Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.112801383G>CCA16023152APCc.834G>C (p.Gln278His)
n.890G>C
c.*840G>C (n.*840G>C)
c.780G>C (p.Gln260His)
c.864G>C (p.Gln288His)
c.759G>C (p.Gln253His)
c.750G>C (p.Gln250His)
c.657G>C (p.Gln219His)
c.-202G>C (n.-202G>C)
dbSNP COSMIC
5g.112801383G>ACA16611754APCc.834G>A (p.Gln278=)
n.890G>A
c.*840G>A (n.*840G>A)
c.780G>A (p.Gln260=)
c.864G>A (p.Gln288=)
c.759G>A (p.Gln253=)
c.750G>A (p.Gln250=)
c.657G>A (p.Gln219=)
c.-202G>A (n.-202G>A)
ClinVar dbSNP
5g.112801383G=CA1573510330APCc.834G= (p.Gln278=)
n.890G=
c.*840G= (n.*840G=)
c.780G= (p.Gln260=)
c.864G= (p.Gln288=)
c.759G= (p.Gln253=)
c.750G= (p.Gln250=)
c.657G= (p.Gln219=)
c.-202G= (n.-202G=)
dbSNP

Number of alleles fetched