ClinVar Miner

List of variants in gene MAP2K2 reported by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Total variants: 76
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HGVS dbSNP
NM_030662.3(MAP2K2):c.*8C>T rs377675706
NM_030662.3(MAP2K2):c.*9G>A rs397517410
NM_030662.3(MAP2K2):c.-27_-25CCG[6] rs397517411
NM_030662.3(MAP2K2):c.1020C>T (p.Pro340=) rs192389729
NM_030662.3(MAP2K2):c.1046+4G>A rs1011864039
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.1065G>A (p.Ala355=) rs374807671
NM_030662.3(MAP2K2):c.1093-6T>C rs369681843
NM_030662.3(MAP2K2):c.1140C>T (p.Ala380=) rs146618055
NM_030662.3(MAP2K2):c.1162C>T (p.Arg388Trp) rs144383241
NM_030662.3(MAP2K2):c.1187C>T (p.Thr396Met) rs117945277
NM_030662.3(MAP2K2):c.1194C>T (p.Thr398=) rs144850779
NM_030662.3(MAP2K2):c.169T>A (p.Phe57Ile) rs121434498
NM_030662.3(MAP2K2):c.174C>T (p.Leu58=) rs876657504
NM_030662.3(MAP2K2):c.183A>T (p.Lys61Asn) rs886041310
NM_030662.3(MAP2K2):c.192C>T (p.Val64=) rs8157
NM_030662.3(MAP2K2):c.246C>T (p.Asn82=) rs150942310
NM_030662.3(MAP2K2):c.258C>A (p.Val86=) rs148437150
NM_030662.3(MAP2K2):c.281C>T (p.Ser94Leu) rs202220799
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.303+11C>T rs200405512
NM_030662.3(MAP2K2):c.303+12G>A rs376432107
NM_030662.3(MAP2K2):c.303+8C>G rs199612401
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.33G>A (p.Ala11=) rs368233443
NM_030662.3(MAP2K2):c.383C>G (p.Pro128Arg) rs267607230
NM_030662.3(MAP2K2):c.384G>A (p.Pro128=) rs727503156
NM_030662.3(MAP2K2):c.391G>A (p.Val131Met) rs397517413
NM_030662.3(MAP2K2):c.400T>C (p.Tyr134His) rs121434499
NM_030662.3(MAP2K2):c.401A>G (p.Tyr134Cys) rs727504370
NM_030662.3(MAP2K2):c.405G>C (p.Gly135=) rs10424722
NM_030662.3(MAP2K2):c.420C>T (p.Asp140=) rs369925884
NM_030662.3(MAP2K2):c.450+13G>A rs572847821
NM_030662.3(MAP2K2):c.450+14G>A rs397517414
NM_030662.3(MAP2K2):c.450+15G>T rs10424545
NM_030662.3(MAP2K2):c.453C>T (p.Asp151=) rs17851657
NM_030662.3(MAP2K2):c.474G>A (p.Val158=) rs370736371
NM_030662.3(MAP2K2):c.498C>T (p.Pro166=) rs139404261
NM_030662.3(MAP2K2):c.49A>G (p.Thr17Ala) rs397517415
NM_030662.3(MAP2K2):c.525C>T (p.Ile175=) rs150833333
NM_030662.3(MAP2K2):c.529-12G>A rs375701469
NM_030662.3(MAP2K2):c.564C>T (p.His188=) rs546749336
NM_030662.3(MAP2K2):c.578G>A (p.Arg193Gln) rs530342723
NM_030662.3(MAP2K2):c.580+6G>A rs201435249
NM_030662.3(MAP2K2):c.581-8G>A rs369262004
NM_030662.3(MAP2K2):c.603C>T (p.Leu201=) rs148291450
NM_030662.3(MAP2K2):c.619G>A (p.Glu207Lys) rs727504382
NM_030662.3(MAP2K2):c.621G>A (p.Glu207=) rs397517416
NM_030662.3(MAP2K2):c.639C>T (p.Phe213=) rs727504818
NM_030662.3(MAP2K2):c.658A>G (p.Ile220Val) rs727504363
NM_030662.3(MAP2K2):c.660C>A (p.Ile220=) rs10250
NM_030662.3(MAP2K2):c.678C>T (p.Ser226=) rs200874968
NM_030662.3(MAP2K2):c.705+10C>T rs372898071
NM_030662.3(MAP2K2):c.705+11G>A rs202086678
NM_030662.3(MAP2K2):c.705+11G>C rs202086678
NM_030662.3(MAP2K2):c.706-1_706delinsTT
NM_030662.3(MAP2K2):c.784G>A (p.Val262Ile) rs138873805
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.823C>T (p.Leu275=) rs145934142
NM_030662.3(MAP2K2):c.834C>A (p.Ile278=) rs766540227
NM_030662.3(MAP2K2):c.844C>T (p.Pro282Ser) rs142307980
NM_030662.3(MAP2K2):c.846C>T (p.Pro282=) rs11539506
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.893C>T (p.Pro298Leu) rs200371894
NM_030662.3(MAP2K2):c.919+12A>G rs350911
NM_030662.3(MAP2K2):c.93-6C>T rs727504836
NM_030662.3(MAP2K2):c.938G>A (p.Arg313Gln) rs151133017
NM_030662.3(MAP2K2):c.939G>T (p.Arg313=) rs397517417
NM_030662.3(MAP2K2):c.981C>T (p.Asn327=) rs143275018
NM_030662.3(MAP2K2):c.985C>T (p.Pro329Ser) rs727504353

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