Protein level identifier (n.a.):
p.Asp613His
cDNA level identifier (n.a.):
c.1837G>C
Gene level identifier:
g.90872G>C
Reference, alternative allele:
G, C
Genomic location
not available
Gene name:
Consequence:
missense
Pathogenicity scoring:
Probably pathogenic
CADD score:
29
Positive functional evidence:
not available
Number of all included cases:
3 heterozygous (3 in total).