C20orf96[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2235232	NM_153269.3(C20orf96):c.541G>A (p.Glu181Lys)	C20orf96 (E180K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259571	NM_153269.3(C20orf96):c.427C>A (p.His143Asn)	C20orf96 (H143N +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2406223	NM_153269.3(C20orf96):c.424C>G (p.Leu142Val)	C20orf96 (L141V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245013	NM_153269.3(C20orf96):c.338G>T (p.Arg113Leu)	C20orf96 (R112L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 783855	NM_153269.3(C20orf96):c.183A>G (p.Gln61=)	C20orf96	Single nucleotide variant (synonymous variant)	not provided	GBenign

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