Protein level identifier (n.a.):
p.Asp441Val
cDNA level identifier (n.a.):
c.1322A>T
Gene level identifier:
g.73267A>T
Reference, alternative allele:
A, T
Genomic location
not available
Gene name:
Consequence:
missense
Pathogenicity scoring:
Possibly pathogenic
CADD score:
34
Positive functional evidence:
not available
Number of all included cases:
1 heterozygous (1 in total).