"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "GAPVD1"[ge - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1335738	NM_001282680.3(GAPVD1):c.265T>C (p.Leu89=)	GAPVD1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 771429	NM_001282680.3(GAPVD1):c.850G>A (p.Val284Met)	GAPVD1 (V284M)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign/Likely benign
Select item 3024816	NM_001282680.3(GAPVD1):c.2830C>T (p.Pro944Ser)	GAPVD1 (P923S +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GLikely benign
Select item 2659496	NM_001282680.3(GAPVD1):c.3774C>T (p.Thr1258=)	GAPVD1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign

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