ClinVar Miner

List of variants in gene KMT2C reported as likely benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 66
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_170606.3(KMT2C):c.10763C>T (p.Ser3588Leu) rs148585727 0.00295
NM_170606.3(KMT2C):c.5587C>G (p.Pro1863Ala) rs142070663 0.00239
NM_170606.3(KMT2C):c.14022A>T (p.Ile4674=) rs143292008 0.00224
NM_170606.3(KMT2C):c.6073T>A (p.Ser2025Thr) rs141338021 0.00208
NM_170606.3(KMT2C):c.7443-9T>A rs768567502 0.00146
NM_170606.3(KMT2C):c.816C>T (p.Asn272=) rs143544942 0.00103
NM_170606.3(KMT2C):c.5532T>C (p.Asp1844=) rs151322246 0.00087
NM_170606.3(KMT2C):c.9138T>A (p.Leu3046=) rs138871839 0.00079
NM_170606.3(KMT2C):c.7388G>A (p.Arg2463His) rs140834550 0.00064
NM_170606.3(KMT2C):c.5683A>G (p.Met1895Val) rs144021585 0.00053
NM_170606.3(KMT2C):c.8488A>C (p.Asn2830His) rs147851738 0.00048
NM_170606.3(KMT2C):c.12434G>A (p.Arg4145His) rs143770207 0.00046
NM_170606.3(KMT2C):c.9931C>T (p.Leu3311Phe) rs139610952 0.00043
NM_170606.3(KMT2C):c.12093G>A (p.Pro4031=) rs149293494 0.00040
NM_170606.3(KMT2C):c.7829G>A (p.Arg2610Gln) rs139770288 0.00038
NM_170606.3(KMT2C):c.10513A>G (p.Asn3505Asp) rs140626076 0.00036
NM_170606.3(KMT2C):c.10723A>G (p.Thr3575Ala) rs142997680 0.00035
NM_170606.3(KMT2C):c.13931T>G (p.Val4644Gly) rs142657994 0.00033
NM_170606.3(KMT2C):c.7489C>T (p.Arg2497Cys) rs150994342 0.00027
NM_170606.3(KMT2C):c.10403C>T (p.Pro3468Leu) rs565114967 0.00025
NM_170606.3(KMT2C):c.10395T>G (p.Pro3465=) rs146083360 0.00021
NM_170606.3(KMT2C):c.13311G>A (p.Thr4437=) rs149554388 0.00021
NM_170606.3(KMT2C):c.12557G>A (p.Gly4186Asp) rs201079078 0.00017
NM_170606.3(KMT2C):c.4154A>G (p.Asn1385Ser) rs61730535 0.00014
NM_170606.3(KMT2C):c.11613C>T (p.Asp3871=) rs369567780 0.00012
NM_170606.3(KMT2C):c.7443-8T>A rs749396012 0.00012
NM_170606.3(KMT2C):c.12552T>C (p.Ser4184=) rs369593556 0.00011
NM_170606.3(KMT2C):c.6383A>C (p.Gln2128Pro) rs368424013 0.00011
NM_170606.3(KMT2C):c.6530A>G (p.Gln2177Arg) rs201637035 0.00011
NM_170606.3(KMT2C):c.10040A>G (p.Asn3347Ser) rs536894778 0.00010
NM_170606.3(KMT2C):c.486A>G (p.Pro162=) rs141143474 0.00009
NM_170606.3(KMT2C):c.6910A>G (p.Met2304Val) rs754015217 0.00009
NM_170606.3(KMT2C):c.4188A>G (p.Lys1396=) rs201433194 0.00008
NM_170606.3(KMT2C):c.9987G>A (p.Met3329Ile) rs200804156 0.00008
NM_170606.3(KMT2C):c.5634A>C (p.Ser1878=) rs558012126 0.00007
NM_170606.3(KMT2C):c.12443C>T (p.Pro4148Leu) rs141718495 0.00006
NM_170606.3(KMT2C):c.13522C>T (p.Pro4508Ser) rs182572555 0.00006
NM_170606.3(KMT2C):c.5198C>T (p.Ser1733Leu) rs146495785 0.00005
NM_170606.3(KMT2C):c.5861C>G (p.Ser1954Cys) rs563948892 0.00005
NM_170606.3(KMT2C):c.6372G>A (p.Arg2124=) rs565855077 0.00005
NM_170606.3(KMT2C):c.6477C>T (p.Tyr2159=) rs761097508 0.00005
NM_170606.3(KMT2C):c.7150-6A>G rs746330866 0.00005
NM_170606.3(KMT2C):c.12755C>T (p.Ala4252Val) rs537579296 0.00004
NM_170606.3(KMT2C):c.3972G>A (p.Glu1324=) rs746567373 0.00003
NM_170606.3(KMT2C):c.4217C>T (p.Pro1406Leu) rs376997793 0.00003
NM_170606.3(KMT2C):c.4548C>T (p.Gly1516=) rs201322783 0.00003
NM_170606.3(KMT2C):c.9765G>A (p.Gln3255=) rs371631535 0.00003
NM_170606.3(KMT2C):c.5713C>G (p.Pro1905Ala) rs769183090 0.00002
NM_170606.3(KMT2C):c.13302G>A (p.Leu4434=) rs776793326 0.00001
NM_170606.3(KMT2C):c.14280G>A (p.Ser4760=) rs924742192 0.00001
NM_170606.3(KMT2C):c.7077G>A (p.Val2359=) rs201191473 0.00001
NM_170606.3(KMT2C):c.8459A>G (p.Asn2820Ser) rs587778500 0.00001
NM_170606.3(KMT2C):c.9072C>T (p.Ser3024=) rs763751547 0.00001
NM_170606.3(KMT2C):c.12444G>A (p.Pro4148=) rs147957197
NM_170606.3(KMT2C):c.12898T>C (p.Ser4300Pro) rs199880787
NM_170606.3(KMT2C):c.13779T>C (p.Asn4593=) rs2091323883
NM_170606.3(KMT2C):c.14154T>C (p.His4718=) rs2129093244
NM_170606.3(KMT2C):c.372T>G (p.Gly124=) rs1016157370
NM_170606.3(KMT2C):c.4389T>C (p.Pro1463=) rs753575812
NM_170606.3(KMT2C):c.591-18ATTTT[2] rs552048274
NM_170606.3(KMT2C):c.6339A>G (p.Ser2113=) rs73161892
NM_170606.3(KMT2C):c.6751C>T (p.Leu2251=) rs771211866
NM_170606.3(KMT2C):c.7443-15_7443-6del rs746018833
NM_170606.3(KMT2C):c.7443-6_7443-5insTA rs1491309235
NM_170606.3(KMT2C):c.9109_9111del (p.Leu3037del) rs772433974
NM_170606.3(KMT2C):c.9159A>G (p.Leu3053=) rs559730393

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.