ClinVar Miner

List of variants in gene combination MUTYH, TOE1 reported as uncertain significance by Color Diagnostics, LLC DBA Color Health

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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_001128425.2(MUTYH):c.17C>A (p.Ser6Tyr) rs587782837 0.00002
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.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>T (p.Leu4Phe) rs587782404
NM_001128425.2(MUTYH):c.13G>A (p.Val5Ile) rs786201933
NM_001128425.2(MUTYH):c.13G>T (p.Val5Phe) rs786201933
NM_001128425.2(MUTYH):c.28C>T (p.Arg10Cys) rs1570591700
NM_001128425.2(MUTYH):c.29G>C (p.Arg10Pro) rs755928199
NM_001128425.2(MUTYH):c.3G>A (p.Met1Ile) rs757906591
NM_001128425.2(MUTYH):c.8C>T (p.Pro3Leu) rs745424307
NM_025077.4(TOE1):c.-38dup rs1557517901
NM_025077.4(TOE1):c.-40G>C rs1553136962
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

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