Protein level identifier (n.a.):
p. Ser467Gly
cDNA level identifier (n.a.):
c.1399A>G
Gene level identifier:
g.6618A>G
Reference, alternative allele:
T, C
Genomic location hg(0)
11:2186490 (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).