Protein level identifier (NP_000208):
p.Val404Ile
cDNA level identifier (NM_000217):
c.1210G>A
Gene level identifier:
g.2684G>A
Reference, alternative allele:
G, A
Genomic location hg(19)
12:5021754 (not available on ExAC)
Gene name:
Consequence:
missense
Pathogenicity scoring:
Probably pathogenic
CADD score:
27
Positive functional evidence:
not available
Number of all included cases:
1 heterozygous (1 in total).