ClinVar Miner

List of variants in gene MSH3 reported as uncertain significance by Quest Diagnostics Nichols Institute San Juan Capistrano

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Total variants: 71
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HGVS dbSNP gnomAD frequency
NM_002439.5(MSH3):c.2016T>G (p.Ile672Met) rs139593361 0.00046
NM_002439.5(MSH3):c.1394A>G (p.Tyr465Cys) rs35009542 0.00032
NM_002439.5(MSH3):c.287C>T (p.Pro96Leu) rs373436584 0.00028
NM_002439.5(MSH3):c.421T>C (p.Cys141Arg) rs143733332 0.00023
NM_002439.5(MSH3):c.2438A>G (p.Lys813Arg) rs150446804 0.00022
NM_002439.5(MSH3):c.3350A>G (p.Gln1117Arg) rs946137864 0.00014
NM_002439.5(MSH3):c.562C>T (p.Arg188Cys) rs147289289 0.00013
NM_002439.5(MSH3):c.2044G>C (p.Val682Leu) rs145657887 0.00012
NM_002439.5(MSH3):c.3000T>G (p.Asp1000Glu) rs139205893 0.00010
NM_002439.5(MSH3):c.2281G>T (p.Val761Leu) rs376555325 0.00009
NM_002439.5(MSH3):c.2695A>G (p.Met899Val) rs756956247 0.00007
NM_002439.5(MSH3):c.1847G>A (p.Arg616His) rs764683130 0.00005
NM_002439.5(MSH3):c.2069A>G (p.Asn690Ser) rs575779178 0.00005
NM_002439.5(MSH3):c.2386C>T (p.Arg796Trp) rs372431614 0.00005
NM_002439.5(MSH3):c.3136G>A (p.Ala1046Thr) rs144603433 0.00005
NM_002439.5(MSH3):c.331_333del (p.Ser111del) rs753775000 0.00005
NM_002439.5(MSH3):c.353A>T (p.Asn118Ile) rs372970933 0.00005
NM_002439.5(MSH3):c.1361G>A (p.Arg454Gln) rs144798521 0.00004
NM_002439.5(MSH3):c.1655C>T (p.Thr552Ile) rs749862056 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.3130+4T>G rs764306633 0.00004
NM_002439.5(MSH3):c.692C>T (p.Pro231Leu) rs201748817 0.00004
NM_002439.5(MSH3):c.1870G>A (p.Gly624Arg) rs756300808 0.00003
NM_002439.5(MSH3):c.1910A>C (p.Glu637Ala) rs376488647 0.00003
NM_002439.5(MSH3):c.2762A>G (p.Tyr921Cys) rs190723980 0.00003
NM_002439.5(MSH3):c.2774A>G (p.Glu925Gly) rs764219762 0.00003
NM_002439.5(MSH3):c.3166C>T (p.Leu1056Phe) rs188074706 0.00003
NM_002439.5(MSH3):c.358+5G>A rs200850015 0.00003
NM_002439.5(MSH3):c.1381A>G (p.Ile461Val) rs201589579 0.00002
NM_002439.5(MSH3):c.2075A>G (p.Gln692Arg) rs771378744 0.00002
NM_002439.5(MSH3):c.2135T>C (p.Ile712Thr) rs369015749 0.00002
NM_002439.5(MSH3):c.512A>G (p.Asp171Gly) rs767478058 0.00002
NM_002439.5(MSH3):c.1195G>A (p.Glu399Lys) rs200365261 0.00001
NM_002439.5(MSH3):c.1366G>A (p.Glu456Lys) rs963234468 0.00001
NM_002439.5(MSH3):c.1472G>T (p.Gly491Val) rs749116282 0.00001
NM_002439.5(MSH3):c.1492C>G (p.Pro498Ala) rs746541629 0.00001
NM_002439.5(MSH3):c.1523A>G (p.Lys508Arg) rs763370550 0.00001
NM_002439.5(MSH3):c.1661T>C (p.Met554Thr) rs755514051 0.00001
NM_002439.5(MSH3):c.2288G>T (p.Cys763Phe) rs373251342 0.00001
NM_002439.5(MSH3):c.2370A>G (p.Arg790=) rs1278142628 0.00001
NM_002439.5(MSH3):c.2410A>G (p.Ser804Gly) rs1165114619 0.00001
NM_002439.5(MSH3):c.2684C>A (p.Thr895Asn) rs1745046566 0.00001
NM_002439.5(MSH3):c.2697G>A (p.Met899Ile) rs1745047109 0.00001
NM_002439.5(MSH3):c.2741T>C (p.Ile914Thr) rs757861627 0.00001
NM_002439.5(MSH3):c.2803A>G (p.Ile935Val) rs1490213002 0.00001
NM_002439.5(MSH3):c.2857A>T (p.Met953Leu) rs528928531 0.00001
NM_002439.5(MSH3):c.3191C>T (p.Ala1064Val) rs1354644574 0.00001
NM_002439.5(MSH3):c.3335C>T (p.Thr1112Met) rs576204286 0.00001
NM_002439.5(MSH3):c.580-5G>T rs770150309 0.00001
NM_002439.5(MSH3):c.909G>C (p.Lys303Asn) rs757164724 0.00001
GRCh37/hg19 5q14.1(chr5:80019759-80167254)x1
NM_002439.5(MSH3):c.1113C>T (p.Ile371=)
NM_002439.5(MSH3):c.1412C>A (p.Ala471Glu) rs1353600849
NM_002439.5(MSH3):c.1642C>G (p.Leu548Val) rs2112866851
NM_002439.5(MSH3):c.1684T>C (p.Trp562Arg)
NM_002439.5(MSH3):c.1910A>G (p.Glu637Gly) rs376488647
NM_002439.5(MSH3):c.1911G>A (p.Glu637=) rs1005120343
NM_002439.5(MSH3):c.2315G>A (p.Gly772Glu) rs2112890215
NM_002439.5(MSH3):c.2408G>C (p.Cys803Ser)
NM_002439.5(MSH3):c.2464T>C (p.Cys822Arg) rs1744531800
NM_002439.5(MSH3):c.2632G>T (p.Val878Phe)
NM_002439.5(MSH3):c.2716A>G (p.Ile906Val) rs767359174
NM_002439.5(MSH3):c.2751G>T (p.Gln917His) rs377380366
NM_002439.5(MSH3):c.2833A>T (p.Ile945Leu) rs1486734790
NM_002439.5(MSH3):c.3003G>A (p.Val1001=)
NM_002439.5(MSH3):c.3062A>G (p.Tyr1021Cys) rs1561503554
NM_002439.5(MSH3):c.3244A>G (p.Ile1082Val) rs1746252809
NM_002439.5(MSH3):c.427G>A (p.Asp143Asn) rs138381683
NM_002439.5(MSH3):c.641A>G (p.Gln214Arg) rs1749671715
NM_002439.5(MSH3):c.889C>G (p.Leu297Val) rs1299382957

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