Gene >> ARHGAP9
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000393791 |
| Start |
57479112:57479112(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.295G>A |
| AA Mutation |
p.Gly99Ser(p.G99S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000393791 |
| Start |
57477480:57477480(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs548695816
|
| CDS Mutation |
c.735G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |