Variant: 1-69334-C-T



Variant

Variant ID Effect Gene AC AN AF NS NHOM
1-69334-C-T missense_variant OR4F5 1 22676 4.4099488E-5 11338 0


Annotation

Effect Gene Transcript HGVS_c HGVS_p PolyPhen
missense_variant OR4F5 ENST00000335137 c.244C>T p.Arg82Cys benign


External AF

ExAC Genome Asia gnomAD Exome gnomAD Genome GME Variome Iranome TOPMED
NA NA 1.73376E-5 NA NA NA NA


Carrier

Gender count:
1 Male
0 Female
0 Ambiguous
0 NA
Ethnicity count:
0 African
1 Caucasian
0 EastAsian
0 Hispanic
0 MiddleEastern
0 SouthAsian
0 NA

Public Available Gender Phenotype Ethnicity GT DP GQ FILTER
Yes M epilepsy Caucasian HET 26 99 FAIL