cDNA level identifier (n.a.):
c.1004+1G>T
Gene level identifier:
g.52226G>T
Archive identifier/Other designation:
IVS6+1G>T
Reference, alternative allele:
G, T
Genomic location
not available
Gene name:
Consequence:
splice site
Pathogenicity scoring:
Probably pathogenic
CADD score:
33
Positive functional evidence:
not available
Number of all included cases:
4 heterozygous (4 in total).