Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
22 | g.20242778G>A | CA117118 | RTN4R | c.355C>T (p.Arg119Trp) c.414C>T c.612C>T n.491C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
22 | g.20242778G>C | CA322184024 | RTN4R | c.355C>G (p.Arg119Gly) c.414C>G c.612C>G n.491C>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
22 | g.20242778G= | CA2396269199 | RTN4R | c.355C= (p.Arg119=) c.414C= c.612C= n.491C= | dbSNP |