Protein level identifier (n.a.):
p.Gly294Arg
cDNA level identifier (n.a.):
c.880G>C
Gene level identifier:
g.4937G>C
Reference, alternative allele:
C, G
Genomic location hg(0)
11:2188171 (not available on ExAC)
Gene name:
Consequence:
missense
Pathogenicity scoring:
Possibly pathogenic
CADD score:
not available
Positive functional evidence:
not available
Number of all included cases:
1 compound heterozygous (1 in total).