Gene >> UGT2B4
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000305107 |
| Start |
69485415:69485415(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1103C>A |
| AA Mutation |
p.Thr368Asn(p.T368N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000305107 |
| Start |
69495379:69495379(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs777267648
|
| CDS Mutation |
c.483C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |