Primary Site >> Stomach Cancer
Gene >> CRHR2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000471646 |
| Start | 30653473:30653473(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140591778 |
| CDS Mutation | c.1223C>T |
| AA Mutation | p.Thr408Met(p.T408M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000471646 |
| Start | 30681933:30681933(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.211G>A |
| AA Mutation | p.Val71Ile(p.V71I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000471646 |
| Start | 30653560:30653560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1136A>G |
| AA Mutation | p.Asp379Gly(p.D379G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000471646 |
| Start | 30655927:30655927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.917G>T |
| AA Mutation | p.Arg306Met(p.R306M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000471646 |
| Start | 30655689:30655689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.944T>C |
| AA Mutation | p.Leu315Pro(p.L315P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000471646 |
| Start | 30655643:30655643(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774059129 |
| CDS Mutation | c.990C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000471646 |
| Start | 30681967:30681967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.177C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |