Gene >> ACVR2A
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000241416 |
| Start |
147918519:147918519(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.889G>A |
| AA Mutation |
p.Ala297Thr(p.A297T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000241416 |
| Start |
147896350:147896350(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.105T>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |