Primary Site >> Stomach Cancer
Gene >> CLDN17
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286808 |
| Start | 30166436:30166436(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773823219 |
| CDS Mutation | c.182G>A |
| AA Mutation | p.Arg61Gln(p.R61Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286808 |
| Start | 30166359:30166359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.259G>A |
| AA Mutation | p.Ala87Thr(p.A87T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286808 |
| Start | 30166380:30166380(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.238G>T |
| AA Mutation | p.Ala80Ser(p.A80S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286808 |
| Start | 30166120:30166120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.498C>A |
| AA Mutation | p.Phe166Leu(p.F166L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286808 |
| Start | 30165987:30165987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.631A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000286808 |
| Start | 30166452:30166452(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148594408 |
| CDS Mutation | c.166C>T |
| AA Mutation | p.Arg56Ter(p.R56*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |