Gene >> NFX1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000379540 |
| Start |
33364104:33364104(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2968G>A |
| AA Mutation |
p.Ala990Thr(p.A990T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000379540 |
| Start |
33311170:33311170(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1441C>T |
| AA Mutation |
p.Arg481Ter(p.R481*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |