Gene >> NAPSA
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000253719 |
| Start |
50360953:50360953(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.656T>C |
| AA Mutation |
p.Phe219Ser(p.F219S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000253719 |
| Start |
50358647:50358647(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1169T>G |
| AA Mutation |
p.Met390Arg(p.M390R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |