ClinVar Miner

List of variants in gene combination MUTYH, TOE1 reported by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 46
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HGVS dbSNP
NC_000001.10:g.(?_45794968)_(45805936_?)dup
NC_000001.11:g.(?_45329306)_(45343656_?)dup
NC_000001.11:g.(?_45340209)_(45343656_?)dup
NM_025077.4(TOE1):c.-10G>A
NM_025077.4(TOE1):c.-12A>G rs1553137063
NM_025077.4(TOE1):c.-13G>T rs1553137062
NM_025077.4(TOE1):c.-15G>C rs587782837
NM_025077.4(TOE1):c.-15G>T rs587782837
NM_025077.4(TOE1):c.-17G>A rs1382218222
NM_025077.4(TOE1):c.-17G>C
NM_025077.4(TOE1):c.-18C>A rs1114167687
NM_025077.4(TOE1):c.-20G>A rs753502884
NM_025077.4(TOE1):c.-24C>T rs1570591736
NM_025077.4(TOE1):c.-27C>G rs755928199
NM_025077.4(TOE1):c.-27C>T rs755928199
NM_025077.4(TOE1):c.-29G>A rs878854188
NM_025077.4(TOE1):c.-29G>C rs878854188
NM_025077.4(TOE1):c.-2T>G
NM_025077.4(TOE1):c.-32A>G rs1060501343
NM_025077.4(TOE1):c.-32A>T
NM_025077.4(TOE1):c.-33C>G rs1064795596
NM_025077.4(TOE1):c.-33C>T rs1064795596
NM_025077.4(TOE1):c.-37T>A rs759654665
NM_025077.4(TOE1):c.-37T>C
NM_025077.4(TOE1):c.-38G>A 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.-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.-4_3dup (p.Ala2fs)
NM_025077.4(TOE1):c.-6G>A rs745424307
NM_025077.4(TOE1):c.-6G>C rs745424307
NM_025077.4(TOE1):c.-7C>A rs958040221
NM_025077.4(TOE1):c.-7C>T rs958040221
NM_025077.4(TOE1):c.-8G>A rs587782404
NM_025077.4(TOE1):c.1A>C (p.Met1Leu) rs865954220
NM_025077.4(TOE1):c.1A>G (p.Met1Val) rs865954220
NM_025077.4(TOE1):c.1A>T (p.Met1Leu)
NM_025077.4(TOE1):c.2T>C (p.Met1Thr)

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