Primary Site >> Stomach Cancer
Gene >> CLDN5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000618236 |
| Start | 19523611:19523611(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.645G>T |
| AA Mutation | p.Lys215Asn(p.K215N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000618236 |
| Start | 19523648:19523648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.608C>T |
| AA Mutation | p.Pro203Leu(p.P203L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000618236 |
| Start | 19524207:19524207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.49G>A |
| AA Mutation | p.Gly17Ser(p.G17S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000618236 |
| Start | 19523837:19523837(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.419C>T |
| AA Mutation | p.Ala140Val(p.A140V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000618236 |
| Start | 19523767:19523767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.489G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000618236 |
| Start | 19524197:19524197(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs771945073 |
| CDS Mutation | c.59delG |
| AA Mutation | p.Gly20ValfsTer2(p.G20Vfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |