ClinVar Miner

List of variants reported as uncertain significance for colorectal cancer, hereditary nonpolyposis, type 7 by Illumina Laboratory Services, Illumina

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 86
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HGVS dbSNP gnomAD frequency
NM_001040108.2(MLH3):c.*1376C>T rs117160510 0.00527
NM_001040108.2(MLH3):c.*3206C>T rs188135545 0.00201
NM_001040108.2(MLH3):c.2425A>G (p.Met809Val) rs61752722 0.00197
NM_001040108.2(MLH3):c.*1448G>A rs185975350 0.00185
NM_001040108.2(MLH3):c.*3258T>C rs138812028 0.00182
NM_001040108.2(MLH3):c.1939C>T (p.Arg647Cys) rs28756987 0.00171
NM_001040108.2(MLH3):c.*1470C>T rs181758061 0.00154
NM_001040108.2(MLH3):c.4351G>A (p.Glu1451Lys) rs28939071 0.00104
NM_001040108.2(MLH3):c.423C>T (p.Ser141=) rs142179277 0.00100
NM_001040108.2(MLH3):c.*1159A>C rs549461634 0.00081
NM_001040108.2(MLH3):c.2838C>A (p.Ser946=) rs181990057 0.00073
NM_001040108.2(MLH3):c.2911G>A (p.Val971Ile) rs41555714 0.00048
NM_001040108.2(MLH3):c.*2469A>G rs764557856 0.00046
NM_001040108.2(MLH3):c.*888C>T rs181069483 0.00043
NM_001040108.2(MLH3):c.-124A>C rs566279601 0.00041
NM_001040108.2(MLH3):c.3440A>T (p.Asn1147Ile) rs142124529 0.00035
NM_001040108.2(MLH3):c.*1291G>A rs543186188 0.00031
NM_001040108.2(MLH3):c.*1073A>C rs1032410483 0.00026
NM_001040108.2(MLH3):c.*889G>A rs886050772 0.00022
NM_001040108.2(MLH3):c.*1235T>C rs189021867 0.00019
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.3752G>A (p.Arg1251Gln) rs201721635 0.00014
NM_001040108.2(MLH3):c.*1110T>C rs774420872 0.00009
NM_001040108.2(MLH3):c.*1447C>T rs1351576949 0.00007
NM_001040108.2(MLH3):c.*646G>A rs754358704 0.00007
NM_001040108.2(MLH3):c.3576C>T (p.Leu1192=) rs376981545 0.00007
NM_001040108.2(MLH3):c.277C>G (p.Arg93Gly) rs28756978 0.00006
NM_001040108.2(MLH3):c.*772T>A rs182733472 0.00005
NM_001040108.2(MLH3):c.-149G>C rs886050783 0.00004
NM_001040108.2(MLH3):c.2093A>G (p.Gln698Arg) rs148876417 0.00004
NM_001040108.2(MLH3):c.2373G>A (p.Leu791=) rs764724825 0.00004
NM_001040108.2(MLH3):c.4032C>T (p.Gly1344=) rs565238806 0.00004
NM_001040108.2(MLH3):c.*1990T>A rs886050769 0.00003
NM_001040108.2(MLH3):c.*2679A>G rs1018604766 0.00003
NM_001040108.2(MLH3):c.*3105C>G rs543449865 0.00003
NM_001040108.2(MLH3):c.1940G>A (p.Arg647His) rs61755653 0.00003
NM_001040108.2(MLH3):c.2684G>A (p.Arg895His) rs186838169 0.00003
NM_001040108.2(MLH3):c.3103G>A (p.Glu1035Lys) rs143865811 0.00003
NM_001040108.2(MLH3):c.3136C>T (p.Arg1046Trp) rs765313787 0.00003
NM_001040108.2(MLH3):c.3405C>T (p.Ser1135=) rs746155226 0.00003
NM_001040108.2(MLH3):c.*1312G>A rs559234350 0.00002
NM_001040108.2(MLH3):c.124G>A (p.Ala42Thr) rs748676497 0.00002
NM_001040108.2(MLH3):c.3020A>G (p.Asn1007Ser) rs776639203 0.00002
NM_001040108.2(MLH3):c.1125T>C (p.Asp375=) rs781394261 0.00001
NM_001040108.2(MLH3):c.1300A>G (p.Asn434Asp) rs886050777 0.00001
NM_001040108.2(MLH3):c.1427T>C (p.Ile476Thr) rs759144160 0.00001
NM_001040108.2(MLH3):c.1560G>T (p.Glu520Asp) rs886050776 0.00001
NM_001040108.2(MLH3):c.1736C>T (p.Thr579Ile) rs1479954154 0.00001
NM_001040108.2(MLH3):c.3384T>C (p.Thr1128=) rs370951929 0.00001
NM_001040108.2(MLH3):c.3689G>A (p.Arg1230His) rs781739661 0.00001
NM_001040108.2(MLH3):c.3751C>T (p.Arg1251Trp) rs754799700 0.00001
NM_001040108.1(MLH3):c.-202A>C rs886050784
NM_001040108.1(MLH3):c.-208G>A rs886050785
NM_001040108.2(MLH3):c.*1381T>C rs1889846337
NM_001040108.2(MLH3):c.*1452G>T rs886050771
NM_001040108.2(MLH3):c.*1566G>A rs1555386072
NM_001040108.2(MLH3):c.*1628G>A rs571716035
NM_001040108.2(MLH3):c.*1674T>C rs1889836174
NM_001040108.2(MLH3):c.*187T>C rs1889916394
NM_001040108.2(MLH3):c.*2058G>T rs190537801
NM_001040108.2(MLH3):c.*2086C>T rs886050768
NM_001040108.2(MLH3):c.*2398C>A rs1889806410
NM_001040108.2(MLH3):c.*2470C>T rs1889802435
NM_001040108.2(MLH3):c.*2495C>T rs1889801175
NM_001040108.2(MLH3):c.*3047G>T rs1033159745
NM_001040108.2(MLH3):c.*3094C>T rs1243766498
NM_001040108.2(MLH3):c.*3140C>G rs77514025
NM_001040108.2(MLH3):c.*541A>G rs1889895952
NM_001040108.2(MLH3):c.*563A>G rs765593107
NM_001040108.2(MLH3):c.*744A>G rs886050774
NM_001040108.2(MLH3):c.*755T>C rs1889885062
NM_001040108.2(MLH3):c.*884C>G rs1889877324
NM_001040108.2(MLH3):c.-120G>A rs886050782
NM_001040108.2(MLH3):c.-27G>A rs886050780
NM_001040108.2(MLH3):c.1144G>T (p.Val382Leu) rs558393444
NM_001040108.2(MLH3):c.1481A>G (p.His494Arg) rs760778201
NM_001040108.2(MLH3):c.149T>A (p.Phe50Tyr) rs148409389
NM_001040108.2(MLH3):c.1814C>T (p.Ser605Phe) rs1892361991
NM_001040108.2(MLH3):c.206T>C (p.Val69Ala) rs886050779
NM_001040108.2(MLH3):c.2128T>C (p.Leu710=) rs1892333159
NM_001040108.2(MLH3):c.2987G>A (p.Gly996Glu) rs886050775
NM_001040108.2(MLH3):c.3465+14A>G rs775972214
NM_001040108.2(MLH3):c.4091-2A>C rs906969002
NM_001040108.2(MLH3):c.4239A>G (p.Lys1413=) rs975447813
NM_001040108.2(MLH3):c.961A>G (p.Met321Val) rs886050778

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