ClinVar Miner

List of variants in gene MSH3 reported as uncertain significance for not specified

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Gene type:
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Total variants: 52
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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.1571A>C (p.Asn524Thr) rs55724159 0.00220
NM_002439.5(MSH3):c.2480A>G (p.His827Arg) rs138339194 0.00191
NM_002439.5(MSH3):c.2041C>T (p.Pro681Ser) rs115198722 0.00112
NM_002439.5(MSH3):c.1453+15T>C rs200717987 0.00096
NM_002439.5(MSH3):c.1394A>G (p.Tyr465Cys) rs35009542 0.00032
NM_002439.5(MSH3):c.2262A>G (p.Ile754Met) rs200819607 0.00028
NM_002439.5(MSH3):c.3174A>G (p.Gln1058=) rs758314489 0.00016
NM_002439.5(MSH3):c.1177G>A (p.Val393Met) rs761779919 0.00013
NM_002439.5(MSH3):c.1194C>T (p.Gly398=) rs141118996 0.00013
NM_002439.5(MSH3):c.2336G>A (p.Arg779His) rs199791286 0.00013
NM_002439.5(MSH3):c.562C>T (p.Arg188Cys) rs147289289 0.00013
NM_002439.5(MSH3):c.3072G>C (p.Gln1024His) rs147640909 0.00012
NM_002439.5(MSH3):c.2180G>A (p.Arg727Gln) rs148896355 0.00010
NM_002439.5(MSH3):c.3000T>G (p.Asp1000Glu) rs139205893 0.00010
NM_002439.5(MSH3):c.1258A>G (p.Ser420Gly) rs55660516 0.00006
NM_002439.5(MSH3):c.1858G>A (p.Asp620Asn) rs200337887 0.00004
NM_002439.5(MSH3):c.2173G>A (p.Glu725Lys) rs200612739 0.00004
NM_002439.5(MSH3):c.2557G>C (p.Glu853Gln) rs200185323 0.00004
NM_002439.5(MSH3):c.845C>T (p.Thr282Ile) rs202184623 0.00004
NM_002439.5(MSH3):c.358+5G>A rs200850015 0.00003
NM_002439.5(MSH3):c.582C>G (p.Asp194Glu) rs749446559 0.00003
NM_002439.5(MSH3):c.3035C>T (p.Pro1012Leu) rs371367632 0.00002
NM_002439.5(MSH3):c.3338T>C (p.Met1113Thr) rs747331232 0.00002
NM_002439.5(MSH3):c.1210A>G (p.Ser404Gly) rs753497335 0.00001
NM_002439.5(MSH3):c.1523A>G (p.Lys508Arg) rs763370550 0.00001
NM_002439.5(MSH3):c.1834G>A (p.Glu612Lys) rs759247521 0.00001
NM_002439.5(MSH3):c.2342A>T (p.His781Leu) rs753129920 0.00001
NM_002439.5(MSH3):c.2383C>T (p.Leu795Phe) rs768661033 0.00001
NM_002439.5(MSH3):c.2442C>G (p.Phe814Leu) rs759094395 0.00001
NM_002439.5(MSH3):c.2857A>T (p.Met953Leu) rs528928531 0.00001
NM_002439.5(MSH3):c.3069C>G (p.His1023Gln) rs771861205 0.00001
NM_002439.5(MSH3):c.307A>G (p.Lys103Glu) rs759128700 0.00001
NM_002439.5(MSH3):c.590T>G (p.Leu197Arg) rs1181059079 0.00001
NM_002439.5(MSH3):c.670C>T (p.Arg224Trp) rs748207601 0.00001
NM_002439.5(MSH3):c.886C>T (p.Arg296Cys) rs201216791 0.00001
NM_002439.5(MSH3):c.909G>C (p.Lys303Asn) rs757164724 0.00001
NM_002439.5(MSH3):c.1148A>G (p.Lys383Arg) rs71539687
NM_002439.5(MSH3):c.1972G>C (p.Ala658Pro) rs2112884378
NM_002439.5(MSH3):c.2084+5G>A rs1580034045
NM_002439.5(MSH3):c.2089G>A (p.Gly697Arg) rs2112885086
NM_002439.5(MSH3):c.2686G>A (p.Gly896Arg) rs777054839
NM_002439.5(MSH3):c.272T>G (p.Leu91Trp)
NM_002439.5(MSH3):c.2745G>A (p.Met915Ile)
NM_002439.5(MSH3):c.2992A>G (p.Ile998Val) rs548030451
NM_002439.5(MSH3):c.3127C>A (p.Pro1043Thr)
NM_002439.5(MSH3):c.3244A>G (p.Ile1082Val) rs1746252809
NM_002439.5(MSH3):c.3331T>C (p.Trp1111Arg) rs1459678591
NM_002439.5(MSH3):c.3385G>A (p.Glu1129Lys)
NM_002439.5(MSH3):c.419T>G (p.Phe140Cys)
NM_002439.5(MSH3):c.427G>A (p.Asp143Asn) rs138381683
NM_002439.5(MSH3):c.634A>C (p.Asn212His) rs756439715

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