ClinVar Miner

List of variants in gene combination MUTYH, TOE1 reported as uncertain significance for Hereditary cancer-predisposing syndrome

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Total variants: 37
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HGVS dbSNP
NM_025077.4(TOE1):c.-11C>A
NM_025077.4(TOE1):c.-11C>G rs786201933
NM_025077.4(TOE1):c.-11C>T rs786201933
NM_025077.4(TOE1):c.-15G>C rs587782837
NM_025077.4(TOE1):c.-15G>T rs587782837
NM_025077.4(TOE1):c.-18C>A rs1114167687
NM_025077.4(TOE1):c.-1C>T
NM_025077.4(TOE1):c.-21A>C rs1570591840
NM_025077.4(TOE1):c.-26G>A
NM_025077.4(TOE1):c.-27C>G rs755928199
NM_025077.4(TOE1):c.-27C>T rs755928199
NM_025077.4(TOE1):c.-29G>C rs878854188
NM_025077.4(TOE1):c.-30A>C rs752665489
NM_025077.4(TOE1):c.-33C>G rs1064795596
NM_025077.4(TOE1):c.-37T>A rs759654665
NM_025077.4(TOE1):c.-38G>A rs774530388
NM_025077.4(TOE1):c.-38G>C rs774530388
NM_025077.4(TOE1):c.-38dup rs1557517901
NM_025077.4(TOE1):c.-39C>T rs876658588
NM_025077.4(TOE1):c.-40G>C rs1553136962
NM_025077.4(TOE1):c.-5G>C rs876659091
NM_025077.4(TOE1):c.-6G>A rs745424307
NM_025077.4(TOE1):c.-6G>C rs745424307
NM_025077.4(TOE1):c.-8G>A rs587782404
NM_025077.4(TOE1):c.-8G>C rs587782404
NM_025077.4(TOE1):c.13A>G (p.Ser5Gly)
NM_025077.4(TOE1):c.15T>A (p.Ser5Arg)
NM_025077.4(TOE1):c.15T>G (p.Ser5Arg) rs1057520831
NM_025077.4(TOE1):c.17A>G (p.Asp6Gly)
NM_025077.4(TOE1):c.1A>G (p.Met1Val) rs865954220
NM_025077.4(TOE1):c.21T>C (p.Asp7=) rs1216403097
NM_025077.4(TOE1):c.2T>C (p.Met1Thr)
NM_025077.4(TOE1):c.4G>C (p.Ala2Pro) rs781609463
NM_025077.4(TOE1):c.52+77G>A rs3219466
NM_025077.4(TOE1):c.5C>A (p.Ala2Asp) rs748689064
NM_025077.4(TOE1):c.5C>T (p.Ala2Val)
NM_025077.4(TOE1):c.6C>T (p.Ala2=) rs876659248

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