List of variants in gene PRF1 reported as pathogenic for lymphoid neoplasm

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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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001083116.3(PRF1):c.50del (p.Leu17fs)	rs147035858	0.00100
NM_001083116.3(PRF1):c.445G>A (p.Gly149Ser)	rs147462227	0.00007
NM_001083116.3(PRF1):c.1122G>A (p.Trp374Ter)	rs104894176	0.00003
NM_001083116.3(PRF1):c.1090_1091del (p.Leu364fs)	rs771552960	0.00001
NM_001083116.3(PRF1):c.658G>A (p.Gly220Ser)	rs776571416	0.00001
NM_001083116.3(PRF1):c.916G>A (p.Gly306Ser)	rs763002067	0.00001
NM_001083116.3(PRF1):c.1168C>T (p.Arg390Ter)	rs760379846
NM_001083116.3(PRF1):c.150del (p.Thr51fs)
NM_001083116.3(PRF1):c.657C>A (p.Tyr219Ter)
NM_001083116.3(PRF1):c.694C>T (p.Arg232Cys)
NM_001083116.3(PRF1):c.844AAG[3] (p.Lys285del)	rs745902829
NM_001083116.3(PRF1):c.916G>T (p.Gly306Cys)

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