Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.56875191G>TCA3272867MAP3K1c.1846G>T (p.Gly616Trp)
c.1468G>T (p.Gly490Trp)
c.1591G>T (p.Gly531Trp)
c.1686+2186G>T (p.=)
c.1435G>T (p.Gly479Trp)
c.1357G>T (p.Gly453Trp)
n.1877G>T
n.1846G>T (p.Gly616Trp)
dbSNP ExAC gnomAD
5g.56875191G>CCA3272865MAP3K1c.1846G>C (p.Gly616Arg)
c.1468G>C (p.Gly490Arg)
c.1591G>C (p.Gly531Arg)
c.1686+2186G>C (p.=)
c.1435G>C (p.Gly479Arg)
c.1357G>C (p.Gly453Arg)
n.1877G>C
n.1846G>C (p.Gly616Arg)
dbSNP ExAC gnomAD
5g.56875191G>ACA3272866MAP3K1c.1846G>A (p.Gly616Arg)
c.1468G>A (p.Gly490Arg)
c.1591G>A (p.Gly531Arg)
c.1686+2186G>A (p.=)
c.1435G>A (p.Gly479Arg)
c.1357G>A (p.Gly453Arg)
n.1877G>A
n.1846G>A (p.Gly616Arg)
ClinVar dbSNP ExAC gnomAD

Number of alleles fetched