"PreventionGenetics, part of Exact Sciences"[submitter] AND "VEGFC"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3040254	NM_005429.5(VEGFC):c.1167G>A (p.Thr389=)	HAFML, VEGFC	Single nucleotide variant (synonymous variant)	VEGFC-related disorder	GLikely benign
Select item 2629790	NM_005429.5(VEGFC):c.913G>T (p.Gly305Ter)	HAFML, VEGFC (G305*)	Single nucleotide variant (nonsense)	VEGFC-related disorder	GUncertain significance
Select item 3049599	NM_005429.5(VEGFC):c.501T>C (p.Asn167=)	VEGFC	Single nucleotide variant (synonymous variant)	VEGFC-related disorder	GLikely benign
Select item 3034798	NM_005429.5(VEGFC):c.495C>T (p.Cys165=)	VEGFC	Single nucleotide variant (synonymous variant)	VEGFC-related disorder	GLikely benign
Select item 3036644	NM_005429.5(VEGFC):c.148-9C>T	VEGFC	Single nucleotide variant (intron variant)	VEGFC-related disorder	GLikely benign
Select item 3043806	NM_005429.5(VEGFC):c.148-10T>C	VEGFC	Single nucleotide variant (intron variant)	VEGFC-related disorder	GLikely benign
Select item 3037341	NM_005429.5(VEGFC):c.79GCC[4] (p.Ala31del)	VEGFC (A31del)	Microsatellite (inframe deletion)	VEGFC-related disorder	GLikely benign

ClinVar