ClinVar Miner

List of variants in gene combination MUTYH, TOE1 studied for Hereditary cancer-predisposing syndrome

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Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_025077.4(TOE1):c.52+77G>A rs3219466 0.02177
NM_025077.4(TOE1):c.-45G>A rs2275602 0.00299
NM_025077.4(TOE1):c.-41A>G rs1211077933 0.00005
NM_001128425.2(MUTYH):c.17C>A (p.Ser6Tyr) rs587782837 0.00002
NM_001128425.2(MUTYH):c.36+1G>A rs1553136984 0.00001
NM_001128425.2(MUTYH):c.8C>G (p.Pro3Arg) rs745424307 0.00001
NM_025077.4(TOE1):c.-37T>A rs759654665 0.00001
NM_025077.4(TOE1):c.-38G>C rs774530388 0.00001
NM_025077.4(TOE1):c.-39C>T rs876658588 0.00001
NM_025077.4(TOE1):c.1A>G (p.Met1Val) rs865954220 0.00001
NM_025077.4(TOE1):c.21T>C (p.Asp7=) rs1216403097 0.00001
NM_025077.4(TOE1):c.5C>T (p.Ala2Val) rs748689064 0.00001
NM_025077.4(TOE1):c.6C>T (p.Ala2=) rs876659248 0.00001
NM_001128425.2(MUTYH):c.10C>G (p.Leu4Val) rs587782404
NM_001128425.2(MUTYH):c.10C>T (p.Leu4Phe) rs587782404
NM_001128425.2(MUTYH):c.12C>A (p.Leu4=) rs876659717
NM_001128425.2(MUTYH):c.12C>T (p.Leu4=) rs876659717
NM_001128425.2(MUTYH):c.13G>A (p.Val5Ile) rs786201933
NM_001128425.2(MUTYH):c.13G>C (p.Val5Leu) rs786201933
NM_001128425.2(MUTYH):c.13G>T (p.Val5Phe) rs786201933
NM_001128425.2(MUTYH):c.17C>G (p.Ser6Cys) rs587782837
NM_001128425.2(MUTYH):c.20G>T (p.Arg7Leu) rs1114167687
NM_001128425.2(MUTYH):c.22C>T (p.Leu8=) rs753502884
NM_001128425.2(MUTYH):c.23T>C (p.Leu8Pro)
NM_001128425.2(MUTYH):c.23T>G (p.Leu8Arg) rs1570591840
NM_001128425.2(MUTYH):c.24G>C (p.Leu8=) rs1570591790
NM_001128425.2(MUTYH):c.28C>A (p.Arg10Ser) rs1570591700
NM_001128425.2(MUTYH):c.28C>T (p.Arg10Cys) rs1570591700
NM_001128425.2(MUTYH):c.29G>A (p.Arg10His) rs755928199
NM_001128425.2(MUTYH):c.29G>C (p.Arg10Pro) rs755928199
NM_001128425.2(MUTYH):c.31C>G (p.Leu11Val) rs878854188
NM_001128425.2(MUTYH):c.31C>T (p.Leu11=) rs878854188
NM_001128425.2(MUTYH):c.32T>G (p.Leu11Arg) rs752665489
NM_001128425.2(MUTYH):c.33G>A (p.Leu11=)
NM_001128425.2(MUTYH):c.35G>A (p.Trp12Ter) rs1064795596
NM_001128425.2(MUTYH):c.35G>C (p.Trp12Ser) rs1064795596
NM_001128425.2(MUTYH):c.36+2T>C
NM_001128425.2(MUTYH):c.36G>A (p.Trp12Ter) rs767402084
NM_001128425.2(MUTYH):c.3G>A (p.Met1Ile) rs757906591
NM_001128425.2(MUTYH):c.3G>C (p.Met1Ile)
NM_001128425.2(MUTYH):c.7C>G (p.Pro3Ala) rs876659091
NM_001128425.2(MUTYH):c.8C>T (p.Pro3Leu) rs745424307
NM_001128425.2(MUTYH):c.9G>A (p.Pro3=) rs958040221
NM_001128425.2(MUTYH):c.9G>C (p.Pro3=) rs958040221
NM_001128425.2(MUTYH):c.9G>T (p.Pro3=) rs958040221
NM_001128425.2(MUTYH):c.9_10delinsAA (p.Leu4Ile) rs1064794772
NM_025077.4(TOE1):c.-38G>A rs774530388
NM_025077.4(TOE1):c.-38dup rs1557517901
NM_025077.4(TOE1):c.-40G>C rs1553136962
NM_025077.4(TOE1):c.-43C>A rs766584437
NM_025077.4(TOE1):c.-43C>T rs766584437
NM_025077.4(TOE1):c.-44T>G rs201746729
NM_025077.4(TOE1):c.-45G>C rs2275602
NM_025077.4(TOE1):c.-52A>G rs1553136902
NM_025077.4(TOE1):c.-54G>A rs540793556
NM_025077.4(TOE1):c.-54G>C rs540793556
NM_025077.4(TOE1):c.-54G>T rs540793556
NM_025077.4(TOE1):c.13A>G (p.Ser5Gly) rs1646825989
NM_025077.4(TOE1):c.15T>A (p.Ser5Arg) rs1057520831
NM_025077.4(TOE1):c.15T>G (p.Ser5Arg) rs1057520831
NM_025077.4(TOE1):c.17A>G (p.Asp6Gly) rs562733690
NM_025077.4(TOE1):c.2T>C (p.Met1Thr) rs1646823787
NM_025077.4(TOE1):c.4G>C (p.Ala2Pro) rs781609463
NM_025077.4(TOE1):c.5C>A (p.Ala2Asp) rs748689064
NM_025077.4(TOE1):c.7G>A (p.Ala3Thr)
NM_025077.4(TOE1):c.9C>T (p.Ala3=)

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