Gene >> CHGA
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000216492 |
| Start |
92932415:92932415(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.854C>T |
| AA Mutation |
p.Ala285Val(p.A285V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000216492 |
| Start |
92926619:92926619(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs376854650
|
| CDS Mutation |
c.108C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |