ClinVar Miner

List of variants in gene SDHB reported as uncertain significance for cardiovascular organ benign neoplasm

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 213
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HGVS dbSNP
NC_000001.10:g.(?_17345217)_(17345453_?)del
NC_000001.10:g.(?_17345217)_(17380665_?)dup
NC_000001.10:g.(?_17345366)_(17380524_?)dup
NC_000001.10:g.(?_17345370)_(17355237_?)dup
NC_000001.10:g.(?_17359545)_(17380524_?)dup
NC_000001.10:g.(?_17371246)_(17380524_?)dup
NM_003000.2(SDHB):c.*102A>G rs201155896
NM_003000.2(SDHB):c.*133T>C rs111686611
NM_003000.2(SDHB):c.-135G>A rs886045587
NM_003000.2(SDHB):c.-142A>G rs886045588
NM_003000.2(SDHB):c.-81G>T rs886045586
NM_003000.2(SDHB):c.106G>T (p.Ala36Ser) rs1204932232
NM_003000.2(SDHB):c.112C>T (p.Arg38Cys) rs202119350
NM_003000.2(SDHB):c.113G>C (p.Arg38Pro)
NM_003000.2(SDHB):c.120G>C (p.Lys40Asn)
NM_003000.2(SDHB):c.130A>G (p.Ile44Val) rs200418115
NM_003000.2(SDHB):c.138A>G (p.Arg46=)
NM_003000.2(SDHB):c.13G>C (p.Val5Leu) rs962717797
NM_003000.2(SDHB):c.13G>T (p.Val5Phe)
NM_003000.2(SDHB):c.148G>C (p.Asp50His) rs1060503765
NM_003000.2(SDHB):c.14T>C (p.Val5Ala)
NM_003000.2(SDHB):c.14T>G (p.Val5Gly) rs760565241
NM_003000.2(SDHB):c.150C>A (p.Asp50Glu)
NM_003000.2(SDHB):c.155C>A (p.Ala52Asp) rs878854573
NM_003000.2(SDHB):c.161A>T (p.Asp54Val) rs1553178735
NM_003000.2(SDHB):c.164A>G (p.Lys55Arg)
NM_003000.2(SDHB):c.172A>G (p.Met58Val) rs1201188410
NM_003000.2(SDHB):c.177G>C (p.Gln59His) rs1277374324
NM_003000.2(SDHB):c.178A>G (p.Thr60Ala) rs34599281
NM_003000.2(SDHB):c.179C>T (p.Thr60Ile)
NM_003000.2(SDHB):c.188T>C (p.Val63Ala) rs1230335211
NM_003000.2(SDHB):c.192C>A (p.Asp64Glu)
NM_003000.2(SDHB):c.193C>T (p.Leu65Phe) rs786202185
NM_003000.2(SDHB):c.194T>C (p.Leu65Pro) rs876659329
NM_003000.2(SDHB):c.19C>T (p.Leu7Phe) rs745664191
NM_003000.2(SDHB):c.200+4A>G
NM_003000.2(SDHB):c.201-10T>A
NM_003000.2(SDHB):c.203G>A (p.Cys68Tyr) rs587782904
NM_003000.2(SDHB):c.208C>A (p.Pro70Thr) rs200890320
NM_003000.2(SDHB):c.214G>A (p.Val72Ile) rs1060503766
NM_003000.2(SDHB):c.220G>A (p.Asp74Asn)
NM_003000.2(SDHB):c.231C>G (p.Ile77Met)
NM_003000.2(SDHB):c.233A>G (p.Lys78Arg) rs774960237
NM_003000.2(SDHB):c.234G>T (p.Lys78Asn)
NM_003000.2(SDHB):c.23C>T (p.Ser8Phe)
NM_003000.2(SDHB):c.248T>C (p.Val83Ala) rs763547482
NM_003000.2(SDHB):c.256A>G (p.Thr86Ala)
NM_003000.2(SDHB):c.25T>G (p.Leu9Val) rs1060503768
NM_003000.2(SDHB):c.260T>C (p.Leu87Ser) rs727504457
NM_003000.2(SDHB):c.263C>G (p.Thr88Ser) rs915794675
NM_003000.2(SDHB):c.267C>G (p.Phe89Leu) rs1553178042
NM_003000.2(SDHB):c.269G>A (p.Arg90Gln) rs570278423
NM_003000.2(SDHB):c.277T>C (p.Cys93Arg) rs727503415
NM_003000.2(SDHB):c.287G>A (p.Gly96Asp) rs778952116
NM_003000.2(SDHB):c.289A>T (p.Ile97Phe) rs1553177769
NM_003000.2(SDHB):c.293G>A (p.Cys98Tyr) rs1553177768
NM_003000.2(SDHB):c.299C>G (p.Ser100Cys) rs121917755
NM_003000.2(SDHB):c.307A>G (p.Met103Val) rs140178341
NM_003000.2(SDHB):c.308T>C (p.Met103Thr) rs1553177765
NM_003000.2(SDHB):c.309G>A (p.Met103Ile)
NM_003000.2(SDHB):c.316A>G (p.Asn106Asp) rs1557741510
NM_003000.2(SDHB):c.317A>G (p.Asn106Ser) rs934514080
NM_003000.2(SDHB):c.31C>T (p.Arg11Cys) rs200868378
NM_003000.2(SDHB):c.323G>A (p.Gly108Asp)
NM_003000.2(SDHB):c.326A>G (p.Asn109Ser)
NM_003000.2(SDHB):c.335C>G (p.Ala112Gly) rs1553177762
NM_003000.2(SDHB):c.34C>T (p.Arg12Trp) rs761996626
NM_003000.2(SDHB):c.350T>C (p.Ile117Thr) rs1553177755
NM_003000.2(SDHB):c.352G>A (p.Asp118Asn) rs200021702
NM_003000.2(SDHB):c.356C>A (p.Thr119Asn)
NM_003000.2(SDHB):c.359A>G (p.Asn120Ser) rs1553177746
NM_003000.2(SDHB):c.35G>C (p.Arg12Pro) rs1293365726
NM_003000.2(SDHB):c.361C>T (p.Leu121Phe) rs1194401420
NM_003000.2(SDHB):c.368A>C (p.Lys123Thr) rs1557741464
NM_003000.2(SDHB):c.371T>C (p.Val124Ala) rs1557741456
NM_003000.2(SDHB):c.376A>G (p.Lys126Glu)
NM_003000.2(SDHB):c.379A>C (p.Ile127Leu) rs201372280
NM_003000.2(SDHB):c.383A>G (p.Tyr128Cys) rs772158627
NM_003000.2(SDHB):c.385C>G (p.Pro129Ala) rs1553177740
NM_003000.2(SDHB):c.395A>G (p.His132Arg) rs74315372
NM_003000.2(SDHB):c.397A>G (p.Met133Val)
NM_003000.2(SDHB):c.398T>C (p.Met133Thr)
NM_003000.2(SDHB):c.39G>C (p.Leu13Phe)
NM_003000.2(SDHB):c.39G>T (p.Leu13Phe) rs201745731
NM_003000.2(SDHB):c.403G>A (p.Val135Met) rs201585157
NM_003000.2(SDHB):c.413A>G (p.Asp138Gly)
NM_003000.2(SDHB):c.41C>T (p.Pro14Leu) rs764089231
NM_003000.2(SDHB):c.422C>G (p.Pro141Arg) rs1553177734
NM_003000.2(SDHB):c.423C>T (p.Pro141=) rs150542357
NM_003000.2(SDHB):c.424-16_424-14dup rs34261028
NM_003000.2(SDHB):c.424-19_424-14delTTCTTC rs34261028
NM_003000.2(SDHB):c.424-3C>G rs1557741166
NM_003000.2(SDHB):c.424-5C>G rs1553177690
NM_003000.2(SDHB):c.425A>T (p.Asp142Val)
NM_003000.2(SDHB):c.436T>G (p.Phe146Val) rs1553177689
NM_003000.2(SDHB):c.440A>G (p.Tyr147Cys) rs774568101
NM_003000.2(SDHB):c.446A>G (p.Gln149Arg)
NM_003000.2(SDHB):c.454T>C (p.Ser152Pro) rs886045584
NM_003000.2(SDHB):c.455C>T (p.Ser152Phe) rs200414835
NM_003000.2(SDHB):c.457A>T (p.Ile153Phe) rs1450956956
NM_003000.2(SDHB):c.463C>T (p.Pro155Ser) rs763008243
NM_003000.2(SDHB):c.464C>T (p.Pro155Leu) rs1553177686
NM_003000.2(SDHB):c.46A>C (p.Thr16Pro) rs1433760506
NM_003000.2(SDHB):c.46A>G (p.Thr16Ala)
NM_003000.2(SDHB):c.472_474AAG[2] (p.Lys160del) rs1173714647
NM_003000.2(SDHB):c.47C>G (p.Thr16Arg) rs775350144
NM_003000.2(SDHB):c.47C>T (p.Thr16Ile)
NM_003000.2(SDHB):c.481G>A (p.Asp161Asn) rs1553177682
NM_003000.2(SDHB):c.482A>G (p.Asp161Gly) rs1049317868
NM_003000.2(SDHB):c.482A>T (p.Asp161Val)
NM_003000.2(SDHB):c.488C>T (p.Ser163Phe) rs769687734
NM_003000.2(SDHB):c.497G>A (p.Gly166Asp) rs1060503760
NM_003000.2(SDHB):c.49A>G (p.Thr17Ala) rs1060503756
NM_003000.2(SDHB):c.50C>A (p.Thr17Asn) rs138979875
NM_003000.2(SDHB):c.50C>T (p.Thr17Ile) rs138979875
NM_003000.2(SDHB):c.520A>G (p.Ile174Val)
NM_003000.2(SDHB):c.521T>C (p.Ile174Thr) rs200301019
NM_003000.2(SDHB):c.523G>A (p.Glu175Lys)
NM_003000.2(SDHB):c.523G>C (p.Glu175Gln) rs202203339
NM_003000.2(SDHB):c.527A>G (p.Glu176Gly) rs201082445
NM_003000.2(SDHB):c.529C>A (p.Arg177Ser) rs149091125
NM_003000.2(SDHB):c.529C>T (p.Arg177Cys) rs149091125
NM_003000.2(SDHB):c.530G>A (p.Arg177His) rs150437793
NM_003000.2(SDHB):c.536A>T (p.Lys179Ile) rs1553177670
NM_003000.2(SDHB):c.540+4A>G rs1557741074
NM_003000.2(SDHB):c.540+5T>C rs1557741072
NM_003000.2(SDHB):c.541-3C>T rs751920183
NM_003000.2(SDHB):c.541-8C>G
NM_003000.2(SDHB):c.541G>A (p.Asp181Asn) rs201385062
NM_003000.2(SDHB):c.544G>A (p.Gly182Arg) rs201928318
NM_003000.2(SDHB):c.544G>T (p.Gly182Trp)
NM_003000.2(SDHB):c.547C>T (p.Leu183Phe) rs1557740003
NM_003000.2(SDHB):c.553G>A (p.Glu185Lys) rs1045881797
NM_003000.2(SDHB):c.557G>C (p.Cys186Ser) rs1553177440
NM_003000.2(SDHB):c.559A>G (p.Ile187Val) rs1557739989
NM_003000.2(SDHB):c.562C>G (p.Leu188Val) rs1392463987
NM_003000.2(SDHB):c.581C>G (p.Thr194Ser) rs200535030
NM_003000.2(SDHB):c.584G>C (p.Ser195Thr)
NM_003000.2(SDHB):c.593G>C (p.Ser198Thr)
NM_003000.2(SDHB):c.5C>T (p.Ala2Val) rs199948437
NM_003000.2(SDHB):c.607G>A (p.Gly203Arg) rs201517260
NM_003000.2(SDHB):c.608G>C (p.Gly203Ala) rs1553177435
NM_003000.2(SDHB):c.612C>G (p.Asp204Glu) rs1553177433
NM_003000.2(SDHB):c.614A>G (p.Lys205Arg) rs774090318
NM_003000.2(SDHB):c.634C>T (p.Leu212Phe) rs1228560456
NM_003000.2(SDHB):c.637A>G (p.Met213Val) rs770622939
NM_003000.2(SDHB):c.638T>C (p.Met213Thr) rs202014362
NM_003000.2(SDHB):c.641A>G (p.Gln214Arg) rs781590955
NM_003000.2(SDHB):c.642+3G>A rs878854577
NM_003000.2(SDHB):c.642+4A>G rs1225871505
NM_003000.2(SDHB):c.642+5G>A
NM_003000.2(SDHB):c.642G>C (p.Gln214His) rs1278834014
NM_003000.2(SDHB):c.644C>T (p.Ala215Val) rs1060503761
NM_003000.2(SDHB):c.647A>G (p.Tyr216Cys) rs1553177291
NM_003000.2(SDHB):c.649C>G (p.Arg217Gly) rs200245469
NM_003000.2(SDHB):c.650G>A (p.Arg217His) rs747518441
NM_003000.2(SDHB):c.658A>G (p.Ile220Val) rs1188548211
NM_003000.2(SDHB):c.659T>C (p.Ile220Thr) rs878854578
NM_003000.2(SDHB):c.65G>A (p.Cys22Tyr) rs141230910
NM_003000.2(SDHB):c.65G>C (p.Cys22Ser) rs141230910
NM_003000.2(SDHB):c.65G>T (p.Cys22Phe) rs141230910
NM_003000.2(SDHB):c.661G>A (p.Asp221Asn) rs1553177288
NM_003000.2(SDHB):c.673G>A (p.Asp225Asn)
NM_003000.2(SDHB):c.676T>C (p.Phe226Leu)
NM_003000.2(SDHB):c.679A>G (p.Thr227Ala)
NM_003000.2(SDHB):c.67C>G (p.Leu23Val) rs1553179319
NM_003000.2(SDHB):c.687G>C (p.Glu229Asp) rs1060503754
NM_003000.2(SDHB):c.695C>T (p.Ala232Val) rs746224555
NM_003000.2(SDHB):c.704A>G (p.Gln235Arg)
NM_003000.2(SDHB):c.709C>T (p.Pro237Ser) rs186768244
NM_003000.2(SDHB):c.710C>G (p.Pro237Arg) rs878854579
NM_003000.2(SDHB):c.714C>A (p.Phe238Leu) rs1553177278
NM_003000.2(SDHB):c.716C>A (p.Ser239Tyr)
NM_003000.2(SDHB):c.716C>G (p.Ser239Cys) rs201098090
NM_003000.2(SDHB):c.716C>T (p.Ser239Phe) rs201098090
NM_003000.2(SDHB):c.71A>C (p.Gln24Pro) rs878854580
NM_003000.2(SDHB):c.72+3G>A rs569245129
NM_003000.2(SDHB):c.72+5G>A rs878854581
NM_003000.2(SDHB):c.721T>G (p.Tyr241Asp) rs1060503758
NM_003000.2(SDHB):c.722A>G (p.Tyr241Cys) rs878854582
NM_003000.2(SDHB):c.72G>A (p.Gln24=) rs1553179312
NM_003000.2(SDHB):c.73-6T>A
NM_003000.2(SDHB):c.73-?_*159+?dup
NM_003000.2(SDHB):c.736A>G (p.Ile246Val) rs146800605
NM_003000.2(SDHB):c.739A>G (p.Met247Val) rs200896502
NM_003000.2(SDHB):c.73G>A (p.Ala25Thr)
NM_003000.2(SDHB):c.73G>C (p.Ala25Pro) rs768101924
NM_003000.2(SDHB):c.749C>T (p.Thr250Ile) rs1057517537
NM_003000.2(SDHB):c.756_765+4delCTGTCCTAAGGTAC rs1553177267
NM_003000.2(SDHB):c.761C>T (p.Pro254Leu) rs948484408
NM_003000.2(SDHB):c.763A>G (p.Lys255Glu)
NM_003000.2(SDHB):c.765+4C>A
NM_003000.2(SDHB):c.765+4C>T
NM_003000.2(SDHB):c.765+5G>A rs199945904
NM_003000.2(SDHB):c.765G>C (p.Lys255Asn)
NM_003000.2(SDHB):c.769C>G (p.Leu257Val)
NM_003000.2(SDHB):c.770T>G (p.Leu257Arg)
NM_003000.2(SDHB):c.773A>C (p.Asn258Thr)
NM_003000.2(SDHB):c.782A>C (p.Lys261Thr) rs1553176980
NM_003000.2(SDHB):c.791C>A (p.Ala264Glu) rs1557738283
NM_003000.2(SDHB):c.79C>G (p.Arg27Gly) rs74315369
NM_003000.2(SDHB):c.801G>C (p.Lys267Asn)
NM_003000.2(SDHB):c.802A>T (p.Lys268Ter) rs1060503755
NM_003000.2(SDHB):c.805A>G (p.Met269Val)
NM_003000.2(SDHB):c.808A>G (p.Met270Val) rs878854584
NM_003000.2(SDHB):c.80G>A (p.Arg27Gln) rs373976827
NM_003000.2(SDHB):c.814A>G (p.Thr272Ala) rs545681543
NM_003000.2(SDHB):c.819T>A (p.Tyr273Ter) rs1553176966
NM_003000.2(SDHB):c.820A>G (p.Lys274Glu) rs1273897502
NM_003000.2(SDHB):c.835T>A (p.Ser279Thr)
NM_003000.2(SDHB):c.8C>T (p.Ala3Val) rs11203289
NM_003000.2(SDHB):c.92C>T (p.Thr31Ile) rs1553178750
NM_003000.2(SDHB):c.95C>T (p.Ala32Val)

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