ClinVar Miner

List of variants in gene MAP2K2 reported as uncertain significance for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 78
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_030662.4(MAP2K2):c.498C>T (p.Pro166=) rs139404261 0.00076
NM_030662.4(MAP2K2):c.678C>T (p.Ser226=) rs200874968 0.00026
NM_030662.4(MAP2K2):c.919+4C>T rs763424788 0.00009
NM_030662.4(MAP2K2):c.1112G>A (p.Arg371Gln) rs730880514 0.00006
NM_030662.4(MAP2K2):c.856G>A (p.Gly286Arg) rs730880523 0.00006
NM_030662.4(MAP2K2):c.890G>A (p.Arg297Gln) rs140111079 0.00006
NM_030662.4(MAP2K2):c.281C>T (p.Ser94Leu) rs202220799 0.00005
NM_030662.4(MAP2K2):c.1187C>T (p.Thr396Met) rs117945277 0.00004
NM_030662.4(MAP2K2):c.274A>G (p.Arg92Gly) rs759061964 0.00004
NM_030662.4(MAP2K2):c.289A>T (p.Ile97Phe) rs373579939 0.00004
NM_030662.4(MAP2K2):c.648C>T (p.Ser216=) rs147276536 0.00004
NM_030662.4(MAP2K2):c.743C>T (p.Ser248Leu) rs761669626 0.00004
NM_030662.4(MAP2K2):c.938G>A (p.Arg313Gln) rs151133017 0.00004
NM_030662.4(MAP2K2):c.1189C>T (p.Arg397Cys) rs730880516 0.00002
NM_030662.4(MAP2K2):c.326C>T (p.Pro109Leu) rs544242665 0.00002
NM_030662.4(MAP2K2):c.449T>C (p.Met150Thr) rs1441349097 0.00002
NM_030662.4(MAP2K2):c.454G>A (p.Gly152Ser) rs910514546 0.00002
NM_030662.4(MAP2K2):c.485C>T (p.Ala162Val) rs376299424 0.00002
NM_030662.4(MAP2K2):c.535C>T (p.Arg179Trp) rs370799450 0.00002
NM_030662.4(MAP2K2):c.692G>A (p.Arg231His) rs730880511 0.00002
NM_030662.4(MAP2K2):c.787G>A (p.Gly263Arg) rs730880522 0.00002
NM_030662.4(MAP2K2):c.1036G>A (p.Val346Ile) rs1015139062 0.00001
NM_030662.4(MAP2K2):c.1061C>T (p.Pro354Leu) rs879819202 0.00001
NM_030662.4(MAP2K2):c.1064C>T (p.Ala355Val) rs768826287 0.00001
NM_030662.4(MAP2K2):c.1141G>A (p.Gly381Ser) rs565860695 0.00001
NM_030662.4(MAP2K2):c.1180A>T (p.Thr394Ser) rs730880515 0.00001
NM_030662.4(MAP2K2):c.143A>G (p.Glu48Gly) rs1064793306 0.00001
NM_030662.4(MAP2K2):c.247G>A (p.Gly83Ser) rs765755554 0.00001
NM_030662.4(MAP2K2):c.529-5T>C rs766943752 0.00001
NM_030662.4(MAP2K2):c.682G>A (p.Val228Met) rs999810842 0.00001
NM_030662.4(MAP2K2):c.707C>T (p.Pro236Leu) rs1309234276 0.00001
NM_030662.4(MAP2K2):c.811G>A (p.Asp271Asn) rs758031424 0.00001
NM_030662.4(MAP2K2):c.842G>A (p.Arg281Gln) rs1332074575 0.00001
NM_030662.4(MAP2K2):c.913G>A (p.Val305Ile) rs730880509 0.00001
NM_030662.4(MAP2K2):c.928A>G (p.Met310Val) rs766715536 0.00001
NM_030662.4(MAP2K2):c.937C>T (p.Arg313Trp) rs772831628 0.00001
NM_030662.4(MAP2K2):c.971A>G (p.Tyr324Cys) rs730880512 0.00001
NM_030662.4(MAP2K2):c.1111C>T (p.Arg371Trp) rs1003521922
NM_030662.4(MAP2K2):c.1151G>A (p.Cys384Tyr) rs2040846395
NM_030662.4(MAP2K2):c.1192A>C (p.Thr398Pro)
NM_030662.4(MAP2K2):c.159del (p.Leu54fs) rs777549760
NM_030662.4(MAP2K2):c.170T>A (p.Phe57Tyr) rs121434497
NM_030662.4(MAP2K2):c.198A>T (p.Glu66Asp) rs1568263766
NM_030662.4(MAP2K2):c.206del (p.Asp69fs) rs2145080289
NM_030662.4(MAP2K2):c.250G>A (p.Gly84Arg) rs1006857816
NM_030662.4(MAP2K2):c.253G>T (p.Val85Leu) rs142503093
NM_030662.4(MAP2K2):c.260C>A (p.Thr87Asn) rs2145079918
NM_030662.4(MAP2K2):c.287_288delinsGT (p.Leu96Arg) rs397517412
NM_030662.4(MAP2K2):c.313C>G (p.Leu105Val) rs730880521
NM_030662.4(MAP2K2):c.317A>C (p.Glu106Ala)
NM_030662.4(MAP2K2):c.331A>T (p.Ile111Phe) rs1555698031
NM_030662.4(MAP2K2):c.360G>T (p.Gln120His)
NM_030662.4(MAP2K2):c.380C>T (p.Ser127Leu) rs1568260052
NM_030662.4(MAP2K2):c.403G>A (p.Gly135Arg)
NM_030662.4(MAP2K2):c.453C>G (p.Asp151Glu) rs17851657
NM_030662.4(MAP2K2):c.455G>A (p.Gly152Asp)
NM_030662.4(MAP2K2):c.475C>G (p.Leu159Val) rs755613777
NM_030662.4(MAP2K2):c.479A>G (p.Lys160Arg) rs2041027193
NM_030662.4(MAP2K2):c.520A>G (p.Ser174Gly)
NM_030662.4(MAP2K2):c.528+1dup
NM_030662.4(MAP2K2):c.538G>T (p.Gly180Cys) rs1336312423
NM_030662.4(MAP2K2):c.580+5G>A rs886041663
NM_030662.4(MAP2K2):c.605T>G (p.Val202Gly) rs1568253689
NM_030662.4(MAP2K2):c.627G>C (p.Lys209Asn) rs1555696933
NM_030662.4(MAP2K2):c.653A>T (p.Gln218Leu)
NM_030662.4(MAP2K2):c.674A>C (p.Asn225Thr)
NM_030662.4(MAP2K2):c.687C>T (p.Gly229=)
NM_030662.4(MAP2K2):c.692G>T (p.Arg231Leu) rs730880511
NM_030662.4(MAP2K2):c.757A>T (p.Met253Leu)
NM_030662.4(MAP2K2):c.763C>T (p.Leu255=) rs794727877
NM_030662.4(MAP2K2):c.806C>T (p.Pro269Leu) rs368064728
NM_030662.4(MAP2K2):c.829G>A (p.Ala277Thr)
NM_030662.4(MAP2K2):c.860AAG[1] (p.Glu288del) rs763469132
NM_030662.4(MAP2K2):c.899_900insT (p.Gly302fs) rs1064793436
NM_030662.4(MAP2K2):c.904G>C (p.Gly302Arg) rs759148204
NM_030662.4(MAP2K2):c.908G>T (p.Arg303Leu) rs1251433138
NM_030662.4(MAP2K2):c.974T>C (p.Ile325Thr) rs2145046473
NM_030662.4(MAP2K2):c.991C>T (p.Pro331Ser) rs1427321403

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.