Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.94478782G>A | CA167765 | MRE11 | c.497C>T (p.Pro166Leu) c.506C>T (p.Pro169Leu) n.573C>T c.29C>T (p.Pro10Leu) n.793C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.94478782G= | CA1992436673 | MRE11 | c.497C= (p.Pro166=) c.506C= (p.Pro169=) n.573C= c.29C= (p.Pro10=) n.793C= | dbSNP |
11 | g.94478782G>T | CA382377408 | MRE11 | c.497C>A (p.Pro166Gln) c.506C>A (p.Pro169Gln) n.573C>A c.29C>A (p.Pro10Gln) n.793C>A | dbSNP gnomAD v4 |