ClinVar Miner

List of variants in gene KMT2C reported as not provided

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Total variants: 84
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HGVS dbSNP
NM_170606.3(KMT2C):c.10024G>T (p.Ala3342Ser) rs144376311
NM_170606.3(KMT2C):c.10163A>G (p.Asn3388Ser) rs200302468
NM_170606.3(KMT2C):c.10403C>T (p.Pro3468Leu) rs565114967
NM_170606.3(KMT2C):c.10432C>G (p.Gln3478Glu) rs142835638
NM_170606.3(KMT2C):c.10444G>A (p.Val3482Ile) rs587778505
NM_170606.3(KMT2C):c.10513A>G (p.Asn3505Asp) rs140626076
NM_170606.3(KMT2C):c.10639T>C (p.Ser3547Pro) rs78004519
NM_170606.3(KMT2C):c.10723A>G (p.Thr3575Ala) rs142997680
NM_170606.3(KMT2C):c.10763C>T (p.Ser3588Leu) rs148585727
NM_170606.3(KMT2C):c.10894C>T (p.Pro3632Ser) rs587778503
NM_170606.3(KMT2C):c.10928C>T (p.Thr3643Ile) rs587778504
NM_170606.3(KMT2C):c.10979C>T (p.Ser3660Leu) rs74483926
NM_170606.3(KMT2C):c.11149G>C (p.Glu3717Gln) rs587778506
NM_170606.3(KMT2C):c.11167G>C (p.Ala3723Pro) rs115580901
NM_170606.3(KMT2C):c.11173A>C (p.Thr3725Pro) rs143269206
NM_170606.3(KMT2C):c.11242G>A (p.Ala3748Thr) rs148366561
NM_170606.3(KMT2C):c.11374C>A (p.Gln3792Lys) rs75191113
NM_170606.3(KMT2C):c.11493T>G (p.Phe3831Leu) rs587778507
NM_170606.3(KMT2C):c.11528G>C (p.Gly3843Ala) rs201952980
NM_170606.3(KMT2C):c.11570C>T (p.Thr3857Met) rs577099359
NM_170606.3(KMT2C):c.11581G>A (p.Ala3861Thr) rs147946863
NM_170606.3(KMT2C):c.11614G>A (p.Glu3872Lys) rs201674711
NM_170606.3(KMT2C):c.11942A>C (p.Asn3981Thr) rs587778508
NM_170606.3(KMT2C):c.12370A>G (p.Met4124Val) rs587778509
NM_170606.3(KMT2C):c.12655C>G (p.Leu4219Val) rs139111507
NM_170606.3(KMT2C):c.12755C>T (p.Ala4252Val) rs537579296
NM_170606.3(KMT2C):c.12964C>T (p.Pro4322Ser) rs587778511
NM_170606.3(KMT2C):c.13246C>T (p.Pro4416Ser) rs201443050
NM_170606.3(KMT2C):c.1344G>T (p.Gln448His) rs149250254
NM_170606.3(KMT2C):c.13522C>T (p.Pro4508Ser) rs182572555
NM_170606.3(KMT2C):c.1365A>G (p.Ile455Met) rs77652527
NM_170606.3(KMT2C):c.13967C>A (p.Ala4656Glu) rs587778512
NM_170606.3(KMT2C):c.14017C>T (p.Arg4673Cys) rs370620314
NM_170606.3(KMT2C):c.1402C>A (p.Pro468Thr) rs140919432
NM_170606.3(KMT2C):c.14107G>A (p.Val4703Ile) rs369684496
NM_170606.3(KMT2C):c.1421_1423ATC[1] (p.His475del) rs587778488
NM_170606.3(KMT2C):c.1577G>A (p.Arg526His) rs3735156
NM_170606.3(KMT2C):c.1577G>C (p.Arg526Pro) rs3735156
NM_170606.3(KMT2C):c.1645G>A (p.Glu549Lys) rs587778489
NM_170606.3(KMT2C):c.1700A>G (p.Asn567Ser) rs12674022
NM_170606.3(KMT2C):c.1795G>T (p.Asp599Tyr) rs141579002
NM_170606.3(KMT2C):c.181A>G (p.Thr61Ala) rs111826855
NM_170606.3(KMT2C):c.3275G>A (p.Arg1092Gln) rs150747860
NM_170606.3(KMT2C):c.3487G>C (p.Val1163Leu) rs142546291
NM_170606.3(KMT2C):c.3955G>C (p.Asp1319His) rs138119145
NM_170606.3(KMT2C):c.4154A>G (p.Asn1385Ser) rs61730535
NM_170606.3(KMT2C):c.4442G>A (p.Arg1481Gln) rs587778490
NM_170606.3(KMT2C):c.4592C>T (p.Ala1531Val) rs587778491
NM_170606.3(KMT2C):c.5171G>T (p.Ser1724Ile) rs138819584
NM_170606.3(KMT2C):c.5352_5354ACA[3] (p.Gln1787dup) rs587778492
NM_170606.3(KMT2C):c.5587C>G (p.Pro1863Ala) rs142070663
NM_170606.3(KMT2C):c.5792C>T (p.Ser1931Leu) rs200297010
NM_170606.3(KMT2C):c.5809C>G (p.Gln1937Glu) rs374061571
NM_170606.3(KMT2C):c.5861C>G (p.Ser1954Cys) rs563948892
NM_170606.3(KMT2C):c.5903A>G (p.Asp1968Gly) rs587778493
NM_170606.3(KMT2C):c.6008C>T (p.Thr2003Ile) rs587778495
NM_170606.3(KMT2C):c.6022A>G (p.Thr2008Ala) rs6951159
NM_170606.3(KMT2C):c.6073T>A (p.Ser2025Thr) rs141338021
NM_170606.3(KMT2C):c.6197G>A (p.Arg2066Gln) rs587778498
NM_170606.3(KMT2C):c.6275A>T (p.Asp2092Val) rs140719911
NM_170606.3(KMT2C):c.6461C>G (p.Ser2154Cys) rs587778496
NM_170606.3(KMT2C):c.6634C>G (p.Pro2212Ala) rs587778497
NM_170606.3(KMT2C):c.6667G>A (p.Ala2223Thr) rs140432708
NM_170606.3(KMT2C):c.6896A>G (p.Tyr2299Cys) rs587778494
NM_170606.3(KMT2C):c.6965T>C (p.Val2322Ala) rs373237480
NM_170606.3(KMT2C):c.709A>G (p.Ile237Val) rs587778510
NM_170606.3(KMT2C):c.7234C>A (p.Pro2412Thr) rs13231116
NM_170606.3(KMT2C):c.7259T>G (p.Leu2420Arg) rs200810583
NM_170606.3(KMT2C):c.7829G>A (p.Arg2610Gln) rs139770288
NM_170606.3(KMT2C):c.7846C>T (p.Pro2616Ser) rs142938767
NM_170606.3(KMT2C):c.7957C>G (p.Leu2653Val) rs149373512
NM_170606.3(KMT2C):c.7958T>C (p.Leu2653Pro) rs61730547
NM_170606.3(KMT2C):c.8449A>G (p.Thr2817Ala) rs587778499
NM_170606.3(KMT2C):c.8459A>G (p.Asn2820Ser) rs587778500
NM_170606.3(KMT2C):c.8488A>C (p.Asn2830His) rs147851738
NM_170606.3(KMT2C):c.8502A>T (p.Glu2834Asp) rs138845109
NM_170606.3(KMT2C):c.8507A>G (p.Lys2836Arg) rs142267328
NM_170606.3(KMT2C):c.8552C>G (p.Thr2851Ser) rs151261105
NM_170606.3(KMT2C):c.9071G>C (p.Ser3024Thr) rs587778501
NM_170606.3(KMT2C):c.9245C>T (p.Pro3082Leu) rs61730545
NM_170606.3(KMT2C):c.9425A>G (p.Gln3142Arg) rs587778502
NM_170606.3(KMT2C):c.9931C>T (p.Leu3311Phe) rs139610952
NM_170606.3(KMT2C):c.9974G>T (p.Ser3325Ile) rs202148187
NM_170606.3(KMT2C):c.9989C>G (p.Pro3330Arg) rs545625106

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