Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.94470575G>A | CA331852 | MRE11 | c.913C>T (p.Arg305Trp) c.922C>T (p.Arg308Trp) c.445C>T (p.Arg149Trp) n.1209C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.94470575G= | CA1992475865 | MRE11 | c.913C= (p.Arg305=) c.922C= (p.Arg308=) c.445C= (p.Arg149=) n.1209C= | dbSNP |
11 | g.94470575G>C | CA382374493 | MRE11 | c.913C>G (p.Arg305Gly) c.922C>G (p.Arg308Gly) c.445C>G (p.Arg149Gly) n.1209C>G | ClinVar dbSNP gnomAD v4 |
11 | g.94470575G>T | CA476284019 | MRE11 | c.913C>A (p.Arg305=) c.922C>A (p.Arg308=) c.445C>A (p.Arg149=) n.1209C>A | ClinVar dbSNP |