ClinVar Miner

List of variants in gene MAP2K2 reported as likely pathogenic

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Total variants: 19
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NM_030662.3(MAP2K2):c.103G>A (p.Val35Met) rs1057519810
NM_030662.3(MAP2K2):c.136C>T (p.Leu46Phe) rs1057519809
NM_030662.3(MAP2K2):c.169T>G (p.Phe57Val) rs121434498
NM_030662.3(MAP2K2):c.171T>G (p.Phe57Leu) rs1057519910
NM_030662.3(MAP2K2):c.179A>C (p.Gln60Pro) rs1057519808
NM_030662.3(MAP2K2):c.181A>G (p.Lys61Glu) rs730880517
NM_030662.3(MAP2K2):c.183A>C (p.Lys61Asn) rs886041310
NM_030662.3(MAP2K2):c.190G>T (p.Val64Phe) rs730880518
NM_030662.3(MAP2K2):c.191T>G (p.Val64Gly) rs1135401787
NM_030662.3(MAP2K2):c.373T>A (p.Cys125Ser) rs1057519807
NM_030662.3(MAP2K2):c.376A>G (p.Asn126Asp) rs1057519806
NM_030662.3(MAP2K2):c.395G>A (p.Gly132Asp) rs387906800
NM_030662.3(MAP2K2):c.692G>T (p.Arg231Leu) rs730880511
NM_030662.3(MAP2K2):c.787G>A (p.Gly263Arg) rs730880522
NM_030662.4(MAP2K2):c.187_192del (p.Lys63_Val64del) rs1599307313
NM_030662.4(MAP2K2):c.335G>T (p.Arg112Leu)
NM_030662.4(MAP2K2):c.400T>C (p.Tyr134His) rs121434499
NM_030662.4(MAP2K2):c.401A>G (p.Tyr134Cys) rs727504370
NM_030662.4(MAP2K2):c.619G>A (p.Glu207Lys) rs727504382

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