ClinVar Miner

List of variants in gene SDHB studied for Hereditary Paraganglioma-Pheochromocytoma Syndromes

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Total variants: 86
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HGVS dbSNP
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.-139G>T rs114522228
NM_003000.2(SDHB):c.-142A>G rs886045588
NM_003000.2(SDHB):c.-37T>C rs143031690
NM_003000.2(SDHB):c.113G>A (p.Arg38His) rs143058777
NM_003000.2(SDHB):c.136C>T (p.Arg46Ter) rs74315370
NM_003000.2(SDHB):c.158G>A (p.Gly53Glu) rs34916635
NM_003000.2(SDHB):c.178A>G (p.Thr60Ala) rs34599281
NM_003000.2(SDHB):c.183T>G (p.Tyr61Ter) rs760169139
NM_003000.2(SDHB):c.1A>T (p.Met1Leu) rs1131691049
NM_003000.2(SDHB):c.1_72del (p.Met1_Gln24del) rs1553179313
NM_003000.2(SDHB):c.1_843del
NM_003000.2(SDHB):c.21C>T (p.Leu7=) rs147815442
NM_003000.2(SDHB):c.24C>T (p.Ser8=) rs148738139
NM_003000.2(SDHB):c.26T>A (p.Leu9Ter) rs786203800
NM_003000.2(SDHB):c.271A>T (p.Arg91Ter) rs878854575
NM_003000.2(SDHB):c.274T>C (p.Ser92Pro) rs1553178041
NM_003000.2(SDHB):c.275C>A (p.Ser92Ter) rs1553178040
NM_003000.2(SDHB):c.286+1G>A rs786201063
NM_003000.2(SDHB):c.286+2T>A rs587781270
NM_003000.2(SDHB):c.286G>A (p.Gly96Ser) rs587782243
NM_003000.2(SDHB):c.287-3C>G rs1553177772
NM_003000.2(SDHB):c.287G>A (p.Gly96Asp) rs778952116
NM_003000.2(SDHB):c.287_540del
NM_003000.2(SDHB):c.299C>G (p.Ser100Cys) rs121917755
NM_003000.2(SDHB):c.329_330CT[1] (p.Leu111fs) rs1060503751
NM_003000.2(SDHB):c.344G>A (p.Arg115Gln) rs200973284
NM_003000.2(SDHB):c.348_352del (p.Ile117fs) rs1480267715
NM_003000.2(SDHB):c.369_370insA (p.Val124fs) rs1553177742
NM_003000.2(SDHB):c.380T>G (p.Ile127Ser) rs786201095
NM_003000.2(SDHB):c.392del (p.Pro131fs) rs1553177739
NM_003000.2(SDHB):c.395A>G (p.His132Arg) rs74315372
NM_003000.2(SDHB):c.418G>T (p.Val140Phe) rs267607032
NM_003000.2(SDHB):c.423+1G>A rs398122805
NM_003000.2(SDHB):c.445C>T (p.Gln149Ter) rs876658451
NM_003000.2(SDHB):c.445_447delinsGGTATCT (p.Gln149fs) rs1553177687
NM_003000.2(SDHB):c.454T>C (p.Ser152Pro) rs886045584
NM_003000.2(SDHB):c.490C>T (p.Gln164Ter) rs1553177679
NM_003000.2(SDHB):c.523_527delinsAAGG (p.Glu175fs) rs1553177672
NM_003000.2(SDHB):c.526G>T (p.Glu176Ter) rs794728946
NM_003000.2(SDHB):c.540G>A (p.Leu180=) rs528442805
NM_003000.2(SDHB):c.541-2A>G rs786201161
NM_003000.2(SDHB):c.541-3C>T rs751920183
NM_003000.2(SDHB):c.553G>T (p.Glu185Ter) rs1045881797
NM_003000.2(SDHB):c.566G>T (p.Cys189Phe) rs876658540
NM_003000.2(SDHB):c.574T>C (p.Cys192Arg) rs786202732
NM_003000.2(SDHB):c.575G>A (p.Cys192Tyr) rs397516835
NM_003000.2(SDHB):c.587G>A (p.Cys196Tyr) rs876658367
NM_003000.2(SDHB):c.590C>G (p.Pro197Arg) rs74315367
NM_003000.2(SDHB):c.600G>T (p.Trp200Cys) rs397516836
NM_003000.2(SDHB):c.640C>T (p.Gln214Ter) rs876658461
NM_003000.2(SDHB):c.642+1G>A rs1131691052
NM_003000.2(SDHB):c.642G>C (p.Gln214His) rs1278834014
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.683_684delAG rs762812025
NM_003000.2(SDHB):c.688C>T (p.Arg230Cys) rs138996609
NM_003000.2(SDHB):c.689G>A (p.Arg230His) rs587782604
NM_003000.2(SDHB):c.700C>T (p.Leu234=) rs201728852
NM_003000.2(SDHB):c.716C>T (p.Ser239Phe) rs201098090
NM_003000.2(SDHB):c.72+1G>T rs587782703
NM_003000.2(SDHB):c.725G>A (p.Arg242His) rs74315368
NM_003000.2(SDHB):c.73-9A>G rs1553178757
NM_003000.2(SDHB):c.736A>T (p.Ile246Phe) rs146800605
NM_003000.2(SDHB):c.761dup (p.Pro254_Lys255insTer) rs34309090
NM_003000.2(SDHB):c.79C>T (p.Arg27Ter) rs74315369
NM_003000.2(SDHB):c.80G>A (p.Arg27Gln) rs373976827
NM_003000.2(SDHB):c.88del (p.Gln30fs) rs747198089
NM_003000.2:c.73_846del
NM_003000.3(SDHB):c.137G>A (p.Arg46Gln) rs772551056
NM_003000.3(SDHB):c.170A>G (p.His57Arg) rs35962811
NM_003000.3(SDHB):c.18C>A (p.Ala6=) rs2746462
NM_003000.3(SDHB):c.260T>C (p.Leu87Ser) rs727504457
NM_003000.3(SDHB):c.268C>T (p.Arg90Ter) rs74315366
NM_003000.3(SDHB):c.277T>C (p.Cys93Arg) rs727503415
NM_003000.3(SDHB):c.287-1G>C rs397516833
NM_003000.3(SDHB):c.300T>C (p.Ser100=) rs11541235
NM_003000.3(SDHB):c.32G>A (p.Arg11His) rs111430410
NM_003000.3(SDHB):c.343C>T (p.Arg115Ter) rs751000085
NM_003000.3(SDHB):c.445_446insTATGG (p.Gln149fs) rs1553177688
NM_003000.3(SDHB):c.487T>C (p.Ser163Pro) rs33927012
NM_003000.3(SDHB):c.540+8G>T
NM_003000.3(SDHB):c.600G>A (p.Trp200Ter) rs397516836
NM_003000.3(SDHB):c.8C>G (p.Ala3Gly) rs11203289

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