"PreventionGenetics, part of Exact Sciences"[submitter] AND "PLD3"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3046314	NM_012268.4(PLD3):c.45G>A (p.Glu15=)	PLD3	Single nucleotide variant (synonymous variant)	PLD3-related disorder	GLikely benign
Select item 2046591	NM_012268.4(PLD3):c.187G>A (p.Gly63Ser)	PLD3 (G63S)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 3054549	NM_012268.4(PLD3):c.489C>G (p.Ile163Met)	PLD3 (I163M)	Single nucleotide variant (missense variant)	PLD3-related disorder	GLikely benign
Select item 3044348	NM_012268.4(PLD3):c.655A>G (p.Met219Val)	PLD3 (M219V)	Single nucleotide variant (missense variant)	PLD3-related disorder	GUncertain significance
Select item 1985142	NM_012268.4(PLD3):c.880-8G>A	PLD3	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 2060536	NM_012268.4(PLD3):c.899G>A (p.Cys300Tyr)	PLD3 (C300Y)	Single nucleotide variant (missense variant)	PLD3-related disorder +1 more	GBenign/Likely benign
Select item 777476	NM_012268.4(PLD3):c.1062C>T (p.Tyr354=)	PLD3	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign

ClinVar