ClinVar Miner

List of variants in gene MSH2 reported as uncertain significance by Quest Diagnostics Nichols Institute San Juan Capistrano

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Total variants: 77
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HGVS dbSNP
NM_000251.2(MSH2):c.-3G>C rs587779960
NM_000251.2(MSH2):c.-68-5G>A rs552303079
NM_000251.2(MSH2):c.-9G>C rs547444746
NM_000251.2(MSH2):c.1048C>G (p.Leu350Val) rs771126636
NM_000251.2(MSH2):c.1077-3C>A rs758182607
NM_000251.2(MSH2):c.1275A>G (p.Glu425=) rs63751650
NM_000251.2(MSH2):c.1277-6T>C
NM_000251.2(MSH2):c.1294T>C (p.Leu432=) rs937218360
NM_000251.2(MSH2):c.1331G>A (p.Arg444His) rs557339938
NM_000251.2(MSH2):c.1379T>C (p.Met460Thr) rs1553361303
NM_000251.2(MSH2):c.1382A>C (p.Asp461Ala) rs730881756
NM_000251.2(MSH2):c.1387-4G>C rs376796243
NM_000251.2(MSH2):c.1462T>G (p.Leu488Val) rs587781314
NM_000251.2(MSH2):c.1570C>T (p.Arg524Cys) rs755818010
NM_000251.2(MSH2):c.1600C>T (p.Arg534Cys) rs63750029
NM_000251.2(MSH2):c.1661+5G>T rs267607972
NM_000251.2(MSH2):c.1677A>C (p.Leu559Phe)
NM_000251.2(MSH2):c.16A>G (p.Lys6Glu) rs777351049
NM_000251.2(MSH2):c.1730T>C (p.Ile577Thr) rs63749910
NM_000251.2(MSH2):c.1748A>G (p.Asn583Ser) rs201118107
NM_000251.2(MSH2):c.174C>A (p.Phe58Leu) rs372189599
NM_000251.2(MSH2):c.1760-3C>T rs786202843
NM_000251.2(MSH2):c.1790A>C (p.Asp597Ala) rs548407418
NM_000251.2(MSH2):c.1821C>T (p.Ser607=)
NM_000251.2(MSH2):c.1865C>G (p.Pro622Arg) rs28929483
NM_000251.2(MSH2):c.1873T>C (p.Leu625=) rs63750669
NM_000251.2(MSH2):c.188T>A (p.Val63Glu)
NM_000251.2(MSH2):c.1897A>G (p.Ile633Val) rs771695599
NM_000251.2(MSH2):c.1937A>G (p.Asp646Gly) rs41295290
NM_000251.2(MSH2):c.1972G>C (p.Glu658Gln)
NM_000251.2(MSH2):c.1A>C (p.Met1Leu) rs267607911
NM_000251.2(MSH2):c.2005+10C>T
NM_000251.2(MSH2):c.2014A>G (p.Met672Val) rs763690339
NM_000251.2(MSH2):c.2039G>A (p.Arg680Gln)
NM_000251.2(MSH2):c.2043A>G (p.Gln681=) rs730881763
NM_000251.2(MSH2):c.2048G>T (p.Gly683Val) rs755920849
NM_000251.2(MSH2):c.2055A>G (p.Ile685Met) rs989001878
NM_000251.2(MSH2):c.206C>T (p.Pro69Leu) rs983555044
NM_000251.2(MSH2):c.2152C>G (p.Gln718Glu) rs587779139
NM_000251.2(MSH2):c.2178G>C (p.Met726Ile) rs587782396
NM_000251.2(MSH2):c.2211-6C>A rs267608003
NM_000251.2(MSH2):c.2218A>G (p.Thr740Ala) rs1553369627
NM_000251.2(MSH2):c.2228C>T (p.Ser743Leu) rs63751155
NM_000251.2(MSH2):c.2266A>G (p.Thr756Ala) rs750646335
NM_000251.2(MSH2):c.228G>T (p.Gln76His) rs587782857
NM_000251.2(MSH2):c.2308A>G (p.Ile770Val) rs63750684
NM_000251.2(MSH2):c.2309T>C (p.Ile770Thr) rs371718349
NM_000251.2(MSH2):c.2503A>C (p.Asn835His) rs41295296
NM_000251.2(MSH2):c.2537A>G (p.Gln846Arg) rs140754514
NM_000251.2(MSH2):c.2556G>C (p.Glu852Asp) rs587781453
NM_000251.2(MSH2):c.2606C>A (p.Ala869Glu) rs730881772
NM_000251.2(MSH2):c.2786G>A (p.Arg929Gln) rs587779967
NM_000251.2(MSH2):c.330G>C (p.Lys110Asn)
NM_000251.2(MSH2):c.339G>C (p.Lys113Asn)
NM_000251.2(MSH2):c.374C>T (p.Pro125Leu) rs876659113
NM_000251.2(MSH2):c.409G>C (p.Gly137Arg) rs587781795
NM_000251.2(MSH2):c.416A>G (p.Asn139Ser) rs1553350676
NM_000251.2(MSH2):c.422T>C (p.Met141Thr) rs768313658
NM_000251.2(MSH2):c.435T>G (p.Ile145Met) rs63750124
NM_000251.2(MSH2):c.439G>A (p.Val147Ile) rs773125415
NM_000251.2(MSH2):c.43G>A (p.Ala15Thr) rs1183892581
NM_000251.2(MSH2):c.508C>G (p.Gln170Glu) rs63750843
NM_000251.2(MSH2):c.554C>T (p.Ser185Phe) rs878853819
NM_000251.2(MSH2):c.557A>G (p.Asn186Ser) rs151129360
NM_000251.2(MSH2):c.55T>C (p.Phe19Leu) rs141711342
NM_000251.2(MSH2):c.565G>A (p.Ala189Thr) rs63750821
NM_000251.2(MSH2):c.5C>T (p.Ala2Val) rs587778521
NM_000251.2(MSH2):c.618T>G (p.Thr206=)
NM_000251.2(MSH2):c.646-4A>G rs587779974
NM_000251.2(MSH2):c.766G>A (p.Ala256Thr) rs377403073
NM_000251.2(MSH2):c.775C>T (p.Pro259Ser) rs587781294
NM_000251.2(MSH2):c.815C>T (p.Ala272Val) rs34136999
NM_000251.2(MSH2):c.835C>G (p.Leu279Val) rs375351205
NM_000251.2(MSH2):c.855C>G (p.Asn285Lys) rs759242666
NM_000251.2(MSH2):c.889A>G (p.Ser297Gly)
NM_000251.2(MSH2):c.891C>G (p.Ser297Arg) rs551236465
NM_000251.2(MSH2):c.913G>A (p.Ala305Thr) rs63751454

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