Primary Site >> Stomach Cancer
Gene >> BMP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306385 |
| Start | 22194749:22194749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1469A>G |
| AA Mutation | p.Tyr490Cys(p.Y490C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306385 |
| Start | 22207378:22207378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780689541 |
| CDS Mutation | c.2437G>A |
| AA Mutation | p.Ala813Thr(p.A813T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306385 |
| Start | 22211628:22211628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2861T>G |
| AA Mutation | p.Val954Gly(p.V954G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306385 |
| Start | 22195491:22195491(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756176995 |
| CDS Mutation | c.1669G>A |
| AA Mutation | p.Gly557Arg(p.G557R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306385 |
| Start | 22195506:22195506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775940520 |
| CDS Mutation | c.1684C>T |
| AA Mutation | p.Arg562Trp(p.R562W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306385 |
| Start | 22194107:22194107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746237859 |
| CDS Mutation | c.1230C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306385 |
| Start | 22195490:22195490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752676983 |
| CDS Mutation | c.1668C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306385 |
| Start | 22176636:22176636(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.537C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306385 |
| Start | 22197374:22197374(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755344067 |
| CDS Mutation | c.2061C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306385 |
| Start | 22179816:22179816(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.948T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306385 |
| Start | 22207479:22207479(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763570635 |
| CDS Mutation | c.2538G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306385 |
| Start | 22209449:22209449(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372744146 |
| CDS Mutation | c.2580C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306385 |
| Start | 22207377:22207377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs112461266 |
| CDS Mutation | c.2436C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |