ClinVar Miner

List of variants in gene combination ILK, TAF10 reported as likely benign for cardiovascular disorder

Included ClinVar conditions (1426):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 113
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HGVS dbSNP gnomAD frequency
NM_004517.4(ILK):c.631C>T (p.Arg211Cys) rs140322345 0.00121
NM_004517.4(ILK):c.669G>T (p.Lys223Asn) rs147368550 0.00046
NM_006284.4(TAF10):c.*2414T>A rs183392482 0.00026
NM_004517.4(ILK):c.707A>G (p.Asn236Ser) rs145571020 0.00018
NM_006284.4(TAF10):c.*1417G>T rs375371977 0.00014
NM_006284.4(TAF10):c.*1865C>T rs377346771 0.00010
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_006284.4(TAF10):c.*2707G>A rs371539613 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_004517.4(ILK):c.885G>A (p.Val295=) rs767184450 0.00005
NM_004517.4(ILK):c.924A>G (p.Leu308=) rs758354683 0.00005
NM_006284.4(TAF10):c.*2692C>T rs201214821 0.00005
NM_004517.4(ILK):c.1066G>A (p.Val356Ile) rs199558648 0.00004
NM_004517.4(ILK):c.1263G>T (p.Val421=) rs146642176 0.00004
NM_004517.4(ILK):c.503T>G (p.Phe168Cys) rs747974626 0.00004
NM_006284.4(TAF10):c.*2423G>A rs781209717 0.00004
NM_006284.4(TAF10):c.*2701T>C rs757579795 0.00004
NM_004517.4(ILK):c.1266T>C (p.Cys422=) rs952639348 0.00003
NM_004517.4(ILK):c.93C>T (p.Asp31=) rs56057203 0.00003
NM_006284.4(TAF10):c.*1632C>T rs1235027162 0.00003
NM_004517.4(ILK):c.1041T>C (p.Pro347=) rs748450237 0.00002
NM_004517.4(ILK):c.1338T>C (p.Leu446=) rs144996026 0.00002
NM_004517.4(ILK):c.288G>A (p.Val96=) rs148059090 0.00002
NM_004517.4(ILK):c.501A>G (p.Thr167=) rs1446758399 0.00002
NM_004517.4(ILK):c.555C>T (p.His185=) rs770369647 0.00002
NM_006284.4(TAF10):c.*2237A>C rs372657109 0.00002
NM_006284.4(TAF10):c.*2881G>A rs201421009 0.00002
NM_006284.4(TAF10):c.*465G>A rs755264665 0.00002
NM_006284.4(TAF10):c.*631G>A rs1159966605 0.00002
NM_006284.4(TAF10):c.*782G>A rs972559469 0.00002
NM_004517.4(ILK):c.1122C>T (p.Asp374=) rs1237951284 0.00001
NM_004517.4(ILK):c.1188C>A (p.Ser396=) rs769331209 0.00001
NM_004517.4(ILK):c.1197G>A (p.Glu399=) rs1057522211 0.00001
NM_004517.4(ILK):c.171G>A (p.Gly57=) rs199880663 0.00001
NM_004517.4(ILK):c.231T>C (p.His77=) rs757605280 0.00001
NM_004517.4(ILK):c.234A>G (p.Gly78=) rs376885008 0.00001
NM_004517.4(ILK):c.468C>A (p.Gly156=) rs775797550 0.00001
NM_004517.4(ILK):c.600C>T (p.Asn200=) rs760482273 0.00001
NM_004517.4(ILK):c.654C>T (p.Val218=) rs770261491 0.00001
NM_004517.4(ILK):c.801C>T (p.Leu267=) rs769777649 0.00001
NM_004517.4(ILK):c.861C>T (p.Phe287=) rs779980137 0.00001
NM_004517.4(ILK):c.909G>A (p.Arg303=) rs372479913 0.00001
NM_004517.4(ILK):c.930A>T (p.Thr310=) rs1855316786 0.00001
NM_006284.4(TAF10):c.*1269A>G rs1855301341 0.00001
NM_006284.4(TAF10):c.*1501C>T rs368709206 0.00001
NM_006284.4(TAF10):c.*2049A>G rs1465056090 0.00001
NM_006284.4(TAF10):c.*2053C>T rs368896352 0.00001
NM_004517.4(ILK):c.1014T>C (p.Ala338=) rs1336585654
NM_004517.4(ILK):c.1074C>T (p.Pro358=)
NM_004517.4(ILK):c.111C>A (p.Pro37=)
NM_004517.4(ILK):c.111C>T (p.Pro37=) rs1444626441
NM_004517.4(ILK):c.1137A>T (p.Ala379=)
NM_004517.4(ILK):c.117C>T (p.His39=) rs903002123
NM_004517.4(ILK):c.1216T>C (p.Leu406=)
NM_004517.4(ILK):c.1227T>C (p.Leu409=) rs1855398103
NM_004517.4(ILK):c.1263G>A (p.Val421=)
NM_004517.4(ILK):c.1305G>A (p.Lys435=)
NM_004517.4(ILK):c.1356G>A (p.Lys452=)
NM_004517.4(ILK):c.183T>C (p.Asn61=) rs1420119164
NM_004517.4(ILK):c.207C>T (p.Thr69=) rs751471922
NM_004517.4(ILK):c.261G>A (p.Leu87=)
NM_004517.4(ILK):c.354C>T (p.Asp118=)
NM_004517.4(ILK):c.387T>C (p.Cys129=) rs1049786548
NM_004517.4(ILK):c.489A>G (p.Pro163=)
NM_004517.4(ILK):c.522C>T (p.Arg174=) rs2134559961
NM_004517.4(ILK):c.588G>A (p.Leu196=) rs2134561396
NM_004517.4(ILK):c.690G>A (p.Arg230=)
NM_004517.4(ILK):c.708T>C (p.Asn236=) rs766701483
NM_004517.4(ILK):c.714G>A (p.Glu238=) rs1346943702
NM_004517.4(ILK):c.738G>C (p.Ser246=) rs369519432
NM_004517.4(ILK):c.777T>C (p.Ser259=)
NM_004517.4(ILK):c.818C>G (p.Pro273Arg) rs774113906
NM_004517.4(ILK):c.819G>C (p.Pro273=)
NM_004517.4(ILK):c.837T>C (p.Asn279=) rs1441279272
NM_004517.4(ILK):c.846T>C (p.His282=)
NM_004517.4(ILK):c.876C>T (p.Ser292=)
NM_004517.4(ILK):c.945C>T (p.Ile315=)
NM_004517.4(ILK):c.972T>C (p.Ser324=)
NM_006284.4(TAF10):c.*1000A>G
NM_006284.4(TAF10):c.*1003dup rs1554899641
NM_006284.4(TAF10):c.*1006T>C rs2134569653
NM_006284.4(TAF10):c.*1064C>T
NM_006284.4(TAF10):c.*1067G>C rs1440762009
NM_006284.4(TAF10):c.*1208G>A rs1589940447
NM_006284.4(TAF10):c.*1208G>C rs1589940447
NM_006284.4(TAF10):c.*1210C>G
NM_006284.4(TAF10):c.*1215_*1217del
NM_006284.4(TAF10):c.*1267C>A
NM_006284.4(TAF10):c.*1424G>A
NM_006284.4(TAF10):c.*1425G>A
NM_006284.4(TAF10):c.*1636T>G
NM_006284.4(TAF10):c.*1641G>C rs377752465
NM_006284.4(TAF10):c.*1747del
NM_006284.4(TAF10):c.*1748AAG[1]
NM_006284.4(TAF10):c.*1867G>A
NM_006284.4(TAF10):c.*1942A>G
NM_006284.4(TAF10):c.*2052_*2055del
NM_006284.4(TAF10):c.*2121G>C rs1855196418
NM_006284.4(TAF10):c.*2236G>A rs2134557160
NM_006284.4(TAF10):c.*2415T>C rs1663195410
NM_006284.4(TAF10):c.*2694A>C
NM_006284.4(TAF10):c.*471A>C
NM_006284.4(TAF10):c.*471A>G
NM_006284.4(TAF10):c.*473G>C rs2134575533
NM_006284.4(TAF10):c.*477A>T
NM_006284.4(TAF10):c.*478A>G
NM_006284.4(TAF10):c.*480A>T rs2134575363
NM_006284.4(TAF10):c.*626A>G
NM_006284.4(TAF10):c.*629C>G
NM_006284.4(TAF10):c.*784T>G rs769283883
NM_006284.4(TAF10):c.*789C>T rs553103939

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