Gene >> HMOX1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000216117 |
| Start |
35386905:35386905(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.365G>T |
| AA Mutation |
p.Gly122Val(p.G122V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000216117 |
| Start |
35393571:35393571(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.840A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |