"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "PLEKHG4B"[ - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2655236	NM_052909.5(PLEKHG4B):c.1312C>A (p.Arg438=)	PLEKHG4B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2655237	NM_052909.5(PLEKHG4B):c.4041C>T (p.Arg1347=)	PLEKHG4B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 624532	GRCh37/hg19 5p15.33(chr5:52186-4163906)x1	AHRR, BRD9 +27 more	Copy number loss	not provided	GLikely pathogenic

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