ClinVar Miner

List of variants in gene SDHD reported as likely benign for Hereditary cancer-predisposing syndrome

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Gene type:
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Total variants: 64
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HGVS dbSNP gnomAD frequency
NM_003002.4(SDHD):c.314+124T>C rs118074328 0.00706
NM_003002.4(SDHD):c.101T>G (p.Phe34Cys) rs141802836 0.00016
NM_003002.4(SDHD):c.255G>C (p.Leu85Phe) rs199517389 0.00013
NM_003002.4(SDHD):c.80G>A (p.Arg27Lys) rs200671534 0.00006
NM_003002.4(SDHD):c.282C>T (p.Ser94=) rs781182616 0.00003
NM_003002.4(SDHD):c.228C>T (p.Leu76=) rs148634289 0.00002
NM_003002.4(SDHD):c.366A>G (p.Lys122=) rs780764151 0.00002
NM_003002.4(SDHD):c.435C>T (p.His145=) rs200062830 0.00002
NM_003002.4(SDHD):c.438T>C (p.Asp146=) rs201328474 0.00002
NM_003002.4(SDHD):c.141G>A (p.Gln47=) rs1217254088 0.00001
NM_003002.4(SDHD):c.231G>C (p.Leu77=) rs1187106228 0.00001
NM_003002.4(SDHD):c.243G>A (p.Pro81=) rs575262156 0.00001
NM_003002.4(SDHD):c.243G>C (p.Pro81=) rs575262156 0.00001
NM_003002.4(SDHD):c.264C>T (p.Cys88=) rs761615413 0.00001
NM_003002.4(SDHD):c.270G>A (p.Ala90=) rs766656463 0.00001
NM_003002.4(SDHD):c.331G>A (p.Val111Ile) rs201869798 0.00001
NM_003002.4(SDHD):c.342T>C (p.Tyr114=) rs1050032491 0.00001
NM_003002.4(SDHD):c.112C>A (p.Arg38=)
NM_003002.4(SDHD):c.118A>C (p.Ile40Leu) rs146276662
NM_003002.4(SDHD):c.120C>T (p.Ile40=)
NM_003002.4(SDHD):c.123A>C (p.Pro41=)
NM_003002.4(SDHD):c.125A>G (p.Glu42Gly)
NM_003002.4(SDHD):c.126A>G (p.Glu42=) rs2135267333
NM_003002.4(SDHD):c.138G>A (p.Val46=) rs2135267384
NM_003002.4(SDHD):c.177C>T (p.Ser59=) rs764869982
NM_003002.4(SDHD):c.180G>A (p.Lys60=) rs750688879
NM_003002.4(SDHD):c.183T>C (p.Ala61=) rs2135269188
NM_003002.4(SDHD):c.202A>G (p.Ser68Gly) rs2135269276
NM_003002.4(SDHD):c.216C>T (p.Val72=)
NM_003002.4(SDHD):c.249T>A (p.Ala83=)
NM_003002.4(SDHD):c.252T>C (p.Tyr84=)
NM_003002.4(SDHD):c.255G>T (p.Leu85Phe) rs199517389
NM_003002.4(SDHD):c.269C>A (p.Ala90Glu) rs200255724
NM_003002.4(SDHD):c.269C>T (p.Ala90Val) rs200255724
NM_003002.4(SDHD):c.279T>C (p.Tyr93=)
NM_003002.4(SDHD):c.282C>G (p.Ser94=) rs781182616
NM_003002.4(SDHD):c.283C>T (p.Leu95=) rs1865691704
NM_003002.4(SDHD):c.288T>G (p.Ala96=)
NM_003002.4(SDHD):c.291A>C (p.Ala97=) rs1592780682
NM_003002.4(SDHD):c.306T>C (p.His102=)
NM_003002.4(SDHD):c.351G>A (p.Gly117=)
NM_003002.4(SDHD):c.354T>C (p.Asp118=) rs911663426
NM_003002.4(SDHD):c.369T>C (p.Ala123=) rs747779190
NM_003002.4(SDHD):c.369T>G (p.Ala123=)
NM_003002.4(SDHD):c.372C>G (p.Ala124=) rs2135277535
NM_003002.4(SDHD):c.381G>T (p.Gly127=)
NM_003002.4(SDHD):c.396A>T (p.Ser132=)
NM_003002.4(SDHD):c.411T>C (p.Ala137=) rs1298909305
NM_003002.4(SDHD):c.414G>A (p.Gly138=) rs1174448545
NM_003002.4(SDHD):c.432T>C (p.Tyr144=)
NM_003002.4(SDHD):c.450C>T (p.Cys150=) rs201337439
NM_003002.4(SDHD):c.468G>A (p.Leu156=) rs2135277845
NM_003002.4(SDHD):c.479G>A (p.Ter160=) rs201372601
NM_003002.4(SDHD):c.57G>A (p.Leu19=) rs560625389
NM_003002.4(SDHD):c.58T>C (p.Leu20=) rs1298878168
NM_003002.4(SDHD):c.60G>A (p.Leu20=) rs2135266996
NM_003002.4(SDHD):c.66A>G (p.Arg22=) rs2135267028
NM_003002.4(SDHD):c.70C>T (p.Pro24Ser) rs775986509
NM_003002.4(SDHD):c.72A>C (p.Pro24=) rs1413100881
NM_003002.4(SDHD):c.72A>G (p.Pro24=) rs1413100881
NM_003002.4(SDHD):c.90T>C (p.His30=)
NM_003002.4(SDHD):c.91A>G (p.Ile31Val) rs1865653068
NM_003002.4(SDHD):c.93C>T (p.Ile31=) rs766096986
NM_003002.4(SDHD):c.96A>C (p.Ser32=)

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