Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.43119587C>GCA376556205RETc.2053C>G (p.Arg685Gly)
n.2023C>G
n.2014C>G
c.2449C>G (p.Arg817Gly)
c.*1043C>G (n.*1043C>G)
c.1290-115C>G (n.1290-115C>G)
c.1687C>G (p.Arg563Gly)
dbSNP
10g.43119587C>TCA008792RETc.2053C>T (p.Arg685Cys)
n.2023C>T
n.2014C>T
c.2449C>T (p.Arg817Cys)
c.*1043C>T (n.*1043C>T)
c.1290-115C>T (n.1290-115C>T)
c.1687C>T (p.Arg563Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.43119587C>ACA376556203RETc.2053C>A (p.Arg685Ser)
n.2023C>A
n.2014C>A
c.2449C>A (p.Arg817Ser)
c.*1043C>A (n.*1043C>A)
c.1290-115C>A (n.1290-115C>A)
c.1687C>A (p.Arg563Ser)
dbSNP

Number of alleles fetched