Gene >> ARL4C
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000390645 |
| Start |
234496027:234496027(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.560A>C |
| AA Mutation |
p.Lys187Thr(p.K187T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000390645 |
| Start |
234496091:234496091(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.496G>C |
| AA Mutation |
p.Glu166Gln(p.E166Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |