ClinVar Miner

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

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Gene type:
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Total variants: 29
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HGVS dbSNP
NM_001035511.2(SDHC):c.*1052C>T
NM_001035511.2(SDHC):c.*1074G>T
NM_001035511.2(SDHC):c.*1543A>C
NM_001035511.2(SDHC):c.*1913A>G
NM_001035511.2(SDHC):c.*2133C>A
NM_001035511.2(SDHC):c.*748C>T
NM_001035511.2(SDHC):c.*763G>C
NM_001035511.2(SDHC):c.*945G>C
NM_003001.3(SDHC):c.*1889T>C rs746551127
NM_003001.3(SDHC):c.*1918G>A rs867593097
NM_003001.3(SDHC):c.*2274G>A rs886045497
NM_003001.3(SDHC):c.*780G>A rs886045483
NM_003001.3(SDHC):c.*863G>A rs570400725
NM_003001.5(SDHC):c.*115T>G rs886045478
NM_003001.5(SDHC):c.*174G>A rs886045479
NM_003001.5(SDHC):c.*251C>T rs886045480
NM_003001.5(SDHC):c.*252G>A
NM_003001.5(SDHC):c.*34A>G rs886045477
NM_003001.5(SDHC):c.*409G>A rs186995249
NM_003001.5(SDHC):c.*540A>G
NM_003001.5(SDHC):c.*632A>G rs886045482
NM_003001.5(SDHC):c.*707G>A
NM_003001.5(SDHC):c.*728C>G
NM_003001.5(SDHC):c.*773A>G
NM_003001.5(SDHC):c.*78G>A rs182629842
NM_003001.5(SDHC):c.128A>G (p.Asn43Ser) rs747349777
NM_003001.5(SDHC):c.15G>T (p.Leu5Phe) rs771746264
NM_003001.5(SDHC):c.218G>A (p.Gly73Asp) rs1553264219
NM_003001.5(SDHC):c.54T>G (p.Phe18Leu) rs200761743

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