Primary Site >> Stomach Cancer
Gene >> ASIC2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359872 |
| Start | 33021242:33021242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1265C>T |
| AA Mutation | p.Ala422Val(p.A422V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359872 |
| Start | 33025952:33025952(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1016A>G |
| AA Mutation | p.His339Arg(p.H339R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359872 |
| Start | 34156058:34156058(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.475C>T |
| AA Mutation | p.Arg159Cys(p.R159C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000359872 |
| Start | 33111919:33111919(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.704C>T |
| AA Mutation | p.Thr235Ile(p.T235I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359872 |
| Start | 33015986:33015986(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1422C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359872 |
| Start | 33021241:33021241(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759168920 |
| CDS Mutation | c.1266G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359872 |
| Start | 34156464:34156464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.69C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359872 |
| Start | 33088983:33088983(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs556982917 |
| CDS Mutation | c.714G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |