ClinVar Miner

List of variants in gene MLH3 reported as uncertain significance for Lynch syndrome

Included ClinVar conditions (18):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 54
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HGVS dbSNP
NM_001040108.1(MLH3):c.*1237A>G rs114347490
NM_001040108.1(MLH3):c.*1347T>G rs539246160
NM_001040108.1(MLH3):c.*1376C>T rs117160510
NM_001040108.1(MLH3):c.*1452G>T rs886050771
NM_001040108.1(MLH3):c.*1701delA rs886050770
NM_001040108.1(MLH3):c.*1990T>A rs886050769
NM_001040108.1(MLH3):c.*2086C>T rs886050768
NM_001040108.1(MLH3):c.*2174C>T rs28757060
NM_001040108.1(MLH3):c.*2590T>C rs138458771
NM_001040108.1(MLH3):c.*3048delC rs886050767
NM_001040108.1(MLH3):c.*3105C>G rs543449865
NM_001040108.1(MLH3):c.*3206C>T rs188135545
NM_001040108.1(MLH3):c.*744A>G rs886050774
NM_001040108.1(MLH3):c.*772T>A rs182733472
NM_001040108.1(MLH3):c.*797dupT rs886050773
NM_001040108.1(MLH3):c.*889G>A rs886050772
NM_001040108.1(MLH3):c.*957_*958delCGinsAT rs386778871
NM_001040108.1(MLH3):c.-120G>A rs886050782
NM_001040108.1(MLH3):c.-149G>C rs886050783
NM_001040108.1(MLH3):c.-202A>C rs886050784
NM_001040108.1(MLH3):c.-208G>A rs886050785
NM_001040108.1(MLH3):c.-27G>A rs886050780
NM_001040108.1(MLH3):c.-4T>G rs28756977
NM_001040108.1(MLH3):c.-63-10dupT rs886050781
NM_001040108.1(MLH3):c.1144G>T (p.Val382Leu) rs558393444
NM_001040108.1(MLH3):c.1300A>G (p.Asn434Asp) rs886050777
NM_001040108.1(MLH3):c.1496A>G (p.Asn499Ser) rs28937871
NM_001040108.1(MLH3):c.149T>A (p.Phe50Tyr) rs148409389
NM_001040108.1(MLH3):c.1560G>T (p.Glu520Asp) rs886050776
NM_001040108.1(MLH3):c.1870G>C (p.Glu624Gln) rs28756986
NM_001040108.1(MLH3):c.206T>C (p.Val69Ala) rs886050779
NM_001040108.1(MLH3):c.2167G>A (p.Val723Ile) rs28756989
NM_001040108.1(MLH3):c.2373G>A (p.Leu791=) rs764724825
NM_001040108.1(MLH3):c.2791_2792GA[1] (p.Asn932fs) rs754716792
NM_001040108.1(MLH3):c.2838C>A (p.Ser946=) rs181990057
NM_001040108.1(MLH3):c.2911G>A (p.Val971Ile) rs41555714
NM_001040108.1(MLH3):c.2924A>G (p.Asn975Ser) rs141066164
NM_001040108.1(MLH3):c.2987G>A (p.Gly996Glu) rs886050775
NM_001040108.1(MLH3):c.3136C>T (p.Arg1046Trp) rs765313787
NM_001040108.1(MLH3):c.3280+14A>T rs142042839
NM_001040108.1(MLH3):c.3384T>C (p.Thr1128=) rs370951929
NM_001040108.1(MLH3):c.3405C>T (p.Ser1135=) rs746155226
NM_001040108.1(MLH3):c.3440A>T (p.Asn1147Ile) rs142124529
NM_001040108.1(MLH3):c.3576C>T (p.Leu1192=) rs376981545
NM_001040108.1(MLH3):c.3784C>T (p.Pro1262Ser) rs372912259
NM_001040108.1(MLH3):c.3987+15C>T rs117251698
NM_001040108.1(MLH3):c.408T>C (p.Asp136=) rs61755655
NM_001040108.1(MLH3):c.4091-2A>C rs906969002
NM_001040108.1(MLH3):c.429G>A (p.Gly143=) rs138943686
NM_001040108.1(MLH3):c.4351G>A (p.Glu1451Lys) rs28939071
NM_001040108.1(MLH3):c.70C>G (p.Gln24Glu) rs28937870
NM_001040108.1(MLH3):c.713A>C (p.Tyr238Ser) rs144707485
NM_001040108.1(MLH3):c.837C>T (p.Cys279=) rs149962294
NM_001040108.1(MLH3):c.961A>G (p.Met321Val) rs886050778

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