Gene >> SNX10
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000338523 |
| Start |
26361023:26361023(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.73T>G |
| AA Mutation |
p.Phe25Val(p.F25V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000338523 |
| Start |
26371931:26371931(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.422C>G |
| AA Mutation |
p.Ser141Cys(p.S141C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |