Gene >> CA11
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000084798 |
| Start |
48639596:48639596(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.593T>A |
| AA Mutation |
p.Leu198His(p.L198H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000084798 |
| Start |
48638931:48638931(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.918G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |