Gene >> IMMP2L
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000331762 |
| Start |
111521426:111521426(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.22G>T |
| AA Mutation |
p.Val8Leu(p.V8L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000331762 |
| Start |
110663656:110663656(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs779329257
|
| CDS Mutation |
c.474A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |