List of variants in gene PRF1 reported as likely benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_001083116.3(PRF1):c.726C>T (p.Cys242=)	rs35329429	0.01263
NM_001083116.3(PRF1):c.755A>G (p.Asn252Ser)	rs28933375	0.00756
NM_001083116.3(PRF1):c.10C>T (p.Arg4Cys)	rs12161733	0.00220
NM_001083116.3(PRF1):c.1560C>T (p.Arg520=)	rs147087107	0.00175
NM_001083116.3(PRF1):c.528C>T (p.Cys176=)	rs138588977	0.00113
NM_001083116.3(PRF1):c.615C>T (p.Asn205=)	rs141130900	0.00088
NM_001083116.3(PRF1):c.1041C>T (p.His347=)	rs150104693	0.00045
NM_001083116.3(PRF1):c.807C>T (p.His269=)	rs147453010	0.00039
NM_001083116.3(PRF1):c.1140G>A (p.Pro380=)	rs144926997	0.00035
NM_001083116.3(PRF1):c.1164C>T (p.Ser388=)
NM_001083116.3(PRF1):c.1212C>T (p.Thr404=)
NM_001083116.3(PRF1):c.519G>C (p.Thr173=)	rs112883709
NM_001083116.3(PRF1):c.539+22G>C	rs12263464
NM_001083116.3(PRF1):c.54C>T (p.Pro18=)
NM_001083116.3(PRF1):c.948C>T (p.Phe316=)	rs201235771

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