Mutation details:

cDNA level identifier:

c.1084-3859_1167+1618del

Genome level identifier:

g.1337036_1342596del

Archive identifier/Other designation:

deletion of exon 10

Reference, alternative allele:

A+5561, A

Genetic location (hg19):

chr6:161806207 (not available on ExAC)

Gene name:

Parkin

Consequence:

structural variation

Pathogenicity scoring:

probably pathogenic

CADD score:

not available

Positive functional evidence:

not available

Diseases reported for this mutation:

PARK-Parkin

Number of all included cases:

1 homozygous (1 in total).

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