Protein level identifier (NP_065753):
p.Gln445*
cDNA level identifier (NM_020702):
c.1333C>T
Gene level identifier:
g.5243C>T
Archive identifier/Other designation:
p.Q445*
Reference, alternative allele:
G, A
Genomic location hg(19)
9:34371609 (not available on ExAC)
Gene name:
Consequence:
nonsense
Pathogenicity scoring:
Possibly pathogenic
CADD score:
not available
Positive functional evidence:
not available
Number of all included cases:
1 homozygous (1 in total).