Gene >> HS3ST2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261374 |
| Start |
22915017:22915017(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs767795389
|
| CDS Mutation |
c.559G>A |
| AA Mutation |
p.Ala187Thr(p.A187T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261374 |
| Start |
22915547:22915547(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1089C>A |
| AA Mutation |
p.Asp363Glu(p.D363E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |