Variant: 1-69334-C-T



Variant

Variant ID Consequence Effect Gene AC AN AF NS NHOM maxEAF
1-69334-C-T p.Arg82Cys missense OR4F5 1 23036 4.3410313E-5 11518 0 1.73376E-5


Annotation

Effect Gene Transcript HGVS_c HGVS_p PolyPhen
missense 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:
Ancestry count:

Public Available Gender Phenotype Ancestry GT DP Percent Alt Read GQ FILTER
Yes M epilepsy Caucasian HET 26 0.42307693 99 FAIL