Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.99132634C>TCA16612807TGFBR1c.262C>T (p.Arg88Ter)
c.274C>T (p.Arg92Ter)
c.136+3534C>T (n.136+3534C>T)
c.*265C>T (n.*265C>T)
c.469C>T (p.Arg157Ter)
c.343+3534C>T (n.343+3534C>T)
c.481C>T (p.Arg161Ter)
ClinVar dbSNP gnomAD v4 COSMIC
9g.99132634C=CA1867274582TGFBR1c.262C= (p.Arg88=)
c.274C= (p.Arg92=)
c.136+3534C= (n.136+3534C=)
c.*265C= (n.*265C=)
c.469C= (p.Arg157=)
c.343+3534C= (n.343+3534C=)
c.481C= (p.Arg161=)
dbSNP

Number of alleles fetched