Gene >> ARHGAP19
| ID |
1 |
| Mutation Consequence |
missense_variant;splice_region_variant |
| Transcription ID |
ENST00000358531 |
| Start |
97229873:97229873(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs368334954
|
| CDS Mutation |
c.1286G>A |
| AA Mutation |
p.Arg429Gln(p.R429Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000358531 |
| Start |
97264842:97264842(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.387T>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |