Gene >> NAT8
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000272425 |
| Start |
73641511:73641511(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.118C>A |
| AA Mutation |
p.Pro40Thr(p.P40T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000272425 |
| Start |
73641150:73641150(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs766541577
|
| CDS Mutation |
c.479C>A |
| AA Mutation |
p.Thr160Asn(p.T160N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |