ClinVar Miner

List of variants in gene combination TBCEL-TECTA, TECTA reported as likely benign for not specified

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Total variants: 64
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HGVS dbSNP gnomAD frequency
NM_005422.4(TECTA):c.972G>C (p.Val324=) rs147790742 0.00271
NM_005422.4(TECTA):c.3304G>A (p.Val1102Ile) rs34658230 0.00253
NM_005422.4(TECTA):c.1436C>T (p.Pro479Leu) rs35107075 0.00186
NM_005422.4(TECTA):c.701A>G (p.Gln234Arg) rs144682235 0.00179
NM_005422.4(TECTA):c.2061C>G (p.Asn687Lys) rs139165033 0.00171
NM_005422.4(TECTA):c.1834G>A (p.Asp612Asn) rs143730090 0.00160
NM_005422.4(TECTA):c.3097C>T (p.Arg1033Trp) rs142486386 0.00149
NM_005422.4(TECTA):c.2123A>G (p.Lys708Arg) rs144932466 0.00123
NM_005422.4(TECTA):c.4720A>G (p.Ile1574Val) rs147354818 0.00123
NM_005422.4(TECTA):c.1002C>T (p.Asp334=) rs35282525 0.00090
NM_005422.4(TECTA):c.2367+9C>T rs368080945 0.00079
NM_005422.4(TECTA):c.1502C>T (p.Ser501Phe) rs148426950 0.00062
NM_005422.4(TECTA):c.4611C>T (p.Pro1537=) rs138477419 0.00057
NM_005422.4(TECTA):c.1509C>T (p.Cys503=) rs61733565 0.00050
NM_005422.4(TECTA):c.2299C>A (p.Arg767=) rs140534420 0.00041
NM_005422.4(TECTA):c.199-4G>A rs373736415 0.00034
NM_005422.4(TECTA):c.5273-8del rs727504781 0.00034
NM_005422.4(TECTA):c.552C>T (p.Tyr184=) rs148364865 0.00032
NM_005422.4(TECTA):c.4315C>A (p.Leu1439Ile) rs202199158 0.00026
NM_005422.4(TECTA):c.5766A>G (p.Thr1922=) rs149602974 0.00026
NM_005422.4(TECTA):c.6250+12C>T rs199696601 0.00019
NM_005422.4(TECTA):c.33C>A (p.Val11=) rs140393508 0.00015
NM_005422.4(TECTA):c.1320T>C (p.Asp440=) rs141488594 0.00014
NM_005422.4(TECTA):c.1425G>A (p.Pro475=) rs149533095 0.00013
NM_005422.4(TECTA):c.1968C>A (p.Gly656=) rs147246652 0.00013
NM_005422.4(TECTA):c.915C>T (p.Cys305=) rs367974065 0.00011
NM_005422.4(TECTA):c.3315C>T (p.Tyr1105=) rs142573400 0.00010
NM_005422.4(TECTA):c.3511G>A (p.Val1171Met) rs186780639 0.00008
NM_005422.4(TECTA):c.2184C>T (p.Ser728=) rs148638616 0.00007
NM_005422.4(TECTA):c.696T>C (p.Asn232=) rs149758927 0.00007
NM_005422.4(TECTA):c.4044C>T (p.Tyr1348=) rs758718634 0.00006
NM_005422.4(TECTA):c.5304G>A (p.Ala1768=) rs373055342 0.00006
NM_005422.4(TECTA):c.6401C>T (p.Thr2134Met) rs372282487 0.00006
NM_005422.4(TECTA):c.2358G>A (p.Ser786=) rs145498566 0.00004
NM_005422.4(TECTA):c.240C>T (p.Ser80=) rs142064539 0.00004
NM_005422.4(TECTA):c.6444C>A (p.Val2148=) rs752301844 0.00004
NM_005422.4(TECTA):c.3291C>T (p.Asp1097=) rs763928462 0.00003
NM_005422.4(TECTA):c.4167C>T (p.Cys1389=) rs745818507 0.00003
NM_005422.4(TECTA):c.5808C>T (p.Leu1936=) rs377039794 0.00003
NM_005422.4(TECTA):c.6033C>T (p.Ile2011=) rs1350403244 0.00003
NM_005422.4(TECTA):c.6102C>T (p.Asp2034=) rs367736479 0.00003
NM_005422.4(TECTA):c.2322C>T (p.Ala774=) rs200749722 0.00002
NM_005422.4(TECTA):c.487-7C>G rs368627411 0.00002
NM_005422.4(TECTA):c.5540C>T (p.Ser1847Phe) rs1198141646 0.00002
NM_005422.4(TECTA):c.585C>T (p.Gly195=) rs372185673 0.00002
NM_005422.4(TECTA):c.1572C>T (p.Cys524=) rs767426110 0.00001
NM_005422.4(TECTA):c.1871C>T (p.Ala624Val) rs1248649998 0.00001
NM_005422.4(TECTA):c.4047C>T (p.Ala1349=) rs768673774 0.00001
NM_005422.4(TECTA):c.6303G>A (p.Arg2101=) rs727505252 0.00001
NM_005422.4(TECTA):c.2134G>C (p.Val712Leu) rs876657587
NM_005422.4(TECTA):c.2199C>G (p.Ser733=) rs397517145
NM_005422.4(TECTA):c.2271G>A (p.Lys757=) rs369114054
NM_005422.4(TECTA):c.2308C>A (p.Arg770=) rs727503458
NM_005422.4(TECTA):c.3375C>T (p.Ile1125=) rs1946747020
NM_005422.4(TECTA):c.3898C>T (p.Leu1300=) rs527881617
NM_005422.4(TECTA):c.4004G>A (p.Gly1335Glu) rs148619105
NM_005422.4(TECTA):c.4263G>A (p.Leu1421=) rs563775304
NM_005422.4(TECTA):c.4690-15T>C rs727505055
NM_005422.4(TECTA):c.5383+8A>G rs1555128731
NM_005422.4(TECTA):c.5955C>A (p.Thr1985=) rs727503466
NM_005422.4(TECTA):c.6402G>T (p.Thr2134=) rs141203939
NM_005422.4(TECTA):c.6459G>A (p.Thr2153=) rs764337303
NM_005422.4(TECTA):c.888G>A (p.Glu296=) rs876657588
NM_005422.4(TECTA):c.90A>T (p.Pro30=) rs577470721

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