"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "LOC1300632 - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2649102	NM_015015.3(KDM4B):c.1732G>C (p.Ala578Pro)	KDM4B, LOC130063244 (A578P +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 2649103	NM_015015.3(KDM4B):c.1750C>T (p.Arg584Cys)	KDM4B, LOC130063244 (R584C +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign