ClinVar Miner

List of variants in gene TEK reported as benign for cardiovascular disorder

Included ClinVar conditions (1435):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 65
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HGVS dbSNP gnomAD frequency
NM_000459.5(TEK):c.3063-49C>T rs667250 0.85116
NM_000459.5(TEK):c.761-40C>T rs666478 0.51926
NM_000459.5(TEK):c.2209+17A>G rs638203 0.47788
NM_000459.5(TEK):c.1962A>G (p.Ser654=) rs639225 0.45945
NM_000459.5(TEK):c.3123G>A (p.Gly1041=) rs2273719 0.22124
NM_000459.5(TEK):c.*922G>A rs9987817 0.21120
NM_000459.5(TEK):c.3301-15T>C rs2273715 0.20881
NM_000459.5(TEK):c.2322G>A (p.Arg774=) rs542913 0.20752
NM_000459.5(TEK):c.2976T>C (p.Tyr992=) rs3737188 0.17751
NM_000459.5(TEK):c.*314C>G rs7037246 0.16207
NM_000459.5(TEK):c.*556G>A rs857 0.15475
NM_000459.5(TEK):c.-275dup rs3837240 0.09570
NM_000459.5(TEK):c.1456G>A (p.Val486Ile) rs1334811 0.06507
NM_000459.5(TEK):c.1680T>C (p.Asn560=) rs35357088 0.06246
NM_000459.5(TEK):c.*717T>A rs41272851 0.05369
NM_000459.5(TEK):c.1798G>T (p.Val600Leu) rs35030851 0.03365
NM_000459.5(TEK):c.2094G>A (p.Gln698=) rs45563539 0.03360
NM_000459.5(TEK):c.2170G>A (p.Ala724Thr) rs4631561 0.02531
NM_000459.5(TEK):c.*381C>G rs10967789 0.02463
NM_000459.5(TEK):c.234G>A (p.Val78=) rs55892210 0.01590
NM_000459.5(TEK):c.1172C>T (p.Thr391Ile) rs34032300 0.01461
NM_000459.5(TEK):c.443T>C (p.Ile148Thr) rs35969327 0.01365
NM_000459.5(TEK):c.902-10C>T rs41272241 0.01308
NM_000459.5(TEK):c.2454G>C (p.Val818=) rs55789591 0.01078
NM_000459.5(TEK):c.138C>T (p.Ala46=) rs76223779 0.00772
NM_000459.5(TEK):c.*52T>A rs117748450 0.00729
NM_000459.5(TEK):c.2838C>T (p.Ala946=) rs45505400 0.00725
NM_000459.5(TEK):c.3201-4G>A rs138855043 0.00629
NM_000459.5(TEK):c.*206A>C rs45521836 0.00605
NM_000459.5(TEK):c.*555C>T rs182565061 0.00510
NM_000459.5(TEK):c.1346A>G (p.Asn449Ser) rs149684174 0.00351
NM_000459.5(TEK):c.*579T>C rs138916876 0.00276
NM_000459.5(TEK):c.*484C>G rs192476871 0.00231
NM_000459.5(TEK):c.3090G>A (p.Glu1030=) rs56133834 0.00121
NM_000459.5(TEK):c.1900C>T (p.Leu634Phe) rs35378598 0.00093
NM_000459.5(TEK):c.3200+12C>G rs148623971 0.00056
NM_000459.5(TEK):c.3315C>T (p.Thr1105=) rs148842789 0.00052
NM_000459.5(TEK):c.677C>T (p.Ala226Val) rs35814893 0.00051
NM_000459.5(TEK):c.3151C>T (p.Leu1051=) rs2273718 0.00046
NM_000459.5(TEK):c.1869G>A (p.Gly623=) rs55979986 0.00042
NM_000459.5(TEK):c.1507A>G (p.Thr503Ala) rs200574110 0.00033
NM_000459.5(TEK):c.882G>C (p.Lys294Asn) rs146169480 0.00015
NM_000459.5(TEK):c.3309G>A (p.Val1103=) rs199954698 0.00014
NM_000459.5(TEK):c.2052C>T (p.His684=) rs35818764 0.00013
NM_000459.5(TEK):c.12A>C (p.Leu4Phe) rs146485295 0.00010
NM_000459.5(TEK):c.1387A>G (p.Ile463Val) rs200857533 0.00009
NM_000459.5(TEK):c.3153G>C (p.Leu1051=) rs377362798 0.00007
NM_000459.5(TEK):c.1313A>G (p.Asn438Ser) rs189543659 0.00006
NM_000459.5(TEK):c.3104-15C>G rs766232720 0.00006
NM_000459.5(TEK):c.1146A>G (p.Glu382=) rs146464819 0.00005
NM_000459.5(TEK):c.776C>T (p.Thr259Met) rs138708761 0.00005
NM_000459.5(TEK):c.2546G>A (p.Arg849Gln) rs376225163 0.00004
NM_000459.5(TEK):c.3369G>A (p.Ala1123=) rs544322437 0.00004
NM_000459.5(TEK):c.1390A>C (p.Asn464His) rs746069957 0.00002
NM_000459.5(TEK):c.1734G>A (p.Val578=) rs146405482 0.00002
NM_000459.5(TEK):c.2877+8C>T rs201140196 0.00002
NM_000459.5(TEK):c.*536C>T rs535524868 0.00001
NM_000459.5(TEK):c.-21G>A rs571331918 0.00001
NM_000459.5(TEK):c.1199A>G (p.His400Arg) rs573051752 0.00001
NM_000459.5(TEK):c.*556G>C rs857
NM_000459.5(TEK):c.1037A>C (p.Gln346Pro) rs682632
NM_000459.5(TEK):c.1565G>T (p.Arg522Leu) rs138894008
NM_000459.5(TEK):c.2796C>T (p.Thr932=) rs770991197
NM_000459.5(TEK):c.3062+38dup rs57300282
NM_000459.5(TEK):c.309A>C (p.Glu103Asp) rs572527340

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