ClinVar Miner

Variants in gene TNXB with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 49
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HGVS dbSNP gnomAD frequency
NM_001365276.2(TNXB):c.8791+35G>A rs11969759 0.10162
NM_001365276.2(TNXB):c.7680C>T (p.Asp2560=) rs12196385 0.10077
NM_001365276.2(TNXB):c.3764G>A (p.Arg1255His) rs12211410 0.08362
NM_001365276.2(TNXB):c.8132T>C (p.Ile2711Thr) rs28361051 0.00963
NM_001365276.2(TNXB):c.6024A>G (p.Thr2008=) rs61744966 0.00962
NM_001365276.2(TNXB):c.7720A>G (p.Lys2574Glu) rs187409250 0.00902
NM_001365276.2(TNXB):c.7711C>G (p.Gln2571Glu) rs188116087 0.00897
NM_001365276.2(TNXB):c.7704T>C (p.Val2568=) rs370919547 0.00888
NM_001365276.2(TNXB):c.113G>A (p.Arg38Gln) rs149502087 0.00797
NM_001365276.2(TNXB):c.9849G>A (p.Thr3283=) rs147118175 0.00795
NM_001365276.2(TNXB):c.7297G>A (p.Val2433Ile) rs17207902 0.00594
NM_001365276.2(TNXB):c.2373C>T (p.Ser791=) rs112581362 0.00587
NM_001365276.2(TNXB):c.10018G>A (p.Gly3340Ser) rs61737606 0.00542
NM_001365276.2(TNXB):c.9072C>T (p.His3024=) rs61729739 0.00518
NM_001365276.2(TNXB):c.1837A>G (p.Ser613Gly) rs61744970 0.00512
NM_001365276.2(TNXB):c.7168+19C>A rs11752495 0.00484
NM_001365276.2(TNXB):c.5746A>G (p.Thr1916Ala) rs17207916 0.00455
NM_001365276.2(TNXB):c.3445+8A>G rs201624002 0.00326
NM_001365276.2(TNXB):c.4562C>T (p.Ala1521Val) rs146120469 0.00316
NM_001365276.2(TNXB):c.6811G>C (p.Val2271Leu) rs140770834 0.00309
NM_001365276.2(TNXB):c.8594T>C (p.Met2865Thr) rs373158501 0.00294
NM_001365276.2(TNXB):c.10368C>T (p.Thr3456=) rs116701346 0.00261
NM_001365276.2(TNXB):c.9612C>T (p.Asp3204=) rs61746872 0.00253
NM_001365276.2(TNXB):c.909C>G (p.Gly303=) rs111244635 0.00214
NM_001365276.2(TNXB):c.9438G>A (p.Thr3146=) rs202162469 0.00200
NM_001365276.2(TNXB):c.7647T>C (p.Phe2549=) rs571377258 0.00183
NM_001365276.2(TNXB):c.4444G>A (p.Val1482Met) rs61740336 0.00179
NM_001365276.2(TNXB):c.7051G>A (p.Gly2351Arg) rs201638755 0.00166
NM_001365276.2(TNXB):c.2030A>G (p.Asp677Gly) rs141190850 0.00158
NM_001365276.2(TNXB):c.10046-4C>T rs41267134 0.00141
NM_001365276.2(TNXB):c.2242+18C>G rs117489305 0.00139
NM_001365276.2(TNXB):c.7866C>T (p.Thr2622=) rs4711284 0.00104
NM_001365276.2(TNXB):c.9663G>A (p.Val3221=) rs2242569 0.00102
NM_001365276.2(TNXB):c.7413T>C (p.Pro2471=) rs375764263 0.00072
NM_001365276.2(TNXB):c.86G>A (p.Arg29Gln) rs184878358 0.00060
NM_001365276.2(TNXB):c.9762C>T (p.Pro3254=) rs190855421 0.00058
NM_001365276.2(TNXB):c.6074A>T (p.Asp2025Val) rs201397168 0.00055
NM_001365276.2(TNXB):c.7802C>T (p.Pro2601Leu) rs575866552 0.00053
NM_001365276.2(TNXB):c.6276C>T (p.Pro2092=) rs376343294 0.00050
NM_001365276.2(TNXB):c.1927A>G (p.Thr643Ala) rs201703963 0.00049
NM_001365276.2(TNXB):c.6608G>A (p.Arg2203Lys) rs150876029 0.00049
NM_001365276.2(TNXB):c.6135G>C (p.Leu2045=) rs149376928 0.00031
NM_001365276.2(TNXB):c.7352G>A (p.Arg2451Gln) rs201131695 0.00027
NM_001365276.2(TNXB):c.2485G>A (p.Gly829Ser) rs147172260 0.00024
NM_001365276.2(TNXB):c.9661G>A (p.Val3221Met) rs367685759 0.00019
NM_001365276.2(TNXB):c.9488C>G (p.Ala3163Gly) rs561810058 0.00005
NM_001365276.2(TNXB):c.5442C>G (p.Asp1814Glu) rs181025235
NM_001365276.2(TNXB):c.7395C>T (p.Thr2465=) rs759303131
NM_001365276.2(TNXB):c.7620T>C (p.Leu2540=) rs547463127

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