ClinVar Miner

List of variants in gene MSH2 reported as uncertain significance by PreventionGenetics, part of Exact Sciences

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Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_000251.3(MSH2):c.435T>G (p.Ile145Met) rs63750124 0.00031
NM_000251.3(MSH2):c.1275A>G (p.Glu425=) rs63751650 0.00016
NM_000251.3(MSH2):c.2537A>G (p.Gln846Arg) rs140754514 0.00015
NM_000251.3(MSH2):c.1748A>G (p.Asn583Ser) rs201118107 0.00014
NM_000251.3(MSH2):c.-3G>C rs587779960 0.00013
NM_000251.3(MSH2):c.128A>G (p.Tyr43Cys) rs17217723 0.00011
NM_000251.3(MSH2):c.1461C>G (p.Asp487Glu) rs35107951 0.00011
NM_000251.3(MSH2):c.1790A>C (p.Asp597Ala) rs548407418 0.00011
NM_000251.3(MSH2):c.2203A>G (p.Ile735Val) rs2229061 0.00011
NM_000251.3(MSH2):c.-181G>A rs786201698 0.00010
NM_000251.3(MSH2):c.1505A>G (p.Asp502Gly) rs148192104 0.00009
NM_000251.3(MSH2):c.820A>G (p.Ile274Val) rs371944271 0.00008
NM_000251.3(MSH2):c.2732T>G (p.Leu911Arg) rs41295182 0.00007
NM_000251.3(MSH2):c.1530G>C (p.Gln510His) rs587782355 0.00004
NM_000251.3(MSH2):c.1366A>G (p.Thr456Ala) rs758636279 0.00003
NM_000251.3(MSH2):c.1724A>G (p.Asp575Gly) rs370330868 0.00003
NM_000251.3(MSH2):c.1847C>G (p.Pro616Arg) rs587779965 0.00003
NM_000251.3(MSH2):c.2558A>C (p.Glu853Ala) rs63750797 0.00003
NM_000251.3(MSH2):c.409G>C (p.Gly137Arg) rs587781795 0.00003
NM_000251.3(MSH2):c.1200C>G (p.Asn400Lys) rs1301023135 0.00002
NM_000251.3(MSH2):c.2158A>G (p.Lys720Glu) rs747265823 0.00002
NM_000251.3(MSH2):c.2178G>C (p.Met726Ile) rs587782396 0.00002
NM_000251.3(MSH2):c.2621A>G (p.Tyr874Cys) rs775390721 0.00002
NM_000251.3(MSH2):c.2650A>T (p.Ile884Phe) rs774732579 0.00002
NM_000251.3(MSH2):c.2717T>C (p.Ile906Thr) rs587780687 0.00002
NM_000251.3(MSH2):c.1148G>A (p.Arg383Gln) rs376934727 0.00001
NM_000251.3(MSH2):c.118G>A (p.Gly40Ser) rs63751260 0.00001
NM_000251.3(MSH2):c.1254A>G (p.Ile418Met) rs751431238 0.00001
NM_000251.3(MSH2):c.1424A>T (p.Asp475Val) rs1349765126 0.00001
NM_000251.3(MSH2):c.1622C>T (p.Thr541Ile) rs864622079 0.00001
NM_000251.3(MSH2):c.1796T>C (p.Leu599Ser) rs747504492 0.00001
NM_000251.3(MSH2):c.1825G>T (p.Ala609Ser) rs150980616 0.00001
NM_000251.3(MSH2):c.1927G>A (p.Glu643Lys) rs374840361 0.00001
NM_000251.3(MSH2):c.1967A>G (p.Tyr656Cys) rs185356145 0.00001
NM_000251.3(MSH2):c.2083G>C (p.Val695Leu) rs772491283 0.00001
NM_000251.3(MSH2):c.208G>A (p.Ala70Thr) rs587778522 0.00001
NM_000251.3(MSH2):c.2122A>G (p.Ile708Val) rs750084297 0.00001
NM_000251.3(MSH2):c.2141C>T (p.Ala714Val) rs63751224 0.00001
NM_000251.3(MSH2):c.2197G>A (p.Ala733Thr) rs772662439 0.00001
NM_000251.3(MSH2):c.2376T>A (p.Asn792Lys) rs1281667531 0.00001
NM_000251.3(MSH2):c.2439G>A (p.Met813Ile) rs587781678 0.00001
NM_000251.3(MSH2):c.2569A>G (p.Ile857Val) rs753459308 0.00001
NM_000251.3(MSH2):c.440T>G (p.Val147Gly) rs760851623 0.00001
NM_000251.3(MSH2):c.775C>T (p.Pro259Ser) rs587781294 0.00001
NM_000251.2(MSH2):c.-210T>C
NM_000251.3(MSH2):c.1148G>C (p.Arg383Pro) rs376934727
NM_000251.3(MSH2):c.127T>G (p.Tyr43Asp) rs786202731
NM_000251.3(MSH2):c.1405C>G (p.Leu469Val) rs780702096
NM_000251.3(MSH2):c.1511-41G>T
NM_000251.3(MSH2):c.1593A>C (p.Lys531Asn) rs1553366599
NM_000251.3(MSH2):c.160G>A (p.Ala54Thr) rs749212640
NM_000251.3(MSH2):c.1798G>T (p.Ala600Ser) rs587778526
NM_000251.3(MSH2):c.183G>C (p.Gln61His) rs751082926
NM_000251.3(MSH2):c.1A>C (p.Met1Leu) rs267607911
NM_000251.3(MSH2):c.20A>C (p.Glu7Ala) rs530071578
NM_000251.3(MSH2):c.2595_2597del (p.Ile865del) rs759912716
NM_000251.3(MSH2):c.2680dup (p.Met894fs) rs876658211
NM_000251.3(MSH2):c.2725A>C (p.Lys909Gln) rs879254253
NM_000251.3(MSH2):c.2777T>G (p.Ile926Ser)
NM_000251.3(MSH2):c.2786G>T (p.Arg929Leu) rs587779967
NM_000251.3(MSH2):c.471C>T (p.Gly157=) rs61756463
NM_000251.3(MSH2):c.786G>T (p.Glu262Asp) rs754820584
NM_000251.3(MSH2):c.79C>T (p.Pro27Ser) rs878853826
NM_000251.3(MSH2):c.812C>G (p.Ser271Cys) rs139891783
NM_000251.3(MSH2):c.911T>C (p.Ile304Thr) rs1021303606
NM_000251.3(MSH2):c.968C>T (p.Ser323Phe) rs63750732

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