Protein level identifier (n.a.):
p.Ile580Thr
cDNA level identifier (n.a.):
c.1739T>C
Gene level identifier:
g.90774T>C
Reference, alternative allele:
T, C
Genomic location
not available
Gene name:
Consequence:
missense
Pathogenicity scoring:
Probably pathogenic
CADD score:
27
Positive functional evidence:
not available
Number of all included cases:
2 heterozygous (2 in total).