"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "PLD3"[gene - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1879438	NM_012268.4(PLD3):c.25dup (p.Glu9fs)	PLD3 (E9fs)	Duplication (frameshift variant)	not provided	GUncertain significance
Select item 2649875	NM_012268.4(PLD3):c.348G>A (p.Ala116=)	PLD3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 120224	NM_012268.4(PLD3):c.694G>A (p.Val232Met)	PLD3 (V232M)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 2060536	NM_012268.4(PLD3):c.899G>A (p.Cys300Tyr)	PLD3 (C300Y)	Single nucleotide variant (missense variant)	PLD3-related condition +1 more	GBenign/Likely benign
Select item 2172277	NM_012268.4(PLD3):c.1052G>A (p.Arg351Gln)	PLD3 (R351Q)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 777476	NM_012268.4(PLD3):c.1062C>T (p.Tyr354=)	PLD3	Single nucleotide variant (synonymous variant)	PLD3-related condition +1 more	GBenign/Likely benign
Select item 2649876	NM_012268.4(PLD3):c.1124G>A (p.Arg375Gln)	PLD3 (R375Q)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 403325	NM_012268.4(PLD3):c.1326G>A (p.Ala442=)	PLD3	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign/Likely benign

ClinVar