Gene >> NUP62
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000352066 |
| Start |
49908816:49908816(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs377108835
|
| CDS Mutation |
c.992C>T |
| AA Mutation |
p.Ala331Val(p.A331V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000352066 |
| Start |
49909469:49909469(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.339C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |