ING4[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3109659	NM_016162.4(ING4):c.651C>T (p.Ser217=)	ING4 (P169L)	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 3109658	NM_016162.4(ING4):c.502C>G (p.Pro168Ala)	ING4 (P166A +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2402859	NM_016162.4(ING4):c.493C>T (p.Arg165Cys)	ING4 (R142C +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264064	NM_016162.4(ING4):c.478A>C (p.Lys160Gln)	ING4 (K160Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358026	NM_016162.4(ING4):c.428G>A (p.Arg143His)	ING4 (R120H +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 161520	NM_016162.4(ING4):c.326C>A (p.Ala109Asp)	ING4 (A85D +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 3109657	NM_016162.4(ING4):c.201G>C (p.Gln67His)	ING4 (Q43H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar