Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.45332481C>TCA058781MUTYHc.624G>A (p.Arg208=)
c.614G>A (p.Gly205Asp)
c.*353G>A (p.=)
c.1202G>A (p.Gly401Asp)
c.582G>A (p.Arg194=)
c.*587G>A (p.=)
c.573G>A (p.Arg191=)
c.689G>A (p.Gly230Asp)
c.*311G>A (p.=)
n.642G>A (p.=)
c.617G>A (p.Gly206Asp)
c.659G>A (p.Gly220Asp)
c.656G>A (p.Gly219Asp)
c.230G>A (p.Gly77Asp)
c.647G>A (p.Gly216Asp)
c.698G>A (p.Gly233Asp)
n.305G>A
n.8G>A (p.Gly3Asp)
c.*537G>A (p.=)
c.501G>A (p.Arg167=)
c.*427G>A (p.=)
n.601G>A
c.187+282G>A (p.=)
c.*265G>A (p.=)
c.115+1910G>A (p.=)
n.243G>A (p.Arg81=)
c.338G>A (p.Gly113Asp)
c.674G>A (p.Gly225Asp)
c.236G>A (p.Gly79Asp)
c.227G>A (p.Gly76Asp)
c.242G>A (p.Gly81Asp)
n.745G>A
c.269G>A (p.Gly90Asp)
n.872G>A
n.686G>A
c.98G>A (p.Gly33Asp)
n.659G>A
n.471G>A
n.651G>A
n.1186G>A
n.759G>A
n.842G>A
n.691G>A
ClinVar dbSNP ExAC gnomAD
1g.45332481C>ACA058789MUTYHc.624G>T (p.Arg208=)
c.614G>T (p.Gly205Val)
c.*353G>T (p.=)
c.1202G>T (p.Gly401Val)
c.582G>T (p.Arg194=)
c.*587G>T (p.=)
c.573G>T (p.Arg191=)
c.689G>T (p.Gly230Val)
c.*311G>T (p.=)
n.642G>T (p.=)
c.617G>T (p.Gly206Val)
c.659G>T (p.Gly220Val)
c.656G>T (p.Gly219Val)
c.230G>T (p.Gly77Val)
c.647G>T (p.Gly216Val)
c.698G>T (p.Gly233Val)
n.305G>T
n.8G>T (p.Gly3Val)
c.*537G>T (p.=)
c.501G>T (p.Arg167=)
c.*427G>T (p.=)
n.601G>T
c.187+282G>T (p.=)
c.*265G>T (p.=)
c.115+1910G>T (p.=)
n.243G>T (p.Arg81=)
c.338G>T (p.Gly113Val)
c.674G>T (p.Gly225Val)
c.236G>T (p.Gly79Val)
c.227G>T (p.Gly76Val)
c.242G>T (p.Gly81Val)
n.745G>T
c.269G>T (p.Gly90Val)
n.872G>T
n.686G>T
c.98G>T (p.Gly33Val)
n.659G>T
n.471G>T
n.651G>T
n.1186G>T
n.759G>T
n.842G>T
n.691G>T
dbSNP ExAC

Number of alleles fetched