List of variants in gene PRKN reported as pathogenic for female reproductive organ cancer

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_004562.3(PRKN):c.823C>T (p.Arg275Trp)	rs34424986	0.00226
NM_004562.3(PRKN):c.337_376del (p.Pro113fs)	rs771529549	0.00016
NM_004562.3(PRKN):c.1289G>A (p.Gly430Asp)	rs191486604	0.00013
NM_004562.3(PRKN):c.98G>A (p.Arg33Gln)	rs147757966	0.00006
NM_004562.3(PRKN):c.1321T>C (p.Cys441Arg)	rs778305273	0.00005
NM_004562.3(PRKN):c.758G>A (p.Cys253Tyr)	rs747427602	0.00002
NM_004562.3(PRKN):c.101del (p.Gln34fs)	rs748142049
NM_004562.3(PRKN):c.155del (p.Asn52fs)	rs754809877
NM_004562.3(PRKN):c.220_221dup (p.Trp74fs)	rs746646126
NM_013988.3:c.(?_171+24726)_(424+11283_?)del

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