Gene >> ARHGAP12
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000344936 |
| Start |
31810710:31810710(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1989G>T |
| AA Mutation |
p.Gln663His(p.Q663H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000344936 |
| Start |
31854192:31854192(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.963A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |