Gene >> GNAL
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000269162 |
| Start |
11753929:11753929(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.377A>G |
| AA Mutation |
p.Asp126Gly(p.D126G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000334049 |
| Start |
11689827:11689827(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.264G>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |