Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.94459461G>A | CA6235079 | MRE11 | c.1447C>T (p.Arg483Ter) c.1456C>T (p.Arg486Ter) c.979C>T (p.Arg327Ter) n.1743C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.94459461G= | CA1992461444 | MRE11 | c.1447C= (p.Arg483=) c.1456C= (p.Arg486=) c.979C= (p.Arg327=) n.1743C= | dbSNP |
11 | g.94459461G>T | CA476281863 | MRE11 | c.1447C>A (p.Arg483=) c.1456C>A (p.Arg486=) c.979C>A (p.Arg327=) n.1743C>A | ClinVar dbSNP |