Primary Site >> Stomach Cancer
Gene >> CLDN16
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264734 |
| Start | 190404875:190404875(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs567783618 |
| CDS Mutation | c.541T>C |
| AA Mutation | p.Tyr181His(p.Y181H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264734 |
| Start | 190410013:190410013(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.895T>C |
| AA Mutation | p.Tyr299His(p.Y299H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264734 |
| Start | 190409993:190409993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752758478 |
| CDS Mutation | c.875G>A |
| AA Mutation | p.Arg292His(p.R292H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264734 |
| Start | 190402398:190402398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762831659 |
| CDS Mutation | c.386G>A |
| AA Mutation | p.Arg129His(p.R129H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264734 |
| Start | 190408487:190408487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.766T>C |
| AA Mutation | p.Cys256Arg(p.C256R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264734 |
| Start | 190409955:190409955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745542693 |
| CDS Mutation | c.837C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |