Gene >> IGSF9
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368094 |
| Start |
159930370:159930370(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1883G>A |
| AA Mutation |
p.Arg628Gln(p.R628Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368094 |
| Start |
159929947:159929947(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2093C>T |
| AA Mutation |
p.Ala698Val(p.A698V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |