Gene >> NPY
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000242152 |
| Start |
24285392:24285392(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.152C>T |
| AA Mutation |
p.Ala51Val(p.A51V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000242152 |
| Start |
24285280:24285280(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs535222320
|
| CDS Mutation |
c.40C>A |
| AA Mutation |
p.Leu14Ile(p.L14I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |