List of variants in gene PRNP studied for Inborn genetic diseases

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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_000311.5(PRNP):c.531C>T (p.His177=)	rs200294214	0.00004
NM_000311.5(PRNP):c.628G>A (p.Val210Ile)	rs74315407	0.00002
NM_000311.5(PRNP):c.110G>A (p.Arg37Gln)	rs1313855686	0.00001
NM_000311.5(PRNP):c.214G>C (p.Gly72Arg)	rs1209553535	0.00001
NM_000311.5(PRNP):c.286C>G (p.His96Asp)	rs1922418945	0.00001
NM_000311.5(PRNP):c.166G>A (p.Gly56Ser)
NM_000311.5(PRNP):c.209G>T (p.Gly70Val)
NM_000311.5(PRNP):c.244G>A (p.Gly82Arg)
NM_000311.5(PRNP):c.314C>T (p.Pro105Leu)	rs11538758
NM_000311.5(PRNP):c.350C>T (p.Ala117Val)	rs74315402
NM_000311.5(PRNP):c.40G>T (p.Ala14Ser)
NM_000311.5(PRNP):c.452G>T (p.Arg151Leu)	rs779113268

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