Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.189868635A>GCA16042468TP63c.1048A>G (p.Arg350Gly)
c.766A>G (p.Arg256Gly)
c.511A>G (p.Arg171Gly)
n.872A>G
c.997A>G (p.Arg333Gly)
c.1045A>G (p.Arg349Gly)
c.1042A>G (p.Arg348Gly)
c.1009A>G (p.Arg337Gly)
ClinVar dbSNP
3g.189868635A>TCA355755199TP63c.1048A>T (p.Arg350Ter)
c.766A>T (p.Arg256Ter)
c.511A>T (p.Arg171Ter)
n.872A>T
c.997A>T (p.Arg333Ter)
c.1045A>T (p.Arg349Ter)
c.1042A>T (p.Arg348Ter)
c.1009A>T (p.Arg337Ter)
dbSNP

Number of alleles fetched