"Ambry Genetics"[submitter] AND "LOC126863198"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2333121	NM_004650.3(PNPLA4):c.358A>G (p.Thr120Ala)	LOC126863198, PNPLA4 (T33A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216053	NM_004650.3(PNPLA4):c.352G>A (p.Ala118Thr)	LOC126863198, PNPLA4 (A31T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3216052	NM_004650.3(PNPLA4):c.349A>G (p.Asn117Asp)	LOC126863198, PNPLA4 (N30D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383212	NM_004650.3(PNPLA4):c.329G>A (p.Arg110Gln)	LOC126863198, PNPLA4 (R23Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332076	NM_004650.3(PNPLA4):c.269G>A (p.Arg90Gln)	LOC126863198, PNPLA4 (R3Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2386579	NM_004650.3(PNPLA4):c.251G>A (p.Gly84Asp)	LOC126863198, PNPLA4 (G84D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3216051	NM_004650.3(PNPLA4):c.250G>A (p.Gly84Ser)	LOC126863198, PNPLA4 (G84S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar