ClinVar Miner

List of variants in gene MAP2K1 studied for not specified

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Total variants: 74
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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.6C>T (p.Pro2=) rs377720622 0.00025
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.439-19C>A rs766207567 0.00010
NM_002755.4(MAP2K1):c.292-3C>T rs55694358 0.00007
NM_002755.4(MAP2K1):c.264G>A (p.Lys88=) rs7494832 0.00006
NM_002755.4(MAP2K1):c.569-19T>A rs371099866 0.00006
NM_002755.4(MAP2K1):c.56C>G (p.Ala19Gly) rs727504413 0.00006
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.156C>T (p.Ala52=) rs147489724 0.00003
NM_002755.4(MAP2K1):c.177G>A (p.Lys59=) rs773928828 0.00003
NM_002755.4(MAP2K1):c.693+10G>A rs377034924 0.00003
NM_002755.4(MAP2K1):c.875C>T (p.Thr292Ile) rs397516794 0.00003
NM_002755.4(MAP2K1):c.901G>A (p.Gly301Arg) rs773890369 0.00003
NM_002755.4(MAP2K1):c.378C>T (p.Ile126=) rs369401783 0.00002
NM_002755.4(MAP2K1):c.517-4C>T rs200197244 0.00002
NM_002755.4(MAP2K1):c.1022+10C>T rs397516787 0.00001
NM_002755.4(MAP2K1):c.1039G>A (p.Ala347Thr) rs746354996 0.00001
NM_002755.4(MAP2K1):c.251A>G (p.Lys84Arg) rs774932586 0.00001
NM_002755.4(MAP2K1):c.263A>G (p.Lys88Arg) rs762354445 0.00001
NM_002755.4(MAP2K1):c.39G>A (p.Pro13=) rs876657503 0.00001
NM_002755.4(MAP2K1):c.405C>T (p.Ser135=) rs767989355 0.00001
NM_002755.4(MAP2K1):c.439-14A>G rs754725417 0.00001
NM_002755.4(MAP2K1):c.631G>A (p.Val211Ile) rs727505206 0.00001
NM_002755.4(MAP2K1):c.693+4T>G rs184151283 0.00001
NM_002755.4(MAP2K1):c.804C>G (p.Ala268=) rs371652992 0.00001
NM_002755.4(MAP2K1):c.871A>G (p.Arg291Gly) rs747807884 0.00001
NM_002755.4(MAP2K1):c.879C>T (p.Pro293=) rs370521459 0.00001
NM_002755.4(MAP2K1):c.896-7T>C rs772786705 0.00001
NM_002755.4(MAP2K1):c.939G>C (p.Leu313Phe) rs1361965478 0.00001
NM_002755.4(MAP2K1):c.124C>T (p.Leu42Phe) rs397516789
NM_002755.4(MAP2K1):c.140G>A (p.Arg47Gln) rs1567009054
NM_002755.4(MAP2K1):c.156C>G (p.Ala52=) rs147489724
NM_002755.4(MAP2K1):c.15G>A (p.Lys5=) rs2140511623
NM_002755.4(MAP2K1):c.291+14_291+15inv
NM_002755.4(MAP2K1):c.291+14_291+19delinsTCTCAC
NM_002755.4(MAP2K1):c.291+14_291+20delinsTCTCACCAATCACCA rs1064795401
NM_002755.4(MAP2K1):c.291+17T>C rs1294983448
NM_002755.4(MAP2K1):c.291+18A>T rs577549188
NM_002755.4(MAP2K1):c.291+19A>C rs752759395
NM_002755.4(MAP2K1):c.292-2A>G
NM_002755.4(MAP2K1):c.292-4C>G rs771407622
NM_002755.4(MAP2K1):c.29A>T (p.Gln10Leu) rs2093343985
NM_002755.4(MAP2K1):c.323G>A (p.Arg108Gln) rs727504819
NM_002755.4(MAP2K1):c.516+2T>C rs1057518013
NM_002755.4(MAP2K1):c.519A>T (p.Val173=) rs1471931068
NM_002755.4(MAP2K1):c.546G>A (p.Glu182=) rs1567012356
NM_002755.4(MAP2K1):c.568+1G>A rs730880505
NM_002755.4(MAP2K1):c.568+6A>G rs1430324310
NM_002755.4(MAP2K1):c.569-8C>T rs375614631
NM_002755.4(MAP2K1):c.586A>G (p.Ile196Val) rs2140667372
NM_002755.4(MAP2K1):c.612C>A (p.Ile204=) rs2140667598
NM_002755.4(MAP2K1):c.645C>G (p.Leu215=) rs2140667933
NM_002755.4(MAP2K1):c.694-12TC[4] rs113913469
NM_002755.4(MAP2K1):c.729G>T (p.Gln243His) rs772752167
NM_002755.4(MAP2K1):c.794_860dup (p.Pro287_Pro288insSerArgCysGlnGlyAlaGlyAlaAspValTrpValProGlyGlyArgArgCysGlyTer) rs1893005622
NM_002755.4(MAP2K1):c.802G>A (p.Ala268Thr) rs1555420656
NM_002755.4(MAP2K1):c.803C>T (p.Ala268Val) rs757459909
NM_002755.4(MAP2K1):c.875C>G (p.Thr292Ser) rs397516794
NM_002755.4(MAP2K1):c.961-61_997dup rs1893152621
NM_002755.4(MAP2K1):c.970A>C (p.Lys324Gln) rs762436311

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