"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "ARHGEF35"[ - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2658122	NM_001003702.3(ARHGEF35):c.1371A>G (p.Arg457=)	ARHGEF35	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2658123	NM_001003702.3(ARHGEF35):c.1261C>G (p.Leu421Val)	ARHGEF35 (L421V)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2583057	GRCh37/hg19 7q34-36.1(chr7:140154317-152551638)x1	KRBA1, LLCFC1 +125 more	Copy number loss	not provided	GPathogenic

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