List of variants in gene PUF60 reported as likely benign for Inborn genetic diseases

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_078480.3(PUF60):c.80T>C (p.Val27Ala)	rs767013428	0.00005
NM_078480.3(PUF60):c.1565C>T (p.Ala522Val)	rs374890815	0.00004
NM_078480.3(PUF60):c.1216A>G (p.Ser406Gly)
NM_078480.3(PUF60):c.1289G>A (p.Arg430Gln)
NM_078480.3(PUF60):c.1289G>T (p.Arg430Leu)	rs776847578
NM_078480.3(PUF60):c.47G>C (p.Gly16Ala)

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