Primary Site >> Stomach Cancer
Gene >> BMP10
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295379 |
| Start | 68866074:68866074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.832C>A |
| AA Mutation | p.Gln278Lys(p.Q278K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295379 |
| Start | 68866472:68866472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.434T>G |
| AA Mutation | p.Leu145Arg(p.L145R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295379 |
| Start | 68866326:68866326(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.580A>G |
| AA Mutation | p.Thr194Ala(p.T194A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295379 |
| Start | 68866539:68866539(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.367C>G |
| AA Mutation | p.Leu123Val(p.L123V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295379 |
| Start | 68865849:68865849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1057C>T |
| AA Mutation | p.Arg353Cys(p.R353C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295379 |
| Start | 68865955:68865955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs113361577 |
| CDS Mutation | c.951C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295379 |
| Start | 68866195:68866195(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.711A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295379 |
| Start | 68865655:68865655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750817496 |
| CDS Mutation | c.1251C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295379 |
| Start | 68865865:68865865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs557332981 |
| CDS Mutation | c.1041C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295379 |
| Start | 68866441:68866441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.465T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |