Protein level identifier (NP_055542):
p.Ile2674Thr
cDNA level identifier (NM_014727):
c.8021T>C
Gene level identifier:
g.20411T>C
Reference, alternative allele:
T, C
Genomic location hg(0)
19:36229331 (not available on ExAC)
Gene name:
Consequence:
missense
Pathogenicity scoring:
Possibly pathogenic
CADD score:
25
Positive functional evidence:
not available
Number of all included cases:
1 heterozygous (1 in total).