Gene >> ARHGAP25
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000409202 |
| Start |
68775329:68775329(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.170G>T |
| AA Mutation |
p.Arg57Met(p.R57M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000409202 |
| Start |
68819231:68819231(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1112C>T |
| AA Mutation |
p.Pro371Leu(p.P371L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |