Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.43123783A>CCA469030954RETc.2518A>C (p.Arg840=)
n.2488A>C
c.2914A>C (p.Arg972=)
c.*1508A>C (n.*1508A>C)
c.*263A>C (n.*263A>C)
c.2152A>C (p.Arg718=)
ClinVar dbSNP
10g.43123783A>GCA009130RETc.2518A>G (p.Arg840Gly)
n.2488A>G
c.2914A>G (p.Arg972Gly)
c.*1508A>G (n.*1508A>G)
c.*263A>G (n.*263A>G)
c.2152A>G (p.Arg718Gly)
ClinVar dbSNP
10g.43123783A=CA1905825065RETc.2518A= (p.Arg840=)
n.2488A=
c.2914A= (p.Arg972=)
c.*1508A= (n.*1508A=)
c.*263A= (n.*263A=)
c.2152A= (p.Arg718=)
dbSNP

Number of alleles fetched