ClinVar Miner

List of variants in gene MAP2K1 reported as benign by GeneDx

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Gene type:
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Total variants: 49
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HGVS dbSNP gnomAD frequency
NM_002755.4(MAP2K1):c.439-67C>T rs6494573 0.83820
NM_002755.4(MAP2K1):c.517-253C>T rs6494574 0.30025
NM_002755.4(MAP2K1):c.291+22G>C rs16949924 0.27222
NM_002755.4(MAP2K1):c.292-133A>C rs11637556 0.21057
NM_002755.4(MAP2K1):c.569-118G>A rs41277720 0.17542
NM_002755.4(MAP2K1):c.516+191G>A rs17201019 0.14207
NM_002755.4(MAP2K1):c.291+199C>T rs66975215 0.12011
NM_002755.4(MAP2K1):c.960+68C>T rs41315964 0.09424
NM_002755.4(MAP2K1):c.1023-8C>T rs41306345 0.09409
NM_002755.4(MAP2K1):c.517-311C>A rs112381615 0.07480
NM_002755.4(MAP2K1):c.896-291G>C rs36047146 0.05688
NM_002755.4(MAP2K1):c.961-254_961-251del rs34067330 0.05667
NM_002755.4(MAP2K1):c.693+275T>A rs75586043 0.01746
NM_002755.4(MAP2K1):c.895+181A>G rs77824107 0.01717
NM_002755.4(MAP2K1):c.438+20C>T rs16949939 0.01567
NM_002755.4(MAP2K1):c.80+33C>G rs56149436 0.01549
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.1023-43C>T rs146169356 0.00221
NM_002755.4(MAP2K1):c.648C>T (p.Ile216=) rs148968935 0.00123
NM_002755.4(MAP2K1):c.80+28G>C rs374238278 0.00118
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.516+28A>G rs184208600 0.00050
NM_002755.4(MAP2K1):c.693+50G>C rs58205072 0.00043
NM_002755.4(MAP2K1):c.848C>T (p.Ala283Val) rs144080051 0.00029
NM_002755.4(MAP2K1):c.6C>T (p.Pro2=) rs377720622 0.00025
NM_002755.4(MAP2K1):c.237C>T (p.Gly79=) rs148656020 0.00024
NM_002755.4(MAP2K1):c.636C>T (p.Ser212=) rs138466751 0.00011
NM_002755.4(MAP2K1):c.396G>A (p.Ala132=) rs139364105 0.00006
NM_002755.4(MAP2K1):c.569-19T>A rs371099866 0.00006
NM_002755.4(MAP2K1):c.439-8G>A rs747709090 0.00004
NM_002755.4(MAP2K1):c.156C>T (p.Ala52=) rs147489724 0.00003
NM_002755.4(MAP2K1):c.177G>A (p.Lys59=) rs773928828 0.00003
NM_002755.4(MAP2K1):c.276G>C (p.Leu92=) rs377323150 0.00003
NM_002755.4(MAP2K1):c.569-13C>T rs770040428 0.00003
NM_002755.4(MAP2K1):c.900C>T (p.Tyr300=) rs147333830 0.00002
NM_002755.4(MAP2K1):c.804C>G (p.Ala268=) rs371652992 0.00001
NM_002755.4(MAP2K1):c.291+127_291+129dup rs71139499
NM_002755.4(MAP2K1):c.291+128_291+129dup rs71139499
NM_002755.4(MAP2K1):c.291+18A>T rs577549188
NM_002755.4(MAP2K1):c.516+230_516+231insAG rs72531931
NM_002755.4(MAP2K1):c.694-12TC[4] rs113913469
NM_002755.4(MAP2K1):c.80+195del rs145028363
NM_002755.4(MAP2K1):c.80+33C>T rs56149436
NM_002755.4(MAP2K1):c.80+54G>C rs4483802
NM_002755.4(MAP2K1):c.80+85del rs2140512008
NM_002755.4(MAP2K1):c.80+87del rs71447901

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