List of variants in gene PITPNC1 reported as uncertain significance for not specified

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_012417.4(PITPNC1):c.509G>C (p.Arg170Thr)	rs371727466	0.00003
NM_012417.4(PITPNC1):c.244G>A (p.Val82Met)	rs1419111593	0.00001
NM_012417.4(PITPNC1):c.427G>A (p.Asp143Asn)	rs777936488	0.00001
NM_012417.4(PITPNC1):c.104G>A (p.Arg35Gln)
NM_012417.4(PITPNC1):c.124G>A (p.Val42Ile)
NM_012417.4(PITPNC1):c.155A>G (p.His52Arg)
NM_012417.4(PITPNC1):c.209G>C (p.Ser70Thr)
NM_012417.4(PITPNC1):c.440A>C (p.Glu147Ala)

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