List of variants in gene PRF1 reported as benign for lymphatic system disorder

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: 34

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HGVS	dbSNP	gnomAD frequency
NM_001083116.3(PRF1):c.900C>T (p.His300=)	rs885822	0.67032
NM_001083116.3(PRF1):c.*96G>A	rs1889490	0.51193
NM_001083116.3(PRF1):c.822C>T (p.Ala274=)	rs885821	0.16394
NM_001083116.3(PRF1):c.272C>T (p.Ala91Val)	rs35947132	0.02791
NM_001083116.3(PRF1):c.11G>A (p.Arg4His)	rs35418374	0.02616
NM_001083116.3(PRF1):c.462A>G (p.Ala154=)	rs116554195	0.01461
NM_001083116.3(PRF1):c.726C>T (p.Cys242=)	rs35329429	0.01263
NM_001083116.3(PRF1):c.435G>A (p.Val145=)	rs115281140	0.01164
NM_001083116.3(PRF1):c.702G>A (p.Ser234=)	rs138508223	0.00843
NM_001083116.3(PRF1):c.755A>G (p.Asn252Ser)	rs28933375	0.00756
NM_001083116.3(PRF1):c.96G>A (p.Lys32=)	rs2228018	0.00448
NM_001083116.3(PRF1):c.444C>T (p.Ala148=)	rs61737403	0.00389
NM_001083116.3(PRF1):c.403G>A (p.Val135Met)	rs12263572	0.00293
NM_001083116.3(PRF1):c.1560C>T (p.Arg520=)	rs147087107	0.00175
NM_001083116.3(PRF1):c.873C>T (p.Ser291=)	rs149008090	0.00139
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.1620A>G (p.Gln540=)	rs149776121	0.00083
NM_001083116.3(PRF1):c.1428G>A (p.Gly476=)	rs145695221	0.00061
NM_001083116.3(PRF1):c.1041C>T (p.His347=)	rs150104693	0.00045
NM_001083116.3(PRF1):c.286C>A (p.Arg96=)	rs144024245	0.00045
NM_001083116.3(PRF1):c.82C>T (p.Arg28Cys)	rs141660796	0.00043
NM_001083116.3(PRF1):c.807C>T (p.His269=)	rs147453010	0.00039
NM_001083116.3(PRF1):c.630C>T (p.Pro210=)	rs144004164	0.00014
NM_001083116.3(PRF1):c.363G>A (p.Ala121=)	rs146358730	0.00010
NM_001083116.3(PRF1):c.632C>T (p.Ala211Val)	rs368524364	0.00006
NM_001083116.3(PRF1):c.111C>T (p.Phe37=)	rs547321451	0.00001
NM_001083116.3(PRF1):c.*139C>A	rs56743633
NM_001083116.3(PRF1):c.*139C>T	rs56743633
NM_001083116.3(PRF1):c.*209del	rs34914326
NM_001083116.3(PRF1):c.*89C>T	rs6480459
NM_001083116.3(PRF1):c.434T>C (p.Val145Ala)	rs535296791
NM_001083116.3(PRF1):c.519G>C (p.Thr173=)	rs112883709
NM_001083116.3(PRF1):c.539+22G>C	rs12263464

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