List of variants in gene PRNP studied for acquired Creutzfeldt-Jakob disease

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_000311.5(PRNP):c.385A>G (p.Met129Val)	rs1799990	0.33516
NM_000311.5(PRNP):c.*115G>A	rs746943389	0.00014
NM_000311.5(PRNP):c.306G>A (p.Pro102=)	rs370426100	0.00012
NM_000311.5(PRNP):c.159C>T (p.Gly53=)	rs776188950	0.00004
NM_000311.5(PRNP):c.623G>A (p.Arg208His)	rs74315412	0.00004
NM_000311.5(PRNP):c.538G>A (p.Val180Ile)	rs74315408	0.00003
NM_000311.5(PRNP):c.498G>A (p.Met166Ile)	rs745480639	0.00002
NM_000311.5(PRNP):c.628G>A (p.Val210Ile)	rs74315407	0.00002
NM_000311.5(PRNP):c.636G>A (p.Gln212=)	rs757784308	0.00002
NM_000311.5(PRNP):c.695T>G (p.Met232Arg)	rs74315409	0.00002
NM_000311.5(PRNP):c.443G>A (p.Arg148His)	rs181348299	0.00001
NM_000311.3(PRNP):c.204_227del24 (p.Pro84_Gln91del)	rs193922906
NM_000311.3(PRNP):c.[385A>G;532G>A]
NM_000311.5(PRNP):c.154_177[6_13]	rs193922906
NM_000311.5(PRNP):c.305C>T (p.Pro102Leu)	rs74315401
NM_000311.5(PRNP):c.598G>A (p.Glu200Lys)	rs28933385
NM_000311.5(PRNP):c.631G>C (p.Glu211Gln)	rs398122370

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