Gene >> CEL
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000372080 |
| Start |
133068699:133068699(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.932T>G |
| AA Mutation |
p.Val311Gly(p.V311G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000372080 |
| Start |
133067165:133067165(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.864C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |