Gene >> CEL
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000372080 |
| Start |
133071702:133071702(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2209G>C |
| AA Mutation |
p.Ala737Pro(p.A737P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000372080 |
| Start |
133069158:133069158(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1194A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |