Gene >> IRF7
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000397574 |
| Start |
613572:613572(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.871G>A |
| AA Mutation |
p.Val291Met(p.V291M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000397574 |
| Start |
613476:613476(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.967G>A |
| AA Mutation |
p.Ala323Thr(p.A323T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |