"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "PLVAP"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1694906	NM_031310.3(PLVAP):c.1296T>C (p.Pro432=)	PLVAP	Single nucleotide variant (synonymous variant)	PLVAP-related condition +1 more	GBenign
Select item 2044044	NM_031310.3(PLVAP):c.1121A>C (p.Gln374Pro)	PLVAP (Q374P)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 2188600	NM_031310.3(PLVAP):c.978G>A (p.Glu326=)	PLVAP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1981559	NM_031310.3(PLVAP):c.912C>T (p.Leu304=)	PLVAP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2062220	NM_031310.3(PLVAP):c.796G>C (p.Ala266Pro)	PLVAP (A266P)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2050868	NM_031310.3(PLVAP):c.579G>C (p.Ala193=)	PLVAP	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 2038200	NM_031310.3(PLVAP):c.441C>A (p.Phe147Leu)	PLVAP (F147L)	Single nucleotide variant (missense variant)	not provided	GBenign

ClinVar