Gene >> NCOA3
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000371998 |
| Start |
47627943:47627943(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.743G>T |
| AA Mutation |
p.Cys248Phe(p.C248F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000371998 |
| Start |
47652546:47652546(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.4087A>T |
| AA Mutation |
p.Lys1363Ter(p.K1363*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |