ClinVar Miner

List of variants in gene SDHC reported as likely benign for Pheochromocytoma

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Gene type:
ClinVar version:
Total variants: 14
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NM_001035511.2(SDHC):c.424G>A (p.Ala142Thr) rs182629842
NM_001035511.2(SDHC):c.430G>C (p.Glu144Gln) rs201210474
NM_003001.3(SDHC):c.*1190T>A rs549554302
NM_003001.3(SDHC):c.*1191A>T rs566186299
NM_003001.3(SDHC):c.*1323G>A rs72714986
NM_003001.3(SDHC):c.*1378T>C rs116141910
NM_003001.3(SDHC):c.*1693G>A rs191417790
NM_003001.3(SDHC):c.*1731G>A rs115718047
NM_003001.3(SDHC):c.*2111C>T rs115166758
NM_003001.3(SDHC):c.*409G>A rs186995249
NM_003001.3(SDHC):c.*685C>T rs138085670
NM_003001.3(SDHC):c.*863G>A rs570400725
NM_003001.3(SDHC):c.120G>A (p.Arg40=) rs36097930
NM_003001.3(SDHC):c.489T>C (p.Ser163=) rs559747670

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