Gene >> BMPR1B
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264568 |
| Start |
95131271:95131271(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.835A>G |
| AA Mutation |
p.Thr279Ala(p.T279A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264568 |
| Start |
95131328:95131328(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs373000965
|
| CDS Mutation |
c.892G>A |
| AA Mutation |
p.Ala298Thr(p.A298T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |