Gene >> OGT
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000373719 |
| Start |
71567509:71567509(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2599C>T |
| AA Mutation |
p.Arg867Cys(p.R867C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000373719 |
| Start |
71563189:71563189(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2208G>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |