Primary Site >> Stomach Cancer
Gene >> ADAM8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000445355 |
| Start | 133270897:133270897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1548G>T |
| AA Mutation | p.Gln516His(p.Q516H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000445355 |
| Start | 133270494:133270494(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1651G>A |
| AA Mutation | p.Val551Ile(p.V551I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000445355 |
| Start | 133271063:133271063(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779344892 |
| CDS Mutation | c.1382C>T |
| AA Mutation | p.Pro461Leu(p.P461L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000445355 |
| Start | 133272513:133272513(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757772199 |
| CDS Mutation | c.778G>A |
| AA Mutation | p.Val260Ile(p.V260I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000445355 |
| Start | 133269959:133269959(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs151131324 |
| CDS Mutation | c.1801C>T |
| AA Mutation | p.Arg601Cys(p.R601C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000445355 |
| Start | 133270947:133270947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1498G>T |
| AA Mutation | p.Gly500Trp(p.G500W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000445355 |
| Start | 133271936:133271936(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370951632 |
| CDS Mutation | c.976G>A |
| AA Mutation | p.Val326Met(p.V326M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000445355 |
| Start | 133270458:133270458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779346703 |
| CDS Mutation | c.1687C>T |
| AA Mutation | p.Arg563Cys(p.R563C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000445355 |
| Start | 133271224:133271224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143338248 |
| CDS Mutation | c.1350C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000445355 |
| Start | 133270495:133270495(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780965691 |
| CDS Mutation | c.1650C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000445355 |
| Start | 133270426:133270426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770651639 |
| CDS Mutation | c.1719G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |