Gene >> UGT2B15
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000338206 |
| Start |
68654153:68654153(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1197T>A |
| AA Mutation |
p.Asp399Glu(p.D399E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000338206 |
| Start |
68669949:68669949(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.670T>C |
| AA Mutation |
p.Trp224Arg(p.W224R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |