ClinVar Miner

List of variants in gene MAP2K1 reported by PreventionGenetics, part of Exact Sciences

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Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_002755.4(MAP2K1):c.291+22G>C rs16949924 0.27222
NM_002755.4(MAP2K1):c.1023-8C>T rs41306345 0.09409
NM_002755.4(MAP2K1):c.438+20C>T rs16949939 0.01567
NM_002755.4(MAP2K1):c.711G>A (p.Gly237=) rs17586159 0.01226
NM_002755.4(MAP2K1):c.-2A>G rs77796976 0.00820
NM_002755.4(MAP2K1):c.927A>T (p.Ala309=) rs146869577 0.00357
NM_002755.4(MAP2K1):c.648C>T (p.Ile216=) rs148968935 0.00123
NM_002755.4(MAP2K1):c.315C>T (p.Pro105=) rs144166521 0.00061
NM_002755.4(MAP2K1):c.69C>T (p.Thr23=) rs140749690 0.00054
NM_002755.4(MAP2K1):c.848C>T (p.Ala283Val) rs144080051 0.00029
NM_002755.4(MAP2K1):c.237C>T (p.Gly79=) rs148656020 0.00024
NM_002755.4(MAP2K1):c.726G>T (p.Val242=) rs373745627 0.00013
NM_002755.4(MAP2K1):c.636C>T (p.Ser212=) rs138466751 0.00011
NM_002755.4(MAP2K1):c.292-3C>T rs55694358 0.00007
NM_002755.4(MAP2K1):c.957C>T (p.Asn319=) rs143019052 0.00005
NM_002755.4(MAP2K1):c.439-8G>A rs747709090 0.00004
NM_002755.4(MAP2K1):c.1023-20C>T rs200542677 0.00003
NM_002755.4(MAP2K1):c.276G>C (p.Leu92=) rs377323150 0.00003
NM_002755.4(MAP2K1):c.80+9G>A rs1219385230 0.00003
NM_002755.4(MAP2K1):c.804C>G (p.Ala268=) rs371652992 0.00001
NM_002755.4(MAP2K1):c.15G>T (p.Lys5Asn)
NM_002755.4(MAP2K1):c.389A>G (p.Tyr130Cys) rs121908595
NM_002755.4(MAP2K1):c.672G>A (p.Val224=)
NM_002755.4(MAP2K1):c.694-12TC[4] rs113913469
NM_002755.4(MAP2K1):c.828G>A (p.Gly276=)
NM_002755.4(MAP2K1):c.904A>C (p.Met302Leu) rs1023593707

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