cDNA level identifier (n.a.):
c.(1083+1_1084-1)_(1167+1_1168-1)del
Archive identifier/Other designation:
deletion of exon 10
Genomic location hg(19)
not available
Gene name:
Consequence:
structural variation includes copy number variants inversions and translocations
Pathogenicity scoring:
Probably pathogenic
CADD score:
not available
Positive functional evidence:
not available
Number of all included cases:
2 homozygous (2 in total).