Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.31068276C>T | CA4704137 | WRN | c.673C>T (p.Arg225Ter) c.*287C>T (n.*287C>T) n.946C>T c.463C>T (p.Arg155Ter) n.974C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.31068276C= | CA3156157383 | WRN | c.673C= (p.Arg225=) c.*287C= (n.*287C=) n.946C= c.463C= (p.Arg155=) n.974C= | dbSNP |