Gene >> B3GAT1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000312527 |
| Start |
134382823:134382823(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.805A>C |
| AA Mutation |
p.Ser269Arg(p.S269R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000312527 |
| Start |
134384028:134384028(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.273C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |