Protein level identifier (n.a.):
p.Ala376Val
cDNA level identifier (n.a.):
c.1127C>T
Gene level identifier:
g.5385C>T
Reference, alternative allele:
G, A
Genomic location hg(0)
11:2187723 (not available on ExAC)
Gene name:
Consequence:
missense
Pathogenicity scoring:
Probably pathogenic
CADD score:
not available
Positive functional evidence:
not available
Number of all included cases:
2 compound heterozygous (2 in total).