"Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, E - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1166101	NM_006284.4(TAF10):c.2120_2123=	ILK, TAF10	Variation (no sequence alteration +1 more)	Primary familial hypertrophic cardiomyopathy	GBenign
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 1299856	NM_004517.4(ILK):c.647A>G (p.Asp216Gly)	ILK, TAF10 (D155G +2 more)	Single nucleotide variant (missense variant +1 more)	Primary familial hypertrophic cardiomyopathy	GUncertain significance
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)	not specified +1 more	GBenign
Select item 681788	NM_006284.4(TAF10):c.*784T>G	ILK, TAF10	Single nucleotide variant (3 prime UTR variant +1 more)	not provided +2 more	GLikely benign

ClinVar