ClinVar Miner

List of variants in gene MAP2K2 reported as likely benign by GeneDx

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Gene type:
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Total variants: 67
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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.-23C>A rs1057522728
NM_030662.3(MAP2K2):c.-406C>A
NM_030662.3(MAP2K2):c.-419C>A
NM_030662.3(MAP2K2):c.-42C>T rs886041258
NM_030662.3(MAP2K2):c.-47A>G rs1057520422
NM_030662.3(MAP2K2):c.-4C>G rs747742961
NM_030662.3(MAP2K2):c.-50C>A rs760176331
NM_030662.3(MAP2K2):c.-9G>A rs1057523493
NM_030662.3(MAP2K2):c.1046+16C>A rs906888337
NM_030662.3(MAP2K2):c.1046+200C>T
NM_030662.3(MAP2K2):c.1046+303del rs574248280
NM_030662.3(MAP2K2):c.1046+91_1046+92del rs559885397
NM_030662.3(MAP2K2):c.1047-212G>A
NM_030662.3(MAP2K2):c.1092A>G (p.Thr364=) rs779378237
NM_030662.3(MAP2K2):c.1093-273C>T
NM_030662.3(MAP2K2):c.1093-6T>C rs369681843
NM_030662.3(MAP2K2):c.1112G>A (p.Arg371Gln) rs730880514
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.1197C>T (p.Ala399=) rs987393686
NM_030662.3(MAP2K2):c.168C>T (p.Ala56=) rs147814905
NM_030662.3(MAP2K2):c.240G>A (p.Ala80=) rs543217722
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.291C>G (p.Ile97Met) rs200918323
NM_030662.3(MAP2K2):c.303+15del rs758256765
NM_030662.3(MAP2K2):c.304-7C>T rs561127903
NM_030662.3(MAP2K2):c.327G>A (p.Pro109=) rs369156025
NM_030662.3(MAP2K2):c.351C>G (p.Arg117=) rs777670871
NM_030662.3(MAP2K2):c.42C>T (p.Ile14=) rs1057522557
NM_030662.3(MAP2K2):c.450+12C>T rs750513646
NM_030662.3(MAP2K2):c.450+17C>T rs199892711
NM_030662.3(MAP2K2):c.450+20G>A rs374143146
NM_030662.3(MAP2K2):c.450+307C>A
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.528+11C>T rs369913089
NM_030662.3(MAP2K2):c.529-10T>C rs551098822
NM_030662.3(MAP2K2):c.529-14G>A rs756414078
NM_030662.3(MAP2K2):c.580+14C>T rs544557960
NM_030662.3(MAP2K2):c.580+15G>A rs370921720
NM_030662.3(MAP2K2):c.581-11G>A rs758442973
NM_030662.3(MAP2K2):c.581-19C>T rs573730409
NM_030662.3(MAP2K2):c.581-20C>T rs1057523179
NM_030662.3(MAP2K2):c.581-8G>A rs369262004
NM_030662.3(MAP2K2):c.581-9C>T rs539611844
NM_030662.3(MAP2K2):c.639C>T (p.Phe213=) rs727504818
NM_030662.3(MAP2K2):c.705+10C>T rs372898071
NM_030662.3(MAP2K2):c.705+128C>T
NM_030662.3(MAP2K2):c.706-17C>T rs754737193
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.818A>G (p.Lys273Arg) rs539555837
NM_030662.3(MAP2K2):c.853G>A (p.Asp285Asn) rs150369301
NM_030662.3(MAP2K2):c.889C>T (p.Arg297Trp) rs562352756
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+10G>A rs780890887
NM_030662.3(MAP2K2):c.919+10_919+12delinsAAG rs1064794489
NM_030662.3(MAP2K2):c.919+4C>T rs763424788
NM_030662.3(MAP2K2):c.92+11A>C rs1228838756
NM_030662.3(MAP2K2):c.92+266G>A
NM_030662.3(MAP2K2):c.920-17T>A rs1057524145
NM_030662.3(MAP2K2):c.93-6C>T rs727504836

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