Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.66435132_66435146delCA16042894MAP2K1c.186_200del (p.Glu62_Asp66del)
n.697_711del
c.120_134del (p.Glu40_Asp44del)
ClinVar dbSNP
15g.66435133_66435147delCA645570540MAP2K1c.187_201del (p.Leu63_Asp67del)
n.698_712del
c.121_135del (p.Leu41_Asp45del)
COSMIC
15g.66435145G>ACA180743MAP2K1c.199G>A (p.Asp67Asn)
n.710G>A
c.133G>A (p.Asp45Asn)
ClinVar dbSNP COSMIC
15g.66435145G>CCA392929317MAP2K1c.199G>C (p.Asp67His)
n.710G>C
c.133G>C (p.Asp45His)
15g.66435145G=CA2184071757MAP2K1c.199G= (p.Asp67=)
n.710G=
c.133G= (p.Asp45=)
15g.66435145G>TCA392929318MAP2K1c.199G>T (p.Asp67Tyr)
n.710G>T
c.133G>T (p.Asp45Tyr)
COSMIC
15g.66435146A>CCA392929319MAP2K1c.200A>C (p.Asp67Ala)
n.711A>C
c.134A>C (p.Asp45Ala)
15g.66435146A>GCA392929320MAP2K1c.200A>G (p.Asp67Gly)
n.711A>G
c.134A>G (p.Asp45Gly)
15g.66435146A>TCA392929321MAP2K1c.200A>T (p.Asp67Val)
n.711A>T
c.134A>T (p.Asp45Val)
15g.66435147C>ACA392929322MAP2K1c.201C>A (p.Asp67Glu)
n.712C>A
c.135C>A (p.Asp45Glu)
15g.66435147C>GCA392929323MAP2K1c.201C>G (p.Asp67Glu)
n.712C>G
c.135C>G (p.Asp45Glu)
15g.66435147C>TCA490855981MAP2K1c.201C>T (p.Asp67=)
n.712C>T
c.135C>T (p.Asp45=)
15g.66435148T>ACA392929324MAP2K1c.202T>A (p.Phe68Ile)
n.713T>A
c.136T>A (p.Phe46Ile)
15g.66435148T>CCA392929325MAP2K1c.202T>C (p.Phe68Leu)
n.713T>C
c.136T>C (p.Phe46Leu)
15g.66435148T>GCA392929326MAP2K1c.202T>G (p.Phe68Val)
n.713T>G
c.136T>G (p.Phe46Val)
15g.66435149T>ACA392929328MAP2K1c.203T>A (p.Phe68Tyr)
n.714T>A
c.137T>A (p.Phe46Tyr)
15g.66435149T>CCA392929329MAP2K1c.203T>C (p.Phe68Ser)
n.714T>C
c.137T>C (p.Phe46Ser)
15g.66435149T>GCA392929327MAP2K1c.203T>G (p.Phe68Cys)
n.714T>G
c.137T>G (p.Phe46Cys)
15g.66435150T>ACA392929330MAP2K1c.204T>A (p.Phe68Leu)
n.715T>A
c.138T>A (p.Phe46Leu)
15g.66435150T>CCA490855986MAP2K1c.204T>C (p.Phe68=)
n.715T>C
c.138T>C (p.Phe46=)
15g.66435150T>GCA392929331MAP2K1c.204T>G (p.Phe68Leu)
n.715T>G
c.138T>G (p.Phe46Leu)
15g.66435151G>ACA392929332MAP2K1c.205G>A (p.Glu69Lys)
n.716G>A
c.139G>A (p.Glu47Lys)
ClinVar
15g.66435151G>CCA392929333MAP2K1c.205G>C (p.Glu69Gln)
n.716G>C
c.139G>C (p.Glu47Gln)
15g.66435151G=CA2184071758MAP2K1c.205G= (p.Glu69=)
n.716G=
c.139G= (p.Glu47=)
15g.66435151G>TCA392929334MAP2K1c.205G>T (p.Glu69Ter)
n.716G>T
c.139G>T (p.Glu47Ter)
15g.66435152A>CCA392929335MAP2K1c.206A>C (p.Glu69Ala)
n.717A>C
c.140A>C (p.Glu47Ala)
15g.66435152A>GCA392929336MAP2K1c.206A>G (p.Glu69Gly)
n.717A>G
c.140A>G (p.Glu47Gly)
15g.66435152A>TCA392929337MAP2K1c.206A>T (p.Glu69Val)
n.717A>T
c.140A>T (p.Glu47Val)
15g.66435153G>ACA490855989MAP2K1c.207G>A (p.Glu69=)
n.718G>A
c.141G>A (p.Glu47=)
15g.66435153G>CCA392929338MAP2K1c.207G>C (p.Glu69Asp)
n.718G>C
c.141G>C (p.Glu47Asp)
15g.66435153G>TCA392929339MAP2K1c.207G>T (p.Glu69Asp)
n.718G>T
c.141G>T (p.Glu47Asp)
15g.66435154A>CCA392929340MAP2K1c.208A>C (p.Lys70Gln)
n.719A>C
c.142A>C (p.Lys48Gln)
15g.66435154A>GCA392929341MAP2K1c.208A>G (p.Lys70Glu)
n.719A>G
c.142A>G (p.Lys48Glu)
15g.66435154A>TCA392929342MAP2K1c.208A>T (p.Lys70Ter)
n.719A>T
c.142A>T (p.Lys48Ter)
15g.66435155A>CCA392929345MAP2K1c.209A>C (p.Lys70Thr)
n.720A>C
c.143A>C (p.Lys48Thr)
15g.66435155A>GCA392929344MAP2K1c.209A>G (p.Lys70Arg)
n.720A>G
c.143A>G (p.Lys48Arg)
15g.66435155A>TCA392929343MAP2K1c.209A>T (p.Lys70Met)
n.720A>T
c.143A>T (p.Lys48Met)
15g.66435156G>ACA490855997MAP2K1c.210G>A (p.Lys70=)
n.721G>A
c.144G>A (p.Lys48=)
15g.66435156G>CCA392929346MAP2K1c.210G>C (p.Lys70Asn)
n.721G>C
c.144G>C (p.Lys48Asn)
15g.66435156G>TCA392929347MAP2K1c.210G>T (p.Lys70Asn)
n.721G>T
c.144G>T (p.Lys48Asn)
15g.66435157A>CCA392929348MAP2K1c.211A>C (p.Ile71Leu)
n.722A>C
c.145A>C (p.Ile49Leu)
15g.66435157A>GCA392929349MAP2K1c.211A>G (p.Ile71Val)
n.722A>G
c.145A>G (p.Ile49Val)
15g.66435157A>TCA392929350MAP2K1c.211A>T (p.Ile71Phe)
n.722A>T
c.145A>T (p.Ile49Phe)
15g.66435158T>ACA392929351MAP2K1c.212T>A (p.Ile71Asn)
n.723T>A
c.146T>A (p.Ile49Asn)
15g.66435158T>CCA392929352MAP2K1c.212T>C (p.Ile71Thr)
n.723T>C
c.146T>C (p.Ile49Thr)
15g.66435158T>GCA392929353MAP2K1c.212T>G (p.Ile71Ser)
n.723T>G
c.146T>G (p.Ile49Ser)
15g.66435159C>ACA490855999MAP2K1c.213C>A (p.Ile71=)
n.724C>A
c.147C>A (p.Ile49=)
15g.66435159C>GCA392929354MAP2K1c.213C>G (p.Ile71Met)
n.724C>G
c.147C>G (p.Ile49Met)
15g.66435159C>TCA490856000MAP2K1c.213C>T (p.Ile71=)
n.724C>T
c.147C>T (p.Ile49=)
15g.66435160A=CA2184071759MAP2K1c.214A= (p.Ser72=)
n.725A=
c.148A= (p.Ser50=)

Number of alleles fetched