ClinVar Miner

List of variants in gene CUL7 reported as uncertain significance by Eurofins NTD LLC (GA)

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Gene type:
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Total variants: 62
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HGVS dbSNP gnomAD frequency
NM_014780.5(CUL7):c.2645G>A (p.Arg882Gln) rs45574335 0.00185
NM_014780.5(CUL7):c.2614G>A (p.Gly872Ser) rs61750320 0.00170
NM_014780.5(CUL7):c.1859C>T (p.Pro620Leu) rs147326417 0.00115
NM_014780.5(CUL7):c.1067G>A (p.Arg356His) rs146227929 0.00114
NM_014780.5(CUL7):c.136C>T (p.Arg46Trp) rs141692693 0.00108
NM_014780.5(CUL7):c.4659G>A (p.Glu1553=) rs139243761 0.00107
NM_014780.5(CUL7):c.2115C>T (p.His705=) rs143128153 0.00098
NM_014780.5(CUL7):c.2163T>C (p.Asp721=) rs145572983 0.00061
NM_014780.5(CUL7):c.2563A>G (p.Lys855Glu) rs140218677 0.00053
NM_014780.5(CUL7):c.2318G>A (p.Arg773Gln) rs144619494 0.00047
NM_014780.5(CUL7):c.3432G>A (p.Thr1144=) rs144556973 0.00036
NM_014780.5(CUL7):c.2682T>C (p.Ala894=) rs138043979 0.00034
NM_014780.5(CUL7):c.3273G>A (p.Ser1091=) rs144269675 0.00031
NM_014780.5(CUL7):c.5080T>G (p.Phe1694Val) rs150979209 0.00031
NM_014780.5(CUL7):c.2802C>A (p.Leu934=) rs144926293 0.00025
NM_014780.5(CUL7):c.981C>T (p.Pro327=) rs144880219 0.00022
NM_014780.5(CUL7):c.3097G>A (p.Glu1033Lys) rs543762437 0.00019
NM_014780.5(CUL7):c.4003G>C (p.Asp1335His) rs142830307 0.00014
NM_014780.5(CUL7):c.139C>T (p.Arg47Cys) rs371627402 0.00013
NM_014780.5(CUL7):c.3548G>T (p.Ser1183Ile) rs138726142 0.00013
NM_014780.5(CUL7):c.25G>C (p.Glu9Gln) rs375192347 0.00012
NM_014780.5(CUL7):c.3834C>T (p.Gly1278=) rs141756281 0.00011
NM_014780.5(CUL7):c.1570-8G>A rs372757013 0.00010
NM_014780.5(CUL7):c.4482C>T (p.Ser1494=) rs760462179 0.00008
NM_014780.5(CUL7):c.3747G>A (p.Leu1249=) rs141211365 0.00006
NM_014780.5(CUL7):c.3769G>A (p.Gly1257Ser) rs769005642 0.00006
NM_014780.5(CUL7):c.4625G>A (p.Arg1542Gln) rs189054608 0.00006
NM_014780.5(CUL7):c.4713C>T (p.Ile1571=) rs368539088 0.00006
NM_014780.5(CUL7):c.509T>G (p.Leu170Trp) rs138430226 0.00006
NM_014780.5(CUL7):c.4146T>C (p.Tyr1382=) rs760451045 0.00005
NM_014780.5(CUL7):c.156C>T (p.Asp52=) rs368209176 0.00004
NM_014780.5(CUL7):c.2644C>T (p.Arg882Trp) rs746022422 0.00004
NM_014780.5(CUL7):c.2885G>A (p.Arg962Gln) rs761386869 0.00004
NM_014780.5(CUL7):c.2586G>T (p.Lys862Asn) rs749595977 0.00003
NM_014780.5(CUL7):c.2753C>T (p.Thr918Met) rs368479196 0.00003
NM_014780.5(CUL7):c.785C>T (p.Ser262Leu) rs764858516 0.00003
NM_014780.5(CUL7):c.2384G>A (p.Gly795Glu) rs1305192331 0.00002
NM_014780.5(CUL7):c.3861C>T (p.Ala1287=) rs745678508 0.00002
NM_014780.5(CUL7):c.79C>T (p.Arg27Cys) rs199974831 0.00002
NM_014780.5(CUL7):c.935G>A (p.Arg312His) rs201422720 0.00002
NM_014780.5(CUL7):c.1005G>A (p.Leu335=) rs201310376 0.00001
NM_014780.5(CUL7):c.1047C>T (p.Pro349=) rs771240549 0.00001
NM_014780.5(CUL7):c.1073G>A (p.Arg358His) rs750045772 0.00001
NM_014780.5(CUL7):c.4068A>G (p.Glu1356=) rs886043610 0.00001
NM_014780.5(CUL7):c.4258G>A (p.Gly1420Ser) rs369391720 0.00001
NM_014780.5(CUL7):c.4936T>C (p.Tyr1646His) rs1228984654 0.00001
NM_014780.5(CUL7):c.934C>T (p.Arg312Cys) rs746206896 0.00001
NM_014780.5(CUL7):c.1686C>T (p.Cys562=) rs754838245
NM_014780.5(CUL7):c.1782G>A (p.Ala594=) rs369092411
NM_014780.5(CUL7):c.2229C>G (p.Ala743=) rs188565648
NM_014780.5(CUL7):c.2472C>T (p.Leu824=) rs886043579
NM_014780.5(CUL7):c.2647G>A (p.Gly883Ser) rs368465274
NM_014780.5(CUL7):c.2688G>A (p.Glu896=) rs886042208
NM_014780.5(CUL7):c.2754G>A (p.Thr918=) rs138777262
NM_014780.5(CUL7):c.2767-17_2767-13dup rs886042144
NM_014780.5(CUL7):c.2885G>T (p.Arg962Leu) rs761386869
NM_014780.5(CUL7):c.2901A>G (p.Leu967=) rs1554137586
NM_014780.5(CUL7):c.314C>T (p.Ser105Phe) rs755714598
NM_014780.5(CUL7):c.3610G>A (p.Ala1204Thr) rs1554136798
NM_014780.5(CUL7):c.4419G>A (p.Leu1473=) rs1358843733
NM_014780.5(CUL7):c.594G>A (p.Gln198=) rs886042561
NM_014780.5(CUL7):c.618A>G (p.Gln206=) rs1561896171

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