Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.66481706_66481749del | CA2184097348 | MAP2K1 | c.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 |
15 | g.66481741T>C | CA2731111625 | MAP2K1 | c.503-14T>C (n.503-14T>C) c.569-14T>C (n.569-14T>C) c.422-14T>C (n.422-14T>C) c.569-5487T>C (n.569-5487T>C) n.927-14T>C c.620-14T>C (n.620-14T>C) c.569-3253T>C (n.569-3253T>C) c.425-14T>C (n.425-14T>C) c.41-14T>C (n.41-14T>C) c.491-14T>C (n.491-14T>C) | dbSNP |
15 | g.66481742C>A | CA2730917801 | MAP2K1 | c.503-13C>A (n.503-13C>A) c.569-13C>A (n.569-13C>A) c.422-13C>A (n.422-13C>A) c.569-5486C>A (n.569-5486C>A) n.927-13C>A c.620-13C>A (n.620-13C>A) c.569-3252C>A (n.569-3252C>A) c.425-13C>A (n.425-13C>A) c.41-13C>A (n.41-13C>A) c.491-13C>A (n.491-13C>A) | dbSNP |
15 | g.66481742C= | CA2184097374 | MAP2K1 | c.503-13C= (n.503-13C=) c.569-13C= (n.569-13C=) c.422-13C= (n.422-13C=) c.569-5486C= (n.569-5486C=) n.927-13C= c.620-13C= (n.620-13C=) c.569-3252C= (n.569-3252C=) c.425-13C= (n.425-13C=) c.41-13C= (n.41-13C=) c.491-13C= (n.491-13C=) | |
15 | g.66481742C>T | CA7623987 | MAP2K1 | c.503-13C>T (n.503-13C>T) c.569-13C>T (n.569-13C>T) c.422-13C>T (n.422-13C>T) c.569-5486C>T (n.569-5486C>T) n.927-13C>T c.620-13C>T (n.620-13C>T) c.569-3252C>T (n.569-3252C>T) c.425-13C>T (n.425-13C>T) c.41-13C>T (n.41-13C>T) c.491-13C>T (n.491-13C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.66481744C= | CA2184097376 | MAP2K1 | c.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=) | |
15 | g.66481744C>T | CA2184097377 | MAP2K1 | c.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 |
15 | g.66481745T>C | CA7623988 | MAP2K1 | c.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 |
15 | g.66481745T= | CA2184097378 | MAP2K1 | c.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=) | |
15 | g.66481746T>C | CA2731111632 | MAP2K1 | c.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 |
15 | g.66481747C>A | CA2730913082 | MAP2K1 | c.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 |
15 | g.66481747C= | CA2184097380 | MAP2K1 | c.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=) | |
15 | g.66481747C>G | CA7623989 | MAP2K1 | c.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 |
15 | g.66481747C>T | CA658798392 | MAP2K1 | c.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 |
15 | g.66481748C>A | CA618679507 | MAP2K1 | c.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 |
15 | g.66481748C= | CA2184097382 | MAP2K1 | c.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=) | |
15 | g.66481748C>G | CA618679509 | MAP2K1 | c.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 |
15 | g.66481748C>T | CA7623990 | MAP2K1 | c.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 |
15 | g.66481749C>A | CA2731111652 | MAP2K1 | c.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 |
15 | g.66481749C>T | CA2731111651 | MAP2K1 | c.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 |
15 | g.66481751G>A | CA2573151055 | MAP2K1 | c.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 |
15 | g.66481751G>C | CA2731111657 | MAP2K1 | c.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 |
15 | g.66481751G>T | CA2731111656 | MAP2K1 | c.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 |
15 | g.66481752C>G | CA2731111694 | MAP2K1 | c.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 |
15 | g.66481752C>T | CA2731111692 | MAP2K1 | c.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 |
15 | g.66481753A>C | CA392936029 | MAP2K1 | c.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 |
15 | g.66481753A>G | CA392936031 | MAP2K1 | c.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 |
15 | g.66481753A>T | CA392936033 | MAP2K1 | c.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 |
15 | g.66481754G>A | CA392936035 | MAP2K1 | c.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 |
15 | g.66481754G>C | CA392936036 | MAP2K1 | c.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 |
15 | g.66481754G>T | CA392936038 | MAP2K1 | c.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 |
15 | g.66481755A>C | CA392936041 | MAP2K1 | c.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) | |
15 | g.66481755A>G | CA392936043 | MAP2K1 | c.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) | |
15 | g.66481755A>T | CA392936040 | MAP2K1 | c.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 |
15 | g.66481756T>A | CA392936045 | MAP2K1 | c.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) | |
15 | g.66481756T>C | CA490858374 | MAP2K1 | c.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 |
15 | g.66481756T>G | CA392936046 | MAP2K1 | c.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 |
15 | g.66481757G>A | CA392936049 | MAP2K1 | c.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 |
15 | g.66481757G>C | CA392936051 | MAP2K1 | c.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 |
15 | g.66481757G>T | CA392936053 | MAP2K1 | c.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 |
15 | g.66481758T>A | CA392936059 | MAP2K1 | c.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 |
15 | g.66481758T>C | CA392936055 | MAP2K1 | c.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 |
15 | g.66481758T>G | CA392936057 | MAP2K1 | c.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 |
15 | g.66481759C>A | CA490858375 | MAP2K1 | c.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 |
15 | g.66481759C>G | CA490858376 | MAP2K1 | c.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 |
15 | g.66481759C>T | CA490858377 | MAP2K1 | c.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 |
15 | g.66481760A>C | CA392936061 | MAP2K1 | c.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) | |
15 | g.66481760A>G | CA392936064 | MAP2K1 | c.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 |
15 | g.66481760A>T | CA392936066 | MAP2K1 | c.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 |
15 | g.66481761A>C | CA392936068 | MAP2K1 | c.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) | |
15 | g.66481761A>G | CA392936070 | MAP2K1 | c.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 |
15 | g.66481761A>T | CA392936071 | MAP2K1 | c.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 |
15 | g.66481762G>A | CA490858378 | MAP2K1 | c.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 |
15 | g.66481762G>C | CA392936073 | MAP2K1 | c.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 |
15 | g.66481762G>T | CA392936075 | MAP2K1 | c.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) | |
15 | g.66481763C>A | CA392936077 | MAP2K1 | c.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 |
15 | g.66481763C= | CA2184097385 | MAP2K1 | c.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=) | |
15 | g.66481763C>G | CA392936079 | MAP2K1 | c.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 |
15 | g.66481763C>T | CA392936081 | MAP2K1 | c.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 |
15 | g.66481764C>A | CA392936082 | MAP2K1 | c.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) | |
15 | g.66481764C>G | CA392936084 | MAP2K1 | c.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 |
15 | g.66481764C>T | CA392936086 | MAP2K1 | c.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 |
15 | g.66481765C>A | CA490858380 | MAP2K1 | c.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=) | |
15 | g.66481765C>G | CA490858381 | MAP2K1 | c.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=) | |
15 | g.66481765C>T | CA490858379 | MAP2K1 | c.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 |
15 | g.66481766T>A | CA392936092 | MAP2K1 | c.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) | |
15 | g.66481766T>C | CA392936090 | MAP2K1 | c.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) | |
15 | g.66481766T>G | CA392936088 | MAP2K1 | c.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) | |
15 | g.66481766T= | CA2184097388 | MAP2K1 | c.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=) | |
15 | g.66481766_66481767insAG | CA970939411 | MAP2K1 | c.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 |
15 | g.66481767C>A | CA392936095 | MAP2K1 | c.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 |
15 | g.66481767C= | CA2184097390 | MAP2K1 | c.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=) | |
15 | g.66481767C>G | CA392936097 | MAP2K1 | c.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 |
15 | g.66481767C>T | CA392936098 | MAP2K1 | c.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 |
15 | g.66481768C>A | CA490858383 | MAP2K1 | c.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=) | |
15 | g.66481768C>G | CA490858382 | MAP2K1 | c.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=) | |
15 | g.66481768C>T | CA490858384 | MAP2K1 | c.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 |
15 | g.66481769A>C | CA392936100 | MAP2K1 | c.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) | |
15 | g.66481769A>G | CA392936102 | MAP2K1 | c.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) | |
15 | g.66481769A>T | CA392936104 | MAP2K1 | c.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 |
15 | g.66481770A>C | CA392936107 | MAP2K1 | c.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 |
15 | g.66481770A>G | CA392936109 | MAP2K1 | c.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 |
15 | g.66481770A>T | CA392936108 | MAP2K1 | c.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 |
15 | g.66481771C>A | CA392936111 | MAP2K1 | c.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) | |
15 | g.66481771C= | CA2184097392 | MAP2K1 | c.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=) | |
15 | g.66481771C>G | CA392936113 | MAP2K1 | c.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 |
15 | g.66481771C>T | CA490858385 | MAP2K1 | c.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 |
15 | g.66481772A>C | CA392936115 | MAP2K1 | c.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) | |
15 | g.66481772A>G | CA392936116 | MAP2K1 | c.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 |
15 | g.66481772A>T | CA392936118 | MAP2K1 | c.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 |
15 | g.66481773T>A | CA392936120 | MAP2K1 | c.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 |
15 | g.66481773T>C | CA392936122 | MAP2K1 | c.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) | |
15 | g.66481773T>G | CA392936124 | MAP2K1 | c.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) | |
15 | g.66481774C>A | CA490858387 | MAP2K1 | c.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=) | |
15 | g.66481774C>G | CA392936126 | MAP2K1 | c.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 |
15 | g.66481774C>T | CA490858386 | MAP2K1 | c.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 |
15 | g.66481775C>A | CA392936128 | MAP2K1 | c.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 |
15 | g.66481775C= | CA2184097393 | MAP2K1 | c.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=) | |
15 | g.66481775C>G | CA392936130 | MAP2K1 | c.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 |
15 | g.66481775C>T | CA490858388 | MAP2K1 | c.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 |
15 | g.66481776T>A | CA392936132 | MAP2K1 | c.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 |
15 | g.66481776T>C | CA392936136 | MAP2K1 | c.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) | |
15 | g.66481776T>G | CA392936134 | MAP2K1 | c.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) | |
15 | g.66481777A>C | CA490858391 | MAP2K1 | c.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=) | |
15 | g.66481777A>G | CA490858389 | MAP2K1 | c.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 |
15 | g.66481777A>T | CA490858390 | MAP2K1 | c.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 |
15 | g.66481778G>A | CA392936138 | MAP2K1 | c.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 |
15 | g.66481778G>C | CA7623991 | MAP2K1 | c.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 |
15 | g.66481778G= | CA2184097395 | MAP2K1 | c.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=) | |
15 | g.66481778G>T | CA392936140 | MAP2K1 | c.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) | |
15 | g.66481779T>A | CA392936143 | MAP2K1 | c.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 |
15 | g.66481779T>C | CA392936145 | MAP2K1 | c.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 |
15 | g.66481779T>G | CA392936147 | MAP2K1 | c.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 |
15 | g.66481780C>A | CA490858393 | MAP2K1 | c.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 |
15 | g.66481780C= | CA2184097398 | MAP2K1 | c.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=) | |
15 | g.66481780C>G | CA490858392 | MAP2K1 | c.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 |
15 | g.66481780C>T | CA490858394 | MAP2K1 | c.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 |
15 | g.66481781A>C | CA392936150 | MAP2K1 | c.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) | |
15 | g.66481781A>G | CA392936151 | MAP2K1 | c.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) | |
15 | g.66481781A>T | CA392936153 | MAP2K1 | c.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) | |
15 | g.66481782A= | CA2184097400 | MAP2K1 | c.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=) | |
15 | g.66481782A>C | CA392936156 | MAP2K1 | c.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 |
15 | g.66481782A>G | CA392936157 | MAP2K1 | c.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 |
15 | g.66481782A>T | CA392936160 | MAP2K1 | c.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 |
15 | g.66481783C>A | CA392936162 | MAP2K1 | c.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) | |
15 | g.66481783C>G | CA392936163 | MAP2K1 | c.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 |
15 | g.66481783C>T | CA490858395 | MAP2K1 | c.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 |
15 | g.66481784T>A | CA392936169 | MAP2K1 | c.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) | |
15 | g.66481784T>C | CA392936167 | MAP2K1 | c.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 |
15 | g.66481784T>G | CA392936165 | MAP2K1 | c.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) | |
15 | g.66481785C>A | CA392936171 | MAP2K1 | c.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 |
15 | g.66481785C>G | CA392936172 | MAP2K1 | c.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 |
15 | g.66481785C>T | CA392936174 | MAP2K1 | c.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 |
15 | g.66481786C>A | CA490858396 | MAP2K1 | c.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 |
15 | g.66481786C>G | CA490858397 | MAP2K1 | c.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 |
15 | g.66481786C>T | CA490858398 | MAP2K1 | c.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 |
15 | g.66481787C>A | CA392936176 | MAP2K1 | c.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 |
15 | g.66481787C= | CA2184097402 | MAP2K1 | c.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=) | |
15 | g.66481787C>G | CA392936178 | MAP2K1 | c.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 |
15 | g.66481787C>T | CA7623992 | MAP2K1 | c.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 |
15 | g.66481788G>A | CA392936181 | MAP2K1 | c.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 |
15 | g.66481788G>C | CA392936183 | MAP2K1 | c.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 |
15 | g.66481788G>T | CA392936184 | MAP2K1 | c.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 |
15 | g.66481789T>A | CA490858400 | MAP2K1 | c.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 |
15 | g.66481789T>C | CA490858401 | MAP2K1 | c.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 |
15 | g.66481789T>G | CA490858399 | MAP2K1 | c.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=) | |
15 | g.66481789T= | CA2184097405 | MAP2K1 | c.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=) | |
15 | g.66481790G>A | CA392936185 | MAP2K1 | c.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 |
15 | g.66481790G>C | CA392936187 | MAP2K1 | c.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 |
15 | g.66481790G>T | CA392936189 | MAP2K1 | c.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 |
15 | g.66481791G>A | CA392936194 | MAP2K1 | c.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 |
15 | g.66481791G>C | CA392936192 | MAP2K1 | c.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 |
15 | g.66481791G>T | CA392936191 | MAP2K1 | c.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 |
15 | g.66481792G>A | CA7623993 | MAP2K1 | c.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 |
15 | g.66481792G>C | CA490858402 | MAP2K1 | c.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 |
15 | g.66481792G= | CA2184097407 | MAP2K1 | c.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=) | |
15 | g.66481792G>T | CA490858403 | MAP2K1 | c.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 |
15 | g.66481793G>A | CA16602457 | MAP2K1 | c.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 |
15 | g.66481793G>C | CA392936198 | MAP2K1 | c.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 |
15 | g.66481793G= | CA2184097409 | MAP2K1 | c.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=) | |
15 | g.66481793G>T | CA392936200 | MAP2K1 | c.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 |
15 | g.66481794A= | CA2184097414 | MAP2K1 | c.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=) | |
15 | g.66481794A>C | CA392936203 | MAP2K1 | c.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 |
15 | g.66481794A>G | CA234222 | MAP2K1 | c.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 |
15 | g.66481794A>T | CA392936205 | MAP2K1 | c.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 |
15 | g.66481795G>A | CA490858404 | MAP2K1 | c.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 |
15 | g.66481795G>C | CA392936207 | MAP2K1 | c.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 |
15 | g.66481795G>T | CA392936208 | MAP2K1 | c.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 |
15 | g.66481796A>C | CA392936210 | MAP2K1 | c.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 |
15 | g.66481796A>G | CA392936212 | MAP2K1 | c.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 |
15 | g.66481796A>T | CA392936214 | MAP2K1 | c.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 |
15 | g.66481797T>A | CA392936218 | MAP2K1 | c.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 |
15 | g.66481797T>C | CA392936220 | MAP2K1 | c.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 |
15 | g.66481797T>G | CA392936216 | MAP2K1 | c.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 |
15 | g.66481798C>A | CA490858406 | MAP2K1 | c.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 |
15 | g.66481798C>G | CA392936222 | MAP2K1 | c.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 |
15 | g.66481798C>T | CA490858405 | MAP2K1 | c.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 |
15 | g.66481799A>C | CA392936224 | MAP2K1 | c.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) | |
15 | g.66481799A>G | CA392936226 | MAP2K1 | c.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 |
15 | g.66481799A>T | CA392936228 | MAP2K1 | c.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 |
15 | g.66481800A>C | CA392936234 | MAP2K1 | c.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) | |
15 | g.66481800A>G | CA392936232 | MAP2K1 | c.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 |
15 | g.66481800A>T | CA392936230 | MAP2K1 | c.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 |
15 | g.66481801G>A | CA7623994 | MAP2K1 | c.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 |
15 | g.66481801G>C | CA392936236 | MAP2K1 | c.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 |
15 | g.66481801G= | CA2184097415 | MAP2K1 | c.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=) | |
15 | g.66481801G>T | CA392936237 | MAP2K1 | c.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) | |
15 | g.66481802C>A | CA392936240 | MAP2K1 | c.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 |
15 | g.66481802C>G | CA392936241 | MAP2K1 | c.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 |
15 | g.66481802C>T | CA392936242 | MAP2K1 | c.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) | |
15 | g.66481803T>A | CA392936245 | MAP2K1 | c.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 |
15 | g.66481803T>C | CA392936249 | MAP2K1 | c.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) | |
15 | g.66481803T>G | CA392936247 | MAP2K1 | c.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) | |
15 | g.66481804C>A | CA490858407 | MAP2K1 | c.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 |
15 | g.66481804C>G | CA490858408 | MAP2K1 | c.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 |
15 | g.66481804C>T | CA490858409 | MAP2K1 | c.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 |
15 | g.66481805T>A | CA392936251 | MAP2K1 | c.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 |
15 | g.66481805T>C | CA392936255 | MAP2K1 | c.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 |
15 | g.66481805T>G | CA392936253 | MAP2K1 | c.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) | |
15 | g.66481806del | CA2629083409 | MAP2K1 | c.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 |
15 | g.66481806G>A | CA392936257 | MAP2K1 | c.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 |
15 | g.66481806G>C | CA392936258 | MAP2K1 | c.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 |
15 | g.66481806G>T | CA392936261 | MAP2K1 | c.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) | |
15 | g.66481807T>A | CA392936263 | MAP2K1 | c.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 |
15 | g.66481807T>C | CA490858410 | MAP2K1 | c.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 |
15 | g.66481807T>G | CA392936264 | MAP2K1 | c.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 |
15 | g.66481808G>A | CA392936271 | MAP2K1 | c.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 |
15 | g.66481808G>C | CA392936269 | MAP2K1 | c.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 |
15 | g.66481808G>T | CA392936267 | MAP2K1 | c.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) | |
15 | g.66481809A>C | CA392936273 | MAP2K1 | c.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 |
15 | g.66481809A>G | CA392936275 | MAP2K1 | c.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 |
15 | g.66481809A>T | CA392936277 | MAP2K1 | c.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 |
15 | g.66481810C>A | CA392936279 | MAP2K1 | c.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 |
15 | g.66481810C= | CA2184097417 | MAP2K1 | c.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=) | |
15 | g.66481810C>G | CA392936281 | MAP2K1 | c.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) | |
15 | g.66481810C>T | CA7623995 | MAP2K1 | c.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 |
15 | g.66481811T>A | CA392936288 | MAP2K1 | c.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 |
15 | g.66481811T>C | CA392936285 | MAP2K1 | c.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) | |
15 | g.66481811T>G | CA392936286 | MAP2K1 | c.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) | |
15 | g.66481812T>A | CA392936289 | MAP2K1 | c.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 |
15 | g.66481812T>C | CA392936291 | MAP2K1 | c.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) | |
15 | g.66481812T>G | CA392936292 | MAP2K1 | c.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) | |
15 | g.66481813T>A | CA392936294 | MAP2K1 | c.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) | |
15 | g.66481813T>C | CA271671668 | MAP2K1 | c.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 |
15 | g.66481813T>G | CA392936297 | MAP2K1 | c.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 |
15 | g.66481813T= | CA2184097420 | MAP2K1 | c.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=) | |
15 | g.66481814G>A | CA392936300 | MAP2K1 | c.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 |
15 | g.66481814G>C | CA392936302 | MAP2K1 | c.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 |
15 | g.66481814G>T | CA392936304 | MAP2K1 | c.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 |
15 | g.66481815G>A | CA392936306 | MAP2K1 | c.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 |
15 | g.66481815G>C | CA392936307 | MAP2K1 | c.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 |
15 | g.66481815G>T | CA392936309 | MAP2K1 | c.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 |
15 | g.66481816G>A | CA490858412 | MAP2K1 | c.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 |
15 | g.66481816G>C | CA490858411 | MAP2K1 | c.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 |
15 | g.66481816G= | CA2184097422 | MAP2K1 | c.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=) | |
15 | g.66481816G>T | CA490858413 | MAP2K1 | c.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 |
15 | g.66481817G>A | CA185378 | MAP2K1 | c.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 |
15 | g.66481817G>C | CA392936313 | MAP2K1 | c.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 |
15 | g.66481817G= | CA2184097424 | MAP2K1 | c.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=) | |
15 | g.66481817G>T | CA392936312 | MAP2K1 | c.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 |
15 | g.66481818T>A | CA16602653 | MAP2K1 | c.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 |
15 | g.66481818T>C | CA392936316 | MAP2K1 | c.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 |
15 | g.66481818T>G | CA392936317 | MAP2K1 | c.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 |
15 | g.66481818T= | CA2184097428 | MAP2K1 | c.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=) | |
15 | g.66481819C>A | CA490858414 | MAP2K1 | c.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 |
15 | g.66481819C= | CA2184097430 | MAP2K1 | c.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=) | |
15 | g.66481819C>G | CA490858416 | MAP2K1 | c.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 |
15 | g.66481819C>T | CA490858415 | MAP2K1 | c.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 |
15 | g.66481820A>C | CA392936319 | MAP2K1 | c.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) | |
15 | g.66481820A>G | CA392936321 | MAP2K1 | c.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 |
15 | g.66481820A>T | CA392936322 | MAP2K1 | c.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 |
15 | g.66481821G>A | CA392936324 | MAP2K1 | c.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 |
15 | g.66481821G>C | CA271671674 | MAP2K1 | c.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 |
15 | g.66481821G= | CA2184097432 | MAP2K1 | c.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=) | |
15 | g.66481821G>T | CA392936327 | MAP2K1 | c.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) | |
15 | g.66481822C>A | CA392936329 | MAP2K1 | c.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 |
15 | g.66481822C= | CA2184097434 | MAP2K1 | c.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=) | |
15 | g.66481822C>G | CA392936331 | MAP2K1 | c.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 |
15 | g.66481822C>T | CA291989 | MAP2K1 | c.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 |
15 | g.66481823G>A | CA392936338 | MAP2K1 | c.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 |
15 | g.66481823G>C | CA392936335 | MAP2K1 | c.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 |
15 | g.66481823G= | CA2184097436 | MAP2K1 | c.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=) | |
15 | g.66481823G>T | CA392936337 | MAP2K1 | c.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 |
15 | g.66481824G>A | CA392936341 | MAP2K1 | c.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 |
15 | g.66481824G>C | CA392936343 | MAP2K1 | c.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 |
15 | g.66481824G>T | CA392936345 | MAP2K1 | c.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 |
15 | g.66481825G>A | CA271671679 | MAP2K1 | c.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 |
15 | g.66481825G>C | CA490858417 | MAP2K1 | c.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 |
15 | g.66481825G= | CA2184097439 | MAP2K1 | c.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=) | |
15 | g.66481825G>T | CA490858418 | MAP2K1 | c.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 |
15 | g.66481826C>A | CA392936347 | MAP2K1 | c.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) | |
15 | g.66481826C>G | CA392936349 | MAP2K1 | c.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 |
15 | g.66481826C>T | CA392936351 | MAP2K1 | c.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 |
15 | g.66481827A>C | CA392936353 | MAP2K1 | c.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) | |
15 | g.66481827A>G | CA392936355 | MAP2K1 | c.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 |
15 | g.66481827A>T | CA392936357 | MAP2K1 | c.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 |
15 | g.66481828G>A | CA271671685 | MAP2K1 | c.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 |
15 | g.66481828G>C | CA392936358 | MAP2K1 | c.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 |
15 | g.66481828G= | CA2184097440 | MAP2K1 | c.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=) | |
15 | g.66481828G>T | CA392936360 | MAP2K1 | c.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) | |
15 | g.66481829C>A | CA392936366 | MAP2K1 | c.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 |
15 | g.66481829C>G | CA392936364 | MAP2K1 | c.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 |
15 | g.66481829C>T | CA392936362 | MAP2K1 | c.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 |
15 | g.66481830T>A | CA392936369 | MAP2K1 | c.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 |
15 | g.66481830T>C | CA16602654 | MAP2K1 | c.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 |
15 | g.66481830T>G | CA392936370 | MAP2K1 | c.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) | |
15 | g.66481830T= | CA2184097442 | MAP2K1 | c.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=) | |
15 | g.66481831C>A | CA490858419 | MAP2K1 | c.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=) | |
15 | g.66481831C>G | CA490858421 | MAP2K1 | c.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 |
15 | g.66481831C>T | CA490858420 | MAP2K1 | c.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 |
15 | g.66481832A>C | CA392936372 | MAP2K1 | c.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 |
15 | g.66481832A>G | CA392936374 | MAP2K1 | c.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 |
15 | g.66481832A>T | CA392936376 | MAP2K1 | c.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 |
15 | g.66481833T>A | CA392936378 | MAP2K1 | c.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 |
15 | g.66481833T>C | CA392936380 | MAP2K1 | c.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 |
15 | g.66481833T>G | CA392936382 | MAP2K1 | c.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 |
15 | g.66481834C>A | CA490858422 | MAP2K1 | c.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=) | |
15 | g.66481834C= | CA2184097445 | MAP2K1 | c.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=) | |
15 | g.66481834C>G | CA392936383 | MAP2K1 | c.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 |
15 | g.66481834C>T | CA134607 | MAP2K1 | c.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 |
15 | g.66481835G>A | CA7623996 | MAP2K1 | c.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 |
15 | g.66481835G>C | CA392936386 | MAP2K1 | c.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 |
15 | g.66481835G= | CA2184097448 | MAP2K1 | c.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=) | |
15 | g.66481835G>T | CA392936387 | MAP2K1 | c.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) | |
15 | g.66481836A>C | CA392936393 | MAP2K1 | c.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 |
15 | g.66481836A>G | CA392936390 | MAP2K1 | c.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 |
15 | g.66481836A>T | CA392936391 | MAP2K1 | c.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 |
15 | g.66481837C>A | CA392936395 | MAP2K1 | c.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) | |
15 | g.66481837C>G | CA392936397 | MAP2K1 | c.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 |
15 | g.66481837C>T | CA490858423 | MAP2K1 | c.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=) | |
15 | g.66481838T>A | CA392936400 | MAP2K1 | c.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 |
15 | g.66481838T>C | CA392936402 | MAP2K1 | c.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 |
15 | g.66481838T>G | CA392936403 | MAP2K1 | c.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) | |
15 | g.66481839C>A | CA392936405 | MAP2K1 | c.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 |
15 | g.66481839C>G | CA392936406 | MAP2K1 | c.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 |
15 | g.66481839C>T | CA392936408 | MAP2K1 | c.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 |
15 | g.66481840C>A | CA490858425 | MAP2K1 | c.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 |
15 | g.66481840C>G | CA490858424 | MAP2K1 | c.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 |
15 | g.66481840C>T | CA490858426 | MAP2K1 | c.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 |
15 | g.66481841A= | CA2184097451 | MAP2K1 | c.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=) | |
15 | g.66481841A>C | CA392936410 | MAP2K1 | c.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 |
15 | g.66481841A>G | CA392936412 | MAP2K1 | c.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 |
15 | g.66481841A>T | CA392936414 | MAP2K1 | c.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 |