Primary Site >> Stomach Cancer
Gene >> CADM2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000407528 |
| Start | 85912453:85912453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.583A>T |
| AA Mutation | p.Ser195Cys(p.S195C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000407528 |
| Start | 85912406:85912406(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.536G>A |
| AA Mutation | p.Arg179His(p.R179H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000407528 |
| Start | 85883329:85883329(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.250T>A |
| AA Mutation | p.Trp84Arg(p.W84R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000407528 |
| Start | 86065632:86065632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1091G>A |
| AA Mutation | p.Gly364Asp(p.G364D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000407528 |
| Start | 86065605:86065605(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752725804 |
| CDS Mutation | c.1064A>G |
| AA Mutation | p.Asp355Gly(p.D355G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000407528 |
| Start | 85883322:85883322(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747906551 |
| CDS Mutation | c.243C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |