ClinVar Miner

List of variants in gene MAP2K2 reported as likely benign for not specified

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Total variants: 69
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HGVS dbSNP
NM_030662.3(MAP2K2):c.*14C>T rs374728969
NM_030662.3(MAP2K2):c.*20G>A rs377441764
NM_030662.3(MAP2K2):c.*2A>T rs1057521556
NM_030662.3(MAP2K2):c.*9G>A rs397517410
NM_030662.3(MAP2K2):c.-21_-16dupCCGCCG rs397517411
NM_030662.3(MAP2K2):c.-4C>G rs747742961
NM_030662.3(MAP2K2):c.-50C>A rs760176331
NM_030662.3(MAP2K2):c.1046+16C>A rs906888337
NM_030662.3(MAP2K2):c.1065G>A (p.Ala355=) rs374807671
NM_030662.3(MAP2K2):c.1092A>G (p.Thr364=) rs779378237
NM_030662.3(MAP2K2):c.1093-6T>C rs369681843
NM_030662.3(MAP2K2):c.1112G>A (p.Arg371Gln) rs730880514
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.1167G>A (p.Leu389=) rs1473228474
NM_030662.3(MAP2K2):c.1176C>T (p.Pro392=) rs529064753
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.1197C>T (p.Ala399=) rs987393686
NM_030662.3(MAP2K2):c.168C>T (p.Ala56=) rs147814905
NM_030662.3(MAP2K2):c.174C>T (p.Leu58=) rs876657504
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.258C>T (p.Val86=) rs148437150
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.303+12G>A rs376432107
NM_030662.3(MAP2K2):c.33G>A (p.Ala11=) rs368233443
NM_030662.3(MAP2K2):c.351C>G (p.Arg117=) rs777670871
NM_030662.3(MAP2K2):c.384G>A (p.Pro128=) rs727503156
NM_030662.3(MAP2K2):c.450+13G>A rs572847821
NM_030662.3(MAP2K2):c.450+14G>A rs397517414
NM_030662.3(MAP2K2):c.450+20G>A rs374143146
NM_030662.3(MAP2K2):c.456C>T (p.Gly152=) rs143106439
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.516A>G (p.Lys172=) rs886038699
NM_030662.3(MAP2K2):c.525C>T (p.Ile175=) rs150833333
NM_030662.3(MAP2K2):c.529-10T>C rs551098822
NM_030662.3(MAP2K2):c.529-12G>A rs375701469
NM_030662.3(MAP2K2):c.529-15C>T rs778783152
NM_030662.3(MAP2K2):c.529-5T>C rs766943752
NM_030662.3(MAP2K2):c.546G>A (p.Ala182=) rs141402203
NM_030662.3(MAP2K2):c.564C>T (p.His188=) rs546749336
NM_030662.3(MAP2K2):c.580+6G>A rs201435249
NM_030662.3(MAP2K2):c.581-11G>A rs758442973
NM_030662.3(MAP2K2):c.581-8G>A rs369262004
NM_030662.3(MAP2K2):c.581-9C>T rs539611844
NM_030662.3(MAP2K2):c.603C>T (p.Leu201=) rs148291450
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.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.784G>A (p.Val262Ile) rs138873805
NM_030662.3(MAP2K2):c.804C>T (p.Pro268=) rs886038700
NM_030662.3(MAP2K2):c.818A>G (p.Lys273Arg) rs539555837
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.863_865delAAG (p.Glu288del) rs763469132
NM_030662.3(MAP2K2):c.894G>A (p.Pro298=) rs374526051
NM_030662.3(MAP2K2):c.913G>A (p.Val305Ile) rs730880509
NM_030662.3(MAP2K2):c.919+4C>T rs763424788
NM_030662.3(MAP2K2):c.92+11A>C rs1228838756
NM_030662.3(MAP2K2):c.93-6C>T rs727504836
NM_030662.3(MAP2K2):c.939G>T (p.Arg313=) rs397517417

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