Protein level identifier (n.a.):
p.Arg562Gln
cDNA level identifier (n.a.):
c.1685G>A
Gene level identifier:
g.81395G>A
Reference, alternative allele:
G, A
Genomic location
not available
Gene name:
Consequence:
missense
Pathogenicity scoring:
Probably pathogenic
CADD score:
31
Positive functional evidence:
not available
Number of all included cases:
5 heterozygous (5 in total).