Protein level identifier (n.a.):
p.Leu367Ser
cDNA level identifier (n.a.):
c.1100T>C
Gene level identifier:
g.63339T>C
Reference, alternative allele:
T, C
Genomic location
not available
Gene name:
Consequence:
missense
Pathogenicity scoring:
Probably pathogenic
CADD score:
33
Positive functional evidence:
not available
Number of all included cases:
1 heterozygous (1 in total).