Gene >> IRF4
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000380956 |
| Start |
401770:401770(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1092C>A |
| AA Mutation |
p.Phe364Leu(p.F364L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000380956 |
| Start |
401644:401644(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs113364548
|
| CDS Mutation |
c.966C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |