ClinVar Miner

List of variants in gene SDHB studied for Pheochromocytoma

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Total variants: 35
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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.-81G>T rs886045586
NM_003000.2(SDHB):c.113G>A (p.Arg38His) rs143058777
NM_003000.2(SDHB):c.131_139del (p.Ile44_Trp47delinsArg) rs864321639
NM_003000.2(SDHB):c.136C>G (p.Arg46Gly) rs74315370
NM_003000.2(SDHB):c.158G>A (p.Gly53Glu) rs34916635
NM_003000.2(SDHB):c.170A>G (p.His57Arg) rs35962811
NM_003000.2(SDHB):c.18C>A (p.Ala6=) rs2746462
NM_003000.2(SDHB):c.21C>T (p.Leu7=) rs147815442
NM_003000.2(SDHB):c.227T>G (p.Leu76Ter) rs864321638
NM_003000.2(SDHB):c.24C>T (p.Ser8=) rs148738139
NM_003000.2(SDHB):c.251A>C (p.Asp84Ala) rs864321637
NM_003000.2(SDHB):c.299C>T (p.Ser100Phe) rs121917755
NM_003000.2(SDHB):c.300T>C (p.Ser100=) rs11541235
NM_003000.2(SDHB):c.302G>A (p.Cys101Tyr) rs74315371
NM_003000.2(SDHB):c.338G>C (p.Cys113Ser) rs864321636
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.424-37TTC[10] rs34261028
NM_003000.2(SDHB):c.454T>C (p.Ser152Pro) rs886045584
NM_003000.2(SDHB):c.47C>G (p.Thr16Arg) rs775350144
NM_003000.2(SDHB):c.487T>C (p.Ser163Pro) rs33927012
NM_003000.2(SDHB):c.591del (p.Ser198fs) rs1060503757
NM_003000.2(SDHB):c.700C>T (p.Leu234=) rs201728852
NM_003000.2(SDHB):c.716C>G (p.Ser239Cys) rs201098090
NM_003000.2(SDHB):c.716_719delCTCT rs587781266
NM_003000.2(SDHB):c.725G>A (p.Arg242His) rs74315368
NM_003000.2(SDHB):c.79C>G (p.Arg27Gly) rs74315369
NM_003000.2(SDHB):c.79C>T (p.Arg27Ter) rs74315369
NM_003000.2(SDHB):c.8C>G (p.Ala3Gly) rs11203289

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