Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.66435165G>ACA490856002MAP2K1c.153G>A (p.Glu51=)
c.219G>A (p.Glu73=)
n.655G>A
n.730G>A
 COSMIC
15g.66435165G>CCA392929369MAP2K1c.153G>C (p.Glu51Asp)
c.219G>C (p.Glu73Asp)
n.655G>C
n.730G>C
 dbSNP
15g.66435165G>TCA392929370MAP2K1c.153G>T (p.Glu51Asp)
c.219G>T (p.Glu73Asp)
n.655G>T
n.730G>T
15g.66435166C>ACA392929371MAP2K1c.154C>A (p.Leu52Met)
c.220C>A (p.Leu74Met)
n.656C>A
n.731C>A
 dbSNP
15g.66435166C>GCA392929372MAP2K1c.154C>G (p.Leu52Val)
c.220C>G (p.Leu74Val)
n.656C>G
n.731C>G
 dbSNP
15g.66435166C>TCA490856003MAP2K1c.154C>T (p.Leu52=)
c.220C>T (p.Leu74=)
n.656C>T
n.731C>T
 dbSNP
15g.66435167T>ACA392929373MAP2K1c.155T>A (p.Leu52Gln)
c.221T>A (p.Leu74Gln)
n.657T>A
n.732T>A
15g.66435167T>CCA392929374MAP2K1c.155T>C (p.Leu52Pro)
c.221T>C (p.Leu74Pro)
n.657T>C
n.732T>C
15g.66435167T>GCA392929375MAP2K1c.155T>G (p.Leu52Arg)
c.221T>G (p.Leu74Arg)
n.657T>G
n.732T>G
15g.66435168G>ACA490856005MAP2K1c.156G>A (p.Leu52=)
c.222G>A (p.Leu74=)
n.658G>A
n.733G>A
 dbSNP
15g.66435168G>CCA490856004MAP2K1c.156G>C (p.Leu52=)
c.222G>C (p.Leu74=)
n.658G>C
n.733G>C
 dbSNP
15g.66435168G=CA2184071762MAP2K1c.156G= (p.Leu52=)
c.222G= (p.Leu74=)
n.658G=
n.733G=
15g.66435168G>TCA490856006MAP2K1c.156G>T (p.Leu52=)
c.222G>T (p.Leu74=)
n.658G>T
n.733G>T
15g.66435172dupCA2731115417MAP2K1c.160dup (p.Ala54GlyfsTer?)
c.226dup (p.Ala76GlyfsTer?)
n.662dup
n.737dup
 dbSNP
15g.66435169G>ACA392929376MAP2K1c.157G>A (p.Gly53Arg)
c.223G>A (p.Gly75Arg)
n.659G>A
n.734G>A
15g.66435169G>CCA392929378MAP2K1c.157G>C (p.Gly53Arg)
c.223G>C (p.Gly75Arg)
n.659G>C
n.734G>C
15g.66435169G>TCA392929377MAP2K1c.157G>T (p.Gly53Trp)
c.223G>T (p.Gly75Trp)
n.659G>T
n.734G>T
15g.66435170G>ACA392929381MAP2K1c.158G>A (p.Gly53Glu)
c.224G>A (p.Gly75Glu)
n.660G>A
n.735G>A
 dbSNP
15g.66435170G>CCA392929383MAP2K1c.158G>C (p.Gly53Ala)
c.224G>C (p.Gly75Ala)
n.660G>C
n.735G>C
 dbSNP
15g.66435170G>TCA392929384MAP2K1c.158G>T (p.Gly53Val)
c.224G>T (p.Gly75Val)
n.660G>T
n.735G>T
15g.66435171G>ACA490856007MAP2K1c.159G>A (p.Gly53=)
c.225G>A (p.Gly75=)
n.661G>A
n.736G>A
15g.66435171G>CCA490856008MAP2K1c.159G>C (p.Gly53=)
c.225G>C (p.Gly75=)
n.661G>C
n.736G>C
15g.66435171G>TCA490856009MAP2K1c.159G>T (p.Gly53=)
c.225G>T (p.Gly75=)
n.661G>T
n.736G>T
15g.66435172G>ACA392929387MAP2K1c.160G>A (p.Ala54Thr)
c.226G>A (p.Ala76Thr)
n.662G>A
n.737G>A
 dbSNP
15g.66435172G>CCA392929388MAP2K1c.160G>C (p.Ala54Pro)
c.226G>C (p.Ala76Pro)
n.662G>C
n.737G>C
 dbSNP
15g.66435172G>TCA392929390MAP2K1c.160G>T (p.Ala54Ser)
c.226G>T (p.Ala76Ser)
n.662G>T
n.737G>T
 dbSNP gnomAD v4
15g.66435173C>ACA392929392MAP2K1c.161C>A (p.Ala54Asp)
c.227C>A (p.Ala76Asp)
n.663C>A
n.738C>A
 dbSNP
15g.66435173C>GCA392929394MAP2K1c.161C>G (p.Ala54Gly)
c.227C>G (p.Ala76Gly)
n.663C>G
n.738C>G
 dbSNP
15g.66435173C>TCA392929396MAP2K1c.161C>T (p.Ala54Val)
c.227C>T (p.Ala76Val)
n.663C>T
n.738C>T
 dbSNP COSMIC
15g.66435174T>ACA490856011MAP2K1c.162T>A (p.Ala54=)
c.228T>A (p.Ala76=)
n.664T>A
n.739T>A
15g.66435174T>CCA490856010MAP2K1c.162T>C (p.Ala54=)
c.228T>C (p.Ala76=)
n.664T>C
n.739T>C
15g.66435174T>GCA490856012MAP2K1c.162T>G (p.Ala54=)
c.228T>G (p.Ala76=)
n.664T>G
n.739T>G
15g.66435175G>ACA392929399MAP2K1c.163G>A (p.Gly55Ser)
c.229G>A (p.Gly77Ser)
n.665G>A
n.740G>A
 dbSNP gnomAD v4
15g.66435175G>CCA392929400MAP2K1c.163G>C (p.Gly55Arg)
c.229G>C (p.Gly77Arg)
n.665G>C
n.740G>C
15g.66435175G>TCA392929402MAP2K1c.163G>T (p.Gly55Cys)
c.229G>T (p.Gly77Cys)
n.665G>T
n.740G>T
15g.66435176G>ACA392929405MAP2K1c.164G>A (p.Gly55Asp)
c.230G>A (p.Gly77Asp)
n.666G>A
n.741G>A
15g.66435176G>CCA392929409MAP2K1c.164G>C (p.Gly55Ala)
c.230G>C (p.Gly77Ala)
n.666G>C
n.741G>C
15g.66435176G>TCA392929406MAP2K1c.164G>T (p.Gly55Val)
c.230G>T (p.Gly77Val)
n.666G>T
n.741G>T
 dbSNP
15g.66435177C>ACA490856014MAP2K1c.165C>A (p.Gly55=)
c.231C>A (p.Gly77=)
n.667C>A
n.742C>A
15g.66435177C=CA2184071763MAP2K1c.165C= (p.Gly55=)
c.231C= (p.Gly77=)
n.667C=
n.742C=
15g.66435177C>GCA490856013MAP2K1c.165C>G (p.Gly55=)
c.231C>G (p.Gly77=)
n.667C>G
n.742C>G
 dbSNP gnomAD v4
15g.66435177C>TCA490856015MAP2K1c.165C>T (p.Gly55=)
c.231C>T (p.Gly77=)
n.667C>T
n.742C>T
15g.66435178A>CCA392929411MAP2K1c.166A>C (p.Asn56His)
c.232A>C (p.Asn78His)
n.668A>C
n.743A>C
15g.66435178A>GCA392929413MAP2K1c.166A>G (p.Asn56Asp)
c.232A>G (p.Asn78Asp)
n.668A>G
n.743A>G
15g.66435178A>TCA392929415MAP2K1c.166A>T (p.Asn56Tyr)
c.232A>T (p.Asn78Tyr)
n.668A>T
n.743A>T
 dbSNP
15g.66435179A>CCA392929417MAP2K1c.167A>C (p.Asn56Thr)
c.233A>C (p.Asn78Thr)
n.669A>C
n.744A>C
 dbSNP
15g.66435179A>GCA392929419MAP2K1c.167A>G (p.Asn56Ser)
c.233A>G (p.Asn78Ser)
n.669A>G
n.744A>G
15g.66435179A>TCA392929420MAP2K1c.167A>T (p.Asn56Ile)
c.233A>T (p.Asn78Ile)
n.669A>T
n.744A>T
 dbSNP
15g.66435180T>ACA392929421MAP2K1c.168T>A (p.Asn56Lys)
c.234T>A (p.Asn78Lys)
n.670T>A
n.745T>A
 dbSNP
15g.66435180T>CCA490856016MAP2K1c.168T>C (p.Asn56=)
c.234T>C (p.Asn78=)
n.670T>C
n.745T>C
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched