ClinVar Miner

List of variants in gene combination MUTYH, TOE1 reported as likely benign

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Gene type:
ClinVar version:
Total variants: 31
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HGVS dbSNP
NM_001128425.2(MUTYH):c.36+179G>T rs1418696430
NM_001128425.2(MUTYH):c.36+214G>C rs568514678
NM_025077.4(TOE1):c.-10G>A
NM_025077.4(TOE1):c.-10G>T rs876659717
NM_025077.4(TOE1):c.-13G>T rs1553137062
NM_025077.4(TOE1):c.-20G>A rs753502884
NM_025077.4(TOE1):c.-22C>G rs1570591790
NM_025077.4(TOE1):c.-26G>T rs1570591700
NM_025077.4(TOE1):c.-29G>A rs878854188
NM_025077.4(TOE1):c.-41A>C rs1211077933
NM_025077.4(TOE1):c.-41A>G rs1211077933
NM_025077.4(TOE1):c.-42C>T rs1060504202
NM_025077.4(TOE1):c.-43C>A rs766584437
NM_025077.4(TOE1):c.-43C>T
NM_025077.4(TOE1):c.-44T>C rs201746729
NM_025077.4(TOE1):c.-44T>G rs201746729
NM_025077.4(TOE1):c.-45G>A rs2275602
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.-7C>A rs958040221
NM_025077.4(TOE1):c.-7C>G rs958040221
NM_025077.4(TOE1):c.-7C>T rs958040221
NM_025077.4(TOE1):c.15T>G (p.Ser5Arg) rs1057520831
NM_025077.4(TOE1):c.39C>T (p.Pro13=) rs749548330
NM_025077.4(TOE1):c.52+130A>G rs1215187269
NM_025077.4(TOE1):c.52+76A>G rs547694371
NM_025077.4(TOE1):c.52+77G>A rs3219466
NM_025077.4(TOE1):c.52+97G>A rs992028783

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