List of variants in gene C14orf39 reported as likely benign for not provided

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_174978.3(C14orf39):c.462A>G (p.Ala154=)	rs35543839	0.00447
NM_174978.3(C14orf39):c.1386A>C (p.Glu462Asp)	rs139054454	0.00298
NM_174978.3(C14orf39):c.1279T>C (p.Phe427Leu)	rs149339653	0.00229
NM_174978.3(C14orf39):c.1704T>G (p.Ser568=)	rs145164745	0.00042
NM_174978.3(C14orf39):c.1575G>A (p.Glu525=)

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