ClinVar Miner

List of variants in gene MAP2K2 reported as uncertain significance by Integrated Genetics/Laboratory Corporation of America

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Total variants: 16
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HGVS dbSNP
NM_030662.3(MAP2K2):c.1092A>C (p.Thr364=) rs779378237
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.170T>A (p.Phe57Tyr) rs121434497
NM_030662.3(MAP2K2):c.207C>T (p.Asp69=) rs199850535
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.399C>T (p.Phe133=) rs145524962
NM_030662.3(MAP2K2):c.39C>T (p.Thr13=) rs752951050
NM_030662.3(MAP2K2):c.529-5T>C rs766943752
NM_030662.3(MAP2K2):c.531T>C (p.Val177=) rs528169616
NM_030662.3(MAP2K2):c.581-5T>C rs757662989
NM_030662.3(MAP2K2):c.581-9C>T rs539611844
NM_030662.3(MAP2K2):c.627G>C (p.Lys209Asn) rs1555696933
NM_030662.3(MAP2K2):c.699C>T (p.Tyr233=) rs1044588100
NM_030662.3(MAP2K2):c.806C>T (p.Pro269Leu) rs368064728

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