Gene >> ARHGAP9
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000393791 |
| Start |
57474920:57474920(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1606G>T |
| AA Mutation |
p.Val536Leu(p.V536L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000393791 |
| Start |
57477473:57477473(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.742A>T |
| AA Mutation |
p.Ser248Cys(p.S248C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |