"Institute of Human Genetics, University Hospital Muenster"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2430318	NM_001378418.1(TCF20):c.1933A>G (p.Lys645Glu)	TCF20 (K645E)	Single nucleotide variant (missense variant)	See cases	GUncertain significance
Select item 1708328	NM_001378418.1(TCF20):c.1545G>A (p.Met515Ile)	TCF20 (M515I)	Single nucleotide variant (missense variant)	See cases	GUncertain significance
Select item 1708365	NM_001378418.1(TCF20):c.792C>A (p.Tyr264Ter)	TCF20 (Y264*)	Single nucleotide variant (nonsense)	See cases	GPathogenic

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