Mutation details:

cDNA level identifier (n.a.):

c.(933+1_934-1)_(1083+1_1084-1)del

Archive identifier/Other designation:

deletion of exon 9

Genomic location hg(19)

not available

Gene name:

Parkin

Consequence:

structural variation

Pathogenicity scoring:

Definitely pathogenic

CADD score:

not available

Positive functional evidence:

not available

Number of all included cases:

3 homozygous, 5 heterozygous, 11 compound heterozygous (19 in total).

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