ClinVar Miner

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

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Total variants: 41
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HGVS dbSNP
NM_030662.3(MAP2K2):c.*8C>T rs377675706
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.1046+4G>A rs1011864039
NM_030662.3(MAP2K2):c.1047-3C>T rs1002166872
NM_030662.3(MAP2K2):c.1061C>T (p.Pro354Leu) rs879819202
NM_030662.3(MAP2K2):c.1064C>T (p.Ala355Val) rs768826287
NM_030662.3(MAP2K2):c.1085T>C (p.Met362Thr) rs730880513
NM_030662.3(MAP2K2):c.1092A>C (p.Thr364=) rs779378237
NM_030662.3(MAP2K2):c.1187C>T (p.Thr396Met) rs117945277
NM_030662.3(MAP2K2):c.169T>A (p.Phe57Ile) rs121434498
NM_030662.3(MAP2K2):c.183A>T (p.Lys61Asn) rs886041310
NM_030662.3(MAP2K2):c.216C>G (p.Phe72Leu) rs1057517929
NM_030662.3(MAP2K2):c.247G>A (p.Gly83Ser) rs765755554
NM_030662.3(MAP2K2):c.274A>G (p.Arg92Gly) rs759061964
NM_030662.3(MAP2K2):c.287_288delinsGT (p.Leu96Arg) rs397517412
NM_030662.3(MAP2K2):c.289A>T (p.Ile97Phe) rs373579939
NM_030662.3(MAP2K2):c.320T>A (p.Ile107Asn) rs1555698037
NM_030662.3(MAP2K2):c.326C>T (p.Pro109Leu) rs544242665
NM_030662.3(MAP2K2):c.32C>G (p.Ala11Gly) rs1555699410
NM_030662.3(MAP2K2):c.352G>A (p.Glu118Lys) rs756646033
NM_030662.3(MAP2K2):c.357G>A (p.Leu119=) rs1377039329
NM_030662.3(MAP2K2):c.383C>G (p.Pro128Arg) rs267607230
NM_030662.3(MAP2K2):c.391G>A (p.Val131Met) rs397517413
NM_030662.3(MAP2K2):c.531T>C (p.Val177=) rs528169616
NM_030662.3(MAP2K2):c.541T>A (p.Leu181Met) rs1057517898
NM_030662.3(MAP2K2):c.578G>A (p.Arg193Gln) rs530342723
NM_030662.3(MAP2K2):c.581-5T>C rs757662989
NM_030662.3(MAP2K2):c.581-9C>T rs539611844
NM_030662.3(MAP2K2):c.699C>T (p.Tyr233=) rs1044588100
NM_030662.3(MAP2K2):c.706-1_706delinsTT
NM_030662.3(MAP2K2):c.806C>G (p.Pro269Arg) 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.853G>A (p.Asp285Asn) rs150369301
NM_030662.3(MAP2K2):c.860_862AAG[1] (p.Glu288del) rs763469132
NM_030662.3(MAP2K2):c.884C>T (p.Ser295Leu) rs531584619
NM_030662.3(MAP2K2):c.93-6C>T rs727504836
NM_030662.3(MAP2K2):c.938G>A (p.Arg313Gln) rs151133017
NM_030662.3(MAP2K2):c.985C>T (p.Pro329Ser) rs727504353

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