Gene >> ARMC5
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000268314 |
| Start |
31462218:31462218(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.671C>A |
| AA Mutation |
p.Ala224Glu(p.A224E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000268314 |
| Start |
31466857:31466857(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2776G>T |
| AA Mutation |
p.Gly926Trp(p.G926W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |