |
| AA Mutation | p.Asp181Asn(p.D181N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354420 |
| Start | 494914:494914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768887568 |
| CDS Mutation | c.1267C>T |
| AA Mutation | p.Arg423Trp(p.R423W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354420 |
| Start | 498110:498110(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.988T>C |
| AA Mutation | p.Cys330Arg(p.C330R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000354420 |
| Start | 498027:498027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748497432 |
| CDS Mutation | c.1071C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000354420 |
| Start | 494953:494953(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1228C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000354420 |
| Start | 502079:502079(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.84G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000354420 |
| Start | 499909:499909(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769276568 |
| CDS Mutation | c.363C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |