Gene >> HMOX1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000216117 |
| Start |
35386740:35386740(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs753863879
|
| CDS Mutation |
c.200G>A |
| AA Mutation |
p.Arg67His(p.R67H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000216117 |
| Start |
35386908:35386908(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.368G>A |
| AA Mutation |
p.Arg123His(p.R123H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |