"Ambry Genetics"[submitter] AND "APOL4"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2224418	NM_001386885.1(APOL4):c.230A>G (p.Tyr77Cys)	APOL4 (Y77C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2334231	NM_001386885.1(APOL4):c.125A>T (p.Lys42Met)	APOL4 (K45M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2348449	NM_001386885.1(APOL4):c.92G>A (p.Arg31His)	APOL4 (R31H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2249516	NM_001386885.1(APOL4):c.71G>A (p.Gly24Glu)	APOL4 (G24E +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2595123	NM_001386885.1(APOL4):c.37G>A (p.Val13Met)	APOL4 (V16M +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2605721	NM_145660.2(APOL4):c.41T>A (p.Ile14Asn)	APOL4 (I14N)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance

ClinVar