Primary Site >> Stomach Cancer
Gene >> BMP7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395863 |
| Start | 57183740:57183740(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.940C>T |
| AA Mutation | p.Arg314Trp(p.R314W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395863 |
| Start | 57265779:57265779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.344G>A |
| AA Mutation | p.Gly115Asp(p.G115D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395863 |
| Start | 57183784:57183784(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771679633 |
| CDS Mutation | c.896G>A |
| AA Mutation | p.Arg299His(p.R299H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395863 |
| Start | 57228260:57228260(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199551942 |
| CDS Mutation | c.580G>A |
| AA Mutation | p.Val194Ile(p.V194I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395863 |
| Start | 57202589:57202589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.646C>T |
| AA Mutation | p.Leu216Phe(p.L216F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395863 |
| Start | 57171043:57171043(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1212C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395863 |
| Start | 57173230:57173230(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142139866 |
| CDS Mutation | c.1116C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395863 |
| Start | 57228317:57228317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.523C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395863 |
| Start | 57171091:57171091(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751546714 |
| CDS Mutation | c.1164G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |