ClinVar Miner

List of variants in gene SDHD reported as uncertain significance for Hereditary cancer-predisposing syndrome

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Total variants: 125
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HGVS dbSNP gnomAD frequency
NM_003002.4(SDHD):c.278A>G (p.Tyr93Cys) rs142135772 0.00049
NM_003002.4(SDHD):c.*5T>C rs201987672 0.00019
NM_003002.4(SDHD):c.53C>T (p.Ala18Val) rs192332761 0.00011
NM_003002.4(SDHD):c.107A>G (p.Gln36Arg) rs759143732 0.00003
NM_003002.4(SDHD):c.118A>G (p.Ile40Val) rs146276662 0.00003
NM_003002.4(SDHD):c.158C>T (p.Pro53Leu) rs149516118 0.00003
NM_003002.4(SDHD):c.116C>T (p.Pro39Leu) rs752689382 0.00002
NM_003002.4(SDHD):c.122C>T (p.Pro41Leu) rs753724042 0.00002
NM_003002.4(SDHD):c.398C>A (p.Ala133Asp) rs755584530 0.00002
NM_003002.4(SDHD):c.464T>A (p.Met155Lys) rs1060503776 0.00002
NM_003002.4(SDHD):c.56T>C (p.Leu19Pro) rs574698019 0.00002
NM_003002.4(SDHD):c.113G>A (p.Arg38Gln) rs199901239 0.00001
NM_003002.4(SDHD):c.124G>A (p.Glu42Lys) rs756995021 0.00001
NM_003002.4(SDHD):c.167A>C (p.His56Pro) rs1555186817 0.00001
NM_003002.4(SDHD):c.180G>T (p.Lys60Asn) rs750688879 0.00001
NM_003002.4(SDHD):c.217A>G (p.Ser73Gly) rs748545223 0.00001
NM_003002.4(SDHD):c.281C>G (p.Ser94Cys) rs199754684 0.00001
NM_003002.4(SDHD):c.293C>T (p.Ala98Val) rs200980609 0.00001
NM_003002.4(SDHD):c.301C>T (p.Leu101Phe) rs1165258369 0.00001
NM_003002.4(SDHD):c.310C>G (p.His104Asp) rs779863605 0.00001
NM_003002.4(SDHD):c.328G>A (p.Val110Ile) rs1060503771 0.00001
NM_003002.4(SDHD):c.335C>T (p.Thr112Ile) rs199869408 0.00001
NM_003002.4(SDHD):c.344T>C (p.Val115Ala) rs1489012268 0.00001
NM_003002.4(SDHD):c.353A>G (p.Asp118Gly) rs750857413 0.00001
NM_003002.4(SDHD):c.356C>T (p.Ala119Val) rs758784300 0.00001
NM_003002.4(SDHD):c.375G>T (p.Lys125Asn) rs878854595 0.00001
NM_003002.4(SDHD):c.400T>G (p.Leu134Val) rs200851392 0.00001
NM_003002.4(SDHD):c.421T>C (p.Tyr141His) rs1394514096 0.00001
NM_003002.4(SDHD):c.422A>G (p.Tyr141Cys) rs199772639 0.00001
NM_003002.4(SDHD):c.428A>G (p.Asn143Ser) rs770909248 0.00001
NM_003002.4(SDHD):c.430T>C (p.Tyr144His) rs774243340 0.00001
NM_003002.4(SDHD):c.431A>G (p.Tyr144Cys) rs745732631 0.00001
NM_003002.4(SDHD):c.433C>A (p.His145Asn) rs121908984 0.00001
NM_003002.4(SDHD):c.82C>A (p.Pro28Thr) rs541477171 0.00001
NM_003002.4(SDHD):c.82C>T (p.Pro28Ser) rs541477171 0.00001
NM_003002.4(SDHD):c.85G>C (p.Ala29Pro) rs776930864 0.00001
NM_003002.4(SDHD):c.88C>T (p.His30Tyr) rs561759202 0.00001
NM_003002.4(SDHD):c.104T>C (p.Leu35Pro) rs11547892
NM_003002.4(SDHD):c.107A>C (p.Gln36Pro) rs759143732
NM_003002.4(SDHD):c.109G>A (p.Asp37Asn) rs1865654125
NM_003002.4(SDHD):c.109G>T (p.Asp37Tyr)
NM_003002.4(SDHD):c.113G>C (p.Arg38Pro) rs199901239
NM_003002.4(SDHD):c.115C>A (p.Pro39Thr) rs1043566340
NM_003002.4(SDHD):c.133G>A (p.Gly45Arg)
NM_003002.4(SDHD):c.137T>A (p.Val46Glu)
NM_003002.4(SDHD):c.140A>C (p.Gln47Pro)
NM_003002.4(SDHD):c.140A>G (p.Gln47Arg) rs899706404
NM_003002.4(SDHD):c.146T>C (p.Ile49Thr) rs1555186808
NM_003002.4(SDHD):c.148C>A (p.His50Asn) rs779249550
NM_003002.4(SDHD):c.151T>A (p.Leu51Met)
NM_003002.4(SDHD):c.157C>G (p.Pro53Ala) rs1865656629
NM_003002.4(SDHD):c.163C>T (p.His55Tyr)
NM_003002.4(SDHD):c.164A>T (p.His55Leu) rs1865656869
NM_003002.4(SDHD):c.169+3A>G rs1865657168
NM_003002.4(SDHD):c.170-5T>A rs1218549926
NM_003002.4(SDHD):c.170C>G (p.Ser57Cys)
NM_003002.4(SDHD):c.172G>C (p.Gly58Arg)
NM_003002.4(SDHD):c.175T>C (p.Ser59Pro) rs1592780294
NM_003002.4(SDHD):c.176C>T (p.Ser59Phe) rs1592780300
NM_003002.4(SDHD):c.194A>G (p.His65Arg) rs780226013
NM_003002.4(SDHD):c.200C>T (p.Thr67Ile)
NM_003002.4(SDHD):c.202A>G (p.Ser68Gly) rs2135269276
NM_003002.4(SDHD):c.209G>A (p.Arg70Lys) rs755047928
NM_003002.4(SDHD):c.211G>T (p.Val71Phe) rs1428042303
NM_003002.4(SDHD):c.220G>A (p.Val74Ile)
NM_003002.4(SDHD):c.223T>G (p.Leu75Val)
NM_003002.4(SDHD):c.226C>T (p.Leu76Phe) rs1865687801
NM_003002.4(SDHD):c.235C>G (p.Leu79Val)
NM_003002.4(SDHD):c.244G>C (p.Ala82Pro) rs745559875
NM_003002.4(SDHD):c.250T>A (p.Tyr84Asn)
NM_003002.4(SDHD):c.259C>G (p.Pro87Ala)
NM_003002.4(SDHD):c.260C>G (p.Pro87Arg)
NM_003002.4(SDHD):c.260C>T (p.Pro87Leu)
NM_003002.4(SDHD):c.265T>C (p.Ser89Pro)
NM_003002.4(SDHD):c.268G>T (p.Ala90Ser)
NM_003002.4(SDHD):c.268_269delinsTT (p.Ala90Leu) rs1555187033
NM_003002.4(SDHD):c.269C>G (p.Ala90Gly)
NM_003002.4(SDHD):c.270G>C (p.Ala90=) rs766656463
NM_003002.4(SDHD):c.271A>T (p.Met91Leu) rs2135269615
NM_003002.4(SDHD):c.276C>G (p.Asp92Glu)
NM_003002.4(SDHD):c.281C>T (p.Ser94Phe) rs199754684
NM_003002.4(SDHD):c.290C>T (p.Ala97Val) rs756533450
NM_003002.4(SDHD):c.298A>G (p.Thr100Ala) rs1555187065
NM_003002.4(SDHD):c.314+3A>G
NM_003002.4(SDHD):c.315-3T>C rs1555187565
NM_003002.4(SDHD):c.319C>T (p.Leu107Phe) rs1209781530
NM_003002.4(SDHD):c.328G>C (p.Val110Leu)
NM_003002.4(SDHD):c.332T>C (p.Val111Ala) rs1592786183
NM_003002.4(SDHD):c.334A>T (p.Thr112Ser)
NM_003002.4(SDHD):c.338A>T (p.Asp113Val) rs786202513
NM_003002.4(SDHD):c.343G>A (p.Val115Ile)
NM_003002.4(SDHD):c.346C>T (p.His116Tyr) rs2135277443
NM_003002.4(SDHD):c.347A>G (p.His116Arg)
NM_003002.4(SDHD):c.354T>G (p.Asp118Glu) rs911663426
NM_003002.4(SDHD):c.355G>T (p.Ala119Ser) rs930768406
NM_003002.4(SDHD):c.371C>T (p.Ala124Val) rs1865811210
NM_003002.4(SDHD):c.373A>G (p.Lys125Glu)
NM_003002.4(SDHD):c.374A>G (p.Lys125Arg) rs1592786256
NM_003002.4(SDHD):c.376G>A (p.Ala126Thr) rs1592786265
NM_003002.4(SDHD):c.386T>C (p.Leu129Ser) rs201726097
NM_003002.4(SDHD):c.389C>G (p.Ala130Gly) rs1049692537
NM_003002.4(SDHD):c.391C>T (p.Leu131Phe)
NM_003002.4(SDHD):c.394T>G (p.Ser132Ala) rs2135277611
NM_003002.4(SDHD):c.395C>T (p.Ser132Leu)
NM_003002.4(SDHD):c.410C>T (p.Ala137Val) rs749250498
NM_003002.4(SDHD):c.413G>A (p.Gly138Glu) rs1401695686
NM_003002.4(SDHD):c.419G>A (p.Cys140Tyr) rs2135277691
NM_003002.4(SDHD):c.426C>G (p.Phe142Leu) rs2135277712
NM_003002.4(SDHD):c.432T>A (p.Tyr144Ter) rs1355803189
NM_003002.4(SDHD):c.435C>A (p.His145Gln)
NM_003002.4(SDHD):c.443G>A (p.Gly148Asp)
NM_003002.4(SDHD):c.445A>G (p.Ile149Val) rs1865813813
NM_003002.4(SDHD):c.452A>G (p.Lys151Arg)
NM_003002.4(SDHD):c.453A>C (p.Lys151Asn) rs761953172
NM_003002.4(SDHD):c.458T>C (p.Val153Ala) rs1555187644
NM_003002.4(SDHD):c.461C>T (p.Ala154Val)
NM_003002.4(SDHD):c.463del (p.Met155fs) rs587776647
NM_003002.4(SDHD):c.478T>A (p.Ter160Arg) rs1555187655
NM_003002.4(SDHD):c.53-3C>T
NM_003002.4(SDHD):c.59T>C (p.Leu20Ser)
NM_003002.4(SDHD):c.61C>T (p.Leu21Phe) rs1592778703
NM_003002.4(SDHD):c.65G>A (p.Arg22Gln) rs1555186772
NM_003002.4(SDHD):c.73G>T (p.Val25Leu) rs878854597
NM_003002.4(SDHD):c.85G>A (p.Ala29Thr)
NM_003002.4(SDHD):c.93C>G (p.Ile31Met)

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