List of variants in gene ILK, TAF10 studied for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 32

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_004517.4(ILK):c.297C>T (p.His99=)	rs1043388	0.29694
NM_004517.4(ILK):c.819G>A (p.Pro273=)	rs1043390	0.27055
NM_004517.4(ILK):c.918C>T (p.Ala306=)	rs2292195	0.22020
NM_006284.4(TAF10):c.*792G>A	rs111833028	0.00738
NM_006284.4(TAF10):c.*1210C>T	rs145172848	0.00146
NM_004517.4(ILK):c.631C>T (p.Arg211Cys)	rs140322345	0.00121
NM_006284.4(TAF10):c.*2414T>A	rs183392482	0.00026
NM_004517.4(ILK):c.435A>C (p.Arg145Ser)	rs139640491	0.00019
NM_004517.4(ILK):c.279C>A (p.Ile93=)	rs565996441	0.00009
NM_004517.4(ILK):c.1296C>T (p.Asp432=)	rs765285266	0.00008
NM_004517.4(ILK):c.252G>A (p.Gln84=)	rs757818130	0.00007
NM_004517.4(ILK):c.864C>T (p.Val288=)	rs147558204	0.00007
NM_006284.4(TAF10):c.*2423G>A	rs781209717	0.00004
NM_006284.4(TAF10):c.*788G>T	rs776003441	0.00003
NM_004517.4(ILK):c.778C>T (p.Pro260Ser)	rs750354350	0.00002
NM_006284.4(TAF10):c.*782G>A	rs972559469	0.00002
NM_004517.4(ILK):c.1197G>A (p.Glu399=)	rs1057522211	0.00001
NM_004517.4(ILK):c.600C>T (p.Asn200=)	rs760482273	0.00001
NM_004517.4(ILK):c.632G>A (p.Arg211His)	rs200288502	0.00001
NM_006284.4(TAF10):c.*1501C>T	rs368709206	0.00001
NM_006284.4(TAF10):c.*1941C>T	rs776123992	0.00001
NM_006284.4(TAF10):c.*309T>C	rs778105132	0.00001
NM_004517.4(ILK):c.1285A>G (p.Met429Val)	rs1554900131
NM_004517.4(ILK):c.211del (p.Leu71fs)	rs776120061
NM_004517.4(ILK):c.219G>C (p.Leu73=)	rs1057521161
NM_004517.4(ILK):c.222A>T (p.Ala74=)	rs1554898398
NM_004517.4(ILK):c.601G>A (p.Glu201Lys)	rs1057518584
NM_006284.4(TAF10):c.*1003dup	rs1554899641
NM_006284.4(TAF10):c.*1756C>T	rs876657478
NM_006284.4(TAF10):c.2120_2123=
NM_006284.4(TAF10):c.*2123del	rs11314683
NM_006284.4(TAF10):c.*784T>G	rs769283883

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.