Primary Site >> Stomach Cancer
Gene >> BMP3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282701 |
| Start | 81046359:81046359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.938A>C |
| AA Mutation | p.Glu313Ala(p.E313A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282701 |
| Start | 81046500:81046500(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1079G>T |
| AA Mutation | p.Arg360Met(p.R360M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282701 |
| Start | 81046378:81046378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.957G>T |
| AA Mutation | p.Lys319Asn(p.K319N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282701 |
| Start | 81031469:81031469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.185G>A |
| AA Mutation | p.Arg62Gln(p.R62Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282701 |
| Start | 81046170:81046170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.749C>A |
| AA Mutation | p.Ser250Tyr(p.S250Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282701 |
| Start | 81053464:81053464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1347C>A |
| AA Mutation | p.Phe449Leu(p.F449L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282701 |
| Start | 81031597:81031597(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.313G>A |
| AA Mutation | p.Ala105Thr(p.A105T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282701 |
| Start | 81045831:81045831(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.410G>T |
| AA Mutation | p.Gly137Val(p.G137V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282701 |
| Start | 81046260:81046260(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765583405 |
| CDS Mutation | c.839C>T |
| AA Mutation | p.Ala280Val(p.A280V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282701 |
| Start | 81045945:81045945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.524A>C |
| AA Mutation | p.Asn175Thr(p.N175T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282701 |
| Start | 81046483:81046483(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1062G>T |
| AA Mutation | p.Gln354His(p.Q354H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282701 |
| Start | 81046465:81046465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778395597 |
| CDS Mutation | c.1044G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |