Primary Site >> Stomach Cancer
Gene >> BMPR1B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264568 |
| Start | 95131422:95131422(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.986C>T |
| AA Mutation | p.Ala329Val(p.A329V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264568 |
| Start | 95131413:95131413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.977C>T |
| AA Mutation | p.Pro326Leu(p.P326L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264568 |
| Start | 95148797:95148797(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768328319 |
| CDS Mutation | c.1126C>T |
| AA Mutation | p.Arg376Cys(p.R376C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264568 |
| Start | 95114802:95114802(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.226G>T |
| AA Mutation | p.Gly76Cys(p.G76C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264568 |
| Start | 95154627:95154627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1463A>G |
| AA Mutation | p.Lys488Arg(p.K488R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264568 |
| Start | 95154568:95154568(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1404A>C |
| AA Mutation | p.Lys468Asn(p.K468N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264568 |
| Start | 95131399:95131399(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.963T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264568 |
| Start | 95115690:95115690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.252T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264568 |
| Start | 95104526:95104526(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766432447 |
| CDS Mutation | c.102C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |