ClinVar Miner

List of variants in gene CTC1 reported as benign

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Gene type:
ClinVar version:
Total variants: 75
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HGVS dbSNP gnomAD frequency
NM_025099.6(CTC1):c.435+3= rs6503093 0.99999
NM_025099.6(CTC1):c.1077+49T>C rs4791626 0.98988
NM_025099.6(CTC1):c.2458A>G (p.Ile820Val) rs3027238 0.94552
NM_025099.6(CTC1):c.3013A>G (p.Ile1005Val) rs3826543 0.77529
NM_025099.6(CTC1):c.*2338T>C rs8078338 0.40460
NM_025099.6(CTC1):c.1077+37A>G rs66582670 0.29942
NM_025099.6(CTC1):c.793-112T>A rs59922886 0.27836
NM_025099.6(CTC1):c.647+25A>G rs11655903 0.27813
NM_025099.6(CTC1):c.793-100A>G rs58532865 0.27809
NM_025099.6(CTC1):c.*631T>G rs3027247 0.26879
NM_025099.6(CTC1):c.198-182C>T rs9896745 0.24871
NM_025099.6(CTC1):c.1945+132G>A rs3027234 0.15775
NM_025099.6(CTC1):c.990C>T (p.Asp330=) rs74506939 0.15238
NM_025099.6(CTC1):c.198-153C>T rs74252612 0.14992
NM_025099.6(CTC1):c.648-100G>T rs117819634 0.08423
NM_025099.6(CTC1):c.*1807G>T rs3027251 0.06914
NM_025099.6(CTC1):c.3222-37T>G rs73244850 0.05154
NM_025099.6(CTC1):c.2386-13T>G rs3027237 0.04073
NM_025099.6(CTC1):c.2669+80T>C rs3027240 0.04061
NM_025099.6(CTC1):c.2160C>T (p.Thr720=) rs3027235 0.04058
NM_025099.6(CTC1):c.2385+37C>T rs3027236 0.04040
NM_025099.6(CTC1):c.3515-28G>A rs3027244 0.02224
NM_025099.6(CTC1):c.*1450G>A rs3027250 0.02223
NM_025099.6(CTC1):c.366A>G (p.Ala122=) rs73244859 0.02139
NM_025099.6(CTC1):c.197+76A>G rs73244892 0.02138
NM_025099.6(CTC1):c.198-239T>C rs112291297 0.02136
NM_025099.6(CTC1):c.197+138G>T rs78780166 0.02135
NM_025099.6(CTC1):c.*2087A>G rs75503577 0.01557
NM_025099.6(CTC1):c.*43C>T rs3027245 0.01554
NM_025099.6(CTC1):c.3153G>C (p.Arg1051=) rs3027242 0.01548
NM_025099.6(CTC1):c.126A>G (p.Val42=) rs116271319 0.01470
NM_025099.6(CTC1):c.1025A>G (p.Asp342Gly) rs78390421 0.01469
NM_025099.6(CTC1):c.1307G>A (p.Arg436His) rs75790638 0.01383
NM_025099.6(CTC1):c.2162G>C (p.Gly721Ala) rs62620189 0.01383
NM_025099.6(CTC1):c.1383G>A (p.Gln461=) rs145192682 0.01148
NM_025099.6(CTC1):c.3591C>G (p.Ser1197=) rs115990839 0.01042
NM_025099.6(CTC1):c.197+15C>T rs111473388 0.00989
NM_025099.6(CTC1):c.2154T>A (p.Asp718Glu) rs62637610 0.00947
NM_025099.6(CTC1):c.2973T>C (p.Tyr991=) rs62637613 0.00946
NM_025099.6(CTC1):c.*3231A>G rs139845972 0.00670
NM_025099.6(CTC1):c.*2006T>C rs57270818 0.00633
NM_025099.6(CTC1):c.*2848A>C rs73975813 0.00571
NM_025099.6(CTC1):c.1617+11G>A rs114425026 0.00535
NM_025099.6(CTC1):c.*1668G>A rs114198389 0.00519
NM_025099.6(CTC1):c.*1041A>G rs148405704 0.00430
NM_025099.6(CTC1):c.477G>T (p.Leu159=) rs200658590 0.00148
NM_025099.6(CTC1):c.2478A>G (p.Thr826=) rs200643329 0.00136
NM_025099.6(CTC1):c.*1844G>A rs3027252 0.00127
NM_025099.6(CTC1):c.1720C>T (p.Pro574Ser) rs200440641 0.00117
NM_025099.6(CTC1):c.663T>C (p.Gly221=) rs138725914 0.00105
NM_025099.6(CTC1):c.1728G>A (p.Pro576=) rs78320653 0.00083
NM_025099.6(CTC1):c.1401C>T (p.Tyr467=) rs150409406 0.00079
NM_025099.6(CTC1):c.189C>G (p.Leu63=) rs188658691 0.00044
NM_025099.6(CTC1):c.3221+13G>C rs115684610 0.00041
NM_025099.6(CTC1):c.1795C>T (p.Pro599Ser) rs183556317 0.00029
NM_025099.6(CTC1):c.695G>A (p.Arg232Gln) rs201592575 0.00013
NM_025099.6(CTC1):c.3515-17C>T rs376402639 0.00008
NM_025099.6(CTC1):c.3087C>T (p.Cys1029=) rs775991134 0.00007
NM_025099.6(CTC1):c.2353G>A (p.Glu785Lys) rs201561504 0.00002
NM_025099.6(CTC1):c.1548G>A (p.Pro516=) rs781000475 0.00001
NM_025099.6(CTC1):c.233G>A (p.Arg78His) rs369627256 0.00001
NM_025099.6(CTC1):c.*1200T>C rs80097010
NM_025099.6(CTC1):c.*1474G>A rs78517666
NM_025099.6(CTC1):c.*1960C>G rs11650309
NM_025099.6(CTC1):c.*275G>A rs3027246
NM_025099.6(CTC1):c.1207-40T>G rs12603646
NM_025099.6(CTC1):c.1241G>C (p.Gly414Ala) rs62624978
NM_025099.6(CTC1):c.1818+36C>T rs4792621
NM_025099.6(CTC1):c.1819-314del rs34772323
NM_025099.6(CTC1):c.197+150_197+151insTGT rs143793869
NM_025099.6(CTC1):c.197+235A>G rs73244891
NM_025099.6(CTC1):c.248G>C (p.Ser83Thr) rs78870822
NM_025099.6(CTC1):c.3072G>A (p.Gln1024=) rs1279994496
NM_025099.6(CTC1):c.615C>T (p.Tyr205=) rs571035242
NM_025099.6(CTC1):c.647+12del rs755954781

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