ClinVar Miner

List of variants in gene MAP2K1 reported by Ambry Genetics

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Total variants: 67
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HGVS dbSNP gnomAD frequency
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.264G>A (p.Lys88=) rs7494832 0.00006
NM_002755.4(MAP2K1):c.277G>A (p.Val93Ile) rs151207265 0.00006
NM_002755.4(MAP2K1):c.396G>A (p.Ala132=) rs139364105 0.00006
NM_002755.4(MAP2K1):c.729G>A (p.Gln243=) rs772752167 0.00005
NM_002755.4(MAP2K1):c.1038C>T (p.Pro346=) rs547178339 0.00004
NM_002755.4(MAP2K1):c.198C>T (p.Asp66=) rs56200325 0.00004
NM_002755.4(MAP2K1):c.156C>T (p.Ala52=) rs147489724 0.00003
NM_002755.4(MAP2K1):c.771G>A (p.Ala257=) rs767965126 0.00003
NM_002755.4(MAP2K1):c.1005A>G (p.Gln335=) rs1057520833 0.00002
NM_002755.4(MAP2K1):c.12G>A (p.Lys4=) rs1489477346 0.00002
NM_002755.4(MAP2K1):c.279C>T (p.Val93=) rs140387057 0.00002
NM_002755.4(MAP2K1):c.378C>T (p.Ile126=) rs369401783 0.00002
NM_002755.4(MAP2K1):c.900C>T (p.Tyr300=) rs147333830 0.00002
NM_002755.4(MAP2K1):c.255C>T (p.Val85=) rs1052147663 0.00001
NM_002755.4(MAP2K1):c.263A>G (p.Lys88Arg) rs762354445 0.00001
NM_002755.4(MAP2K1):c.372G>A (p.Pro124=) rs750270430 0.00001
NM_002755.4(MAP2K1):c.405C>T (p.Ser135=) rs767989355 0.00001
NM_002755.4(MAP2K1):c.492A>G (p.Gln164=) rs140822439 0.00001
NM_002755.4(MAP2K1):c.792T>G (p.Pro264=) rs764379969 0.00001
NM_002755.4(MAP2K1):c.804C>G (p.Ala268=) rs371652992 0.00001
NM_002755.4(MAP2K1):c.834G>A (p.Gln278=) rs148151221 0.00001
NM_002755.4(MAP2K1):c.871A>G (p.Arg291Gly) rs747807884 0.00001
NM_002755.4(MAP2K1):c.961C>T (p.Pro321Ser) rs771613524 0.00001
NM_002755.4(MAP2K1):c.984A>C (p.Gly328=) rs773755873 0.00001
NM_002755.4(MAP2K1):c.156C>G (p.Ala52=) rs147489724
NM_002755.4(MAP2K1):c.199G>A (p.Asp67Asn) rs727504317
NM_002755.4(MAP2K1):c.280A>G (p.Met94Val)
NM_002755.4(MAP2K1):c.343C>G (p.Leu115Val) rs1428775799
NM_002755.4(MAP2K1):c.388T>C (p.Tyr130His) rs397516793
NM_002755.4(MAP2K1):c.389A>G (p.Tyr130Cys) rs121908595
NM_002755.4(MAP2K1):c.43C>G (p.Pro15Ala)
NM_002755.4(MAP2K1):c.45C>T (p.Pro15=)
NM_002755.4(MAP2K1):c.503A>G (p.Lys168Arg) rs886051366
NM_002755.4(MAP2K1):c.529C>G (p.Leu177Val) rs1891815342
NM_002755.4(MAP2K1):c.537T>C (p.Tyr179=) rs1188803242
NM_002755.4(MAP2K1):c.573C>G (p.Val191=)
NM_002755.4(MAP2K1):c.607G>A (p.Glu203Lys) rs1057519733
NM_002755.4(MAP2K1):c.630G>A (p.Gly210=) rs1595884752
NM_002755.4(MAP2K1):c.753G>A (p.Leu251=)
NM_002755.4(MAP2K1):c.801T>A (p.Asp267Glu)
NM_002755.4(MAP2K1):c.840A>G (p.Glu280=)
NM_002755.4(MAP2K1):c.842_844del (p.Gly281del)
NM_002755.4(MAP2K1):c.849G>A (p.Ala283=)
NM_002755.4(MAP2K1):c.877C>G (p.Pro293Ala)
NM_002755.4(MAP2K1):c.909C>T (p.Asp303=)
NM_002755.4(MAP2K1):c.930T>G (p.Ile310Met)
NM_002755.4(MAP2K1):c.937T>C (p.Leu313=)
NM_002755.4(MAP2K1):c.949A>G (p.Ile317Val)
NM_002755.4(MAP2K1):c.950T>C (p.Ile317Thr)
NM_002755.4(MAP2K1):c.95C>T (p.Ala32Val)
NM_002755.4(MAP2K1):c.967C>T (p.Pro323Ser)
NM_002755.4(MAP2K1):c.969A>C (p.Pro323=)
NM_002755.4(MAP2K1):c.969A>G (p.Pro323=)
NM_002755.4(MAP2K1):c.978C>A (p.Pro326=)
NM_002755.4(MAP2K1):c.984A>T (p.Gly328=)
NM_002755.4(MAP2K1):c.987G>T (p.Val329=)

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