Primary Site >> Stomach Cancer
Gene >> DSC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257198 |
| Start | 31154872:31154872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780160984 |
| CDS Mutation | c.529G>A |
| AA Mutation | p.Val177Met(p.V177M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257198 |
| Start | 31140243:31140243(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1319C>A |
| AA Mutation | p.Ala440Glu(p.A440E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257198 |
| Start | 31156116:31156116(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761035986 |
| CDS Mutation | c.398A>G |
| AA Mutation | p.Lys133Arg(p.K133R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257198 |
| Start | 31130554:31130554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2645C>A |
| AA Mutation | p.Pro882His(p.P882H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257198 |
| Start | 31130653:31130653(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754736071 |
| CDS Mutation | c.2546C>T |
| AA Mutation | p.Ser849Leu(p.S849L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257198 |
| Start | 31140100:31140100(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1462C>A |
| AA Mutation | p.Gln488Lys(p.Q488K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257198 |
| Start | 31134728:31134728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777889677 |
| CDS Mutation | c.1720G>A |
| AA Mutation | p.Ala574Thr(p.A574T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257198 |
| Start | 31131675:31131675(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770954271 |
| CDS Mutation | c.2406C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |