List of variants in gene PIGV reported by Fulgent Genetics, Fulgent Genetics

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_017837.4(PIGV):c.101C>T (p.Pro34Leu)	rs139246652	0.00505
NM_017837.4(PIGV):c.*149G>A	rs3754360	0.00091
NM_017837.4(PIGV):c.1369C>T (p.Leu457Phe)	rs143676075	0.00068
NM_017837.4(PIGV):c.1022C>A (p.Ala341Glu)	rs139073416	0.00014
NM_017837.4(PIGV):c.473G>A (p.Ser158Asn)	rs201332799	0.00014
NM_017837.4(PIGV):c.808C>T (p.Arg270Cys)	rs374158705	0.00006
NM_017837.4(PIGV):c.115G>A (p.Glu39Lys)	rs369275802	0.00005
NM_017837.4(PIGV):c.348_349delinsAG (p.Ile117Val)	rs886044116

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