Gene >> OGT
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000373719 |
| Start |
71537960:71537960(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.350G>A |
| AA Mutation |
p.Arg117His(p.R117H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000373719 |
| Start |
71557243:71557243(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1369A>G |
| AA Mutation |
p.Lys457Glu(p.K457E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |