Gene >> ZNF382
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000292928 |
| Start |
36626973:36626973(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1076A>C |
| AA Mutation |
p.Lys359Thr(p.K359T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000292928 |
| Start |
36627519:36627519(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1622C>T |
| AA Mutation |
p.Thr541Ile(p.T541I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |