Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.66481706_66481749delCA2184097348MAP2K1c.503-49_503-6del (n.503-49_503-6del)
c.569-49_569-6del (n.569-49_569-6del)
c.422-49_422-6del (n.422-49_422-6del)
c.569-5522_569-5479del (n.569-5522_569-5479del)
n.927-49_927-6del
c.620-49_620-6del (n.620-49_620-6del)
c.569-3288_569-3245del (n.569-3288_569-3245del)
c.425-49_425-6del (n.425-49_425-6del)
c.41-49_41-6del (n.41-49_41-6del)
c.491-49_491-6del (n.491-49_491-6del)
ClinVar dbSNP gnomAD v4
15g.66481744C=CA2184097376MAP2K1c.503-11C= (n.503-11C=)
c.569-11C= (n.569-11C=)
c.422-11C= (n.422-11C=)
c.569-5484C= (n.569-5484C=)
n.927-11C=
c.620-11C= (n.620-11C=)
c.569-3250C= (n.569-3250C=)
c.425-11C= (n.425-11C=)
c.41-11C= (n.41-11C=)
c.491-11C= (n.491-11C=)
15g.66481744C>TCA2184097377MAP2K1c.503-11C>T (n.503-11C>T)
c.569-11C>T (n.569-11C>T)
c.422-11C>T (n.422-11C>T)
c.569-5484C>T (n.569-5484C>T)
n.927-11C>T
c.620-11C>T (n.620-11C>T)
c.569-3250C>T (n.569-3250C>T)
c.425-11C>T (n.425-11C>T)
c.41-11C>T (n.41-11C>T)
c.491-11C>T (n.491-11C>T)
ClinVar dbSNP gnomAD v4
15g.66481745T>CCA7623988MAP2K1c.503-10T>C (n.503-10T>C)
c.569-10T>C (n.569-10T>C)
c.422-10T>C (n.422-10T>C)
c.569-5483T>C (n.569-5483T>C)
n.927-10T>C
c.620-10T>C (n.620-10T>C)
c.569-3249T>C (n.569-3249T>C)
c.425-10T>C (n.425-10T>C)
c.41-10T>C (n.41-10T>C)
c.491-10T>C (n.491-10T>C)
dbSNP ExAC gnomAD v2
15g.66481745T=CA2184097378MAP2K1c.503-10T= (n.503-10T=)
c.569-10T= (n.569-10T=)
c.422-10T= (n.422-10T=)
c.569-5483T= (n.569-5483T=)
n.927-10T=
c.620-10T= (n.620-10T=)
c.569-3249T= (n.569-3249T=)
c.425-10T= (n.425-10T=)
c.41-10T= (n.41-10T=)
c.491-10T= (n.491-10T=)
15g.66481746T>CCA2731111632MAP2K1c.503-9T>C (n.503-9T>C)
c.569-9T>C (n.569-9T>C)
c.422-9T>C (n.422-9T>C)
c.569-5482T>C (n.569-5482T>C)
n.927-9T>C
c.620-9T>C (n.620-9T>C)
c.569-3248T>C (n.569-3248T>C)
c.425-9T>C (n.425-9T>C)
c.41-9T>C (n.41-9T>C)
c.491-9T>C (n.491-9T>C)
dbSNP
15g.66481747C>ACA2730913082MAP2K1c.503-8C>A (n.503-8C>A)
c.569-8C>A (n.569-8C>A)
c.422-8C>A (n.422-8C>A)
c.569-5481C>A (n.569-5481C>A)
n.927-8C>A
c.620-8C>A (n.620-8C>A)
c.569-3247C>A (n.569-3247C>A)
c.425-8C>A (n.425-8C>A)
c.41-8C>A (n.41-8C>A)
c.491-8C>A (n.491-8C>A)
dbSNP
15g.66481747C=CA2184097380MAP2K1c.503-8C= (n.503-8C=)
c.569-8C= (n.569-8C=)
c.422-8C= (n.422-8C=)
c.569-5481C= (n.569-5481C=)
n.927-8C=
c.620-8C= (n.620-8C=)
c.569-3247C= (n.569-3247C=)
c.425-8C= (n.425-8C=)
c.41-8C= (n.41-8C=)
c.491-8C= (n.491-8C=)
15g.66481747C>GCA7623989MAP2K1c.503-8C>G (n.503-8C>G)
c.569-8C>G (n.569-8C>G)
c.422-8C>G (n.422-8C>G)
c.569-5481C>G (n.569-5481C>G)
n.927-8C>G
c.620-8C>G (n.620-8C>G)
c.569-3247C>G (n.569-3247C>G)
c.425-8C>G (n.425-8C>G)
c.41-8C>G (n.41-8C>G)
c.491-8C>G (n.491-8C>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.66481747C>TCA658798392MAP2K1c.503-8C>T (n.503-8C>T)
c.569-8C>T (n.569-8C>T)
c.422-8C>T (n.422-8C>T)
c.569-5481C>T (n.569-5481C>T)
n.927-8C>T
c.620-8C>T (n.620-8C>T)
c.569-3247C>T (n.569-3247C>T)
c.425-8C>T (n.425-8C>T)
c.41-8C>T (n.41-8C>T)
c.491-8C>T (n.491-8C>T)
ClinVar dbSNP gnomAD v4
15g.66481748C>ACA618679507MAP2K1c.503-7C>A (n.503-7C>A)
c.569-7C>A (n.569-7C>A)
c.422-7C>A (n.422-7C>A)
c.569-5480C>A (n.569-5480C>A)
n.927-7C>A
c.620-7C>A (n.620-7C>A)
c.569-3246C>A (n.569-3246C>A)
c.425-7C>A (n.425-7C>A)
c.41-7C>A (n.41-7C>A)
c.491-7C>A (n.491-7C>A)
dbSNP gnomAD v2
15g.66481748C=CA2184097382MAP2K1c.503-7C= (n.503-7C=)
c.569-7C= (n.569-7C=)
c.422-7C= (n.422-7C=)
c.569-5480C= (n.569-5480C=)
n.927-7C=
c.620-7C= (n.620-7C=)
c.569-3246C= (n.569-3246C=)
c.425-7C= (n.425-7C=)
c.41-7C= (n.41-7C=)
c.491-7C= (n.491-7C=)
15g.66481748C>GCA618679509MAP2K1c.503-7C>G (n.503-7C>G)
c.569-7C>G (n.569-7C>G)
c.422-7C>G (n.422-7C>G)
c.569-5480C>G (n.569-5480C>G)
n.927-7C>G
c.620-7C>G (n.620-7C>G)
c.569-3246C>G (n.569-3246C>G)
c.425-7C>G (n.425-7C>G)
c.41-7C>G (n.41-7C>G)
c.491-7C>G (n.491-7C>G)
dbSNP gnomAD v2 gnomAD v4
15g.66481748C>TCA7623990MAP2K1c.503-7C>T (n.503-7C>T)
c.569-7C>T (n.569-7C>T)
c.422-7C>T (n.422-7C>T)
c.569-5480C>T (n.569-5480C>T)
n.927-7C>T
c.620-7C>T (n.620-7C>T)
c.569-3246C>T (n.569-3246C>T)
c.425-7C>T (n.425-7C>T)
c.41-7C>T (n.41-7C>T)
c.491-7C>T (n.491-7C>T)
dbSNP ExAC gnomAD v2 gnomAD v4
15g.66481749C>ACA2731111652MAP2K1c.503-6C>A (n.503-6C>A)
c.569-6C>A (n.569-6C>A)
c.422-6C>A (n.422-6C>A)
c.569-5479C>A (n.569-5479C>A)
n.927-6C>A
c.620-6C>A (n.620-6C>A)
c.569-3245C>A (n.569-3245C>A)
c.425-6C>A (n.425-6C>A)
c.41-6C>A (n.41-6C>A)
c.491-6C>A (n.491-6C>A)
dbSNP
15g.66481749C>TCA2731111651MAP2K1c.503-6C>T (n.503-6C>T)
c.569-6C>T (n.569-6C>T)
c.422-6C>T (n.422-6C>T)
c.569-5479C>T (n.569-5479C>T)
n.927-6C>T
c.620-6C>T (n.620-6C>T)
c.569-3245C>T (n.569-3245C>T)
c.425-6C>T (n.425-6C>T)
c.41-6C>T (n.41-6C>T)
c.491-6C>T (n.491-6C>T)
dbSNP
15g.66481751G>ACA2573151055MAP2K1c.503-4G>A (n.503-4G>A)
c.569-4G>A (n.569-4G>A)
c.422-4G>A (n.422-4G>A)
c.569-5477G>A (n.569-5477G>A)
n.927-4G>A
c.620-4G>A (n.620-4G>A)
c.569-3243G>A (n.569-3243G>A)
c.425-4G>A (n.425-4G>A)
c.41-4G>A (n.41-4G>A)
c.491-4G>A (n.491-4G>A)
ClinVar dbSNP
15g.66481751G>CCA2731111657MAP2K1c.503-4G>C (n.503-4G>C)
c.569-4G>C (n.569-4G>C)
c.422-4G>C (n.422-4G>C)
c.569-5477G>C (n.569-5477G>C)
n.927-4G>C
c.620-4G>C (n.620-4G>C)
c.569-3243G>C (n.569-3243G>C)
c.425-4G>C (n.425-4G>C)
c.41-4G>C (n.41-4G>C)
c.491-4G>C (n.491-4G>C)
dbSNP
15g.66481751G>TCA2731111656MAP2K1c.503-4G>T (n.503-4G>T)
c.569-4G>T (n.569-4G>T)
c.422-4G>T (n.422-4G>T)
c.569-5477G>T (n.569-5477G>T)
n.927-4G>T
c.620-4G>T (n.620-4G>T)
c.569-3243G>T (n.569-3243G>T)
c.425-4G>T (n.425-4G>T)
c.41-4G>T (n.41-4G>T)
c.491-4G>T (n.491-4G>T)
dbSNP
15g.66481752C>GCA2731111694MAP2K1c.503-3C>G (n.503-3C>G)
c.569-3C>G (n.569-3C>G)
c.422-3C>G (n.422-3C>G)
c.569-5476C>G (n.569-5476C>G)
n.927-3C>G
c.620-3C>G (n.620-3C>G)
c.569-3242C>G (n.569-3242C>G)
c.425-3C>G (n.425-3C>G)
c.41-3C>G (n.41-3C>G)
c.491-3C>G (n.491-3C>G)
dbSNP
15g.66481752C>TCA2731111692MAP2K1c.503-3C>T (n.503-3C>T)
c.569-3C>T (n.569-3C>T)
c.422-3C>T (n.422-3C>T)
c.569-5476C>T (n.569-5476C>T)
n.927-3C>T
c.620-3C>T (n.620-3C>T)
c.569-3242C>T (n.569-3242C>T)
c.425-3C>T (n.425-3C>T)
c.41-3C>T (n.41-3C>T)
c.491-3C>T (n.491-3C>T)
dbSNP
15g.66481753A>CCA392936029MAP2K1c.503-2A>C (n.503-2A>C)
c.569-2A>C (n.569-2A>C)
c.422-2A>C (n.422-2A>C)
c.569-5475A>C (n.569-5475A>C)
n.927-2A>C
c.620-2A>C (n.620-2A>C)
c.569-3241A>C (n.569-3241A>C)
c.425-2A>C (n.425-2A>C)
c.41-2A>C (n.41-2A>C)
c.491-2A>C (n.491-2A>C)
COSMIC
15g.66481753A>GCA392936031MAP2K1c.503-2A>G (n.503-2A>G)
c.569-2A>G (n.569-2A>G)
c.422-2A>G (n.422-2A>G)
c.569-5475A>G (n.569-5475A>G)
n.927-2A>G
c.620-2A>G (n.620-2A>G)
c.569-3241A>G (n.569-3241A>G)
c.425-2A>G (n.425-2A>G)
c.41-2A>G (n.41-2A>G)
c.491-2A>G (n.491-2A>G)
dbSNP
15g.66481753A>TCA392936033MAP2K1c.503-2A>T (n.503-2A>T)
c.569-2A>T (n.569-2A>T)
c.422-2A>T (n.422-2A>T)
c.569-5475A>T (n.569-5475A>T)
n.927-2A>T
c.620-2A>T (n.620-2A>T)
c.569-3241A>T (n.569-3241A>T)
c.425-2A>T (n.425-2A>T)
c.41-2A>T (n.41-2A>T)
c.491-2A>T (n.491-2A>T)
dbSNP
15g.66481754G>ACA392936035MAP2K1c.503-1G>A (n.503-1G>A)
c.569-1G>A (n.569-1G>A)
c.422-1G>A (n.422-1G>A)
c.569-5474G>A (n.569-5474G>A)
n.927-1G>A
c.620-1G>A (n.620-1G>A)
c.569-3240G>A (n.569-3240G>A)
c.425-1G>A (n.425-1G>A)
c.41-1G>A (n.41-1G>A)
c.491-1G>A (n.491-1G>A)
dbSNP
15g.66481754G>CCA392936036MAP2K1c.503-1G>C (n.503-1G>C)
c.569-1G>C (n.569-1G>C)
c.422-1G>C (n.422-1G>C)
c.569-5474G>C (n.569-5474G>C)
n.927-1G>C
c.620-1G>C (n.620-1G>C)
c.569-3240G>C (n.569-3240G>C)
c.425-1G>C (n.425-1G>C)
c.41-1G>C (n.41-1G>C)
c.491-1G>C (n.491-1G>C)
dbSNP
15g.66481754G>TCA392936038MAP2K1c.503-1G>T (n.503-1G>T)
c.569-1G>T (n.569-1G>T)
c.422-1G>T (n.422-1G>T)
c.569-5474G>T (n.569-5474G>T)
n.927-1G>T
c.620-1G>T (n.620-1G>T)
c.569-3240G>T (n.569-3240G>T)
c.425-1G>T (n.425-1G>T)
c.41-1G>T (n.41-1G>T)
c.491-1G>T (n.491-1G>T)
dbSNP
15g.66481755A>CCA392936041MAP2K1c.503A>C (p.Asp168Ala)
c.569A>C (p.Asp190Ala)
c.422A>C (p.Asp141Ala)
c.569-5473A>C (n.569-5473A>C)
n.927A>C
c.620A>C (p.Asn207Thr)
c.569-3239A>C (n.569-3239A>C)
c.425A>C (p.Asp142Ala)
c.41A>C (p.Asn14Thr)
c.491A>C (p.Asp164Ala)
15g.66481755A>GCA392936043MAP2K1c.503A>G (p.Asp168Gly)
c.569A>G (p.Asp190Gly)
c.422A>G (p.Asp141Gly)
c.569-5473A>G (n.569-5473A>G)
n.927A>G
c.620A>G (p.Asn207Ser)
c.569-3239A>G (n.569-3239A>G)
c.425A>G (p.Asp142Gly)
c.41A>G (p.Asn14Ser)
c.491A>G (p.Asp164Gly)
15g.66481755A>TCA392936040MAP2K1c.503A>T (p.Asp168Val)
c.569A>T (p.Asp190Val)
c.422A>T (p.Asp141Val)
c.569-5473A>T (n.569-5473A>T)
n.927A>T
c.620A>T (p.Asn207Ile)
c.569-3239A>T (n.569-3239A>T)
c.425A>T (p.Asp142Val)
c.41A>T (p.Asn14Ile)
c.491A>T (p.Asp164Val)
dbSNP gnomAD v4
15g.66481756T>ACA392936045MAP2K1c.504T>A (p.Asp168Glu)
c.570T>A (p.Asp190Glu)
c.423T>A (p.Asp141Glu)
c.569-5472T>A (n.569-5472T>A)
n.928T>A
c.621T>A (p.Asn207Lys)
c.569-3238T>A (n.569-3238T>A)
c.426T>A (p.Asp142Glu)
c.42T>A (p.Asn14Lys)
c.492T>A (p.Asp164Glu)
15g.66481756T>CCA490858374MAP2K1c.504T>C (p.Asp168=)
c.570T>C (p.Asp190=)
c.423T>C (p.Asp141=)
c.569-5472T>C (n.569-5472T>C)
n.928T>C
c.621T>C (p.Asn207=)
c.569-3238T>C (n.569-3238T>C)
c.426T>C (p.Asp142=)
c.42T>C (p.Asn14=)
c.492T>C (p.Asp164=)
dbSNP
15g.66481756T>GCA392936046MAP2K1c.504T>G (p.Asp168Glu)
c.570T>G (p.Asp190Glu)
c.423T>G (p.Asp141Glu)
c.569-5472T>G (n.569-5472T>G)
n.928T>G
c.621T>G (p.Asn207Lys)
c.569-3238T>G (n.569-3238T>G)
c.426T>G (p.Asp142Glu)
c.42T>G (p.Asn14Lys)
c.492T>G (p.Asp164Glu)
dbSNP
15g.66481757G>ACA392936049MAP2K1c.505G>A (p.Val169Ile)
c.571G>A (p.Val191Ile)
c.424G>A (p.Val142Ile)
c.569-5471G>A (n.569-5471G>A)
n.929G>A
c.622G>A (p.Val208Ile)
c.569-3237G>A (n.569-3237G>A)
c.427G>A (p.Val143Ile)
c.43G>A (p.Val15Ile)
c.493G>A (p.Val165Ile)
dbSNP
15g.66481757G>CCA392936051MAP2K1c.505G>C (p.Val169Leu)
c.571G>C (p.Val191Leu)
c.424G>C (p.Val142Leu)
c.569-5471G>C (n.569-5471G>C)
n.929G>C
c.622G>C (p.Val208Leu)
c.569-3237G>C (n.569-3237G>C)
c.427G>C (p.Val143Leu)
c.43G>C (p.Val15Leu)
c.493G>C (p.Val165Leu)
dbSNP
15g.66481757G>TCA392936053MAP2K1c.505G>T (p.Val169Phe)
c.571G>T (p.Val191Phe)
c.424G>T (p.Val142Phe)
c.569-5471G>T (n.569-5471G>T)
n.929G>T
c.622G>T (p.Val208Phe)
c.569-3237G>T (n.569-3237G>T)
c.427G>T (p.Val143Phe)
c.43G>T (p.Val15Phe)
c.493G>T (p.Val165Phe)
dbSNP
15g.66481758T>ACA392936059MAP2K1c.506T>A (p.Val169Asp)
c.572T>A (p.Val191Asp)
c.425T>A (p.Val142Asp)
c.569-5470T>A (n.569-5470T>A)
n.930T>A
c.623T>A (p.Val208Asp)
c.569-3236T>A (n.569-3236T>A)
c.428T>A (p.Val143Asp)
c.44T>A (p.Val15Asp)
c.494T>A (p.Val165Asp)
dbSNP
15g.66481758T>CCA392936055MAP2K1c.506T>C (p.Val169Ala)
c.572T>C (p.Val191Ala)
c.425T>C (p.Val142Ala)
c.569-5470T>C (n.569-5470T>C)
n.930T>C
c.623T>C (p.Val208Ala)
c.569-3236T>C (n.569-3236T>C)
c.428T>C (p.Val143Ala)
c.44T>C (p.Val15Ala)
c.494T>C (p.Val165Ala)
dbSNP
15g.66481758T>GCA392936057MAP2K1c.506T>G (p.Val169Gly)
c.572T>G (p.Val191Gly)
c.425T>G (p.Val142Gly)
c.569-5470T>G (n.569-5470T>G)
n.930T>G
c.623T>G (p.Val208Gly)
c.569-3236T>G (n.569-3236T>G)
c.428T>G (p.Val143Gly)
c.44T>G (p.Val15Gly)
c.494T>G (p.Val165Gly)
dbSNP
15g.66481759C>ACA490858375MAP2K1c.507C>A (p.Val169=)
c.573C>A (p.Val191=)
c.426C>A (p.Val142=)
c.569-5469C>A (n.569-5469C>A)
n.931C>A
c.624C>A (p.Val208=)
c.569-3235C>A (n.569-3235C>A)
c.429C>A (p.Val143=)
c.45C>A (p.Val15=)
c.495C>A (p.Val165=)
dbSNP
15g.66481759C>GCA490858376MAP2K1c.507C>G (p.Val169=)
c.573C>G (p.Val191=)
c.426C>G (p.Val142=)
c.569-5469C>G (n.569-5469C>G)
n.931C>G
c.624C>G (p.Val208=)
c.569-3235C>G (n.569-3235C>G)
c.429C>G (p.Val143=)
c.45C>G (p.Val15=)
c.495C>G (p.Val165=)
ClinVar dbSNP
15g.66481759C>TCA490858377MAP2K1c.507C>T (p.Val169=)
c.573C>T (p.Val191=)
c.426C>T (p.Val142=)
c.569-5469C>T (n.569-5469C>T)
n.931C>T
c.624C>T (p.Val208=)
c.569-3235C>T (n.569-3235C>T)
c.429C>T (p.Val143=)
c.45C>T (p.Val15=)
c.495C>T (p.Val165=)
dbSNP
15g.66481760A>CCA392936061MAP2K1c.508A>C (p.Lys170Gln)
c.574A>C (p.Lys192Gln)
c.427A>C (p.Lys143Gln)
c.569-5468A>C (n.569-5468A>C)
n.932A>C
c.625A>C (p.Lys209Gln)
c.569-3234A>C (n.569-3234A>C)
c.430A>C (p.Lys144Gln)
c.46A>C (p.Lys16Gln)
c.496A>C (p.Lys166Gln)
15g.66481760A>GCA392936064MAP2K1c.508A>G (p.Lys170Glu)
c.574A>G (p.Lys192Glu)
c.427A>G (p.Lys143Glu)
c.569-5468A>G (n.569-5468A>G)
n.932A>G
c.625A>G (p.Lys209Glu)
c.569-3234A>G (n.569-3234A>G)
c.430A>G (p.Lys144Glu)
c.46A>G (p.Lys16Glu)
c.496A>G (p.Lys166Glu)
dbSNP
15g.66481760A>TCA392936066MAP2K1c.508A>T (p.Lys170Ter)
c.574A>T (p.Lys192Ter)
c.427A>T (p.Lys143Ter)
c.569-5468A>T (n.569-5468A>T)
n.932A>T
c.625A>T (p.Lys209Ter)
c.569-3234A>T (n.569-3234A>T)
c.430A>T (p.Lys144Ter)
c.46A>T (p.Lys16Ter)
c.496A>T (p.Lys166Ter)
dbSNP
15g.66481761A>CCA392936068MAP2K1c.509A>C (p.Lys170Thr)
c.575A>C (p.Lys192Thr)
c.428A>C (p.Lys143Thr)
c.569-5467A>C (n.569-5467A>C)
n.933A>C
c.626A>C (p.Lys209Thr)
c.569-3233A>C (n.569-3233A>C)
c.431A>C (p.Lys144Thr)
c.47A>C (p.Lys16Thr)
c.497A>C (p.Lys166Thr)
15g.66481761A>GCA392936070MAP2K1c.509A>G (p.Lys170Arg)
c.575A>G (p.Lys192Arg)
c.428A>G (p.Lys143Arg)
c.569-5467A>G (n.569-5467A>G)
n.933A>G
c.626A>G (p.Lys209Arg)
c.569-3233A>G (n.569-3233A>G)
c.431A>G (p.Lys144Arg)
c.47A>G (p.Lys16Arg)
c.497A>G (p.Lys166Arg)
dbSNP
15g.66481761A>TCA392936071MAP2K1c.509A>T (p.Lys170Met)
c.575A>T (p.Lys192Met)
c.428A>T (p.Lys143Met)
c.569-5467A>T (n.569-5467A>T)
n.933A>T
c.626A>T (p.Lys209Met)
c.569-3233A>T (n.569-3233A>T)
c.431A>T (p.Lys144Met)
c.47A>T (p.Lys16Met)
c.497A>T (p.Lys166Met)
dbSNP
15g.66481762G>ACA490858378MAP2K1c.510G>A (p.Lys170=)
c.576G>A (p.Lys192=)
c.429G>A (p.Lys143=)
c.569-5466G>A (n.569-5466G>A)
n.934G>A
c.627G>A (p.Lys209=)
c.569-3232G>A (n.569-3232G>A)
c.432G>A (p.Lys144=)
c.48G>A (p.Lys16=)
c.498G>A (p.Lys166=)
dbSNP
15g.66481762G>CCA392936073MAP2K1c.510G>C (p.Lys170Asn)
c.576G>C (p.Lys192Asn)
c.429G>C (p.Lys143Asn)
c.569-5466G>C (n.569-5466G>C)
n.934G>C
c.627G>C (p.Lys209Asn)
c.569-3232G>C (n.569-3232G>C)
c.432G>C (p.Lys144Asn)
c.48G>C (p.Lys16Asn)
c.498G>C (p.Lys166Asn)
dbSNP COSMIC
15g.66481762G>TCA392936075MAP2K1c.510G>T (p.Lys170Asn)
c.576G>T (p.Lys192Asn)
c.429G>T (p.Lys143Asn)
c.569-5466G>T (n.569-5466G>T)
n.934G>T
c.627G>T (p.Lys209Asn)
c.569-3232G>T (n.569-3232G>T)
c.432G>T (p.Lys144Asn)
c.48G>T (p.Lys16Asn)
c.498G>T (p.Lys166Asn)
15g.66481763C>ACA392936077MAP2K1c.511C>A (p.Pro171Thr)
c.577C>A (p.Pro193Thr)
c.430C>A (p.Pro144Thr)
c.569-5465C>A (n.569-5465C>A)
n.935C>A
c.628C>A (p.Pro210Thr)
c.569-3231C>A (n.569-3231C>A)
c.433C>A (p.Pro145Thr)
c.49C>A (p.Pro17Thr)
c.499C>A (p.Pro167Thr)
dbSNP
15g.66481763C=CA2184097385MAP2K1c.511C= (p.Pro171=)
c.577C= (p.Pro193=)
c.430C= (p.Pro144=)
c.569-5465C= (n.569-5465C=)
n.935C=
c.628C= (p.Pro210=)
c.569-3231C= (n.569-3231C=)
c.433C= (p.Pro145=)
c.49C= (p.Pro17=)
c.499C= (p.Pro167=)
15g.66481763C>GCA392936079MAP2K1c.511C>G (p.Pro171Ala)
c.577C>G (p.Pro193Ala)
c.430C>G (p.Pro144Ala)
c.569-5465C>G (n.569-5465C>G)
n.935C>G
c.628C>G (p.Pro210Ala)
c.569-3231C>G (n.569-3231C>G)
c.433C>G (p.Pro145Ala)
c.49C>G (p.Pro17Ala)
c.499C>G (p.Pro167Ala)
ClinVar dbSNP
15g.66481763C>TCA392936081MAP2K1c.511C>T (p.Pro171Ser)
c.577C>T (p.Pro193Ser)
c.430C>T (p.Pro144Ser)
c.569-5465C>T (n.569-5465C>T)
n.935C>T
c.628C>T (p.Pro210Ser)
c.569-3231C>T (n.569-3231C>T)
c.433C>T (p.Pro145Ser)
c.49C>T (p.Pro17Ser)
c.499C>T (p.Pro167Ser)
dbSNP COSMIC
15g.66481764C>ACA392936082MAP2K1c.512C>A (p.Pro171His)
c.578C>A (p.Pro193His)
c.431C>A (p.Pro144His)
c.569-5464C>A (n.569-5464C>A)
n.936C>A
c.629C>A (p.Pro210His)
c.569-3230C>A (n.569-3230C>A)
c.434C>A (p.Pro145His)
c.50C>A (p.Pro17His)
c.500C>A (p.Pro167His)
15g.66481764C>GCA392936084MAP2K1c.512C>G (p.Pro171Arg)
c.578C>G (p.Pro193Arg)
c.431C>G (p.Pro144Arg)
c.569-5464C>G (n.569-5464C>G)
n.936C>G
c.629C>G (p.Pro210Arg)
c.569-3230C>G (n.569-3230C>G)
c.434C>G (p.Pro145Arg)
c.50C>G (p.Pro17Arg)
c.500C>G (p.Pro167Arg)
dbSNP
15g.66481764C>TCA392936086MAP2K1c.512C>T (p.Pro171Leu)
c.578C>T (p.Pro193Leu)
c.431C>T (p.Pro144Leu)
c.569-5464C>T (n.569-5464C>T)
n.936C>T
c.629C>T (p.Pro210Leu)
c.569-3230C>T (n.569-3230C>T)
c.434C>T (p.Pro145Leu)
c.50C>T (p.Pro17Leu)
c.500C>T (p.Pro167Leu)
dbSNP
15g.66481765C>ACA490858380MAP2K1c.513C>A (p.Pro171=)
c.579C>A (p.Pro193=)
c.432C>A (p.Pro144=)
c.569-5463C>A (n.569-5463C>A)
n.937C>A
c.630C>A (p.Pro210=)
c.569-3229C>A (n.569-3229C>A)
c.435C>A (p.Pro145=)
c.51C>A (p.Pro17=)
c.501C>A (p.Pro167=)
15g.66481765C>GCA490858381MAP2K1c.513C>G (p.Pro171=)
c.579C>G (p.Pro193=)
c.432C>G (p.Pro144=)
c.569-5463C>G (n.569-5463C>G)
n.937C>G
c.630C>G (p.Pro210=)
c.569-3229C>G (n.569-3229C>G)
c.435C>G (p.Pro145=)
c.51C>G (p.Pro17=)
c.501C>G (p.Pro167=)
15g.66481765C>TCA490858379MAP2K1c.513C>T (p.Pro171=)
c.579C>T (p.Pro193=)
c.432C>T (p.Pro144=)
c.569-5463C>T (n.569-5463C>T)
n.937C>T
c.630C>T (p.Pro210=)
c.569-3229C>T (n.569-3229C>T)
c.435C>T (p.Pro145=)
c.51C>T (p.Pro17=)
c.501C>T (p.Pro167=)
dbSNP
15g.66481766T>ACA392936092MAP2K1c.514T>A (p.Ser172Thr)
c.580T>A (p.Ser194Thr)
c.433T>A (p.Ser145Thr)
c.569-5462T>A (n.569-5462T>A)
n.938T>A
c.631T>A (p.Ser211Thr)
c.569-3228T>A (n.569-3228T>A)
c.436T>A (p.Ser146Thr)
c.52T>A (p.Ser18Thr)
c.502T>A (p.Ser168Thr)
15g.66481766T>CCA392936090MAP2K1c.514T>C (p.Ser172Pro)
c.580T>C (p.Ser194Pro)
c.433T>C (p.Ser145Pro)
c.569-5462T>C (n.569-5462T>C)
n.938T>C
c.631T>C (p.Ser211Pro)
c.569-3228T>C (n.569-3228T>C)
c.436T>C (p.Ser146Pro)
c.52T>C (p.Ser18Pro)
c.502T>C (p.Ser168Pro)
15g.66481766T>GCA392936088MAP2K1c.514T>G (p.Ser172Ala)
c.580T>G (p.Ser194Ala)
c.433T>G (p.Ser145Ala)
c.569-5462T>G (n.569-5462T>G)
n.938T>G
c.631T>G (p.Ser211Ala)
c.569-3228T>G (n.569-3228T>G)
c.436T>G (p.Ser146Ala)
c.52T>G (p.Ser18Ala)
c.502T>G (p.Ser168Ala)
15g.66481766T=CA2184097388MAP2K1c.514T= (p.Ser172=)
c.580T= (p.Ser194=)
c.433T= (p.Ser145=)
c.569-5462T= (n.569-5462T=)
n.938T=
c.631T= (p.Ser211=)
c.569-3228T= (n.569-3228T=)
c.436T= (p.Ser146=)
c.52T= (p.Ser18=)
c.502T= (p.Ser168=)
15g.66481766_66481767insAGCA970939411MAP2K1c.514_515insAG (p.Ser172Ter)
c.580_581insAG (p.Ser194Ter)
c.433_434insAG (p.Ser145Ter)
c.569-5462_569-5461insAG (n.569-5462_569-5461insAG)
n.938_939insAG
c.631_632insAG (p.Ser211Ter)
c.569-3228_569-3227insAG (n.569-3228_569-3227insAG)
c.436_437insAG (p.Ser146Ter)
c.52_53insAG (p.Ser18Ter)
c.502_503insAG (p.Ser168Ter)
dbSNP gnomAD v3 gnomAD v4
15g.66481767C>ACA392936095MAP2K1c.515C>A (p.Ser172Tyr)
c.581C>A (p.Ser194Tyr)
c.434C>A (p.Ser145Tyr)
c.569-5461C>A (n.569-5461C>A)
n.939C>A
c.632C>A (p.Ser211Tyr)
c.569-3227C>A (n.569-3227C>A)
c.437C>A (p.Ser146Tyr)
c.53C>A (p.Ser18Tyr)
c.503C>A (p.Ser168Tyr)
dbSNP
15g.66481767C=CA2184097390MAP2K1c.515C= (p.Ser172=)
c.581C= (p.Ser194=)
c.434C= (p.Ser145=)
c.569-5461C= (n.569-5461C=)
n.939C=
c.632C= (p.Ser211=)
c.569-3227C= (n.569-3227C=)
c.437C= (p.Ser146=)
c.53C= (p.Ser18=)
c.503C= (p.Ser168=)
15g.66481767C>GCA392936097MAP2K1c.515C>G (p.Ser172Cys)
c.581C>G (p.Ser194Cys)
c.434C>G (p.Ser145Cys)
c.569-5461C>G (n.569-5461C>G)
n.939C>G
c.632C>G (p.Ser211Cys)
c.569-3227C>G (n.569-3227C>G)
c.437C>G (p.Ser146Cys)
c.53C>G (p.Ser18Cys)
c.503C>G (p.Ser168Cys)
dbSNP
15g.66481767C>TCA392936098MAP2K1c.515C>T (p.Ser172Phe)
c.581C>T (p.Ser194Phe)
c.434C>T (p.Ser145Phe)
c.569-5461C>T (n.569-5461C>T)
n.939C>T
c.632C>T (p.Ser211Phe)
c.569-3227C>T (n.569-3227C>T)
c.437C>T (p.Ser146Phe)
c.53C>T (p.Ser18Phe)
c.503C>T (p.Ser168Phe)
dbSNP gnomAD v3 gnomAD v4
15g.66481768C>ACA490858383MAP2K1c.516C>A (p.Ser172=)
c.582C>A (p.Ser194=)
c.435C>A (p.Ser145=)
c.569-5460C>A (n.569-5460C>A)
n.940C>A
c.633C>A (p.Ser211=)
c.569-3226C>A (n.569-3226C>A)
c.438C>A (p.Ser146=)
c.54C>A (p.Ser18=)
c.504C>A (p.Ser168=)
15g.66481768C>GCA490858382MAP2K1c.516C>G (p.Ser172=)
c.582C>G (p.Ser194=)
c.435C>G (p.Ser145=)
c.569-5460C>G (n.569-5460C>G)
n.940C>G
c.633C>G (p.Ser211=)
c.569-3226C>G (n.569-3226C>G)
c.438C>G (p.Ser146=)
c.54C>G (p.Ser18=)
c.504C>G (p.Ser168=)
15g.66481768C>TCA490858384MAP2K1c.516C>T (p.Ser172=)
c.582C>T (p.Ser194=)
c.435C>T (p.Ser145=)
c.569-5460C>T (n.569-5460C>T)
n.940C>T
c.633C>T (p.Ser211=)
c.569-3226C>T (n.569-3226C>T)
c.438C>T (p.Ser146=)
c.54C>T (p.Ser18=)
c.504C>T (p.Ser168=)
gnomAD v4
15g.66481769A>CCA392936100MAP2K1c.517A>C (p.Asn173His)
c.583A>C (p.Asn195His)
c.436A>C (p.Asn146His)
c.569-5459A>C (n.569-5459A>C)
n.941A>C
c.634A>C (p.Asn212His)
c.569-3225A>C (n.569-3225A>C)
c.439A>C (p.Asn147His)
c.55A>C (p.Asn19His)
c.505A>C (p.Asn169His)
15g.66481769A>GCA392936102MAP2K1c.517A>G (p.Asn173Asp)
c.583A>G (p.Asn195Asp)
c.436A>G (p.Asn146Asp)
c.569-5459A>G (n.569-5459A>G)
n.941A>G
c.634A>G (p.Asn212Asp)
c.569-3225A>G (n.569-3225A>G)
c.439A>G (p.Asn147Asp)
c.55A>G (p.Asn19Asp)
c.505A>G (p.Asn169Asp)
15g.66481769A>TCA392936104MAP2K1c.517A>T (p.Asn173Tyr)
c.583A>T (p.Asn195Tyr)
c.436A>T (p.Asn146Tyr)
c.569-5459A>T (n.569-5459A>T)
n.941A>T
c.634A>T (p.Asn212Tyr)
c.569-3225A>T (n.569-3225A>T)
c.439A>T (p.Asn147Tyr)
c.55A>T (p.Asn19Tyr)
c.505A>T (p.Asn169Tyr)
dbSNP
15g.66481770A>CCA392936107MAP2K1c.518A>C (p.Asn173Thr)
c.584A>C (p.Asn195Thr)
c.437A>C (p.Asn146Thr)
c.569-5458A>C (n.569-5458A>C)
n.942A>C
c.635A>C (p.Asn212Thr)
c.569-3224A>C (n.569-3224A>C)
c.440A>C (p.Asn147Thr)
c.56A>C (p.Asn19Thr)
c.506A>C (p.Asn169Thr)
dbSNP
15g.66481770A>GCA392936109MAP2K1c.518A>G (p.Asn173Ser)
c.584A>G (p.Asn195Ser)
c.437A>G (p.Asn146Ser)
c.569-5458A>G (n.569-5458A>G)
n.942A>G
c.635A>G (p.Asn212Ser)
c.569-3224A>G (n.569-3224A>G)
c.440A>G (p.Asn147Ser)
c.56A>G (p.Asn19Ser)
c.506A>G (p.Asn169Ser)
dbSNP gnomAD v4
15g.66481770A>TCA392936108MAP2K1c.518A>T (p.Asn173Ile)
c.584A>T (p.Asn195Ile)
c.437A>T (p.Asn146Ile)
c.569-5458A>T (n.569-5458A>T)
n.942A>T
c.635A>T (p.Asn212Ile)
c.569-3224A>T (n.569-3224A>T)
c.440A>T (p.Asn147Ile)
c.56A>T (p.Asn19Ile)
c.506A>T (p.Asn169Ile)
dbSNP
15g.66481771C>ACA392936111MAP2K1c.519C>A (p.Asn173Lys)
c.585C>A (p.Asn195Lys)
c.438C>A (p.Asn146Lys)
c.569-5457C>A (n.569-5457C>A)
n.943C>A
c.636C>A (p.Asn212Lys)
c.569-3223C>A (n.569-3223C>A)
c.441C>A (p.Asn147Lys)
c.57C>A (p.Asn19Lys)
c.507C>A (p.Asn169Lys)
15g.66481771C=CA2184097392MAP2K1c.519C= (p.Asn173=)
c.585C= (p.Asn195=)
c.438C= (p.Asn146=)
c.569-5457C= (n.569-5457C=)
n.943C=
c.636C= (p.Asn212=)
c.569-3223C= (n.569-3223C=)
c.441C= (p.Asn147=)
c.57C= (p.Asn19=)
c.507C= (p.Asn169=)
15g.66481771C>GCA392936113MAP2K1c.519C>G (p.Asn173Lys)
c.585C>G (p.Asn195Lys)
c.438C>G (p.Asn146Lys)
c.569-5457C>G (n.569-5457C>G)
n.943C>G
c.636C>G (p.Asn212Lys)
c.569-3223C>G (n.569-3223C>G)
c.441C>G (p.Asn147Lys)
c.57C>G (p.Asn19Lys)
c.507C>G (p.Asn169Lys)
dbSNP
15g.66481771C>TCA490858385MAP2K1c.519C>T (p.Asn173=)
c.585C>T (p.Asn195=)
c.438C>T (p.Asn146=)
c.569-5457C>T (n.569-5457C>T)
n.943C>T
c.636C>T (p.Asn212=)
c.569-3223C>T (n.569-3223C>T)
c.441C>T (p.Asn147=)
c.57C>T (p.Asn19=)
c.507C>T (p.Asn169=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.66481772A>CCA392936115MAP2K1c.520A>C (p.Ile174Leu)
c.586A>C (p.Ile196Leu)
c.439A>C (p.Ile147Leu)
c.569-5456A>C (n.569-5456A>C)
n.944A>C
c.637A>C (p.Ile213Leu)
c.569-3222A>C (n.569-3222A>C)
c.442A>C (p.Ile148Leu)
c.58A>C (p.Ile20Leu)
c.508A>C (p.Ile170Leu)
15g.66481772A>GCA392936116MAP2K1c.520A>G (p.Ile174Val)
c.586A>G (p.Ile196Val)
c.439A>G (p.Ile147Val)
c.569-5456A>G (n.569-5456A>G)
n.944A>G
c.637A>G (p.Ile213Val)
c.569-3222A>G (n.569-3222A>G)
c.442A>G (p.Ile148Val)
c.58A>G (p.Ile20Val)
c.508A>G (p.Ile170Val)
ClinVar dbSNP gnomAD v4
15g.66481772A>TCA392936118MAP2K1c.520A>T (p.Ile174Phe)
c.586A>T (p.Ile196Phe)
c.439A>T (p.Ile147Phe)
c.569-5456A>T (n.569-5456A>T)
n.944A>T
c.637A>T (p.Ile213Phe)
c.569-3222A>T (n.569-3222A>T)
c.442A>T (p.Ile148Phe)
c.58A>T (p.Ile20Phe)
c.508A>T (p.Ile170Phe)
dbSNP
15g.66481773T>ACA392936120MAP2K1c.521T>A (p.Ile174Asn)
c.587T>A (p.Ile196Asn)
c.440T>A (p.Ile147Asn)
c.569-5455T>A (n.569-5455T>A)
n.945T>A
c.638T>A (p.Ile213Asn)
c.569-3221T>A (n.569-3221T>A)
c.443T>A (p.Ile148Asn)
c.59T>A (p.Ile20Asn)
c.509T>A (p.Ile170Asn)
dbSNP
15g.66481773T>CCA392936122MAP2K1c.521T>C (p.Ile174Thr)
c.587T>C (p.Ile196Thr)
c.440T>C (p.Ile147Thr)
c.569-5455T>C (n.569-5455T>C)
n.945T>C
c.638T>C (p.Ile213Thr)
c.569-3221T>C (n.569-3221T>C)
c.443T>C (p.Ile148Thr)
c.59T>C (p.Ile20Thr)
c.509T>C (p.Ile170Thr)
15g.66481773T>GCA392936124MAP2K1c.521T>G (p.Ile174Ser)
c.587T>G (p.Ile196Ser)
c.440T>G (p.Ile147Ser)
c.569-5455T>G (n.569-5455T>G)
n.945T>G
c.638T>G (p.Ile213Ser)
c.569-3221T>G (n.569-3221T>G)
c.443T>G (p.Ile148Ser)
c.59T>G (p.Ile20Ser)
c.509T>G (p.Ile170Ser)
15g.66481774C>ACA490858387MAP2K1c.522C>A (p.Ile174=)
c.588C>A (p.Ile196=)
c.441C>A (p.Ile147=)
c.569-5454C>A (n.569-5454C>A)
n.946C>A
c.639C>A (p.Ile213=)
c.569-3220C>A (n.569-3220C>A)
c.444C>A (p.Ile148=)
c.60C>A (p.Ile20=)
c.510C>A (p.Ile170=)
15g.66481774C>GCA392936126MAP2K1c.522C>G (p.Ile174Met)
c.588C>G (p.Ile196Met)
c.441C>G (p.Ile147Met)
c.569-5454C>G (n.569-5454C>G)
n.946C>G
c.639C>G (p.Ile213Met)
c.569-3220C>G (n.569-3220C>G)
c.444C>G (p.Ile148Met)
c.60C>G (p.Ile20Met)
c.510C>G (p.Ile170Met)
dbSNP
15g.66481774C>TCA490858386MAP2K1c.522C>T (p.Ile174=)
c.588C>T (p.Ile196=)
c.441C>T (p.Ile147=)
c.569-5454C>T (n.569-5454C>T)
n.946C>T
c.639C>T (p.Ile213=)
c.569-3220C>T (n.569-3220C>T)
c.444C>T (p.Ile148=)
c.60C>T (p.Ile20=)
c.510C>T (p.Ile170=)
dbSNP
15g.66481775C>ACA392936128MAP2K1c.523C>A (p.Leu175Ile)
c.589C>A (p.Leu197Ile)
c.442C>A (p.Leu148Ile)
c.569-5453C>A (n.569-5453C>A)
n.947C>A
c.640C>A (p.Leu214Ile)
c.569-3219C>A (n.569-3219C>A)
c.445C>A (p.Leu149Ile)
c.61C>A (p.Leu21Ile)
c.511C>A (p.Leu171Ile)
dbSNP
15g.66481775C=CA2184097393MAP2K1c.523C= (p.Leu175=)
c.589C= (p.Leu197=)
c.442C= (p.Leu148=)
c.569-5453C= (n.569-5453C=)
n.947C=
c.640C= (p.Leu214=)
c.569-3219C= (n.569-3219C=)
c.445C= (p.Leu149=)
c.61C= (p.Leu21=)
c.511C= (p.Leu171=)
15g.66481775C>GCA392936130MAP2K1c.523C>G (p.Leu175Val)
c.589C>G (p.Leu197Val)
c.442C>G (p.Leu148Val)
c.569-5453C>G (n.569-5453C>G)
n.947C>G
c.640C>G (p.Leu214Val)
c.569-3219C>G (n.569-3219C>G)
c.445C>G (p.Leu149Val)
c.61C>G (p.Leu21Val)
c.511C>G (p.Leu171Val)
dbSNP
15g.66481775C>TCA490858388MAP2K1c.523C>T (p.Leu175=)
c.589C>T (p.Leu197=)
c.442C>T (p.Leu148=)
c.569-5453C>T (n.569-5453C>T)
n.947C>T
c.640C>T (p.Leu214=)
c.569-3219C>T (n.569-3219C>T)
c.445C>T (p.Leu149=)
c.61C>T (p.Leu21=)
c.511C>T (p.Leu171=)
ClinVar dbSNP gnomAD v2 gnomAD v4
15g.66481776T>ACA392936132MAP2K1c.524T>A (p.Leu175Gln)
c.590T>A (p.Leu197Gln)
c.443T>A (p.Leu148Gln)
c.569-5452T>A (n.569-5452T>A)
n.948T>A
c.641T>A (p.Leu214Gln)
c.569-3218T>A (n.569-3218T>A)
c.446T>A (p.Leu149Gln)
c.62T>A (p.Leu21Gln)
c.512T>A (p.Leu171Gln)
dbSNP
15g.66481776T>CCA392936136MAP2K1c.524T>C (p.Leu175Pro)
c.590T>C (p.Leu197Pro)
c.443T>C (p.Leu148Pro)
c.569-5452T>C (n.569-5452T>C)
n.948T>C
c.641T>C (p.Leu214Pro)
c.569-3218T>C (n.569-3218T>C)
c.446T>C (p.Leu149Pro)
c.62T>C (p.Leu21Pro)
c.512T>C (p.Leu171Pro)
15g.66481776T>GCA392936134MAP2K1c.524T>G (p.Leu175Arg)
c.590T>G (p.Leu197Arg)
c.443T>G (p.Leu148Arg)
c.569-5452T>G (n.569-5452T>G)
n.948T>G
c.641T>G (p.Leu214Arg)
c.569-3218T>G (n.569-3218T>G)
c.446T>G (p.Leu149Arg)
c.62T>G (p.Leu21Arg)
c.512T>G (p.Leu171Arg)
15g.66481777A>CCA490858391MAP2K1c.525A>C (p.Leu175=)
c.591A>C (p.Leu197=)
c.444A>C (p.Leu148=)
c.569-5451A>C (n.569-5451A>C)
n.949A>C
c.642A>C (p.Leu214=)
c.569-3217A>C (n.569-3217A>C)
c.447A>C (p.Leu149=)
c.63A>C (p.Leu21=)
c.513A>C (p.Leu171=)
15g.66481777A>GCA490858389MAP2K1c.525A>G (p.Leu175=)
c.591A>G (p.Leu197=)
c.444A>G (p.Leu148=)
c.569-5451A>G (n.569-5451A>G)
n.949A>G
c.642A>G (p.Leu214=)
c.569-3217A>G (n.569-3217A>G)
c.447A>G (p.Leu149=)
c.63A>G (p.Leu21=)
c.513A>G (p.Leu171=)
dbSNP
15g.66481777A>TCA490858390MAP2K1c.525A>T (p.Leu175=)
c.591A>T (p.Leu197=)
c.444A>T (p.Leu148=)
c.569-5451A>T (n.569-5451A>T)
n.949A>T
c.642A>T (p.Leu214=)
c.569-3217A>T (n.569-3217A>T)
c.447A>T (p.Leu149=)
c.63A>T (p.Leu21=)
c.513A>T (p.Leu171=)
dbSNP
15g.66481778G>ACA392936138MAP2K1c.526G>A (p.Val176Ile)
c.592G>A (p.Val198Ile)
c.445G>A (p.Val149Ile)
c.569-5450G>A (n.569-5450G>A)
n.950G>A
c.643G>A (p.Val215Ile)
c.569-3216G>A (n.569-3216G>A)
c.448G>A (p.Val150Ile)
c.64G>A (p.Val22Ile)
c.514G>A (p.Val172Ile)
dbSNP
15g.66481778G>CCA7623991MAP2K1c.526G>C (p.Val176Leu)
c.592G>C (p.Val198Leu)
c.445G>C (p.Val149Leu)
c.569-5450G>C (n.569-5450G>C)
n.950G>C
c.643G>C (p.Val215Leu)
c.569-3216G>C (n.569-3216G>C)
c.448G>C (p.Val150Leu)
c.64G>C (p.Val22Leu)
c.514G>C (p.Val172Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
15g.66481778G=CA2184097395MAP2K1c.526G= (p.Val176=)
c.592G= (p.Val198=)
c.445G= (p.Val149=)
c.569-5450G= (n.569-5450G=)
n.950G=
c.643G= (p.Val215=)
c.569-3216G= (n.569-3216G=)
c.448G= (p.Val150=)
c.64G= (p.Val22=)
c.514G= (p.Val172=)
15g.66481778G>TCA392936140MAP2K1c.526G>T (p.Val176Phe)
c.592G>T (p.Val198Phe)
c.445G>T (p.Val149Phe)
c.569-5450G>T (n.569-5450G>T)
n.950G>T
c.643G>T (p.Val215Phe)
c.569-3216G>T (n.569-3216G>T)
c.448G>T (p.Val150Phe)
c.64G>T (p.Val22Phe)
c.514G>T (p.Val172Phe)
15g.66481779T>ACA392936143MAP2K1c.527T>A (p.Val176Asp)
c.593T>A (p.Val198Asp)
c.446T>A (p.Val149Asp)
c.569-5449T>A (n.569-5449T>A)
n.951T>A
c.644T>A (p.Val215Asp)
c.569-3215T>A (n.569-3215T>A)
c.449T>A (p.Val150Asp)
c.65T>A (p.Val22Asp)
c.515T>A (p.Val172Asp)
dbSNP
15g.66481779T>CCA392936145MAP2K1c.527T>C (p.Val176Ala)
c.593T>C (p.Val198Ala)
c.446T>C (p.Val149Ala)
c.569-5449T>C (n.569-5449T>C)
n.951T>C
c.644T>C (p.Val215Ala)
c.569-3215T>C (n.569-3215T>C)
c.449T>C (p.Val150Ala)
c.65T>C (p.Val22Ala)
c.515T>C (p.Val172Ala)
dbSNP
15g.66481779T>GCA392936147MAP2K1c.527T>G (p.Val176Gly)
c.593T>G (p.Val198Gly)
c.446T>G (p.Val149Gly)
c.569-5449T>G (n.569-5449T>G)
n.951T>G
c.644T>G (p.Val215Gly)
c.569-3215T>G (n.569-3215T>G)
c.449T>G (p.Val150Gly)
c.65T>G (p.Val22Gly)
c.515T>G (p.Val172Gly)
dbSNP
15g.66481780C>ACA490858393MAP2K1c.528C>A (p.Val176=)
c.594C>A (p.Val198=)
c.447C>A (p.Val149=)
c.569-5448C>A (n.569-5448C>A)
n.952C>A
c.645C>A (p.Val215=)
c.569-3214C>A (n.569-3214C>A)
c.450C>A (p.Val150=)
c.66C>A (p.Val22=)
c.516C>A (p.Val172=)
dbSNP
15g.66481780C=CA2184097398MAP2K1c.528C= (p.Val176=)
c.594C= (p.Val198=)
c.447C= (p.Val149=)
c.569-5448C= (n.569-5448C=)
n.952C=
c.645C= (p.Val215=)
c.569-3214C= (n.569-3214C=)
c.450C= (p.Val150=)
c.66C= (p.Val22=)
c.516C= (p.Val172=)
15g.66481780C>GCA490858392MAP2K1c.528C>G (p.Val176=)
c.594C>G (p.Val198=)
c.447C>G (p.Val149=)
c.569-5448C>G (n.569-5448C>G)
n.952C>G
c.645C>G (p.Val215=)
c.569-3214C>G (n.569-3214C>G)
c.450C>G (p.Val150=)
c.66C>G (p.Val22=)
c.516C>G (p.Val172=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.66481780C>TCA490858394MAP2K1c.528C>T (p.Val176=)
c.594C>T (p.Val198=)
c.447C>T (p.Val149=)
c.569-5448C>T (n.569-5448C>T)
n.952C>T
c.645C>T (p.Val215=)
c.569-3214C>T (n.569-3214C>T)
c.450C>T (p.Val150=)
c.66C>T (p.Val22=)
c.516C>T (p.Val172=)
dbSNP gnomAD v2 gnomAD v4
15g.66481781A>CCA392936150MAP2K1c.529A>C (p.Asn177His)
c.595A>C (p.Asn199His)
c.448A>C (p.Asn150His)
c.569-5447A>C (n.569-5447A>C)
n.953A>C
c.646A>C (p.Asn216His)
c.569-3213A>C (n.569-3213A>C)
c.451A>C (p.Asn151His)
c.67A>C (p.Asn23His)
c.517A>C (p.Asn173His)
15g.66481781A>GCA392936151MAP2K1c.529A>G (p.Asn177Asp)
c.595A>G (p.Asn199Asp)
c.448A>G (p.Asn150Asp)
c.569-5447A>G (n.569-5447A>G)
n.953A>G
c.646A>G (p.Asn216Asp)
c.569-3213A>G (n.569-3213A>G)
c.451A>G (p.Asn151Asp)
c.67A>G (p.Asn23Asp)
c.517A>G (p.Asn173Asp)
15g.66481781A>TCA392936153MAP2K1c.529A>T (p.Asn177Tyr)
c.595A>T (p.Asn199Tyr)
c.448A>T (p.Asn150Tyr)
c.569-5447A>T (n.569-5447A>T)
n.953A>T
c.646A>T (p.Asn216Tyr)
c.569-3213A>T (n.569-3213A>T)
c.451A>T (p.Asn151Tyr)
c.67A>T (p.Asn23Tyr)
c.517A>T (p.Asn173Tyr)
15g.66481782A=CA2184097400MAP2K1c.530A= (p.Asn177=)
c.596A= (p.Asn199=)
c.449A= (p.Asn150=)
c.569-5446A= (n.569-5446A=)
n.954A=
c.647A= (p.Asn216=)
c.569-3212A= (n.569-3212A=)
c.452A= (p.Asn151=)
c.68A= (p.Asn23=)
c.518A= (p.Asn173=)
15g.66481782A>CCA392936156MAP2K1c.530A>C (p.Asn177Thr)
c.596A>C (p.Asn199Thr)
c.449A>C (p.Asn150Thr)
c.569-5446A>C (n.569-5446A>C)
n.954A>C
c.647A>C (p.Asn216Thr)
c.569-3212A>C (n.569-3212A>C)
c.452A>C (p.Asn151Thr)
c.68A>C (p.Asn23Thr)
c.518A>C (p.Asn173Thr)
dbSNP
15g.66481782A>GCA392936157MAP2K1c.530A>G (p.Asn177Ser)
c.596A>G (p.Asn199Ser)
c.449A>G (p.Asn150Ser)
c.569-5446A>G (n.569-5446A>G)
n.954A>G
c.647A>G (p.Asn216Ser)
c.569-3212A>G (n.569-3212A>G)
c.452A>G (p.Asn151Ser)
c.68A>G (p.Asn23Ser)
c.518A>G (p.Asn173Ser)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.66481782A>TCA392936160MAP2K1c.530A>T (p.Asn177Ile)
c.596A>T (p.Asn199Ile)
c.449A>T (p.Asn150Ile)
c.569-5446A>T (n.569-5446A>T)
n.954A>T
c.647A>T (p.Asn216Ile)
c.569-3212A>T (n.569-3212A>T)
c.452A>T (p.Asn151Ile)
c.68A>T (p.Asn23Ile)
c.518A>T (p.Asn173Ile)
dbSNP
15g.66481783C>ACA392936162MAP2K1c.531C>A (p.Asn177Lys)
c.597C>A (p.Asn199Lys)
c.450C>A (p.Asn150Lys)
c.569-5445C>A (n.569-5445C>A)
n.955C>A
c.648C>A (p.Asn216Lys)
c.569-3211C>A (n.569-3211C>A)
c.453C>A (p.Asn151Lys)
c.69C>A (p.Asn23Lys)
c.519C>A (p.Asn173Lys)
15g.66481783C>GCA392936163MAP2K1c.531C>G (p.Asn177Lys)
c.597C>G (p.Asn199Lys)
c.450C>G (p.Asn150Lys)
c.569-5445C>G (n.569-5445C>G)
n.955C>G
c.648C>G (p.Asn216Lys)
c.569-3211C>G (n.569-3211C>G)
c.453C>G (p.Asn151Lys)
c.69C>G (p.Asn23Lys)
c.519C>G (p.Asn173Lys)
dbSNP
15g.66481783C>TCA490858395MAP2K1c.531C>T (p.Asn177=)
c.597C>T (p.Asn199=)
c.450C>T (p.Asn150=)
c.569-5445C>T (n.569-5445C>T)
n.955C>T
c.648C>T (p.Asn216=)
c.569-3211C>T (n.569-3211C>T)
c.453C>T (p.Asn151=)
c.69C>T (p.Asn23=)
c.519C>T (p.Asn173=)
dbSNP
15g.66481784T>ACA392936169MAP2K1c.532T>A (p.Ser178Thr)
c.598T>A (p.Ser200Thr)
c.451T>A (p.Ser151Thr)
c.569-5444T>A (n.569-5444T>A)
n.956T>A
c.649T>A (p.Ser217Thr)
c.569-3210T>A (n.569-3210T>A)
c.454T>A (p.Ser152Thr)
c.70T>A (p.Ser24Thr)
c.520T>A (p.Ser174Thr)
15g.66481784T>CCA392936167MAP2K1c.532T>C (p.Ser178Pro)
c.598T>C (p.Ser200Pro)
c.451T>C (p.Ser151Pro)
c.569-5444T>C (n.569-5444T>C)
n.956T>C
c.649T>C (p.Ser217Pro)
c.569-3210T>C (n.569-3210T>C)
c.454T>C (p.Ser152Pro)
c.70T>C (p.Ser24Pro)
c.520T>C (p.Ser174Pro)
gnomAD v4
15g.66481784T>GCA392936165MAP2K1c.532T>G (p.Ser178Ala)
c.598T>G (p.Ser200Ala)
c.451T>G (p.Ser151Ala)
c.569-5444T>G (n.569-5444T>G)
n.956T>G
c.649T>G (p.Ser217Ala)
c.569-3210T>G (n.569-3210T>G)
c.454T>G (p.Ser152Ala)
c.70T>G (p.Ser24Ala)
c.520T>G (p.Ser174Ala)
15g.66481785C>ACA392936171MAP2K1c.533C>A (p.Ser178Tyr)
c.599C>A (p.Ser200Tyr)
c.452C>A (p.Ser151Tyr)
c.569-5443C>A (n.569-5443C>A)
n.957C>A
c.650C>A (p.Ser217Tyr)
c.569-3209C>A (n.569-3209C>A)
c.455C>A (p.Ser152Tyr)
c.71C>A (p.Ser24Tyr)
c.521C>A (p.Ser174Tyr)
dbSNP COSMIC
15g.66481785C>GCA392936172MAP2K1c.533C>G (p.Ser178Cys)
c.599C>G (p.Ser200Cys)
c.452C>G (p.Ser151Cys)
c.569-5443C>G (n.569-5443C>G)
n.957C>G
c.650C>G (p.Ser217Cys)
c.569-3209C>G (n.569-3209C>G)
c.455C>G (p.Ser152Cys)
c.71C>G (p.Ser24Cys)
c.521C>G (p.Ser174Cys)
dbSNP
15g.66481785C>TCA392936174MAP2K1c.533C>T (p.Ser178Phe)
c.599C>T (p.Ser200Phe)
c.452C>T (p.Ser151Phe)
c.569-5443C>T (n.569-5443C>T)
n.957C>T
c.650C>T (p.Ser217Phe)
c.569-3209C>T (n.569-3209C>T)
c.455C>T (p.Ser152Phe)
c.71C>T (p.Ser24Phe)
c.521C>T (p.Ser174Phe)
dbSNP gnomAD v4
15g.66481786C>ACA490858396MAP2K1c.534C>A (p.Ser178=)
c.600C>A (p.Ser200=)
c.453C>A (p.Ser151=)
c.569-5442C>A (n.569-5442C>A)
n.958C>A
c.651C>A (p.Ser217=)
c.569-3208C>A (n.569-3208C>A)
c.456C>A (p.Ser152=)
c.72C>A (p.Ser24=)
c.522C>A (p.Ser174=)
dbSNP
15g.66481786C>GCA490858397MAP2K1c.534C>G (p.Ser178=)
c.600C>G (p.Ser200=)
c.453C>G (p.Ser151=)
c.569-5442C>G (n.569-5442C>G)
n.958C>G
c.651C>G (p.Ser217=)
c.569-3208C>G (n.569-3208C>G)
c.456C>G (p.Ser152=)
c.72C>G (p.Ser24=)
c.522C>G (p.Ser174=)
dbSNP
15g.66481786C>TCA490858398MAP2K1c.534C>T (p.Ser178=)
c.600C>T (p.Ser200=)
c.453C>T (p.Ser151=)
c.569-5442C>T (n.569-5442C>T)
n.958C>T
c.651C>T (p.Ser217=)
c.569-3208C>T (n.569-3208C>T)
c.456C>T (p.Ser152=)
c.72C>T (p.Ser24=)
c.522C>T (p.Ser174=)
ClinVar dbSNP
15g.66481787C>ACA392936176MAP2K1c.535C>A (p.Arg179Ser)
c.601C>A (p.Arg201Ser)
c.454C>A (p.Arg152Ser)
c.569-5441C>A (n.569-5441C>A)
n.959C>A
c.652C>A (p.Arg218Ser)
c.569-3207C>A (n.569-3207C>A)
c.457C>A (p.Arg153Ser)
c.73C>A (p.Arg25Ser)
c.523C>A (p.Arg175Ser)
dbSNP gnomAD v4 COSMIC
15g.66481787C=CA2184097402MAP2K1c.535C= (p.Arg179=)
c.601C= (p.Arg201=)
c.454C= (p.Arg152=)
c.569-5441C= (n.569-5441C=)
n.959C=
c.652C= (p.Arg218=)
c.569-3207C= (n.569-3207C=)
c.457C= (p.Arg153=)
c.73C= (p.Arg25=)
c.523C= (p.Arg175=)
15g.66481787C>GCA392936178MAP2K1c.535C>G (p.Arg179Gly)
c.601C>G (p.Arg201Gly)
c.454C>G (p.Arg152Gly)
c.569-5441C>G (n.569-5441C>G)
n.959C>G
c.652C>G (p.Arg218Gly)
c.569-3207C>G (n.569-3207C>G)
c.457C>G (p.Arg153Gly)
c.73C>G (p.Arg25Gly)
c.523C>G (p.Arg175Gly)
dbSNP
15g.66481787C>TCA7623992MAP2K1c.535C>T (p.Arg179Cys)
c.601C>T (p.Arg201Cys)
c.454C>T (p.Arg152Cys)
c.569-5441C>T (n.569-5441C>T)
n.959C>T
c.652C>T (p.Arg218Cys)
c.569-3207C>T (n.569-3207C>T)
c.457C>T (p.Arg153Cys)
c.73C>T (p.Arg25Cys)
c.523C>T (p.Arg175Cys)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
15g.66481788G>ACA392936181MAP2K1c.536G>A (p.Arg179His)
c.602G>A (p.Arg201His)
c.455G>A (p.Arg152His)
c.569-5440G>A (n.569-5440G>A)
n.960G>A
c.653G>A (p.Arg218His)
c.569-3206G>A (n.569-3206G>A)
c.458G>A (p.Arg153His)
c.74G>A (p.Arg25His)
c.524G>A (p.Arg175His)
ClinVar dbSNP gnomAD v4 COSMIC
15g.66481788G>CCA392936183MAP2K1c.536G>C (p.Arg179Pro)
c.602G>C (p.Arg201Pro)
c.455G>C (p.Arg152Pro)
c.569-5440G>C (n.569-5440G>C)
n.960G>C
c.653G>C (p.Arg218Pro)
c.569-3206G>C (n.569-3206G>C)
c.458G>C (p.Arg153Pro)
c.74G>C (p.Arg25Pro)
c.524G>C (p.Arg175Pro)
dbSNP
15g.66481788G>TCA392936184MAP2K1c.536G>T (p.Arg179Leu)
c.602G>T (p.Arg201Leu)
c.455G>T (p.Arg152Leu)
c.569-5440G>T (n.569-5440G>T)
n.960G>T
c.653G>T (p.Arg218Leu)
c.569-3206G>T (n.569-3206G>T)
c.458G>T (p.Arg153Leu)
c.74G>T (p.Arg25Leu)
c.524G>T (p.Arg175Leu)
dbSNP
15g.66481789T>ACA490858400MAP2K1c.537T>A (p.Arg179=)
c.603T>A (p.Arg201=)
c.456T>A (p.Arg152=)
c.569-5439T>A (n.569-5439T>A)
n.961T>A
c.654T>A (p.Arg218=)
c.569-3205T>A (n.569-3205T>A)
c.459T>A (p.Arg153=)
c.75T>A (p.Arg25=)
c.525T>A (p.Arg175=)
dbSNP
15g.66481789T>CCA490858401MAP2K1c.537T>C (p.Arg179=)
c.603T>C (p.Arg201=)
c.456T>C (p.Arg152=)
c.569-5439T>C (n.569-5439T>C)
n.961T>C
c.654T>C (p.Arg218=)
c.569-3205T>C (n.569-3205T>C)
c.459T>C (p.Arg153=)
c.75T>C (p.Arg25=)
c.525T>C (p.Arg175=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.66481789T>GCA490858399MAP2K1c.537T>G (p.Arg179=)
c.603T>G (p.Arg201=)
c.456T>G (p.Arg152=)
c.569-5439T>G (n.569-5439T>G)
n.961T>G
c.654T>G (p.Arg218=)
c.569-3205T>G (n.569-3205T>G)
c.459T>G (p.Arg153=)
c.75T>G (p.Arg25=)
c.525T>G (p.Arg175=)
15g.66481789T=CA2184097405MAP2K1c.537T= (p.Arg179=)
c.603T= (p.Arg201=)
c.456T= (p.Arg152=)
c.569-5439T= (n.569-5439T=)
n.961T=
c.654T= (p.Arg218=)
c.569-3205T= (n.569-3205T=)
c.459T= (p.Arg153=)
c.75T= (p.Arg25=)
c.525T= (p.Arg175=)
15g.66481790G>ACA392936185MAP2K1c.538G>A (p.Gly180Arg)
c.604G>A (p.Gly202Arg)
c.457G>A (p.Gly153Arg)
c.569-5438G>A (n.569-5438G>A)
n.962G>A
c.655G>A (p.Gly219Arg)
c.569-3204G>A (n.569-3204G>A)
c.460G>A (p.Gly154Arg)
c.76G>A (p.Gly26Arg)
c.526G>A (p.Gly176Arg)
dbSNP
15g.66481790G>CCA392936187MAP2K1c.538G>C (p.Gly180Arg)
c.604G>C (p.Gly202Arg)
c.457G>C (p.Gly153Arg)
c.569-5438G>C (n.569-5438G>C)
n.962G>C
c.655G>C (p.Gly219Arg)
c.569-3204G>C (n.569-3204G>C)
c.460G>C (p.Gly154Arg)
c.76G>C (p.Gly26Arg)
c.526G>C (p.Gly176Arg)
dbSNP
15g.66481790G>TCA392936189MAP2K1c.538G>T (p.Gly180Trp)
c.604G>T (p.Gly202Trp)
c.457G>T (p.Gly153Trp)
c.569-5438G>T (n.569-5438G>T)
n.962G>T
c.655G>T (p.Gly219Trp)
c.569-3204G>T (n.569-3204G>T)
c.460G>T (p.Gly154Trp)
c.76G>T (p.Gly26Trp)
c.526G>T (p.Gly176Trp)
dbSNP
15g.66481791G>ACA392936194MAP2K1c.539G>A (p.Gly180Glu)
c.605G>A (p.Gly202Glu)
c.458G>A (p.Gly153Glu)
c.569-5437G>A (n.569-5437G>A)
n.963G>A
c.656G>A (p.Gly219Glu)
c.569-3203G>A (n.569-3203G>A)
c.461G>A (p.Gly154Glu)
c.77G>A (p.Gly26Glu)
c.527G>A (p.Gly176Glu)
dbSNP
15g.66481791G>CCA392936192MAP2K1c.539G>C (p.Gly180Ala)
c.605G>C (p.Gly202Ala)
c.458G>C (p.Gly153Ala)
c.569-5437G>C (n.569-5437G>C)
n.963G>C
c.656G>C (p.Gly219Ala)
c.569-3203G>C (n.569-3203G>C)
c.461G>C (p.Gly154Ala)
c.77G>C (p.Gly26Ala)
c.527G>C (p.Gly176Ala)
dbSNP
15g.66481791G>TCA392936191MAP2K1c.539G>T (p.Gly180Val)
c.605G>T (p.Gly202Val)
c.458G>T (p.Gly153Val)
c.569-5437G>T (n.569-5437G>T)
n.963G>T
c.656G>T (p.Gly219Val)
c.569-3203G>T (n.569-3203G>T)
c.461G>T (p.Gly154Val)
c.77G>T (p.Gly26Val)
c.527G>T (p.Gly176Val)
dbSNP
15g.66481792G>ACA7623993MAP2K1c.540G>A (p.Gly180=)
c.606G>A (p.Gly202=)
c.459G>A (p.Gly153=)
c.569-5436G>A (n.569-5436G>A)
n.964G>A
c.657G>A (p.Gly219=)
c.569-3202G>A (n.569-3202G>A)
c.462G>A (p.Gly154=)
c.78G>A (p.Gly26=)
c.528G>A (p.Gly176=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.66481792G>CCA490858402MAP2K1c.540G>C (p.Gly180=)
c.606G>C (p.Gly202=)
c.459G>C (p.Gly153=)
c.569-5436G>C (n.569-5436G>C)
n.964G>C
c.657G>C (p.Gly219=)
c.569-3202G>C (n.569-3202G>C)
c.462G>C (p.Gly154=)
c.78G>C (p.Gly26=)
c.528G>C (p.Gly176=)
dbSNP
15g.66481792G=CA2184097407MAP2K1c.540G= (p.Gly180=)
c.606G= (p.Gly202=)
c.459G= (p.Gly153=)
c.569-5436G= (n.569-5436G=)
n.964G=
c.657G= (p.Gly219=)
c.569-3202G= (n.569-3202G=)
c.462G= (p.Gly154=)
c.78G= (p.Gly26=)
c.528G= (p.Gly176=)
15g.66481792G>TCA490858403MAP2K1c.540G>T (p.Gly180=)
c.606G>T (p.Gly202=)
c.459G>T (p.Gly153=)
c.569-5436G>T (n.569-5436G>T)
n.964G>T
c.657G>T (p.Gly219=)
c.569-3202G>T (n.569-3202G>T)
c.462G>T (p.Gly154=)
c.78G>T (p.Gly26=)
c.528G>T (p.Gly176=)
dbSNP
15g.66481793G>ACA16602457MAP2K1c.541G>A (p.Glu181Lys)
c.607G>A (p.Glu203Lys)
c.460G>A (p.Glu154Lys)
c.569-5435G>A (n.569-5435G>A)
n.965G>A
c.658G>A (p.Glu220Lys)
c.569-3201G>A (n.569-3201G>A)
c.463G>A (p.Glu155Lys)
c.79G>A (p.Glu27Lys)
c.529G>A (p.Glu177Lys)
ClinVar dbSNP COSMIC
15g.66481793G>CCA392936198MAP2K1c.541G>C (p.Glu181Gln)
c.607G>C (p.Glu203Gln)
c.460G>C (p.Glu154Gln)
c.569-5435G>C (n.569-5435G>C)
n.965G>C
c.658G>C (p.Glu220Gln)
c.569-3201G>C (n.569-3201G>C)
c.463G>C (p.Glu155Gln)
c.79G>C (p.Glu27Gln)
c.529G>C (p.Glu177Gln)
ClinVar dbSNP
15g.66481793G=CA2184097409MAP2K1c.541G= (p.Glu181=)
c.607G= (p.Glu203=)
c.460G= (p.Glu154=)
c.569-5435G= (n.569-5435G=)
n.965G=
c.658G= (p.Glu220=)
c.569-3201G= (n.569-3201G=)
c.463G= (p.Glu155=)
c.79G= (p.Glu27=)
c.529G= (p.Glu177=)
15g.66481793G>TCA392936200MAP2K1c.541G>T (p.Glu181Ter)
c.607G>T (p.Glu203Ter)
c.460G>T (p.Glu154Ter)
c.569-5435G>T (n.569-5435G>T)
n.965G>T
c.658G>T (p.Glu220Ter)
c.569-3201G>T (n.569-3201G>T)
c.463G>T (p.Glu155Ter)
c.79G>T (p.Glu27Ter)
c.529G>T (p.Glu177Ter)
dbSNP
15g.66481794A=CA2184097414MAP2K1c.542A= (p.Glu181=)
c.608A= (p.Glu203=)
c.461A= (p.Glu154=)
c.569-5434A= (n.569-5434A=)
n.966A=
c.659A= (p.Glu220=)
c.569-3200A= (n.569-3200A=)
c.464A= (p.Glu155=)
c.80A= (p.Glu27=)
c.530A= (p.Glu177=)
15g.66481794A>CCA392936203MAP2K1c.542A>C (p.Glu181Ala)
c.608A>C (p.Glu203Ala)
c.461A>C (p.Glu154Ala)
c.569-5434A>C (n.569-5434A>C)
n.966A>C
c.659A>C (p.Glu220Ala)
c.569-3200A>C (n.569-3200A>C)
c.464A>C (p.Glu155Ala)
c.80A>C (p.Glu27Ala)
c.530A>C (p.Glu177Ala)
ClinVar
15g.66481794A>GCA234222MAP2K1c.542A>G (p.Glu181Gly)
c.608A>G (p.Glu203Gly)
c.461A>G (p.Glu154Gly)
c.569-5434A>G (n.569-5434A>G)
n.966A>G
c.659A>G (p.Glu220Gly)
c.569-3200A>G (n.569-3200A>G)
c.464A>G (p.Glu155Gly)
c.80A>G (p.Glu27Gly)
c.530A>G (p.Glu177Gly)
ClinVar dbSNP
15g.66481794A>TCA392936205MAP2K1c.542A>T (p.Glu181Val)
c.608A>T (p.Glu203Val)
c.461A>T (p.Glu154Val)
c.569-5434A>T (n.569-5434A>T)
n.966A>T
c.659A>T (p.Glu220Val)
c.569-3200A>T (n.569-3200A>T)
c.464A>T (p.Glu155Val)
c.80A>T (p.Glu27Val)
c.530A>T (p.Glu177Val)
dbSNP COSMIC
15g.66481795G>ACA490858404MAP2K1c.543G>A (p.Glu181=)
c.609G>A (p.Glu203=)
c.462G>A (p.Glu154=)
c.569-5433G>A (n.569-5433G>A)
n.967G>A
c.660G>A (p.Glu220=)
c.569-3199G>A (n.569-3199G>A)
c.465G>A (p.Glu155=)
c.81G>A (p.Glu27=)
c.531G>A (p.Glu177=)
dbSNP
15g.66481795G>CCA392936207MAP2K1c.543G>C (p.Glu181Asp)
c.609G>C (p.Glu203Asp)
c.462G>C (p.Glu154Asp)
c.569-5433G>C (n.569-5433G>C)
n.967G>C
c.660G>C (p.Glu220Asp)
c.569-3199G>C (n.569-3199G>C)
c.465G>C (p.Glu155Asp)
c.81G>C (p.Glu27Asp)
c.531G>C (p.Glu177Asp)
dbSNP
15g.66481795G>TCA392936208MAP2K1c.543G>T (p.Glu181Asp)
c.609G>T (p.Glu203Asp)
c.462G>T (p.Glu154Asp)
c.569-5433G>T (n.569-5433G>T)
n.967G>T
c.660G>T (p.Glu220Asp)
c.569-3199G>T (n.569-3199G>T)
c.465G>T (p.Glu155Asp)
c.81G>T (p.Glu27Asp)
c.531G>T (p.Glu177Asp)
dbSNP
15g.66481796A>CCA392936210MAP2K1c.544A>C (p.Ile182Leu)
c.610A>C (p.Ile204Leu)
c.463A>C (p.Ile155Leu)
c.569-5432A>C (n.569-5432A>C)
n.968A>C
c.661A>C (p.Ile221Leu)
c.569-3198A>C (n.569-3198A>C)
c.466A>C (p.Ile156Leu)
c.82A>C (p.Ile28Leu)
c.532A>C (p.Ile178Leu)
dbSNP
15g.66481796A>GCA392936212MAP2K1c.544A>G (p.Ile182Val)
c.610A>G (p.Ile204Val)
c.463A>G (p.Ile155Val)
c.569-5432A>G (n.569-5432A>G)
n.968A>G
c.661A>G (p.Ile221Val)
c.569-3198A>G (n.569-3198A>G)
c.466A>G (p.Ile156Val)
c.82A>G (p.Ile28Val)
c.532A>G (p.Ile178Val)
dbSNP
15g.66481796A>TCA392936214MAP2K1c.544A>T (p.Ile182Phe)
c.610A>T (p.Ile204Phe)
c.463A>T (p.Ile155Phe)
c.569-5432A>T (n.569-5432A>T)
n.968A>T
c.661A>T (p.Ile221Phe)
c.569-3198A>T (n.569-3198A>T)
c.466A>T (p.Ile156Phe)
c.82A>T (p.Ile28Phe)
c.532A>T (p.Ile178Phe)
dbSNP
15g.66481797T>ACA392936218MAP2K1c.545T>A (p.Ile182Asn)
c.611T>A (p.Ile204Asn)
c.464T>A (p.Ile155Asn)
c.569-5431T>A (n.569-5431T>A)
n.969T>A
c.662T>A (p.Ile221Asn)
c.569-3197T>A (n.569-3197T>A)
c.467T>A (p.Ile156Asn)
c.83T>A (p.Ile28Asn)
c.533T>A (p.Ile178Asn)
dbSNP
15g.66481797T>CCA392936220MAP2K1c.545T>C (p.Ile182Thr)
c.611T>C (p.Ile204Thr)
c.464T>C (p.Ile155Thr)
c.569-5431T>C (n.569-5431T>C)
n.969T>C
c.662T>C (p.Ile221Thr)
c.569-3197T>C (n.569-3197T>C)
c.467T>C (p.Ile156Thr)
c.83T>C (p.Ile28Thr)
c.533T>C (p.Ile178Thr)
dbSNP COSMIC
15g.66481797T>GCA392936216MAP2K1c.545T>G (p.Ile182Ser)
c.611T>G (p.Ile204Ser)
c.464T>G (p.Ile155Ser)
c.569-5431T>G (n.569-5431T>G)
n.969T>G
c.662T>G (p.Ile221Ser)
c.569-3197T>G (n.569-3197T>G)
c.467T>G (p.Ile156Ser)
c.83T>G (p.Ile28Ser)
c.533T>G (p.Ile178Ser)
dbSNP
15g.66481798C>ACA490858406MAP2K1c.546C>A (p.Ile182=)
c.612C>A (p.Ile204=)
c.465C>A (p.Ile155=)
c.569-5430C>A (n.569-5430C>A)
n.970C>A
c.663C>A (p.Ile221=)
c.569-3196C>A (n.569-3196C>A)
c.468C>A (p.Ile156=)
c.84C>A (p.Ile28=)
c.534C>A (p.Ile178=)
ClinVar dbSNP
15g.66481798C>GCA392936222MAP2K1c.546C>G (p.Ile182Met)
c.612C>G (p.Ile204Met)
c.465C>G (p.Ile155Met)
c.569-5430C>G (n.569-5430C>G)
n.970C>G
c.663C>G (p.Ile221Met)
c.569-3196C>G (n.569-3196C>G)
c.468C>G (p.Ile156Met)
c.84C>G (p.Ile28Met)
c.534C>G (p.Ile178Met)
ClinVar dbSNP
15g.66481798C>TCA490858405MAP2K1c.546C>T (p.Ile182=)
c.612C>T (p.Ile204=)
c.465C>T (p.Ile155=)
c.569-5430C>T (n.569-5430C>T)
n.970C>T
c.663C>T (p.Ile221=)
c.569-3196C>T (n.569-3196C>T)
c.468C>T (p.Ile156=)
c.84C>T (p.Ile28=)
c.534C>T (p.Ile178=)
dbSNP
15g.66481799A>CCA392936224MAP2K1c.547A>C (p.Lys183Gln)
c.613A>C (p.Lys205Gln)
c.466A>C (p.Lys156Gln)
c.569-5429A>C (n.569-5429A>C)
n.971A>C
c.664A>C (p.Lys222Gln)
c.569-3195A>C (n.569-3195A>C)
c.469A>C (p.Lys157Gln)
c.85A>C (p.Lys29Gln)
c.535A>C (p.Lys179Gln)
15g.66481799A>GCA392936226MAP2K1c.547A>G (p.Lys183Glu)
c.613A>G (p.Lys205Glu)
c.466A>G (p.Lys156Glu)
c.569-5429A>G (n.569-5429A>G)
n.971A>G
c.664A>G (p.Lys222Glu)
c.569-3195A>G (n.569-3195A>G)
c.469A>G (p.Lys157Glu)
c.85A>G (p.Lys29Glu)
c.535A>G (p.Lys179Glu)
dbSNP
15g.66481799A>TCA392936228MAP2K1c.547A>T (p.Lys183Ter)
c.613A>T (p.Lys205Ter)
c.466A>T (p.Lys156Ter)
c.569-5429A>T (n.569-5429A>T)
n.971A>T
c.664A>T (p.Lys222Ter)
c.569-3195A>T (n.569-3195A>T)
c.469A>T (p.Lys157Ter)
c.85A>T (p.Lys29Ter)
c.535A>T (p.Lys179Ter)
dbSNP
15g.66481800A>CCA392936234MAP2K1c.548A>C (p.Lys183Thr)
c.614A>C (p.Lys205Thr)
c.467A>C (p.Lys156Thr)
c.569-5428A>C (n.569-5428A>C)
n.972A>C
c.665A>C (p.Lys222Thr)
c.569-3194A>C (n.569-3194A>C)
c.470A>C (p.Lys157Thr)
c.86A>C (p.Lys29Thr)
c.536A>C (p.Lys179Thr)
15g.66481800A>GCA392936232MAP2K1c.548A>G (p.Lys183Arg)
c.614A>G (p.Lys205Arg)
c.467A>G (p.Lys156Arg)
c.569-5428A>G (n.569-5428A>G)
n.972A>G
c.665A>G (p.Lys222Arg)
c.569-3194A>G (n.569-3194A>G)
c.470A>G (p.Lys157Arg)
c.86A>G (p.Lys29Arg)
c.536A>G (p.Lys179Arg)
dbSNP
15g.66481800A>TCA392936230MAP2K1c.548A>T (p.Lys183Met)
c.614A>T (p.Lys205Met)
c.467A>T (p.Lys156Met)
c.569-5428A>T (n.569-5428A>T)
n.972A>T
c.665A>T (p.Lys222Met)
c.569-3194A>T (n.569-3194A>T)
c.470A>T (p.Lys157Met)
c.86A>T (p.Lys29Met)
c.536A>T (p.Lys179Met)
dbSNP
15g.66481801G>ACA7623994MAP2K1c.549G>A (p.Lys183=)
c.615G>A (p.Lys205=)
c.468G>A (p.Lys156=)
c.569-5427G>A (n.569-5427G>A)
n.973G>A
c.666G>A (p.Lys222=)
c.569-3193G>A (n.569-3193G>A)
c.471G>A (p.Lys157=)
c.87G>A (p.Lys29=)
c.537G>A (p.Lys179=)
dbSNP ExAC gnomAD v2 gnomAD v4
15g.66481801G>CCA392936236MAP2K1c.549G>C (p.Lys183Asn)
c.615G>C (p.Lys205Asn)
c.468G>C (p.Lys156Asn)
c.569-5427G>C (n.569-5427G>C)
n.973G>C
c.666G>C (p.Lys222Asn)
c.569-3193G>C (n.569-3193G>C)
c.471G>C (p.Lys157Asn)
c.87G>C (p.Lys29Asn)
c.537G>C (p.Lys179Asn)
dbSNP
15g.66481801G=CA2184097415MAP2K1c.549G= (p.Lys183=)
c.615G= (p.Lys205=)
c.468G= (p.Lys156=)
c.569-5427G= (n.569-5427G=)
n.973G=
c.666G= (p.Lys222=)
c.569-3193G= (n.569-3193G=)
c.471G= (p.Lys157=)
c.87G= (p.Lys29=)
c.537G= (p.Lys179=)
15g.66481801G>TCA392936237MAP2K1c.549G>T (p.Lys183Asn)
c.615G>T (p.Lys205Asn)
c.468G>T (p.Lys156Asn)
c.569-5427G>T (n.569-5427G>T)
n.973G>T
c.666G>T (p.Lys222Asn)
c.569-3193G>T (n.569-3193G>T)
c.471G>T (p.Lys157Asn)
c.87G>T (p.Lys29Asn)
c.537G>T (p.Lys179Asn)
15g.66481802C>ACA392936240MAP2K1c.550C>A (p.Leu184Ile)
c.616C>A (p.Leu206Ile)
c.469C>A (p.Leu157Ile)
c.569-5426C>A (n.569-5426C>A)
n.974C>A
c.667C>A (p.Leu223Ile)
c.569-3192C>A (n.569-3192C>A)
c.472C>A (p.Leu158Ile)
c.88C>A (p.Leu30Ile)
c.538C>A (p.Leu180Ile)
dbSNP
15g.66481802C>GCA392936241MAP2K1c.550C>G (p.Leu184Val)
c.616C>G (p.Leu206Val)
c.469C>G (p.Leu157Val)
c.569-5426C>G (n.569-5426C>G)
n.974C>G
c.667C>G (p.Leu223Val)
c.569-3192C>G (n.569-3192C>G)
c.472C>G (p.Leu158Val)
c.88C>G (p.Leu30Val)
c.538C>G (p.Leu180Val)
dbSNP
15g.66481802C>TCA392936242MAP2K1c.550C>T (p.Leu184Phe)
c.616C>T (p.Leu206Phe)
c.469C>T (p.Leu157Phe)
c.569-5426C>T (n.569-5426C>T)
n.974C>T
c.667C>T (p.Leu223Phe)
c.569-3192C>T (n.569-3192C>T)
c.472C>T (p.Leu158Phe)
c.88C>T (p.Leu30Phe)
c.538C>T (p.Leu180Phe)
15g.66481803T>ACA392936245MAP2K1c.551T>A (p.Leu184His)
c.617T>A (p.Leu206His)
c.470T>A (p.Leu157His)
c.569-5425T>A (n.569-5425T>A)
n.975T>A
c.668T>A (p.Leu223His)
c.569-3191T>A (n.569-3191T>A)
c.473T>A (p.Leu158His)
c.89T>A (p.Leu30His)
c.539T>A (p.Leu180His)
dbSNP
15g.66481803T>CCA392936249MAP2K1c.551T>C (p.Leu184Pro)
c.617T>C (p.Leu206Pro)
c.470T>C (p.Leu157Pro)
c.569-5425T>C (n.569-5425T>C)
n.975T>C
c.668T>C (p.Leu223Pro)
c.569-3191T>C (n.569-3191T>C)
c.473T>C (p.Leu158Pro)
c.89T>C (p.Leu30Pro)
c.539T>C (p.Leu180Pro)
15g.66481803T>GCA392936247MAP2K1c.551T>G (p.Leu184Arg)
c.617T>G (p.Leu206Arg)
c.470T>G (p.Leu157Arg)
c.569-5425T>G (n.569-5425T>G)
n.975T>G
c.668T>G (p.Leu223Arg)
c.569-3191T>G (n.569-3191T>G)
c.473T>G (p.Leu158Arg)
c.89T>G (p.Leu30Arg)
c.539T>G (p.Leu180Arg)
15g.66481804C>ACA490858407MAP2K1c.552C>A (p.Leu184=)
c.618C>A (p.Leu206=)
c.471C>A (p.Leu157=)
c.569-5424C>A (n.569-5424C>A)
n.976C>A
c.669C>A (p.Leu223=)
c.569-3190C>A (n.569-3190C>A)
c.474C>A (p.Leu158=)
c.90C>A (p.Leu30=)
c.540C>A (p.Leu180=)
gnomAD v4
15g.66481804C>GCA490858408MAP2K1c.552C>G (p.Leu184=)
c.618C>G (p.Leu206=)
c.471C>G (p.Leu157=)
c.569-5424C>G (n.569-5424C>G)
n.976C>G
c.669C>G (p.Leu223=)
c.569-3190C>G (n.569-3190C>G)
c.474C>G (p.Leu158=)
c.90C>G (p.Leu30=)
c.540C>G (p.Leu180=)
dbSNP
15g.66481804C>TCA490858409MAP2K1c.552C>T (p.Leu184=)
c.618C>T (p.Leu206=)
c.471C>T (p.Leu157=)
c.569-5424C>T (n.569-5424C>T)
n.976C>T
c.669C>T (p.Leu223=)
c.569-3190C>T (n.569-3190C>T)
c.474C>T (p.Leu158=)
c.90C>T (p.Leu30=)
c.540C>T (p.Leu180=)
ClinVar dbSNP
15g.66481805T>ACA392936251MAP2K1c.553T>A (p.Cys185Ser)
c.619T>A (p.Cys207Ser)
c.472T>A (p.Cys158Ser)
c.569-5423T>A (n.569-5423T>A)
n.977T>A
c.670T>A (p.Cys224Ser)
c.569-3189T>A (n.569-3189T>A)
c.475T>A (p.Cys159Ser)
c.91T>A (p.Cys31Ser)
c.541T>A (p.Cys181Ser)
dbSNP
15g.66481805T>CCA392936255MAP2K1c.553T>C (p.Cys185Arg)
c.619T>C (p.Cys207Arg)
c.472T>C (p.Cys158Arg)
c.569-5423T>C (n.569-5423T>C)
n.977T>C
c.670T>C (p.Cys224Arg)
c.569-3189T>C (n.569-3189T>C)
c.475T>C (p.Cys159Arg)
c.91T>C (p.Cys31Arg)
c.541T>C (p.Cys181Arg)
dbSNP
15g.66481805T>GCA392936253MAP2K1c.553T>G (p.Cys185Gly)
c.619T>G (p.Cys207Gly)
c.472T>G (p.Cys158Gly)
c.569-5423T>G (n.569-5423T>G)
n.977T>G
c.670T>G (p.Cys224Gly)
c.569-3189T>G (n.569-3189T>G)
c.475T>G (p.Cys159Gly)
c.91T>G (p.Cys31Gly)
c.541T>G (p.Cys181Gly)
15g.66481806delCA2629083409MAP2K1c.554del (p.Cys185LeufsTer?)
c.620del (p.Cys207LeufsTer?)
c.473del (p.Cys158LeufsTer?)
c.569-5422del (n.569-5422del)
n.978del
c.671del (p.Cys224LeufsTer?)
c.569-3188del (n.569-3188del)
c.476del (p.Cys159LeufsTer?)
c.92del (p.Cys31LeufsTer?)
c.542del (p.Cys181LeufsTer?)
gnomAD v4
15g.66481806G>ACA392936257MAP2K1c.554G>A (p.Cys185Tyr)
c.620G>A (p.Cys207Tyr)
c.473G>A (p.Cys158Tyr)
c.569-5422G>A (n.569-5422G>A)
n.978G>A
c.671G>A (p.Cys224Tyr)
c.569-3188G>A (n.569-3188G>A)
c.476G>A (p.Cys159Tyr)
c.92G>A (p.Cys31Tyr)
c.542G>A (p.Cys181Tyr)
dbSNP
15g.66481806G>CCA392936258MAP2K1c.554G>C (p.Cys185Ser)
c.620G>C (p.Cys207Ser)
c.473G>C (p.Cys158Ser)
c.569-5422G>C (n.569-5422G>C)
n.978G>C
c.671G>C (p.Cys224Ser)
c.569-3188G>C (n.569-3188G>C)
c.476G>C (p.Cys159Ser)
c.92G>C (p.Cys31Ser)
c.542G>C (p.Cys181Ser)
dbSNP
15g.66481806G>TCA392936261MAP2K1c.554G>T (p.Cys185Phe)
c.620G>T (p.Cys207Phe)
c.473G>T (p.Cys158Phe)
c.569-5422G>T (n.569-5422G>T)
n.978G>T
c.671G>T (p.Cys224Phe)
c.569-3188G>T (n.569-3188G>T)
c.476G>T (p.Cys159Phe)
c.92G>T (p.Cys31Phe)
c.542G>T (p.Cys181Phe)
15g.66481807T>ACA392936263MAP2K1c.555T>A (p.Cys185Ter)
c.621T>A (p.Cys207Ter)
c.474T>A (p.Cys158Ter)
c.569-5421T>A (n.569-5421T>A)
n.979T>A
c.672T>A (p.Cys224Ter)
c.569-3187T>A (n.569-3187T>A)
c.477T>A (p.Cys159Ter)
c.93T>A (p.Cys31Ter)
c.543T>A (p.Cys181Ter)
dbSNP
15g.66481807T>CCA490858410MAP2K1c.555T>C (p.Cys185=)
c.621T>C (p.Cys207=)
c.474T>C (p.Cys158=)
c.569-5421T>C (n.569-5421T>C)
n.979T>C
c.672T>C (p.Cys224=)
c.569-3187T>C (n.569-3187T>C)
c.477T>C (p.Cys159=)
c.93T>C (p.Cys31=)
c.543T>C (p.Cys181=)
dbSNP
15g.66481807T>GCA392936264MAP2K1c.555T>G (p.Cys185Trp)
c.621T>G (p.Cys207Trp)
c.474T>G (p.Cys158Trp)
c.569-5421T>G (n.569-5421T>G)
n.979T>G
c.672T>G (p.Cys224Trp)
c.569-3187T>G (n.569-3187T>G)
c.477T>G (p.Cys159Trp)
c.93T>G (p.Cys31Trp)
c.543T>G (p.Cys181Trp)
dbSNP
15g.66481808G>ACA392936271MAP2K1c.556G>A (p.Asp186Asn)
c.622G>A (p.Asp208Asn)
c.475G>A (p.Asp159Asn)
c.569-5420G>A (n.569-5420G>A)
n.980G>A
c.673G>A (p.Asp225Asn)
c.569-3186G>A (n.569-3186G>A)
c.478G>A (p.Asp160Asn)
c.94G>A (p.Asp32Asn)
c.544G>A (p.Asp182Asn)
dbSNP
15g.66481808G>CCA392936269MAP2K1c.556G>C (p.Asp186His)
c.622G>C (p.Asp208His)
c.475G>C (p.Asp159His)
c.569-5420G>C (n.569-5420G>C)
n.980G>C
c.673G>C (p.Asp225His)
c.569-3186G>C (n.569-3186G>C)
c.478G>C (p.Asp160His)
c.94G>C (p.Asp32His)
c.544G>C (p.Asp182His)
dbSNP
15g.66481808G>TCA392936267MAP2K1c.556G>T (p.Asp186Tyr)
c.622G>T (p.Asp208Tyr)
c.475G>T (p.Asp159Tyr)
c.569-5420G>T (n.569-5420G>T)
n.980G>T
c.673G>T (p.Asp225Tyr)
c.569-3186G>T (n.569-3186G>T)
c.478G>T (p.Asp160Tyr)
c.94G>T (p.Asp32Tyr)
c.544G>T (p.Asp182Tyr)
15g.66481809A>CCA392936273MAP2K1c.557A>C (p.Asp186Ala)
c.623A>C (p.Asp208Ala)
c.476A>C (p.Asp159Ala)
c.569-5419A>C (n.569-5419A>C)
n.981A>C
c.674A>C (p.Asp225Ala)
c.569-3185A>C (n.569-3185A>C)
c.479A>C (p.Asp160Ala)
c.95A>C (p.Asp32Ala)
c.545A>C (p.Asp182Ala)
dbSNP
15g.66481809A>GCA392936275MAP2K1c.557A>G (p.Asp186Gly)
c.623A>G (p.Asp208Gly)
c.476A>G (p.Asp159Gly)
c.569-5419A>G (n.569-5419A>G)
n.981A>G
c.674A>G (p.Asp225Gly)
c.569-3185A>G (n.569-3185A>G)
c.479A>G (p.Asp160Gly)
c.95A>G (p.Asp32Gly)
c.545A>G (p.Asp182Gly)
dbSNP
15g.66481809A>TCA392936277MAP2K1c.557A>T (p.Asp186Val)
c.623A>T (p.Asp208Val)
c.476A>T (p.Asp159Val)
c.569-5419A>T (n.569-5419A>T)
n.981A>T
c.674A>T (p.Asp225Val)
c.569-3185A>T (n.569-3185A>T)
c.479A>T (p.Asp160Val)
c.95A>T (p.Asp32Val)
c.545A>T (p.Asp182Val)
dbSNP
15g.66481810C>ACA392936279MAP2K1c.558C>A (p.Asp186Glu)
c.624C>A (p.Asp208Glu)
c.477C>A (p.Asp159Glu)
c.569-5418C>A (n.569-5418C>A)
n.982C>A
c.675C>A (p.Asp225Glu)
c.569-3184C>A (n.569-3184C>A)
c.480C>A (p.Asp160Glu)
c.96C>A (p.Asp32Glu)
c.546C>A (p.Asp182Glu)
dbSNP
15g.66481810C=CA2184097417MAP2K1c.558C= (p.Asp186=)
c.624C= (p.Asp208=)
c.477C= (p.Asp159=)
c.569-5418C= (n.569-5418C=)
n.982C=
c.675C= (p.Asp225=)
c.569-3184C= (n.569-3184C=)
c.480C= (p.Asp160=)
c.96C= (p.Asp32=)
c.546C= (p.Asp182=)
15g.66481810C>GCA392936281MAP2K1c.558C>G (p.Asp186Glu)
c.624C>G (p.Asp208Glu)
c.477C>G (p.Asp159Glu)
c.569-5418C>G (n.569-5418C>G)
n.982C>G
c.675C>G (p.Asp225Glu)
c.569-3184C>G (n.569-3184C>G)
c.480C>G (p.Asp160Glu)
c.96C>G (p.Asp32Glu)
c.546C>G (p.Asp182Glu)
15g.66481810C>TCA7623995MAP2K1c.558C>T (p.Asp186=)
c.624C>T (p.Asp208=)
c.477C>T (p.Asp159=)
c.569-5418C>T (n.569-5418C>T)
n.982C>T
c.675C>T (p.Asp225=)
c.569-3184C>T (n.569-3184C>T)
c.480C>T (p.Asp160=)
c.96C>T (p.Asp32=)
c.546C>T (p.Asp182=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.66481811T>ACA392936288MAP2K1c.559T>A (p.Phe187Ile)
c.625T>A (p.Phe209Ile)
c.478T>A (p.Phe160Ile)
c.569-5417T>A (n.569-5417T>A)
n.983T>A
c.676T>A (p.Phe226Ile)
c.569-3183T>A (n.569-3183T>A)
c.481T>A (p.Phe161Ile)
c.97T>A (p.Phe33Ile)
c.547T>A (p.Phe183Ile)
dbSNP
15g.66481811T>CCA392936285MAP2K1c.559T>C (p.Phe187Leu)
c.625T>C (p.Phe209Leu)
c.478T>C (p.Phe160Leu)
c.569-5417T>C (n.569-5417T>C)
n.983T>C
c.676T>C (p.Phe226Leu)
c.569-3183T>C (n.569-3183T>C)
c.481T>C (p.Phe161Leu)
c.97T>C (p.Phe33Leu)
c.547T>C (p.Phe183Leu)
15g.66481811T>GCA392936286MAP2K1c.559T>G (p.Phe187Val)
c.625T>G (p.Phe209Val)
c.478T>G (p.Phe160Val)
c.569-5417T>G (n.569-5417T>G)
n.983T>G
c.676T>G (p.Phe226Val)
c.569-3183T>G (n.569-3183T>G)
c.481T>G (p.Phe161Val)
c.97T>G (p.Phe33Val)
c.547T>G (p.Phe183Val)
15g.66481812T>ACA392936289MAP2K1c.560T>A (p.Phe187Tyr)
c.626T>A (p.Phe209Tyr)
c.479T>A (p.Phe160Tyr)
c.569-5416T>A (n.569-5416T>A)
n.984T>A
c.677T>A (p.Phe226Tyr)
c.569-3182T>A (n.569-3182T>A)
c.482T>A (p.Phe161Tyr)
c.98T>A (p.Phe33Tyr)
c.548T>A (p.Phe183Tyr)
dbSNP
15g.66481812T>CCA392936291MAP2K1c.560T>C (p.Phe187Ser)
c.626T>C (p.Phe209Ser)
c.479T>C (p.Phe160Ser)
c.569-5416T>C (n.569-5416T>C)
n.984T>C
c.677T>C (p.Phe226Ser)
c.569-3182T>C (n.569-3182T>C)
c.482T>C (p.Phe161Ser)
c.98T>C (p.Phe33Ser)
c.548T>C (p.Phe183Ser)
15g.66481812T>GCA392936292MAP2K1c.560T>G (p.Phe187Cys)
c.626T>G (p.Phe209Cys)
c.479T>G (p.Phe160Cys)
c.569-5416T>G (n.569-5416T>G)
n.984T>G
c.677T>G (p.Phe226Cys)
c.569-3182T>G (n.569-3182T>G)
c.482T>G (p.Phe161Cys)
c.98T>G (p.Phe33Cys)
c.548T>G (p.Phe183Cys)
15g.66481813T>ACA392936294MAP2K1c.561T>A (p.Phe187Leu)
c.627T>A (p.Phe209Leu)
c.480T>A (p.Phe160Leu)
c.569-5415T>A (n.569-5415T>A)
n.985T>A
c.678T>A (p.Phe226Leu)
c.569-3181T>A (n.569-3181T>A)
c.483T>A (p.Phe161Leu)
c.99T>A (p.Phe33Leu)
c.549T>A (p.Phe183Leu)
15g.66481813T>CCA271671668MAP2K1c.561T>C (p.Phe187=)
c.627T>C (p.Phe209=)
c.480T>C (p.Phe160=)
c.569-5415T>C (n.569-5415T>C)
n.985T>C
c.678T>C (p.Phe226=)
c.569-3181T>C (n.569-3181T>C)
c.483T>C (p.Phe161=)
c.99T>C (p.Phe33=)
c.549T>C (p.Phe183=)
dbSNP
15g.66481813T>GCA392936297MAP2K1c.561T>G (p.Phe187Leu)
c.627T>G (p.Phe209Leu)
c.480T>G (p.Phe160Leu)
c.569-5415T>G (n.569-5415T>G)
n.985T>G
c.678T>G (p.Phe226Leu)
c.569-3181T>G (n.569-3181T>G)
c.483T>G (p.Phe161Leu)
c.99T>G (p.Phe33Leu)
c.549T>G (p.Phe183Leu)
gnomAD v4
15g.66481813T=CA2184097420MAP2K1c.561T= (p.Phe187=)
c.627T= (p.Phe209=)
c.480T= (p.Phe160=)
c.569-5415T= (n.569-5415T=)
n.985T=
c.678T= (p.Phe226=)
c.569-3181T= (n.569-3181T=)
c.483T= (p.Phe161=)
c.99T= (p.Phe33=)
c.549T= (p.Phe183=)
15g.66481814G>ACA392936300MAP2K1c.562G>A (p.Gly188Arg)
c.628G>A (p.Gly210Arg)
c.481G>A (p.Gly161Arg)
c.569-5414G>A (n.569-5414G>A)
n.986G>A
c.679G>A (p.Gly227Arg)
c.569-3180G>A (n.569-3180G>A)
c.484G>A (p.Gly162Arg)
c.100G>A (p.Gly34Arg)
c.550G>A (p.Gly184Arg)
dbSNP
15g.66481814G>CCA392936302MAP2K1c.562G>C (p.Gly188Arg)
c.628G>C (p.Gly210Arg)
c.481G>C (p.Gly161Arg)
c.569-5414G>C (n.569-5414G>C)
n.986G>C
c.679G>C (p.Gly227Arg)
c.569-3180G>C (n.569-3180G>C)
c.484G>C (p.Gly162Arg)
c.100G>C (p.Gly34Arg)
c.550G>C (p.Gly184Arg)
ClinVar dbSNP
15g.66481814G>TCA392936304MAP2K1c.562G>T (p.Gly188Trp)
c.628G>T (p.Gly210Trp)
c.481G>T (p.Gly161Trp)
c.569-5414G>T (n.569-5414G>T)
n.986G>T
c.679G>T (p.Gly227Trp)
c.569-3180G>T (n.569-3180G>T)
c.484G>T (p.Gly162Trp)
c.100G>T (p.Gly34Trp)
c.550G>T (p.Gly184Trp)
dbSNP
15g.66481815G>ACA392936306MAP2K1c.563G>A (p.Gly188Glu)
c.629G>A (p.Gly210Glu)
c.482G>A (p.Gly161Glu)
c.569-5413G>A (n.569-5413G>A)
n.987G>A
c.680G>A (p.Gly227Glu)
c.569-3179G>A (n.569-3179G>A)
c.485G>A (p.Gly162Glu)
c.101G>A (p.Gly34Glu)
c.551G>A (p.Gly184Glu)
dbSNP
15g.66481815G>CCA392936307MAP2K1c.563G>C (p.Gly188Ala)
c.629G>C (p.Gly210Ala)
c.482G>C (p.Gly161Ala)
c.569-5413G>C (n.569-5413G>C)
n.987G>C
c.680G>C (p.Gly227Ala)
c.569-3179G>C (n.569-3179G>C)
c.485G>C (p.Gly162Ala)
c.101G>C (p.Gly34Ala)
c.551G>C (p.Gly184Ala)
dbSNP
15g.66481815G>TCA392936309MAP2K1c.563G>T (p.Gly188Val)
c.629G>T (p.Gly210Val)
c.482G>T (p.Gly161Val)
c.569-5413G>T (n.569-5413G>T)
n.987G>T
c.680G>T (p.Gly227Val)
c.569-3179G>T (n.569-3179G>T)
c.485G>T (p.Gly162Val)
c.101G>T (p.Gly34Val)
c.551G>T (p.Gly184Val)
dbSNP
15g.66481816G>ACA490858412MAP2K1c.564G>A (p.Gly188=)
c.630G>A (p.Gly210=)
c.483G>A (p.Gly161=)
c.569-5412G>A (n.569-5412G>A)
n.988G>A
c.681G>A (p.Gly227=)
c.569-3178G>A (n.569-3178G>A)
c.486G>A (p.Gly162=)
c.102G>A (p.Gly34=)
c.552G>A (p.Gly184=)
ClinVar dbSNP gnomAD v4
15g.66481816G>CCA490858411MAP2K1c.564G>C (p.Gly188=)
c.630G>C (p.Gly210=)
c.483G>C (p.Gly161=)
c.569-5412G>C (n.569-5412G>C)
n.988G>C
c.681G>C (p.Gly227=)
c.569-3178G>C (n.569-3178G>C)
c.486G>C (p.Gly162=)
c.102G>C (p.Gly34=)
c.552G>C (p.Gly184=)
dbSNP
15g.66481816G=CA2184097422MAP2K1c.564G= (p.Gly188=)
c.630G= (p.Gly210=)
c.483G= (p.Gly161=)
c.569-5412G= (n.569-5412G=)
n.988G=
c.681G= (p.Gly227=)
c.569-3178G= (n.569-3178G=)
c.486G= (p.Gly162=)
c.102G= (p.Gly34=)
c.552G= (p.Gly184=)
15g.66481816G>TCA490858413MAP2K1c.564G>T (p.Gly188=)
c.630G>T (p.Gly210=)
c.483G>T (p.Gly161=)
c.569-5412G>T (n.569-5412G>T)
n.988G>T
c.681G>T (p.Gly227=)
c.569-3178G>T (n.569-3178G>T)
c.486G>T (p.Gly162=)
c.102G>T (p.Gly34=)
c.552G>T (p.Gly184=)
dbSNP gnomAD v4
15g.66481817G>ACA185378MAP2K1c.565G>A (p.Val189Ile)
c.631G>A (p.Val211Ile)
c.484G>A (p.Val162Ile)
c.569-5411G>A (n.569-5411G>A)
n.989G>A
c.682G>A (p.Val228Ile)
c.569-3177G>A (n.569-3177G>A)
c.487G>A (p.Val163Ile)
c.103G>A (p.Val35Ile)
c.553G>A (p.Val185Ile)
ClinVar dbSNP gnomAD v3 gnomAD v4
15g.66481817G>CCA392936313MAP2K1c.565G>C (p.Val189Leu)
c.631G>C (p.Val211Leu)
c.484G>C (p.Val162Leu)
c.569-5411G>C (n.569-5411G>C)
n.989G>C
c.682G>C (p.Val228Leu)
c.569-3177G>C (n.569-3177G>C)
c.487G>C (p.Val163Leu)
c.103G>C (p.Val35Leu)
c.553G>C (p.Val185Leu)
dbSNP
15g.66481817G=CA2184097424MAP2K1c.565G= (p.Val189=)
c.631G= (p.Val211=)
c.484G= (p.Val162=)
c.569-5411G= (n.569-5411G=)
n.989G=
c.682G= (p.Val228=)
c.569-3177G= (n.569-3177G=)
c.487G= (p.Val163=)
c.103G= (p.Val35=)
c.553G= (p.Val185=)
15g.66481817G>TCA392936312MAP2K1c.565G>T (p.Val189Phe)
c.631G>T (p.Val211Phe)
c.484G>T (p.Val162Phe)
c.569-5411G>T (n.569-5411G>T)
n.989G>T
c.682G>T (p.Val228Phe)
c.569-3177G>T (n.569-3177G>T)
c.487G>T (p.Val163Phe)
c.103G>T (p.Val35Phe)
c.553G>T (p.Val185Phe)
dbSNP
15g.66481818T>ACA16602653MAP2K1c.566T>A (p.Val189Asp)
c.632T>A (p.Val211Asp)
c.485T>A (p.Val162Asp)
c.569-5410T>A (n.569-5410T>A)
n.990T>A
c.683T>A (p.Val228Asp)
c.569-3176T>A (n.569-3176T>A)
c.488T>A (p.Val163Asp)
c.104T>A (p.Val35Asp)
c.554T>A (p.Val185Asp)
ClinVar dbSNP
15g.66481818T>CCA392936316MAP2K1c.566T>C (p.Val189Ala)
c.632T>C (p.Val211Ala)
c.485T>C (p.Val162Ala)
c.569-5410T>C (n.569-5410T>C)
n.990T>C
c.683T>C (p.Val228Ala)
c.569-3176T>C (n.569-3176T>C)
c.488T>C (p.Val163Ala)
c.104T>C (p.Val35Ala)
c.554T>C (p.Val185Ala)
dbSNP
15g.66481818T>GCA392936317MAP2K1c.566T>G (p.Val189Gly)
c.632T>G (p.Val211Gly)
c.485T>G (p.Val162Gly)
c.569-5410T>G (n.569-5410T>G)
n.990T>G
c.683T>G (p.Val228Gly)
c.569-3176T>G (n.569-3176T>G)
c.488T>G (p.Val163Gly)
c.104T>G (p.Val35Gly)
c.554T>G (p.Val185Gly)
dbSNP
15g.66481818T=CA2184097428MAP2K1c.566T= (p.Val189=)
c.632T= (p.Val211=)
c.485T= (p.Val162=)
c.569-5410T= (n.569-5410T=)
n.990T=
c.683T= (p.Val228=)
c.569-3176T= (n.569-3176T=)
c.488T= (p.Val163=)
c.104T= (p.Val35=)
c.554T= (p.Val185=)
15g.66481819C>ACA490858414MAP2K1c.567C>A (p.Val189=)
c.633C>A (p.Val211=)
c.486C>A (p.Val162=)
c.569-5409C>A (n.569-5409C>A)
n.991C>A
c.684C>A (p.Val228=)
c.569-3175C>A (n.569-3175C>A)
c.489C>A (p.Val163=)
c.105C>A (p.Val35=)
c.555C>A (p.Val185=)
dbSNP
15g.66481819C=CA2184097430MAP2K1c.567C= (p.Val189=)
c.633C= (p.Val211=)
c.486C= (p.Val162=)
c.569-5409C= (n.569-5409C=)
n.991C=
c.684C= (p.Val228=)
c.569-3175C= (n.569-3175C=)
c.489C= (p.Val163=)
c.105C= (p.Val35=)
c.555C= (p.Val185=)
15g.66481819C>GCA490858416MAP2K1c.567C>G (p.Val189=)
c.633C>G (p.Val211=)
c.486C>G (p.Val162=)
c.569-5409C>G (n.569-5409C>G)
n.991C>G
c.684C>G (p.Val228=)
c.569-3175C>G (n.569-3175C>G)
c.489C>G (p.Val163=)
c.105C>G (p.Val35=)
c.555C>G (p.Val185=)
ClinVar dbSNP
15g.66481819C>TCA490858415MAP2K1c.567C>T (p.Val189=)
c.633C>T (p.Val211=)
c.486C>T (p.Val162=)
c.569-5409C>T (n.569-5409C>T)
n.991C>T
c.684C>T (p.Val228=)
c.569-3175C>T (n.569-3175C>T)
c.489C>T (p.Val163=)
c.105C>T (p.Val35=)
c.555C>T (p.Val185=)
dbSNP COSMIC
15g.66481820A>CCA392936319MAP2K1c.568A>C (p.Ser190Arg)
c.634A>C (p.Ser212Arg)
c.487A>C (p.Ser163Arg)
c.569-5408A>C (n.569-5408A>C)
n.992A>C
c.685A>C (p.Ser229Arg)
c.569-3174A>C (n.569-3174A>C)
c.490A>C (p.Ser164Arg)
c.106A>C (p.Ser36Arg)
c.556A>C (p.Ser186Arg)
15g.66481820A>GCA392936321MAP2K1c.568A>G (p.Ser190Gly)
c.634A>G (p.Ser212Gly)
c.487A>G (p.Ser163Gly)
c.569-5408A>G (n.569-5408A>G)
n.992A>G
c.685A>G (p.Ser229Gly)
c.569-3174A>G (n.569-3174A>G)
c.490A>G (p.Ser164Gly)
c.106A>G (p.Ser36Gly)
c.556A>G (p.Ser186Gly)
dbSNP
15g.66481820A>TCA392936322MAP2K1c.568A>T (p.Ser190Cys)
c.634A>T (p.Ser212Cys)
c.487A>T (p.Ser163Cys)
c.569-5408A>T (n.569-5408A>T)
n.992A>T
c.685A>T (p.Ser229Cys)
c.569-3174A>T (n.569-3174A>T)
c.490A>T (p.Ser164Cys)
c.106A>T (p.Ser36Cys)
c.556A>T (p.Ser186Cys)
dbSNP
15g.66481821G>ACA392936324MAP2K1c.569G>A (p.Ser190Asn)
c.635G>A (p.Ser212Asn)
c.488G>A (p.Ser163Asn)
c.569-5407G>A (n.569-5407G>A)
n.993G>A
c.686G>A (p.Ser229Asn)
c.569-3173G>A (n.569-3173G>A)
c.491G>A (p.Ser164Asn)
c.107G>A (p.Ser36Asn)
c.557G>A (p.Ser186Asn)
dbSNP COSMIC
15g.66481821G>CCA271671674MAP2K1c.569G>C (p.Ser190Thr)
c.635G>C (p.Ser212Thr)
c.488G>C (p.Ser163Thr)
c.569-5407G>C (n.569-5407G>C)
n.993G>C
c.686G>C (p.Ser229Thr)
c.569-3173G>C (n.569-3173G>C)
c.491G>C (p.Ser164Thr)
c.107G>C (p.Ser36Thr)
c.557G>C (p.Ser186Thr)
ClinVar dbSNP
15g.66481821G=CA2184097432MAP2K1c.569G= (p.Ser190=)
c.635G= (p.Ser212=)
c.488G= (p.Ser163=)
c.569-5407G= (n.569-5407G=)
n.993G=
c.686G= (p.Ser229=)
c.569-3173G= (n.569-3173G=)
c.491G= (p.Ser164=)
c.107G= (p.Ser36=)
c.557G= (p.Ser186=)
15g.66481821G>TCA392936327MAP2K1c.569G>T (p.Ser190Ile)
c.635G>T (p.Ser212Ile)
c.488G>T (p.Ser163Ile)
c.569-5407G>T (n.569-5407G>T)
n.993G>T
c.686G>T (p.Ser229Ile)
c.569-3173G>T (n.569-3173G>T)
c.491G>T (p.Ser164Ile)
c.107G>T (p.Ser36Ile)
c.557G>T (p.Ser186Ile)
15g.66481822C>ACA392936329MAP2K1c.570C>A (p.Ser190Arg)
c.636C>A (p.Ser212Arg)
c.489C>A (p.Ser163Arg)
c.569-5406C>A (n.569-5406C>A)
n.994C>A
c.687C>A (p.Ser229Arg)
c.569-3172C>A (n.569-3172C>A)
c.492C>A (p.Ser164Arg)
c.108C>A (p.Ser36Arg)
c.558C>A (p.Ser186Arg)
dbSNP
15g.66481822C=CA2184097434MAP2K1c.570C= (p.Ser190=)
c.636C= (p.Ser212=)
c.489C= (p.Ser163=)
c.569-5406C= (n.569-5406C=)
n.994C=
c.687C= (p.Ser229=)
c.569-3172C= (n.569-3172C=)
c.492C= (p.Ser164=)
c.108C= (p.Ser36=)
c.558C= (p.Ser186=)
15g.66481822C>GCA392936331MAP2K1c.570C>G (p.Ser190Arg)
c.636C>G (p.Ser212Arg)
c.489C>G (p.Ser163Arg)
c.569-5406C>G (n.569-5406C>G)
n.994C>G
c.687C>G (p.Ser229Arg)
c.569-3172C>G (n.569-3172C>G)
c.492C>G (p.Ser164Arg)
c.108C>G (p.Ser36Arg)
c.558C>G (p.Ser186Arg)
dbSNP
15g.66481822C>TCA291989MAP2K1c.570C>T (p.Ser190=)
c.636C>T (p.Ser212=)
c.489C>T (p.Ser163=)
c.569-5406C>T (n.569-5406C>T)
n.994C>T
c.687C>T (p.Ser229=)
c.569-3172C>T (n.569-3172C>T)
c.492C>T (p.Ser164=)
c.108C>T (p.Ser36=)
c.558C>T (p.Ser186=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.66481823G>ACA392936338MAP2K1c.571G>A (p.Gly191Arg)
c.637G>A (p.Gly213Arg)
c.490G>A (p.Gly164Arg)
c.569-5405G>A (n.569-5405G>A)
n.995G>A
c.688G>A (p.Gly230Arg)
c.569-3171G>A (n.569-3171G>A)
c.493G>A (p.Gly165Arg)
c.109G>A (p.Gly37Arg)
c.559G>A (p.Gly187Arg)
ClinVar dbSNP gnomAD v3 gnomAD v4
15g.66481823G>CCA392936335MAP2K1c.571G>C (p.Gly191Arg)
c.637G>C (p.Gly213Arg)
c.490G>C (p.Gly164Arg)
c.569-5405G>C (n.569-5405G>C)
n.995G>C
c.688G>C (p.Gly230Arg)
c.569-3171G>C (n.569-3171G>C)
c.493G>C (p.Gly165Arg)
c.109G>C (p.Gly37Arg)
c.559G>C (p.Gly187Arg)
dbSNP
15g.66481823G=CA2184097436MAP2K1c.571G= (p.Gly191=)
c.637G= (p.Gly213=)
c.490G= (p.Gly164=)
c.569-5405G= (n.569-5405G=)
n.995G=
c.688G= (p.Gly230=)
c.569-3171G= (n.569-3171G=)
c.493G= (p.Gly165=)
c.109G= (p.Gly37=)
c.559G= (p.Gly187=)
15g.66481823G>TCA392936337MAP2K1c.571G>T (p.Gly191Trp)
c.637G>T (p.Gly213Trp)
c.490G>T (p.Gly164Trp)
c.569-5405G>T (n.569-5405G>T)
n.995G>T
c.688G>T (p.Gly230Trp)
c.569-3171G>T (n.569-3171G>T)
c.493G>T (p.Gly165Trp)
c.109G>T (p.Gly37Trp)
c.559G>T (p.Gly187Trp)
dbSNP
15g.66481824G>ACA392936341MAP2K1c.572G>A (p.Gly191Glu)
c.638G>A (p.Gly213Glu)
c.491G>A (p.Gly164Glu)
c.569-5404G>A (n.569-5404G>A)
n.996G>A
c.689G>A (p.Gly230Glu)
c.569-3170G>A (n.569-3170G>A)
c.494G>A (p.Gly165Glu)
c.110G>A (p.Gly37Glu)
c.560G>A (p.Gly187Glu)
dbSNP
15g.66481824G>CCA392936343MAP2K1c.572G>C (p.Gly191Ala)
c.638G>C (p.Gly213Ala)
c.491G>C (p.Gly164Ala)
c.569-5404G>C (n.569-5404G>C)
n.996G>C
c.689G>C (p.Gly230Ala)
c.569-3170G>C (n.569-3170G>C)
c.494G>C (p.Gly165Ala)
c.110G>C (p.Gly37Ala)
c.560G>C (p.Gly187Ala)
dbSNP
15g.66481824G>TCA392936345MAP2K1c.572G>T (p.Gly191Val)
c.638G>T (p.Gly213Val)
c.491G>T (p.Gly164Val)
c.569-5404G>T (n.569-5404G>T)
n.996G>T
c.689G>T (p.Gly230Val)
c.569-3170G>T (n.569-3170G>T)
c.494G>T (p.Gly165Val)
c.110G>T (p.Gly37Val)
c.560G>T (p.Gly187Val)
dbSNP
15g.66481825G>ACA271671679MAP2K1c.573G>A (p.Gly191=)
c.639G>A (p.Gly213=)
c.492G>A (p.Gly164=)
c.569-5403G>A (n.569-5403G>A)
n.997G>A
c.690G>A (p.Gly230=)
c.569-3169G>A (n.569-3169G>A)
c.495G>A (p.Gly165=)
c.111G>A (p.Gly37=)
c.561G>A (p.Gly187=)
dbSNP
15g.66481825G>CCA490858417MAP2K1c.573G>C (p.Gly191=)
c.639G>C (p.Gly213=)
c.492G>C (p.Gly164=)
c.569-5403G>C (n.569-5403G>C)
n.997G>C
c.690G>C (p.Gly230=)
c.569-3169G>C (n.569-3169G>C)
c.495G>C (p.Gly165=)
c.111G>C (p.Gly37=)
c.561G>C (p.Gly187=)
dbSNP
15g.66481825G=CA2184097439MAP2K1c.573G= (p.Gly191=)
c.639G= (p.Gly213=)
c.492G= (p.Gly164=)
c.569-5403G= (n.569-5403G=)
n.997G=
c.690G= (p.Gly230=)
c.569-3169G= (n.569-3169G=)
c.495G= (p.Gly165=)
c.111G= (p.Gly37=)
c.561G= (p.Gly187=)
15g.66481825G>TCA490858418MAP2K1c.573G>T (p.Gly191=)
c.639G>T (p.Gly213=)
c.492G>T (p.Gly164=)
c.569-5403G>T (n.569-5403G>T)
n.997G>T
c.690G>T (p.Gly230=)
c.569-3169G>T (n.569-3169G>T)
c.495G>T (p.Gly165=)
c.111G>T (p.Gly37=)
c.561G>T (p.Gly187=)
dbSNP
15g.66481826C>ACA392936347MAP2K1c.574C>A (p.Gln192Lys)
c.640C>A (p.Gln214Lys)
c.493C>A (p.Gln165Lys)
c.569-5402C>A (n.569-5402C>A)
n.998C>A
c.691C>A (p.Gln231Lys)
c.569-3168C>A (n.569-3168C>A)
c.496C>A (p.Gln166Lys)
c.112C>A (p.Gln38Lys)
c.562C>A (p.Gln188Lys)
15g.66481826C>GCA392936349MAP2K1c.574C>G (p.Gln192Glu)
c.640C>G (p.Gln214Glu)
c.493C>G (p.Gln165Glu)
c.569-5402C>G (n.569-5402C>G)
n.998C>G
c.691C>G (p.Gln231Glu)
c.569-3168C>G (n.569-3168C>G)
c.496C>G (p.Gln166Glu)
c.112C>G (p.Gln38Glu)
c.562C>G (p.Gln188Glu)
dbSNP
15g.66481826C>TCA392936351MAP2K1c.574C>T (p.Gln192Ter)
c.640C>T (p.Gln214Ter)
c.493C>T (p.Gln165Ter)
c.569-5402C>T (n.569-5402C>T)
n.998C>T
c.691C>T (p.Gln231Ter)
c.569-3168C>T (n.569-3168C>T)
c.496C>T (p.Gln166Ter)
c.112C>T (p.Gln38Ter)
c.562C>T (p.Gln188Ter)
dbSNP gnomAD v4
15g.66481827A>CCA392936353MAP2K1c.575A>C (p.Gln192Pro)
c.641A>C (p.Gln214Pro)
c.494A>C (p.Gln165Pro)
c.569-5401A>C (n.569-5401A>C)
n.999A>C
c.692A>C (p.Gln231Pro)
c.569-3167A>C (n.569-3167A>C)
c.497A>C (p.Gln166Pro)
c.113A>C (p.Gln38Pro)
c.563A>C (p.Gln188Pro)
15g.66481827A>GCA392936355MAP2K1c.575A>G (p.Gln192Arg)
c.641A>G (p.Gln214Arg)
c.494A>G (p.Gln165Arg)
c.569-5401A>G (n.569-5401A>G)
n.999A>G
c.692A>G (p.Gln231Arg)
c.569-3167A>G (n.569-3167A>G)
c.497A>G (p.Gln166Arg)
c.113A>G (p.Gln38Arg)
c.563A>G (p.Gln188Arg)
dbSNP
15g.66481827A>TCA392936357MAP2K1c.575A>T (p.Gln192Leu)
c.641A>T (p.Gln214Leu)
c.494A>T (p.Gln165Leu)
c.569-5401A>T (n.569-5401A>T)
n.999A>T
c.692A>T (p.Gln231Leu)
c.569-3167A>T (n.569-3167A>T)
c.497A>T (p.Gln166Leu)
c.113A>T (p.Gln38Leu)
c.563A>T (p.Gln188Leu)
dbSNP
15g.66481828G>ACA271671685MAP2K1c.576G>A (p.Gln192=)
c.642G>A (p.Gln214=)
c.495G>A (p.Gln165=)
c.569-5400G>A (n.569-5400G>A)
n.1000G>A
c.693G>A (p.Gln231=)
c.569-3166G>A (n.569-3166G>A)
c.498G>A (p.Gln166=)
c.114G>A (p.Gln38=)
c.564G>A (p.Gln188=)
dbSNP gnomAD v3 gnomAD v4
15g.66481828G>CCA392936358MAP2K1c.576G>C (p.Gln192His)
c.642G>C (p.Gln214His)
c.495G>C (p.Gln165His)
c.569-5400G>C (n.569-5400G>C)
n.1000G>C
c.693G>C (p.Gln231His)
c.569-3166G>C (n.569-3166G>C)
c.498G>C (p.Gln166His)
c.114G>C (p.Gln38His)
c.564G>C (p.Gln188His)
dbSNP
15g.66481828G=CA2184097440MAP2K1c.576G= (p.Gln192=)
c.642G= (p.Gln214=)
c.495G= (p.Gln165=)
c.569-5400G= (n.569-5400G=)
n.1000G=
c.693G= (p.Gln231=)
c.569-3166G= (n.569-3166G=)
c.498G= (p.Gln166=)
c.114G= (p.Gln38=)
c.564G= (p.Gln188=)
15g.66481828G>TCA392936360MAP2K1c.576G>T (p.Gln192His)
c.642G>T (p.Gln214His)
c.495G>T (p.Gln165His)
c.569-5400G>T (n.569-5400G>T)
n.1000G>T
c.693G>T (p.Gln231His)
c.569-3166G>T (n.569-3166G>T)
c.498G>T (p.Gln166His)
c.114G>T (p.Gln38His)
c.564G>T (p.Gln188His)
15g.66481829C>ACA392936366MAP2K1c.577C>A (p.Leu193Ile)
c.643C>A (p.Leu215Ile)
c.496C>A (p.Leu166Ile)
c.569-5399C>A (n.569-5399C>A)
n.1001C>A
c.694C>A (p.Leu232Ile)
c.569-3165C>A (n.569-3165C>A)
c.499C>A (p.Leu167Ile)
c.115C>A (p.Leu39Ile)
c.565C>A (p.Leu189Ile)
COSMIC
15g.66481829C>GCA392936364MAP2K1c.577C>G (p.Leu193Val)
c.643C>G (p.Leu215Val)
c.496C>G (p.Leu166Val)
c.569-5399C>G (n.569-5399C>G)
n.1001C>G
c.694C>G (p.Leu232Val)
c.569-3165C>G (n.569-3165C>G)
c.499C>G (p.Leu167Val)
c.115C>G (p.Leu39Val)
c.565C>G (p.Leu189Val)
dbSNP
15g.66481829C>TCA392936362MAP2K1c.577C>T (p.Leu193Phe)
c.643C>T (p.Leu215Phe)
c.496C>T (p.Leu166Phe)
c.569-5399C>T (n.569-5399C>T)
n.1001C>T
c.694C>T (p.Leu232Phe)
c.569-3165C>T (n.569-3165C>T)
c.499C>T (p.Leu167Phe)
c.115C>T (p.Leu39Phe)
c.565C>T (p.Leu189Phe)
COSMIC
15g.66481830T>ACA392936369MAP2K1c.578T>A (p.Leu193His)
c.644T>A (p.Leu215His)
c.497T>A (p.Leu166His)
c.569-5398T>A (n.569-5398T>A)
n.1002T>A
c.695T>A (p.Leu232His)
c.569-3164T>A (n.569-3164T>A)
c.500T>A (p.Leu167His)
c.116T>A (p.Leu39His)
c.566T>A (p.Leu189His)
dbSNP
15g.66481830T>CCA16602654MAP2K1c.578T>C (p.Leu193Pro)
c.644T>C (p.Leu215Pro)
c.497T>C (p.Leu166Pro)
c.569-5398T>C (n.569-5398T>C)
n.1002T>C
c.695T>C (p.Leu232Pro)
c.569-3164T>C (n.569-3164T>C)
c.500T>C (p.Leu167Pro)
c.116T>C (p.Leu39Pro)
c.566T>C (p.Leu189Pro)
ClinVar dbSNP
15g.66481830T>GCA392936370MAP2K1c.578T>G (p.Leu193Arg)
c.644T>G (p.Leu215Arg)
c.497T>G (p.Leu166Arg)
c.569-5398T>G (n.569-5398T>G)
n.1002T>G
c.695T>G (p.Leu232Arg)
c.569-3164T>G (n.569-3164T>G)
c.500T>G (p.Leu167Arg)
c.116T>G (p.Leu39Arg)
c.566T>G (p.Leu189Arg)
15g.66481830T=CA2184097442MAP2K1c.578T= (p.Leu193=)
c.644T= (p.Leu215=)
c.497T= (p.Leu166=)
c.569-5398T= (n.569-5398T=)
n.1002T=
c.695T= (p.Leu232=)
c.569-3164T= (n.569-3164T=)
c.500T= (p.Leu167=)
c.116T= (p.Leu39=)
c.566T= (p.Leu189=)
15g.66481831C>ACA490858419MAP2K1c.579C>A (p.Leu193=)
c.645C>A (p.Leu215=)
c.498C>A (p.Leu166=)
c.569-5397C>A (n.569-5397C>A)
n.1003C>A
c.696C>A (p.Leu232=)
c.569-3163C>A (n.569-3163C>A)
c.501C>A (p.Leu167=)
c.117C>A (p.Leu39=)
c.567C>A (p.Leu189=)
15g.66481831C>GCA490858421MAP2K1c.579C>G (p.Leu193=)
c.645C>G (p.Leu215=)
c.498C>G (p.Leu166=)
c.569-5397C>G (n.569-5397C>G)
n.1003C>G
c.696C>G (p.Leu232=)
c.569-3163C>G (n.569-3163C>G)
c.501C>G (p.Leu167=)
c.117C>G (p.Leu39=)
c.567C>G (p.Leu189=)
ClinVar dbSNP gnomAD v3 gnomAD v4
15g.66481831C>TCA490858420MAP2K1c.579C>T (p.Leu193=)
c.645C>T (p.Leu215=)
c.498C>T (p.Leu166=)
c.569-5397C>T (n.569-5397C>T)
n.1003C>T
c.696C>T (p.Leu232=)
c.569-3163C>T (n.569-3163C>T)
c.501C>T (p.Leu167=)
c.117C>T (p.Leu39=)
c.567C>T (p.Leu189=)
dbSNP
15g.66481832A>CCA392936372MAP2K1c.580A>C (p.Ile194Leu)
c.646A>C (p.Ile216Leu)
c.499A>C (p.Ile167Leu)
c.569-5396A>C (n.569-5396A>C)
n.1004A>C
c.697A>C (p.Ile233Leu)
c.569-3162A>C (n.569-3162A>C)
c.502A>C (p.Ile168Leu)
c.118A>C (p.Ile40Leu)
c.568A>C (p.Ile190Leu)
dbSNP
15g.66481832A>GCA392936374MAP2K1c.580A>G (p.Ile194Val)
c.646A>G (p.Ile216Val)
c.499A>G (p.Ile167Val)
c.569-5396A>G (n.569-5396A>G)
n.1004A>G
c.697A>G (p.Ile233Val)
c.569-3162A>G (n.569-3162A>G)
c.502A>G (p.Ile168Val)
c.118A>G (p.Ile40Val)
c.568A>G (p.Ile190Val)
dbSNP
15g.66481832A>TCA392936376MAP2K1c.580A>T (p.Ile194Phe)
c.646A>T (p.Ile216Phe)
c.499A>T (p.Ile167Phe)
c.569-5396A>T (n.569-5396A>T)
n.1004A>T
c.697A>T (p.Ile233Phe)
c.569-3162A>T (n.569-3162A>T)
c.502A>T (p.Ile168Phe)
c.118A>T (p.Ile40Phe)
c.568A>T (p.Ile190Phe)
dbSNP
15g.66481833T>ACA392936378MAP2K1c.581T>A (p.Ile194Asn)
c.647T>A (p.Ile216Asn)
c.500T>A (p.Ile167Asn)
c.569-5395T>A (n.569-5395T>A)
n.1005T>A
c.698T>A (p.Ile233Asn)
c.569-3161T>A (n.569-3161T>A)
c.503T>A (p.Ile168Asn)
c.119T>A (p.Ile40Asn)
c.569T>A (p.Ile190Asn)
dbSNP
15g.66481833T>CCA392936380MAP2K1c.581T>C (p.Ile194Thr)
c.647T>C (p.Ile216Thr)
c.500T>C (p.Ile167Thr)
c.569-5395T>C (n.569-5395T>C)
n.1005T>C
c.698T>C (p.Ile233Thr)
c.569-3161T>C (n.569-3161T>C)
c.503T>C (p.Ile168Thr)
c.119T>C (p.Ile40Thr)
c.569T>C (p.Ile190Thr)
ClinVar dbSNP
15g.66481833T>GCA392936382MAP2K1c.581T>G (p.Ile194Ser)
c.647T>G (p.Ile216Ser)
c.500T>G (p.Ile167Ser)
c.569-5395T>G (n.569-5395T>G)
n.1005T>G
c.698T>G (p.Ile233Ser)
c.569-3161T>G (n.569-3161T>G)
c.503T>G (p.Ile168Ser)
c.119T>G (p.Ile40Ser)
c.569T>G (p.Ile190Ser)
dbSNP
15g.66481834C>ACA490858422MAP2K1c.582C>A (p.Ile194=)
c.648C>A (p.Ile216=)
c.501C>A (p.Ile167=)
c.569-5394C>A (n.569-5394C>A)
n.1006C>A
c.699C>A (p.Ile233=)
c.569-3160C>A (n.569-3160C>A)
c.504C>A (p.Ile168=)
c.120C>A (p.Ile40=)
c.570C>A (p.Ile190=)
15g.66481834C=CA2184097445MAP2K1c.582C= (p.Ile194=)
c.648C= (p.Ile216=)
c.501C= (p.Ile167=)
c.569-5394C= (n.569-5394C=)
n.1006C=
c.699C= (p.Ile233=)
c.569-3160C= (n.569-3160C=)
c.504C= (p.Ile168=)
c.120C= (p.Ile40=)
c.570C= (p.Ile190=)
15g.66481834C>GCA392936383MAP2K1c.582C>G (p.Ile194Met)
c.648C>G (p.Ile216Met)
c.501C>G (p.Ile167Met)
c.569-5394C>G (n.569-5394C>G)
n.1006C>G
c.699C>G (p.Ile233Met)
c.569-3160C>G (n.569-3160C>G)
c.504C>G (p.Ile168Met)
c.120C>G (p.Ile40Met)
c.570C>G (p.Ile190Met)
dbSNP
15g.66481834C>TCA134607MAP2K1c.582C>T (p.Ile194=)
c.648C>T (p.Ile216=)
c.501C>T (p.Ile167=)
c.569-5394C>T (n.569-5394C>T)
n.1006C>T
c.699C>T (p.Ile233=)
c.569-3160C>T (n.569-3160C>T)
c.504C>T (p.Ile168=)
c.120C>T (p.Ile40=)
c.570C>T (p.Ile190=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.66481835G>ACA7623996MAP2K1c.583G>A (p.Asp195Asn)
c.649G>A (p.Asp217Asn)
c.502G>A (p.Asp168Asn)
c.569-5393G>A (n.569-5393G>A)
n.1007G>A
c.700G>A (p.Asp234Asn)
c.569-3159G>A (n.569-3159G>A)
c.505G>A (p.Asp169Asn)
c.121G>A (p.Asp41Asn)
c.571G>A (p.Asp191Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.66481835G>CCA392936386MAP2K1c.583G>C (p.Asp195His)
c.649G>C (p.Asp217His)
c.502G>C (p.Asp168His)
c.569-5393G>C (n.569-5393G>C)
n.1007G>C
c.700G>C (p.Asp234His)
c.569-3159G>C (n.569-3159G>C)
c.505G>C (p.Asp169His)
c.121G>C (p.Asp41His)
c.571G>C (p.Asp191His)
dbSNP
15g.66481835G=CA2184097448MAP2K1c.583G= (p.Asp195=)
c.649G= (p.Asp217=)
c.502G= (p.Asp168=)
c.569-5393G= (n.569-5393G=)
n.1007G=
c.700G= (p.Asp234=)
c.569-3159G= (n.569-3159G=)
c.505G= (p.Asp169=)
c.121G= (p.Asp41=)
c.571G= (p.Asp191=)
15g.66481835G>TCA392936387MAP2K1c.583G>T (p.Asp195Tyr)
c.649G>T (p.Asp217Tyr)
c.502G>T (p.Asp168Tyr)
c.569-5393G>T (n.569-5393G>T)
n.1007G>T
c.700G>T (p.Asp234Tyr)
c.569-3159G>T (n.569-3159G>T)
c.505G>T (p.Asp169Tyr)
c.121G>T (p.Asp41Tyr)
c.571G>T (p.Asp191Tyr)
15g.66481836A>CCA392936393MAP2K1c.584A>C (p.Asp195Ala)
c.650A>C (p.Asp217Ala)
c.503A>C (p.Asp168Ala)
c.569-5392A>C (n.569-5392A>C)
n.1008A>C
c.701A>C (p.Asp234Ala)
c.569-3158A>C (n.569-3158A>C)
c.506A>C (p.Asp169Ala)
c.122A>C (p.Asp41Ala)
c.572A>C (p.Asp191Ala)
dbSNP
15g.66481836A>GCA392936390MAP2K1c.584A>G (p.Asp195Gly)
c.650A>G (p.Asp217Gly)
c.503A>G (p.Asp168Gly)
c.569-5392A>G (n.569-5392A>G)
n.1008A>G
c.701A>G (p.Asp234Gly)
c.569-3158A>G (n.569-3158A>G)
c.506A>G (p.Asp169Gly)
c.122A>G (p.Asp41Gly)
c.572A>G (p.Asp191Gly)
dbSNP
15g.66481836A>TCA392936391MAP2K1c.584A>T (p.Asp195Val)
c.650A>T (p.Asp217Val)
c.503A>T (p.Asp168Val)
c.569-5392A>T (n.569-5392A>T)
n.1008A>T
c.701A>T (p.Asp234Val)
c.569-3158A>T (n.569-3158A>T)
c.506A>T (p.Asp169Val)
c.122A>T (p.Asp41Val)
c.572A>T (p.Asp191Val)
dbSNP
15g.66481837C>ACA392936395MAP2K1c.585C>A (p.Asp195Glu)
c.651C>A (p.Asp217Glu)
c.504C>A (p.Asp168Glu)
c.569-5391C>A (n.569-5391C>A)
n.1009C>A
c.702C>A (p.Asp234Glu)
c.569-3157C>A (n.569-3157C>A)
c.507C>A (p.Asp169Glu)
c.123C>A (p.Asp41Glu)
c.573C>A (p.Asp191Glu)
15g.66481837C>GCA392936397MAP2K1c.585C>G (p.Asp195Glu)
c.651C>G (p.Asp217Glu)
c.504C>G (p.Asp168Glu)
c.569-5391C>G (n.569-5391C>G)
n.1009C>G
c.702C>G (p.Asp234Glu)
c.569-3157C>G (n.569-3157C>G)
c.507C>G (p.Asp169Glu)
c.123C>G (p.Asp41Glu)
c.573C>G (p.Asp191Glu)
dbSNP
15g.66481837C>TCA490858423MAP2K1c.585C>T (p.Asp195=)
c.651C>T (p.Asp217=)
c.504C>T (p.Asp168=)
c.569-5391C>T (n.569-5391C>T)
n.1009C>T
c.702C>T (p.Asp234=)
c.569-3157C>T (n.569-3157C>T)
c.507C>T (p.Asp169=)
c.123C>T (p.Asp41=)
c.573C>T (p.Asp191=)
15g.66481838T>ACA392936400MAP2K1c.586T>A (p.Ser196Thr)
c.652T>A (p.Ser218Thr)
c.505T>A (p.Ser169Thr)
c.569-5390T>A (n.569-5390T>A)
n.1010T>A
c.703T>A (p.Ser235Thr)
c.569-3156T>A (n.569-3156T>A)
c.508T>A (p.Ser170Thr)
c.124T>A (p.Ser42Thr)
c.574T>A (p.Ser192Thr)
dbSNP
15g.66481838T>CCA392936402MAP2K1c.586T>C (p.Ser196Pro)
c.652T>C (p.Ser218Pro)
c.505T>C (p.Ser169Pro)
c.569-5390T>C (n.569-5390T>C)
n.1010T>C
c.703T>C (p.Ser235Pro)
c.569-3156T>C (n.569-3156T>C)
c.508T>C (p.Ser170Pro)
c.124T>C (p.Ser42Pro)
c.574T>C (p.Ser192Pro)
ClinVar dbSNP
15g.66481838T>GCA392936403MAP2K1c.586T>G (p.Ser196Ala)
c.652T>G (p.Ser218Ala)
c.505T>G (p.Ser169Ala)
c.569-5390T>G (n.569-5390T>G)
n.1010T>G
c.703T>G (p.Ser235Ala)
c.569-3156T>G (n.569-3156T>G)
c.508T>G (p.Ser170Ala)
c.124T>G (p.Ser42Ala)
c.574T>G (p.Ser192Ala)
15g.66481839C>ACA392936405MAP2K1c.587C>A (p.Ser196Tyr)
c.653C>A (p.Ser218Tyr)
c.506C>A (p.Ser169Tyr)
c.569-5389C>A (n.569-5389C>A)
n.1011C>A
c.704C>A (p.Ser235Tyr)
c.569-3155C>A (n.569-3155C>A)
c.509C>A (p.Ser170Tyr)
c.125C>A (p.Ser42Tyr)
c.575C>A (p.Ser192Tyr)
dbSNP
15g.66481839C>GCA392936406MAP2K1c.587C>G (p.Ser196Cys)
c.653C>G (p.Ser218Cys)
c.506C>G (p.Ser169Cys)
c.569-5389C>G (n.569-5389C>G)
n.1011C>G
c.704C>G (p.Ser235Cys)
c.569-3155C>G (n.569-3155C>G)
c.509C>G (p.Ser170Cys)
c.125C>G (p.Ser42Cys)
c.575C>G (p.Ser192Cys)
dbSNP
15g.66481839C>TCA392936408MAP2K1c.587C>T (p.Ser196Phe)
c.653C>T (p.Ser218Phe)
c.506C>T (p.Ser169Phe)
c.569-5389C>T (n.569-5389C>T)
n.1011C>T
c.704C>T (p.Ser235Phe)
c.569-3155C>T (n.569-3155C>T)
c.509C>T (p.Ser170Phe)
c.125C>T (p.Ser42Phe)
c.575C>T (p.Ser192Phe)
dbSNP
15g.66481840C>ACA490858425MAP2K1c.588C>A (p.Ser196=)
c.654C>A (p.Ser218=)
c.507C>A (p.Ser169=)
c.569-5388C>A (n.569-5388C>A)
n.1012C>A
c.705C>A (p.Ser235=)
c.569-3154C>A (n.569-3154C>A)
c.510C>A (p.Ser170=)
c.126C>A (p.Ser42=)
c.576C>A (p.Ser192=)
dbSNP gnomAD v4
15g.66481840C>GCA490858424MAP2K1c.588C>G (p.Ser196=)
c.654C>G (p.Ser218=)
c.507C>G (p.Ser169=)
c.569-5388C>G (n.569-5388C>G)
n.1012C>G
c.705C>G (p.Ser235=)
c.569-3154C>G (n.569-3154C>G)
c.510C>G (p.Ser170=)
c.126C>G (p.Ser42=)
c.576C>G (p.Ser192=)
dbSNP
15g.66481840C>TCA490858426MAP2K1c.588C>T (p.Ser196=)
c.654C>T (p.Ser218=)
c.507C>T (p.Ser169=)
c.569-5388C>T (n.569-5388C>T)
n.1012C>T
c.705C>T (p.Ser235=)
c.569-3154C>T (n.569-3154C>T)
c.510C>T (p.Ser170=)
c.126C>T (p.Ser42=)
c.576C>T (p.Ser192=)
dbSNP
15g.66481841A=CA2184097451MAP2K1c.589A= (p.Met197=)
c.655A= (p.Met219=)
c.508A= (p.Met170=)
c.569-5387A= (n.569-5387A=)
n.1013A=
c.706A= (p.Met236=)
c.569-3153A= (n.569-3153A=)
c.511A= (p.Met171=)
c.127A= (p.Met43=)
c.577A= (p.Met193=)
15g.66481841A>CCA392936410MAP2K1c.589A>C (p.Met197Leu)
c.655A>C (p.Met219Leu)
c.508A>C (p.Met170Leu)
c.569-5387A>C (n.569-5387A>C)
n.1013A>C
c.706A>C (p.Met236Leu)
c.569-3153A>C (n.569-3153A>C)
c.511A>C (p.Met171Leu)
c.127A>C (p.Met43Leu)
c.577A>C (p.Met193Leu)
dbSNP
15g.66481841A>GCA392936412MAP2K1c.589A>G (p.Met197Val)
c.655A>G (p.Met219Val)
c.508A>G (p.Met170Val)
c.569-5387A>G (n.569-5387A>G)
n.1013A>G
c.706A>G (p.Met236Val)
c.569-3153A>G (n.569-3153A>G)
c.511A>G (p.Met171Val)
c.127A>G (p.Met43Val)
c.577A>G (p.Met193Val)
dbSNP
15g.66481841A>TCA392936414MAP2K1c.589A>T (p.Met197Leu)
c.655A>T (p.Met219Leu)
c.508A>T (p.Met170Leu)
c.569-5387A>T (n.569-5387A>T)
n.1013A>T
c.706A>T (p.Met236Leu)
c.569-3153A>T (n.569-3153A>T)
c.511A>T (p.Met171Leu)
c.127A>T (p.Met43Leu)
c.577A>T (p.Met193Leu)
dbSNP
15g.66481842T>ACA392936418MAP2K1c.590T>A (p.Met197Lys)
c.656T>A (p.Met219Lys)
c.509T>A (p.Met170Lys)
c.569-5386T>A (n.569-5386T>A)
n.1014T>A
c.707T>A (p.Met236Lys)
c.569-3152T>A (n.569-3152T>A)
c.512T>A (p.Met171Lys)
c.128T>A (p.Met43Lys)
c.578T>A (p.Met193Lys)
dbSNP
15g.66481842T>CCA392936419MAP2K1c.590T>C (p.Met197Thr)
c.656T>C (p.Met219Thr)
c.509T>C (p.Met170Thr)
c.569-5386T>C (n.569-5386T>C)
n.1014T>C
c.707T>C (p.Met236Thr)
c.569-3152T>C (n.569-3152T>C)
c.512T>C (p.Met171Thr)
c.128T>C (p.Met43Thr)
c.578T>C (p.Met193Thr)
dbSNP
15g.66481842T>GCA392936416MAP2K1c.590T>G (p.Met197Arg)
c.656T>G (p.Met219Arg)
c.509T>G (p.Met170Arg)
c.569-5386T>G (n.569-5386T>G)
n.1014T>G
c.707T>G (p.Met236Arg)
c.569-3152T>G (n.569-3152T>G)
c.512T>G (p.Met171Arg)
c.128T>G (p.Met43Arg)
c.578T>G (p.Met193Arg)
dbSNP
15g.66481843G>ACA392936422MAP2K1c.591G>A (p.Met197Ile)
c.657G>A (p.Met219Ile)
c.510G>A (p.Met170Ile)
c.569-5385G>A (n.569-5385G>A)
n.1015G>A
c.708G>A (p.Met236Ile)
c.569-3151G>A (n.569-3151G>A)
c.513G>A (p.Met171Ile)
c.129G>A (p.Met43Ile)
c.579G>A (p.Met193Ile)
dbSNP
15g.66481843G>CCA296119MAP2K1c.591G>C (p.Met197Ile)
c.657G>C (p.Met219Ile)
c.510G>C (p.Met170Ile)
c.569-5385G>C (n.569-5385G>C)
n.1015G>C
c.708G>C (p.Met236Ile)
c.569-3151G>C (n.569-3151G>C)
c.513G>C (p.Met171Ile)
c.129G>C (p.Met43Ile)
c.579G>C (p.Met193Ile)
ClinVar dbSNP
15g.66481843G=CA2184097454MAP2K1c.591G= (p.Met197=)
c.657G= (p.Met219=)
c.510G= (p.Met170=)
c.569-5385G= (n.569-5385G=)
n.1015G=
c.708G= (p.Met236=)
c.569-3151G= (n.569-3151G=)
c.513G= (p.Met171=)
c.129G= (p.Met43=)
c.579G= (p.Met193=)
15g.66481843G>TCA392936424MAP2K1c.591G>T (p.Met197Ile)
c.657G>T (p.Met219Ile)
c.510G>T (p.Met170Ile)
c.569-5385G>T (n.569-5385G>T)
n.1015G>T
c.708G>T (p.Met236Ile)
c.569-3151G>T (n.569-3151G>T)
c.513G>T (p.Met171Ile)
c.129G>T (p.Met43Ile)
c.579G>T (p.Met193Ile)
15g.66481843_66481844delinsAACA2766290578MAP2K1c.591_592delinsAA (p.Met197_Ala198delinsIleThr)
c.657_658delinsAA (p.Met219_Ala220delinsIleThr)
c.510_511delinsAA (p.Met170_Ala171delinsIleThr)
c.569-5385_569-5384delinsAA (n.569-5385_569-5384delinsAA)
n.1015_1016delinsAA
c.708_709delinsAA (p.Met236_Ala237delinsIleThr)
c.569-3151_569-3150delinsAA (n.569-3151_569-3150delinsAA)
c.513_514delinsAA (p.Met171_Ala172delinsIleThr)
c.129_130delinsAA (p.Met43_Ala44delinsIleThr)
c.579_580delinsAA (p.Met193_Ala194delinsIleThr)

Number of alleles fetched