ClinVar Miner

List of variants in gene MAP2K2 reported as uncertain significance by GeneDx

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Total variants: 57
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HGVS dbSNP gnomAD frequency
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.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.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.1036G>A (p.Val346Ile) rs1015139062 0.00001
NM_030662.4(MAP2K2):c.1039A>G (p.Asn347Asp) rs1057518088 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.811G>A (p.Asp271Asn) rs758031424 0.00001
NM_030662.4(MAP2K2):c.826G>C (p.Glu276Gln) rs889422963 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.1047-3C>T rs1002166872
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.198A>T (p.Glu66Asp) rs1568263766
NM_030662.4(MAP2K2):c.206del (p.Asp69fs) rs2145080289
NM_030662.4(MAP2K2):c.216C>G (p.Phe72Leu) rs1057517929
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.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.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.541T>A (p.Leu181Met) rs1057517898
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.806C>T (p.Pro269Leu) rs368064728
NM_030662.4(MAP2K2):c.834C>G (p.Ile278Met) rs766540227
NM_030662.4(MAP2K2):c.899_900insT (p.Gly302fs) rs1064793436
NM_030662.4(MAP2K2):c.908G>T (p.Arg303Leu) rs1251433138
NM_030662.4(MAP2K2):c.974T>C (p.Ile325Thr) rs2145046473

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