cDNA level identifier (n.a.):
c.8-61987_171+4006del
Gene level identifier:
g.222312_288468del
Archive identifier/Other designation:
deletion of exon 2
Reference, alternative allele:
C+66157, C
Genomic location hg(19)
6:162860335 (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 compound heterozygous (1 in total).