ClinVar Miner

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

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Total variants: 43
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HGVS dbSNP
NM_030662.3(MAP2K2):c.1036G>A (p.Val346Ile) rs1015139062
NM_030662.3(MAP2K2):c.1039A>G (p.Asn347Asp) rs1057518088
NM_030662.3(MAP2K2):c.1047-2dupA rs1555696233
NM_030662.3(MAP2K2):c.1047-3C>T rs1002166872
NM_030662.3(MAP2K2):c.1085T>C (p.Met362Thr) rs730880513
NM_030662.3(MAP2K2):c.10C>T (p.Arg4Trp) rs730880524
NM_030662.3(MAP2K2):c.1180A>T (p.Thr394Ser) rs730880515
NM_030662.3(MAP2K2):c.1187C>T (p.Thr396Met) rs117945277
NM_030662.3(MAP2K2):c.1189C>T (p.Arg397Cys) rs730880516
NM_030662.3(MAP2K2):c.143A>G (p.Glu48Gly) rs1064793306
NM_030662.3(MAP2K2):c.159del (p.Leu54fs) rs777549760
NM_030662.3(MAP2K2):c.198A>T (p.Glu66Asp) rs1568263766
NM_030662.3(MAP2K2):c.216C>G (p.Phe72Leu) rs1057517929
NM_030662.3(MAP2K2):c.22del (p.Val8fs) rs730880519
NM_030662.3(MAP2K2):c.247G>A (p.Gly83Ser) rs765755554
NM_030662.3(MAP2K2):c.253G>T (p.Val85Leu) rs142503093
NM_030662.3(MAP2K2):c.274A>G (p.Arg92Gly) rs759061964
NM_030662.3(MAP2K2):c.281C>T (p.Ser94Leu) rs202220799
NM_030662.3(MAP2K2):c.289A>T (p.Ile97Phe) rs373579939
NM_030662.3(MAP2K2):c.313C>G (p.Leu105Val) rs730880521
NM_030662.3(MAP2K2):c.326C>T (p.Pro109Leu) rs544242665
NM_030662.3(MAP2K2):c.331A>T (p.Ile111Phe) rs1555698031
NM_030662.3(MAP2K2):c.454G>A (p.Gly152Ser) rs910514546
NM_030662.3(MAP2K2):c.475C>G (p.Leu159Val) rs755613777
NM_030662.3(MAP2K2):c.535C>T (p.Arg179Trp) rs370799450
NM_030662.3(MAP2K2):c.536G>A (p.Arg179Gln) rs776316565
NM_030662.3(MAP2K2):c.541T>A (p.Leu181Met) rs1057517898
NM_030662.3(MAP2K2):c.580+5G>A rs886041663
NM_030662.3(MAP2K2):c.605T>G (p.Val202Gly) rs1568253689
NM_030662.3(MAP2K2):c.71del (p.Pro24fs) rs730880525
NM_030662.3(MAP2K2):c.806C>T (p.Pro269Leu) rs368064728
NM_030662.3(MAP2K2):c.814G>A (p.Ala272Thr) rs757240576
NM_030662.3(MAP2K2):c.826G>C (p.Glu276Gln) rs889422963
NM_030662.3(MAP2K2):c.834C>G (p.Ile278Met) rs766540227
NM_030662.3(MAP2K2):c.83_84delinsAA (p.Gly28Glu) rs730880520
NM_030662.3(MAP2K2):c.856G>A (p.Gly286Arg) rs730880523
NM_030662.3(MAP2K2):c.884C>T (p.Ser295Leu) rs531584619
NM_030662.3(MAP2K2):c.890G>A (p.Arg297Gln) rs140111079
NM_030662.3(MAP2K2):c.899_900insT (p.Gly302fs) rs1064793436
NM_030662.3(MAP2K2):c.937C>T (p.Arg313Trp) rs772831628
NM_030662.3(MAP2K2):c.938G>A (p.Arg313Gln) rs151133017
NM_030662.3(MAP2K2):c.952A>G (p.Ile318Val) rs1064797064
NM_030662.3(MAP2K2):c.971A>G (p.Tyr324Cys) rs730880512

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