Gene >> ALOX5
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000374391 |
| Start |
45443824:45443824(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1670G>A |
| AA Mutation |
p.Gly557Asp(p.G557D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000374391 |
| Start |
45382650:45382650(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs150281723
|
| CDS Mutation |
c.318C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |