Protein level identifier (n.a.):
p.Gly408Arg
cDNA level identifier (n.a.):
c.1222G>C
Gene level identifier:
g.6139G>C
Reference, alternative allele:
C, G
Genomic location hg(0)
11:2186969 (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:
1 compound heterozygous (1 in total).