"Genome Diagnostics Laboratory, University Medical Center Utrecht"[sub - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1174719	NM_004517.4(ILK):c.551A>C (p.Lys184Thr)	TAF10, ILK (K184T +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 239949	NM_006284.4(TAF10):c.*1629G>A	ILK, TAF10	Single nucleotide variant (3 prime UTR variant +1 more)	not provided +2 more	GBenign/Likely benign
Select item 155799	NM_004517.4(ILK):c.631C>T (p.Arg211Cys)	ILK, TAF10 (R211C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 1175020	NM_004517.4(ILK):c.721C>T (p.Arg241Trp)	ILK, TAF10 (R107W +2 more)	Single nucleotide variant (missense variant +1 more)	Primary familial hypertrophic cardiomyopathy	GUncertain significance
Select item 137592	NM_006284.4(TAF10):c.*792G>A	ILK, TAF10	Single nucleotide variant (3 prime UTR variant +1 more)	Primary familial hypertrophic cardiomyopathy +1 more	GBenign
Select item 681788	NM_006284.4(TAF10):c.*784T>G	TAF10, ILK	Single nucleotide variant (3 prime UTR variant +1 more)	ILK-related disorder +2 more	GLikely benign

ClinVar