ClinVar Miner

List of variants in gene SDHB studied for Gastrointestinal stromal tumor

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Total variants: 112
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HGVS dbSNP gnomAD frequency
NM_003000.3(SDHB):c.201-36G>T rs1022580 0.95416
NM_003000.3(SDHB):c.18C>A (p.Ala6=) rs2746462 0.95374
NM_003000.3(SDHB):c.8C>G (p.Ala3Gly) rs11203289 0.01309
NM_003000.3(SDHB):c.487T>C (p.Ser163Pro) rs33927012 0.00921
NM_003000.3(SDHB):c.32G>A (p.Arg11His) rs111430410 0.00185
NM_003000.3(SDHB):c.423+20T>A rs190139590 0.00179
NM_003000.3(SDHB):c.403G>A (p.Val135Met) rs201585157 0.00012
NM_003000.3(SDHB):c.455C>T (p.Ser152Phe) rs200414835 0.00012
NM_003000.3(SDHB):c.440A>G (p.Tyr147Cys) rs774568101 0.00010
NM_003000.3(SDHB):c.178A>G (p.Thr60Ala) rs34599281 0.00007
NM_003000.3(SDHB):c.112C>T (p.Arg38Cys) rs202119350 0.00006
NM_003000.3(SDHB):c.317A>G (p.Asn106Ser) rs934514080 0.00006
NM_003000.3(SDHB):c.200+7A>G rs371329778 0.00005
NM_003000.3(SDHB):c.269G>A (p.Arg90Gln) rs570278423 0.00004
NM_003000.3(SDHB):c.307A>G (p.Met103Val) rs140178341 0.00004
NM_003000.3(SDHB):c.530G>A (p.Arg177His) rs150437793 0.00004
NM_003000.3(SDHB):c.695C>T (p.Ala232Val) rs746224555 0.00004
NM_003000.3(SDHB):c.136C>T (p.Arg46Ter) rs74315370 0.00003
NM_003000.3(SDHB):c.200+4A>C rs774908929 0.00003
NM_003000.3(SDHB):c.344G>A (p.Arg115Gln) rs200973284 0.00003
NM_003000.3(SDHB):c.418G>T (p.Val140Phe) rs267607032 0.00003
NM_003000.3(SDHB):c.650G>A (p.Arg217His) rs747518441 0.00003
NM_003000.3(SDHB):c.79C>T (p.Arg27Ter) rs74315369 0.00003
NM_003000.3(SDHB):c.130A>G (p.Ile44Val) rs200418115 0.00002
NM_003000.3(SDHB):c.400T>C (p.Tyr134His) rs771004483 0.00002
NM_003000.3(SDHB):c.41C>T (p.Pro14Leu) rs764089231 0.00002
NM_003000.3(SDHB):c.529C>T (p.Arg177Cys) rs149091125 0.00002
NM_003000.3(SDHB):c.736A>G (p.Ile246Val) rs146800605 0.00002
NM_003000.3(SDHB):c.739A>G (p.Met247Val) rs200896502 0.00002
NM_003000.3(SDHB):c.820A>G (p.Lys274Glu) rs1273897502 0.00002
NM_003000.3(SDHB):c.137G>A (p.Arg46Gln) rs772551056 0.00001
NM_003000.3(SDHB):c.143A>T (p.Asp48Val) rs202101384 0.00001
NM_003000.3(SDHB):c.14T>G (p.Val5Gly) rs760565241 0.00001
NM_003000.3(SDHB):c.172A>G (p.Met58Val) rs1201188410 0.00001
NM_003000.3(SDHB):c.214G>A (p.Val72Ile) rs1060503766 0.00001
NM_003000.3(SDHB):c.221A>C (p.Asp74Ala) rs876658713 0.00001
NM_003000.3(SDHB):c.286G>A (p.Gly96Ser) rs587782243 0.00001
NM_003000.3(SDHB):c.31C>T (p.Arg11Cys) rs200868378 0.00001
NM_003000.3(SDHB):c.323G>A (p.Gly108Asp) rs767062764 0.00001
NM_003000.3(SDHB):c.343C>T (p.Arg115Ter) rs751000085 0.00001
NM_003000.3(SDHB):c.362T>C (p.Leu121Pro) rs775925040 0.00001
NM_003000.3(SDHB):c.380T>G (p.Ile127Ser) rs786201095 0.00001
NM_003000.3(SDHB):c.423+1G>A rs398122805 0.00001
NM_003000.3(SDHB):c.457A>G (p.Ile153Val) rs1450956956 0.00001
NM_003000.3(SDHB):c.458T>C (p.Ile153Thr) rs1396860069 0.00001
NM_003000.3(SDHB):c.47C>G (p.Thr16Arg) rs775350144 0.00001
NM_003000.3(SDHB):c.482A>G (p.Asp161Gly) rs1049317868 0.00001
NM_003000.3(SDHB):c.527A>G (p.Glu176Gly) rs201082445 0.00001
NM_003000.3(SDHB):c.541G>A (p.Asp181Asn) rs201385062 0.00001
NM_003000.3(SDHB):c.600G>T (p.Trp200Cys) rs397516836 0.00001
NM_003000.3(SDHB):c.607G>A (p.Gly203Arg) rs201517260 0.00001
NM_003000.3(SDHB):c.638T>C (p.Met213Thr) rs202014362 0.00001
NM_003000.3(SDHB):c.649C>T (p.Arg217Cys) rs200245469 0.00001
NM_003000.3(SDHB):c.689G>A (p.Arg230His) rs587782604 0.00001
NM_003000.3(SDHB):c.725G>A (p.Arg242His) rs74315368 0.00001
NM_003000.3(SDHB):c.73-6T>A rs1252798981 0.00001
NM_003000.3(SDHB):c.749C>T (p.Thr250Ile) rs1057517537 0.00001
NM_003000.3(SDHB):c.7G>A (p.Ala3Thr) rs765429934 0.00001
NM_003000.3(SDHB):c.101C>G (p.Ala34Gly) rs867908217
NM_003000.3(SDHB):c.14T>C (p.Val5Ala) rs760565241
NM_003000.3(SDHB):c.166_170del (p.Pro56fs) rs786202100
NM_003000.3(SDHB):c.19C>G (p.Leu7Val) rs745664191
NM_003000.3(SDHB):c.211A>G (p.Met71Val) rs1557742895
NM_003000.3(SDHB):c.233A>G (p.Lys78Arg) rs774960237
NM_003000.3(SDHB):c.23C>T (p.Ser8Phe) rs199848267
NM_003000.3(SDHB):c.241A>T (p.Asn81Tyr) rs1315623287
NM_003000.3(SDHB):c.256A>T (p.Thr86Ser) rs1570951385
NM_003000.3(SDHB):c.263C>G (p.Thr88Ser) rs915794675
NM_003000.3(SDHB):c.269G>T (p.Arg90Leu) rs570278423
NM_003000.3(SDHB):c.286+1G>A rs786201063
NM_003000.3(SDHB):c.286+2T>A rs587781270
NM_003000.3(SDHB):c.286+5G>A rs768966871
NM_003000.3(SDHB):c.287-6T>C
NM_003000.3(SDHB):c.289A>T (p.Ile97Phe) rs1553177769
NM_003000.3(SDHB):c.292T>C (p.Cys98Arg)
NM_003000.3(SDHB):c.29G>A (p.Arg10Lys) rs1570963545
NM_003000.3(SDHB):c.305C>T (p.Ala102Val)
NM_003000.3(SDHB):c.374C>T (p.Ser125Leu) rs786203506
NM_003000.3(SDHB):c.379A>C (p.Ile127Leu) rs201372280
NM_003000.3(SDHB):c.379A>G (p.Ile127Val) rs201372280
NM_003000.3(SDHB):c.395A>G (p.His132Arg) rs74315372
NM_003000.3(SDHB):c.397A>G (p.Met133Val) rs1392546433
NM_003000.3(SDHB):c.398T>C (p.Met133Thr) rs553392349
NM_003000.3(SDHB):c.447G>T (p.Gln149His) rs200353146
NM_003000.3(SDHB):c.472AAG[2] (p.Lys160del) rs1173714647
NM_003000.3(SDHB):c.481G>A (p.Asp161Asn) rs1553177682
NM_003000.3(SDHB):c.493G>A (p.Glu165Lys) rs2101521665
NM_003000.3(SDHB):c.540+11C>T rs1160578491
NM_003000.3(SDHB):c.541-2A>G rs786201161
NM_003000.3(SDHB):c.559A>G (p.Ile187Val) rs1557739989
NM_003000.3(SDHB):c.574T>C (p.Cys192Arg) rs786202732
NM_003000.3(SDHB):c.575G>C (p.Cys192Ser) rs397516835
NM_003000.3(SDHB):c.591del (p.Ser198fs) rs1060503757
NM_003000.3(SDHB):c.5C>T (p.Ala2Val) rs199948437
NM_003000.3(SDHB):c.614A>G (p.Lys205Arg) rs774090318
NM_003000.3(SDHB):c.623G>A (p.Gly208Glu)
NM_003000.3(SDHB):c.637A>T (p.Met213Leu) rs770622939
NM_003000.3(SDHB):c.640C>T (p.Gln214Ter) rs876658461
NM_003000.3(SDHB):c.654G>A (p.Trp218Ter) rs916516745
NM_003000.3(SDHB):c.658A>G (p.Ile220Val) rs1188548211
NM_003000.3(SDHB):c.689G>T (p.Arg230Leu) rs587782604
NM_003000.3(SDHB):c.695C>G (p.Ala232Gly)
NM_003000.3(SDHB):c.708C>G (p.Asp236Glu)
NM_003000.3(SDHB):c.713del (p.Phe238fs) rs876660642
NM_003000.3(SDHB):c.716C>G (p.Ser239Cys) rs201098090
NM_003000.3(SDHB):c.716C>T (p.Ser239Phe) rs201098090
NM_003000.3(SDHB):c.721T>G (p.Tyr241Asp) rs1060503758
NM_003000.3(SDHB):c.724C>T (p.Arg242Cys) rs786203251
NM_003000.3(SDHB):c.73-21G>T rs1311107626
NM_003000.3(SDHB):c.782A>C (p.Lys261Thr) rs1553176980
NM_003000.3(SDHB):c.79C>G (p.Arg27Gly) rs74315369
NM_003000.3(SDHB):c.822G>T (p.Lys274Asn)

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