Protein level identifier (NP_001124162):
p.Phe334Cys
cDNA level identifier (NM_001130690):
c.1001T>G
Gene level identifier:
g.245822T>G
Archive identifier/Other designation:
p.F334C
Reference, alternative allele:
A, C
Genomic location hg(19)
6:165829767 (not available on ExAC)
Gene name:
Consequence:
missense
Pathogenicity scoring:
Probably pathogenic
CADD score:
28
Positive functional evidence:
Number of all included cases:
2 heterozygous (2 in total).