ClinVar Miner

List of variants in gene MAP2K2 reported as uncertain significance by Invitae

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Total variants: 29
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HGVS dbSNP
NC_000019.9:g.(?_4097267)_(4097351_?)del
NM_030662.3(MAP2K2):c.1006G>A (p.Gly336Ser)
NM_030662.3(MAP2K2):c.1085T>C (p.Met362Thr) rs730880513
NM_030662.3(MAP2K2):c.1111C>T (p.Arg371Trp)
NM_030662.3(MAP2K2):c.1112G>A (p.Arg371Gln) rs730880514
NM_030662.3(MAP2K2):c.1190G>A (p.Arg397His)
NM_030662.3(MAP2K2):c.191_192delinsCT (p.Val64Ala) rs1555698682
NM_030662.3(MAP2K2):c.195C>T (p.Gly65=)
NM_030662.3(MAP2K2):c.217G>A (p.Glu73Lys) rs187018595
NM_030662.3(MAP2K2):c.26T>C (p.Leu9Pro)
NM_030662.3(MAP2K2):c.281C>T (p.Ser94Leu) rs202220799
NM_030662.3(MAP2K2):c.288_290CAT[1] (p.Ile97del) rs1555698652
NM_030662.3(MAP2K2):c.289A>T (p.Ile97Phe) rs373579939
NM_030662.3(MAP2K2):c.325C>G (p.Pro109Ala) rs1060502983
NM_030662.3(MAP2K2):c.376A>C (p.Asn126His)
NM_030662.3(MAP2K2):c.380C>T (p.Ser127Leu) rs1568260052
NM_030662.3(MAP2K2):c.453C>G (p.Asp151Glu) rs17851657
NM_030662.3(MAP2K2):c.491G>T (p.Arg164Met)
NM_030662.3(MAP2K2):c.578G>A (p.Arg193Gln) rs530342723
NM_030662.3(MAP2K2):c.692G>A (p.Arg231His) rs730880511
NM_030662.3(MAP2K2):c.692G>T (p.Arg231Leu) rs730880511
NM_030662.3(MAP2K2):c.706-1_706delinsTT
NM_030662.3(MAP2K2):c.784G>A (p.Val262Ile) rs138873805
NM_030662.3(MAP2K2):c.834C>G (p.Ile278Met) rs766540227
NM_030662.3(MAP2K2):c.842G>A (p.Arg281Gln) rs1332074575
NM_030662.3(MAP2K2):c.856G>A (p.Gly286Arg) rs730880523
NM_030662.3(MAP2K2):c.865G>A (p.Gly289Arg) rs1555696725
NM_030662.3(MAP2K2):c.890G>A (p.Arg297Gln) rs140111079
NM_030662.3(MAP2K2):c.918C>T (p.Ser306=) rs777196833

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