Protein level identifier (n.a.):
p.Gln191Arg
cDNA level identifier (n.a.):
c.572A>G
Gene level identifier:
g.61387A>G
Reference, alternative allele:
A, G
Genomic location hg(0)
not available
Gene name:
Consequence:
missense
Pathogenicity scoring:
Probably pathogenic
CADD score:
33
Positive functional evidence:
not available
Number of all included cases:
1 heterozygous (1 in total).