ClinVar Miner

List of variants in gene SDHB studied for Pheochromocytoma

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Total variants: 23
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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.32G>A (p.Arg11His) rs111430410 0.00185
NM_003000.3(SDHB):c.440A>G (p.Tyr147Cys) rs774568101 0.00010
NM_003000.3(SDHB):c.307A>G (p.Met103Val) rs140178341 0.00004
NM_003000.3(SDHB):c.137G>A (p.Arg46Gln) rs772551056 0.00001
NM_003000.3(SDHB):c.47C>G (p.Thr16Arg) rs775350144 0.00001
NM_003000.2(SDHB):c.-81G>T rs886045586
NM_003000.2(SDHB):c.424-16_424-14dup rs34261028
NM_003000.3(SDHB):c.131_139del (p.Ile44_Trp47delinsArg) rs864321639
NM_003000.3(SDHB):c.166_170del (p.Pro56fs) rs786202100
NM_003000.3(SDHB):c.183T>G (p.Tyr61Ter) rs760169139
NM_003000.3(SDHB):c.227T>G (p.Leu76Ter) rs864321638
NM_003000.3(SDHB):c.251A>C (p.Asp84Ala) rs864321637
NM_003000.3(SDHB):c.299C>T (p.Ser100Phe) rs121917755
NM_003000.3(SDHB):c.338G>C (p.Cys113Ser) rs864321636
NM_003000.3(SDHB):c.3G>A (p.Met1Ile) rs1131691061
NM_003000.3(SDHB):c.423+1G>T rs398122805
NM_003000.3(SDHB):c.424-37TTC[10] rs34261028
NM_003000.3(SDHB):c.424-37TTC[6] rs34261028
NM_003000.3(SDHB):c.662A>G (p.Asp221Gly) rs2101513961
NM_003000.3(SDHB):c.716C>G (p.Ser239Cys) rs201098090
NM_003000.3(SDHB):c.79C>G (p.Arg27Gly) rs74315369

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