Primary Site >> Stomach Cancer
Gene >> ADAM12
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368679 |
| Start | 126038263:126038263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369511795 |
| CDS Mutation | c.2336C>T |
| AA Mutation | p.Pro779Leu(p.P779L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368679 |
| Start | 126108624:126108624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.719G>A |
| AA Mutation | p.Arg240Gln(p.R240Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368679 |
| Start | 126019744:126019744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2620G>A |
| AA Mutation | p.Ala874Thr(p.A874T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368679 |
| Start | 126066722:126066722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1417T>G |
| AA Mutation | p.Cys473Gly(p.C473G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368679 |
| Start | 126098472:126098472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.949G>T |
| AA Mutation | p.Gly317Cys(p.G317C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368679 |
| Start | 126049663:126049663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1625A>C |
| AA Mutation | p.Lys542Thr(p.K542T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368679 |
| Start | 126046063:126046063(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1996G>T |
| AA Mutation | p.Gly666Cys(p.G666C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368679 |
| Start | 126064820:126064820(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149776150 |
| CDS Mutation | c.1604C>T |
| AA Mutation | p.Thr535Met(p.T535M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |