Gene >> SIRT3
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000382743 |
| Start |
218900:218900(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1111G>C |
| AA Mutation |
p.Glu371Gln(p.E371Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000382743 |
| Start |
233167:233167(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs148488998
|
| CDS Mutation |
c.522G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |