ClinVar Miner

List of variants in gene SDHC reported as benign for Hereditary Paraganglioma-Pheochromocytoma Syndromes

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Gene type:
ClinVar version:
Total variants: 26
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HGVS dbSNP
NM_001035511.2(SDHC):c.*1256A>C
NM_003001.3(SDHC):c.*1025G>T rs16832859
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.*1335A>G rs3935401
NM_003001.3(SDHC):c.*1378T>C rs116141910
NM_003001.3(SDHC):c.*1379C>T rs114731359
NM_003001.3(SDHC):c.*1731G>A rs115718047
NM_003001.3(SDHC):c.*1800G>C rs72714988
NM_003001.3(SDHC):c.*2052C>G rs12239492
NM_003001.3(SDHC):c.*2111C>T rs115166758
NM_003001.3(SDHC):c.*2156A>C rs116668612
NM_003001.3(SDHC):c.*968A>G rs4600063
NM_003001.3(SDHC):c.77+13G>C rs779727693
NM_003001.5(SDHC):c.*123C>G rs3813632
NM_003001.5(SDHC):c.*247C>G rs540126021
NM_003001.5(SDHC):c.*385G>A rs8266
NM_003001.5(SDHC):c.*469G>A rs148834287
NM_003001.5(SDHC):c.*599A>G
NM_003001.5(SDHC):c.*612C>T rs16865495
NM_003001.5(SDHC):c.*624A>G rs114438179
NM_003001.5(SDHC):c.*685C>T rs138085670
NM_003001.5(SDHC):c.*84G>C rs201210474
NM_003001.5(SDHC):c.120G>A (p.Arg40=) rs36097930
NM_003001.5(SDHC):c.489T>C (p.Ser163=) rs559747670

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