ClinVar Miner

List of variants in gene MLH3 reported by PreventionGenetics, part of Exact Sciences

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Gene type:
ClinVar version:
Total variants: 83
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HGVS dbSNP gnomAD frequency
NM_001040108.2(MLH3):c.2476A>G (p.Asn826Asp) rs175081 0.98791
NM_001040108.2(MLH3):c.4335A>G (p.Gln1445=) rs13712 0.52176
NM_001040108.2(MLH3):c.2531C>T (p.Pro844Leu) rs175080 0.42416
NM_001040108.2(MLH3):c.2159A>G (p.Tyr720Cys) rs28756988 0.02978
NM_001040108.2(MLH3):c.444G>C (p.Val148=) rs11556091 0.01944
NM_001040108.2(MLH3):c.1258G>A (p.Val420Ile) rs28756982 0.01142
NM_001040108.2(MLH3):c.2825C>T (p.Thr942Ile) rs17102999 0.00989
NM_001040108.2(MLH3):c.2490T>G (p.Phe830Leu) rs114015611 0.00177
NM_001040108.2(MLH3):c.2924A>G (p.Asn975Ser) rs141066164 0.00160
NM_001040108.2(MLH3):c.429G>A (p.Gly143=) rs138943686 0.00160
NM_001040108.2(MLH3):c.359T>C (p.Phe120Ser) rs28756979 0.00120
NM_001040108.2(MLH3):c.394G>A (p.Ala132Thr) rs148095325 0.00102
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.2043T>C (p.Tyr681=) rs143573376 0.00056
NM_001040108.2(MLH3):c.2911G>A (p.Val971Ile) rs41555714 0.00048
NM_001040108.2(MLH3):c.902A>T (p.Glu301Val) rs77687901 0.00040
NM_001040108.2(MLH3):c.3344G>A (p.Arg1115Gln) rs78311619 0.00038
NM_001040108.2(MLH3):c.1637G>T (p.Arg546Ile) rs55725216 0.00034
NM_001040108.2(MLH3):c.2449A>G (p.Ser817Gly) rs143278116 0.00032
NM_001040108.2(MLH3):c.2180G>A (p.Ser727Asn) rs116526686 0.00029
NM_001040108.2(MLH3):c.2547T>C (p.Ser849=) rs183078420 0.00018
NM_001040108.2(MLH3):c.2241G>A (p.Leu747=) rs139155264 0.00012
NM_001040108.2(MLH3):c.1500G>A (p.Pro500=) rs554385170 0.00011
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.3248C>A (p.Thr1083Lys) rs561184221 0.00007
NM_001040108.2(MLH3):c.4268G>A (p.Arg1423His) rs752635498 0.00007
NM_001040108.2(MLH3):c.1651C>T (p.Pro551Ser) rs902755970 0.00006
NM_001040108.2(MLH3):c.3455G>A (p.Arg1152His) rs374041909 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.1724A>G (p.His575Arg) rs141572255 0.00004
NM_001040108.2(MLH3):c.3406G>A (p.Glu1136Lys) rs113490514 0.00004
NM_001040108.2(MLH3):c.1017C>T (p.Cys339=) rs368126670 0.00003
NM_001040108.2(MLH3):c.3676G>A (p.Ala1226Thr) rs747817741 0.00003
NM_001040108.2(MLH3):c.4026C>T (p.Thr1342=) rs770765370 0.00003
NM_001040108.2(MLH3):c.4155C>T (p.Ser1385=) rs766537456 0.00003
NM_001040108.2(MLH3):c.958T>G (p.Cys320Gly) rs1334932761 0.00003
NM_001040108.2(MLH3):c.1142G>A (p.Arg381His) rs751375245 0.00002
NM_001040108.2(MLH3):c.184G>A (p.Gly62Arg) rs761501352 0.00002
NM_001040108.2(MLH3):c.2166C>T (p.His722=) rs186533894 0.00002
NM_001040108.2(MLH3):c.2328T>C (p.Asn776=) rs141970415 0.00002
NM_001040108.2(MLH3):c.3117G>A (p.Thr1039=) rs752980464 0.00002
NM_001040108.2(MLH3):c.861T>C (p.Ser287=) rs201745687 0.00002
NM_001040108.2(MLH3):c.121G>A (p.Val41Met) rs770297216 0.00001
NM_001040108.2(MLH3):c.126T>G (p.Ala42=) rs556487716 0.00001
NM_001040108.2(MLH3):c.1306A>G (p.Asn436Asp) rs754824568 0.00001
NM_001040108.2(MLH3):c.1384G>A (p.Asp462Asn) rs369525473 0.00001
NM_001040108.2(MLH3):c.1669G>A (p.Ala557Thr) rs1347649293 0.00001
NM_001040108.2(MLH3):c.2129T>C (p.Leu710Ser) rs1238847805 0.00001
NM_001040108.2(MLH3):c.2218A>G (p.Ile740Val) rs1892322400 0.00001
NM_001040108.2(MLH3):c.3280+9G>A rs766230638 0.00001
NM_001040108.2(MLH3):c.3658G>A (p.Val1220Met) rs560775993 0.00001
NM_001040108.2(MLH3):c.3974A>G (p.Lys1325Arg) rs781013323 0.00001
NM_001040108.2(MLH3):c.4185C>T (p.His1395=) rs145575075 0.00001
NM_001040108.2(MLH3):c.4301A>G (p.Lys1434Arg) rs772866061 0.00001
NM_001040108.2(MLH3):c.*7A>T
NM_001040108.2(MLH3):c.-3A>G
NM_001040108.2(MLH3):c.1223C>A (p.Ser408Ter) rs745988563
NM_001040108.2(MLH3):c.1788_1803dup (p.Lys602Ter)
NM_001040108.2(MLH3):c.1809A>G (p.Leu603=)
NM_001040108.2(MLH3):c.2160T>C (p.Tyr720=)
NM_001040108.2(MLH3):c.2220C>A (p.Ile740=)
NM_001040108.2(MLH3):c.2410T>A (p.Cys804Ser)
NM_001040108.2(MLH3):c.2600A>G (p.Glu867Gly) rs1892287229
NM_001040108.2(MLH3):c.2673G>A (p.Gly891=)
NM_001040108.2(MLH3):c.2784A>G (p.Glu928=)
NM_001040108.2(MLH3):c.3113dup (p.Asn1038fs)
NM_001040108.2(MLH3):c.3186T>C (p.Thr1062=)
NM_001040108.2(MLH3):c.3193A>G (p.Ser1065Gly)
NM_001040108.2(MLH3):c.3246G>C (p.Leu1082=)
NM_001040108.2(MLH3):c.3692T>G (p.Ile1231Arg)
NM_001040108.2(MLH3):c.3731A>C (p.Gln1244Pro)
NM_001040108.2(MLH3):c.3786G>A (p.Pro1262=) rs28757027
NM_001040108.2(MLH3):c.4051C>T (p.Leu1351=)
NM_001040108.2(MLH3):c.4150C>G (p.Leu1384Val) rs1025736417
NM_001040108.2(MLH3):c.4150_4151del (p.Leu1384fs) rs1162704717
NM_001040108.2(MLH3):c.4192C>T (p.Pro1398Ser)
NM_001040108.2(MLH3):c.496C>T (p.Leu166=)
NM_001040108.2(MLH3):c.565T>G (p.Leu189Val)
NM_001040108.2(MLH3):c.713A>G (p.Tyr238Cys) rs144707485
NM_001040108.2(MLH3):c.774A>G (p.Leu258=) rs2139599520

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