cDNA level identifier (n.a.):
c.413-27055_534+20428del
Gene level identifier:
g.499465_547069del
Archive identifier/Other designation:
deletion of exon 4
Reference, alternative allele:
C+47605, C
Genomic location hg(19)
6:162601734 (not available on ExAC)
Gene name:
Consequence:
structural variation includes copy number variants inversions and translocations
Pathogenicity scoring:
Definitely pathogenic
CADD score:
not available
Positive functional evidence:
not available
Number of all included cases:
1 homozygous (1 in total).