Gene >> NCOA1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000348332 |
| Start |
24665879:24665879(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.220G>A |
| AA Mutation |
p.Val74Ile(p.V74I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000348332 |
| Start |
24752099:24752099(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3824C>T |
| AA Mutation |
p.Ser1275Phe(p.S1275F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |