ClinVar Miner

List of variants in gene SDHB studied for not specified

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Gene type:
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Total variants: 74
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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.200+35G>A rs61769190 0.02530
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.24C>T (p.Ser8=) rs148738139 0.00461
NM_003000.3(SDHB):c.-37T>C rs143031690 0.00411
NM_003000.2(SDHB):c.-198G>A rs111873017 0.00383
NM_003000.3(SDHB):c.170A>G (p.His57Arg) rs35962811 0.00231
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.300T>C (p.Ser100=) rs11541235 0.00157
NM_003000.3(SDHB):c.765+29G>A rs41273161 0.00058
NM_003000.3(SDHB):c.21C>T (p.Leu7=) rs147815442 0.00054
NM_003000.3(SDHB):c.158G>A (p.Gly53Glu) rs34916635 0.00041
NM_003000.3(SDHB):c.287-26A>G rs201397253 0.00040
NM_003000.3(SDHB):c.642+17T>C rs200597595 0.00016
NM_003000.3(SDHB):c.403G>A (p.Val135Met) rs201585157 0.00012
NM_003000.3(SDHB):c.113G>A (p.Arg38His) rs143058777 0.00010
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.225T>C (p.Ala75=) rs201762207 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.642+47C>T rs201882049 0.00006
NM_003000.3(SDHB):c.530G>A (p.Arg177His) rs150437793 0.00004
NM_003000.3(SDHB):c.552C>T (p.Tyr184=) rs202098600 0.00004
NM_003000.3(SDHB):c.-5C>T rs200890535 0.00003
NM_003000.3(SDHB):c.-6G>A rs2295056 0.00003
NM_003000.3(SDHB):c.344G>A (p.Arg115Gln) rs200973284 0.00003
NM_003000.3(SDHB):c.541-36G>A rs537705928 0.00003
NM_003000.3(SDHB):c.130A>G (p.Ile44Val) rs200418115 0.00002
NM_003000.3(SDHB):c.765+13G>A rs115561881 0.00002
NM_003000.3(SDHB):c.*30C>T rs199701267 0.00001
NM_003000.3(SDHB):c.286+16C>T rs200305451 0.00001
NM_003000.3(SDHB):c.287-4T>C rs200419171 0.00001
NM_003000.3(SDHB):c.323G>A (p.Gly108Asp) rs767062764 0.00001
NM_003000.3(SDHB):c.482A>G (p.Asp161Gly) rs1049317868 0.00001
NM_003000.3(SDHB):c.642+15A>G rs368427218 0.00001
NM_003000.3(SDHB):c.679A>G (p.Thr227Ala) rs1191046308 0.00001
NM_003000.3(SDHB):c.696C>T (p.Ala232=) rs779143585 0.00001
NM_003000.2(SDHB):c.*159_*184delinsGAACCTGTTCCTTTACTTGCCCCAA rs727503414
NM_003000.2(SDHB):c.-45G>A rs202039513
NM_003000.2(SDHB):c.424-16_424-14dup rs34261028
NM_003000.3(SDHB):c.148G>A (p.Asp50Asn) rs1060503765
NM_003000.3(SDHB):c.166_170del (p.Pro56fs) rs786202100
NM_003000.3(SDHB):c.200+5G>C rs1553178726
NM_003000.3(SDHB):c.234G>A (p.Lys78=) rs776971836
NM_003000.3(SDHB):c.277T>C (p.Cys93Arg) rs727503415
NM_003000.3(SDHB):c.395A>G (p.His132Arg) rs74315372
NM_003000.3(SDHB):c.415C>T (p.Leu139Phe) rs397516834
NM_003000.3(SDHB):c.423+15CT[2] rs778120334
NM_003000.3(SDHB):c.423+28T>C
NM_003000.3(SDHB):c.424-13_424-11dup rs1365741915
NM_003000.3(SDHB):c.424-14_424-9dup rs1064794554
NM_003000.3(SDHB):c.424-37TTC[10] rs34261028
NM_003000.3(SDHB):c.424-37TTC[6] rs34261028
NM_003000.3(SDHB):c.424-37TTC[7] rs34261028
NM_003000.3(SDHB):c.540+31G>A rs2101521469
NM_003000.3(SDHB):c.540+41T>C
NM_003000.3(SDHB):c.541-8_541-7delinsAG
NM_003000.3(SDHB):c.594C>G (p.Ser198Arg)
NM_003000.3(SDHB):c.5C>T (p.Ala2Val) rs199948437
NM_003000.3(SDHB):c.612C>G (p.Asp204Glu) rs1553177433
NM_003000.3(SDHB):c.642G>C (p.Gln214His) rs1278834014
NM_003000.3(SDHB):c.643-49G>A
NM_003000.3(SDHB):c.684G>A (p.Glu228=) rs2101513893
NM_003000.3(SDHB):c.716C>G (p.Ser239Cys) rs201098090
NM_003000.3(SDHB):c.722A>G (p.Tyr241Cys) rs878854582
NM_003000.3(SDHB):c.73-29del rs745905902
NM_003000.3(SDHB):c.73-29dup
NM_003000.3(SDHB):c.73-41C>G
NM_003000.3(SDHB):c.765+45G>A
NM_003000.3(SDHB):c.79C>G (p.Arg27Gly) rs74315369

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