Mutation details:

cDNA level identifier (n.a.):

c.(171+1_172-1)_(534+1_535-1)del

Archive identifier/Other designation:

deletion of exons 3-4

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:

41 homozygous, 43 compound heterozygous (84 in total).

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