ClinVar Miner

List of variants in gene MSH3 reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
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Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_002439.5(MSH3):c.2732T>G (p.Leu911Trp) rs41545019 0.00233
NM_002439.5(MSH3):c.1992G>A (p.Gln664=) rs144019582 0.00143
NM_002439.5(MSH3):c.1794G>A (p.Ser598=) rs61753791 0.00130
NM_002439.5(MSH3):c.2262A>G (p.Ile754Met) rs200819607 0.00028
NM_002439.5(MSH3):c.356C>T (p.Ser119Phe) rs144607594 0.00028
NM_002439.5(MSH3):c.2685C>T (p.Thr895=) rs61753792 0.00024
NM_002439.5(MSH3):c.2438A>G (p.Lys813Arg) rs150446804 0.00022
NM_002439.5(MSH3):c.1194C>T (p.Gly398=) rs141118996 0.00013
NM_002439.5(MSH3):c.562C>T (p.Arg188Cys) rs147289289 0.00013
NM_002439.5(MSH3):c.3181A>G (p.Arg1061Gly) rs746782115 0.00012
NM_002439.5(MSH3):c.1314G>A (p.Ala438=) rs574337805 0.00010
NM_002439.5(MSH3):c.1503C>T (p.Cys501=) rs201057820 0.00004
NM_002439.5(MSH3):c.1896A>G (p.Lys632=) rs201737845 0.00004
NM_002439.5(MSH3):c.2085A>G (p.Lys695=) rs777245977 0.00004
NM_002439.5(MSH3):c.439C>T (p.Pro147Ser) rs977366961 0.00004
NM_002439.5(MSH3):c.517A>G (p.Ser173Gly) rs750311213 0.00004
NM_002439.5(MSH3):c.2436-1G>A rs200639359 0.00003
NM_002439.5(MSH3):c.2520C>T (p.Val840=) rs779973060 0.00003
NM_002439.5(MSH3):c.582C>G (p.Asp194Glu) rs749446559 0.00003
NM_002439.5(MSH3):c.2748T>C (p.Ala916=) rs771253300 0.00002
NM_002439.5(MSH3):c.2179C>T (p.Arg727Ter) rs376667075 0.00001
NM_002439.5(MSH3):c.2845C>T (p.Gln949Ter) rs758546167 0.00001
NM_002439.5(MSH3):c.558G>A (p.Ser186=) rs760604405 0.00001
NM_002439.5(MSH3):c.696A>C (p.Leu232=) rs150903605 0.00001
NM_002439.5(MSH3):c.1035del (p.Pro346_Leu347insTer) rs1580553607
NM_002439.5(MSH3):c.1148dup (p.Asn385fs) rs587776701
NM_002439.5(MSH3):c.1256C>G (p.Ser419Ter) rs578113271
NM_002439.5(MSH3):c.1400A>G (p.His467Arg) rs1316678832
NM_002439.5(MSH3):c.1579C>T (p.Gln527Ter) rs1204734473
NM_002439.5(MSH3):c.1650T>C (p.Asn550=)
NM_002439.5(MSH3):c.1764-9_1764-8del rs41559616
NM_002439.5(MSH3):c.2227_2228del (p.Gln743fs) rs1371600437
NM_002439.5(MSH3):c.2319-1G>A rs866260675
NM_002439.5(MSH3):c.2412T>C (p.Ser804=)
NM_002439.5(MSH3):c.2607G>A (p.Val869=) rs2112026778
NM_002439.5(MSH3):c.2839A>G (p.Lys947Glu) rs1745876734
NM_002439.5(MSH3):c.3027C>T (p.Thr1009=) rs145319344
NM_002439.5(MSH3):c.438_439delinsG (p.Pro147fs)
NM_002439.5(MSH3):c.735T>C (p.Asp245=) rs1161728755

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