Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.43120162C>GCA376557232RETc.2293C>G (p.Arg765Gly)
n.2263C>G
n.2254C>G
c.2689C>G (p.Arg897Gly)
c.*1283C>G (n.*1283C>G)
c.*38C>G (n.*38C>G)
c.1927C>G (p.Arg643Gly)
ClinVar dbSNP
10g.43120162C>TCA16612889RETc.2293C>T (p.Arg765Ter)
n.2263C>T
n.2254C>T
c.2689C>T (p.Arg897Ter)
c.*1283C>T (n.*1283C>T)
c.*38C>T (n.*38C>T)
c.1927C>T (p.Arg643Ter)
ClinVar dbSNP
10g.43120162C>ACA469028911RETc.2293C>A (p.Arg765=)
n.2263C>A
n.2254C>A
c.2689C>A (p.Arg897=)
c.*1283C>A (n.*1283C>A)
c.*38C>A (n.*38C>A)
c.1927C>A (p.Arg643=)
dbSNP

Number of alleles fetched