ClinVar Miner

List of variants in gene MLH3 reported as uncertain significance for not specified

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Gene type:
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Total variants: 71
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HGVS dbSNP gnomAD frequency
NM_001040108.2(MLH3):c.2490T>G (p.Phe830Leu) rs114015611 0.00177
NM_001040108.2(MLH3):c.1939C>T (p.Arg647Cys) rs28756987 0.00171
NM_001040108.2(MLH3):c.1799G>A (p.Arg600Gln) rs28756984 0.00168
NM_001040108.2(MLH3):c.2167G>A (p.Val723Ile) rs28756989 0.00168
NM_001040108.2(MLH3):c.394G>A (p.Ala132Thr) rs148095325 0.00102
NM_001040108.2(MLH3):c.3488G>A (p.Gly1163Asp) rs28757011 0.00100
NM_001040108.2(MLH3):c.2670G>A (p.Met890Ile) rs147021156 0.00093
NM_001040108.2(MLH3):c.1234A>G (p.Lys412Glu) rs61754769 0.00061
NM_001040108.2(MLH3):c.2911G>A (p.Val971Ile) rs41555714 0.00048
NM_001040108.2(MLH3):c.3440A>T (p.Asn1147Ile) rs142124529 0.00035
NM_001040108.2(MLH3):c.1637G>T (p.Arg546Ile) rs55725216 0.00034
NM_001040108.2(MLH3):c.1168T>A (p.Phe390Ile) rs61752721 0.00030
NM_001040108.2(MLH3):c.4180G>A (p.Ala1394Thr) rs138006166 0.00021
NM_001040108.2(MLH3):c.3137G>A (p.Arg1046Gln) rs201303087 0.00018
NM_001040108.2(MLH3):c.713A>C (p.Tyr238Ser) rs144707485 0.00016
NM_001040108.2(MLH3):c.3637G>A (p.Glu1213Lys) rs140899869 0.00014
NM_001040108.2(MLH3):c.3752G>A (p.Arg1251Gln) rs201721635 0.00014
NM_001040108.2(MLH3):c.2638C>G (p.Leu880Val) rs201453923 0.00010
NM_001040108.2(MLH3):c.3367C>T (p.Gln1123Ter) rs151133595 0.00010
NM_001040108.2(MLH3):c.2356G>A (p.Val786Ile) rs372089146 0.00009
NM_001040108.2(MLH3):c.2435G>C (p.Ser812Thr) rs763408801 0.00009
NM_001040108.2(MLH3):c.2224C>T (p.Arg742Cys) rs774817891 0.00006
NM_001040108.2(MLH3):c.3455G>A (p.Arg1152His) rs374041909 0.00006
NM_001040108.2(MLH3):c.3466G>A (p.Val1156Ile) rs184741686 0.00006
NM_001040108.2(MLH3):c.3539G>A (p.Arg1180His) rs377022215 0.00005
NM_001040108.2(MLH3):c.1082A>G (p.Asp361Gly) rs749840648 0.00004
NM_001040108.2(MLH3):c.1827A>G (p.Ile609Met) rs374951352 0.00004
NM_001040108.2(MLH3):c.2093A>G (p.Gln698Arg) rs148876417 0.00004
NM_001040108.2(MLH3):c.3723C>T (p.Tyr1241=) rs145627040 0.00004
NM_001040108.2(MLH3):c.3235A>G (p.Thr1079Ala) rs200350079 0.00003
NM_001040108.2(MLH3):c.4097T>C (p.Ile1366Thr) rs61752724 0.00003
NM_001040108.2(MLH3):c.958T>G (p.Cys320Gly) rs1334932761 0.00003
NM_001040108.2(MLH3):c.4289G>A (p.Arg1430His) rs760305520 0.00002
NM_001040108.2(MLH3):c.1519A>G (p.Met507Val) rs371891794 0.00001
NM_001040108.2(MLH3):c.1955C>T (p.Thr652Ile) rs769332499 0.00001
NM_001040108.2(MLH3):c.3335C>T (p.Pro1112Leu) rs138166592 0.00001
NM_001040108.2(MLH3):c.3751C>T (p.Arg1251Trp) rs754799700 0.00001
NM_001040108.2(MLH3):c.3784C>T (p.Pro1262Ser) rs372912259 0.00001
NM_001040108.2(MLH3):c.3950G>A (p.Arg1317Gln) rs1434472127 0.00001
NM_001040108.2(MLH3):c.4027G>A (p.Gly1343Arg) rs28757040 0.00001
NM_001040108.2(MLH3):c.4127A>G (p.Glu1376Gly) rs748701618 0.00001
NM_001040108.2(MLH3):c.41G>A (p.Arg14His) rs760072474 0.00001
NM_001040108.2(MLH3):c.6C>G (p.Ile2Met) rs776416749 0.00001
NM_001040108.2(MLH3):c.1363G>A (p.Glu455Lys)
NM_001040108.2(MLH3):c.1387A>C (p.Ser463Arg) rs138974583
NM_001040108.2(MLH3):c.1424C>A (p.Thr475Lys) rs376219506
NM_001040108.2(MLH3):c.1484G>T (p.Ser495Ile)
NM_001040108.2(MLH3):c.149T>A (p.Phe50Tyr) rs148409389
NM_001040108.2(MLH3):c.154G>A (p.Val52Ile)
NM_001040108.2(MLH3):c.1732C>G (p.Gln578Glu)
NM_001040108.2(MLH3):c.1860_1862del (p.Thr621del)
NM_001040108.2(MLH3):c.1909C>T (p.Arg637Cys)
NM_001040108.2(MLH3):c.2156G>C (p.Trp719Ser)
NM_001040108.2(MLH3):c.2213A>G (p.Lys738Arg)
NM_001040108.2(MLH3):c.2309C>T (p.Thr770Ile)
NM_001040108.2(MLH3):c.2445T>A (p.Asp815Glu)
NM_001040108.2(MLH3):c.2503G>A (p.Asp835Asn) rs766153131
NM_001040108.2(MLH3):c.2666C>T (p.Thr889Ile) rs1266112326
NM_001040108.2(MLH3):c.2702A>G (p.Asn901Ser)
NM_001040108.2(MLH3):c.2715T>G (p.Ser905Arg)
NM_001040108.2(MLH3):c.2962A>T (p.Ile988Phe) rs1192941281
NM_001040108.2(MLH3):c.376A>G (p.Ser126Gly) rs2139607094
NM_001040108.2(MLH3):c.3786G>T (p.Pro1262=) rs28757027
NM_001040108.2(MLH3):c.3919T>A (p.Cys1307Ser)
NM_001040108.2(MLH3):c.4011+3A>C
NM_001040108.2(MLH3):c.4118G>A (p.Ser1373Asn)
NM_001040108.2(MLH3):c.47G>A (p.Gly16Asp)
NM_001040108.2(MLH3):c.735CAA[1] (p.Asn246del) rs774010757
NM_001040108.2(MLH3):c.755T>G (p.Leu252Trp)
NM_001040108.2(MLH3):c.788A>G (p.Lys263Arg) rs2139599317
NM_001040108.2(MLH3):c.911G>T (p.Gly304Val) rs540533901

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