Gene >> CASP1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000436863 |
| Start |
105034255:105034255(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.227T>G |
| AA Mutation |
p.Ile76Ser(p.I76S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000436863 |
| Start |
105030455:105030455(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs376117763
|
| CDS Mutation |
c.502A>G |
| AA Mutation |
p.Ile168Val(p.I168V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |