| 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= | |
| 22 | g.20242778G>T | CA513693145 | RTN4R | c.355C>A (p.Arg119=) c.414C>A c.612C>A n.491C>A | |
| 22 | g.20242779G>A | CA10109607 | RTN4R | c.354C>T (p.Leu118=) c.413C>T c.611C>T n.490C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 22 | g.20242779G>C | CA513693150 | RTN4R | c.354C>G (p.Leu118=) c.413C>G c.611C>G n.490C>G | gnomAD v4 |
| 22 | g.20242779G= | CA2396269200 | RTN4R | c.354C= (p.Leu118=) c.413C= c.611C= n.490C= | |
| 22 | g.20242779G>T | CA513693151 | RTN4R | c.354C>A (p.Leu118=) c.413C>A c.611C>A n.490C>A | gnomAD v4 |
| 22 | g.20242780A>C | CA410713204 | RTN4R | c.353T>G (p.Leu118Arg) c.412T>G c.610T>G n.489T>G | |
| 22 | g.20242780A>G | CA410713206 | RTN4R | c.353T>C (p.Leu118Pro) c.412T>C c.610T>C n.489T>C | |
| 22 | g.20242780A>T | CA410713208 | RTN4R | c.353T>A (p.Leu118His) c.412T>A c.610T>A n.489T>A | |
| 22 | g.20242781G>A | CA410713209 | RTN4R | c.352C>T (p.Leu118Phe) c.411C>T c.609C>T n.488C>T | gnomAD v4 |
| 22 | g.20242781G>C | CA410713211 | RTN4R | c.352C>G (p.Leu118Val) c.411C>G c.609C>G n.488C>G | |
| 22 | g.20242781G>T | CA410713213 | RTN4R | c.352C>A (p.Leu118Ile) c.411C>A c.609C>A n.488C>A | |
| 22 | g.20242782C>A | CA410713215 | RTN4R | c.351G>T (p.Gln117His) c.410G>T c.608G>T n.487G>T | |
| 22 | g.20242782C>G | CA410713214 | RTN4R | c.351G>C (p.Gln117His) c.410G>C c.608G>C n.487G>C | |
| 22 | g.20242782C>T | CA513693165 | RTN4R | c.351G>A (p.Gln117=) c.410G>A c.608G>A n.487G>A | |
| 22 | g.20242783T>A | CA410713218 | RTN4R | c.350A>T (p.Gln117Leu) c.409A>T c.607A>T n.486A>T | |
| 22 | g.20242783T>C | CA410713219 | RTN4R | c.350A>G (p.Gln117Arg) c.409A>G c.607A>G n.486A>G | dbSNP gnomAD v3 gnomAD v4 |
| 22 | g.20242783T>G | CA410713221 | RTN4R | c.350A>C (p.Gln117Pro) c.409A>C c.607A>C n.486A>C | |
| 22 | g.20242784G>A | CA410713222 | RTN4R | c.349C>T (p.Gln117Ter) c.408C>T c.606C>T n.485C>T | |
| 22 | g.20242784G>C | CA410713224 | RTN4R | c.349C>G (p.Gln117Glu) c.408C>G c.606C>G n.485C>G | |
| 22 | g.20242784G>T | CA410713226 | RTN4R | c.349C>A (p.Gln117Lys) c.408C>A c.606C>A n.485C>A | |
| 22 | g.20242785T>A | CA513693167 | RTN4R | c.348A>T (p.Ala116=) c.407A>T c.605A>T n.484A>T | dbSNP gnomAD v4 |
| 22 | g.20242785T>C | CA513693168 | RTN4R | c.348A>G (p.Ala116=) c.407A>G c.605A>G n.484A>G | dbSNP |
| 22 | g.20242785T>G | CA513693170 | RTN4R | c.348A>C (p.Ala116=) c.407A>C c.605A>C n.484A>C | |
| 22 | g.20242785T= | CA2396269201 | RTN4R | c.348A= (p.Ala116=) c.407A= c.605A= n.484A= | |
| 22 | g.20242786G>A | CA410713228 | RTN4R | c.347C>T (p.Ala116Val) c.406C>T c.604C>T n.483C>T | |
| 22 | g.20242786G>C | CA410713229 | RTN4R | c.347C>G (p.Ala116Gly) c.406C>G c.604C>G n.483C>G | |
| 22 | g.20242786G>T | CA410713231 | RTN4R | c.347C>A (p.Ala116Glu) c.406C>A c.604C>A n.483C>A | |
| 22 | g.20242787C>A | CA10109608 | RTN4R | c.346G>T (p.Ala116Ser) c.405G>T c.603G>T n.482G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 22 | g.20242787C= | CA2396269202 | RTN4R | c.346G= (p.Ala116=) c.405G= c.603G= n.482G= | |
| 22 | g.20242787C>G | CA410713234 | RTN4R | c.346G>C (p.Ala116Pro) c.405G>C c.603G>C n.482G>C | |
| 22 | g.20242787C>T | CA410713235 | RTN4R | c.346G>A (p.Ala116Thr) c.405G>A c.603G>A n.482G>A | |
| 22 | g.20242788A= | CA2396269203 | RTN4R | c.345T= (p.Asn115=) c.404T= c.602T= n.481T= | |
| 22 | g.20242788A>C | CA410713238 | RTN4R | c.345T>G (p.Asn115Lys) c.404T>G c.602T>G n.481T>G | |
| 22 | g.20242788A>G | CA322184050 | RTN4R | c.345T>C (p.Asn115=) c.404T>C c.602T>C n.481T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 22 | g.20242788A>T | CA410713236 | RTN4R | c.345T>A (p.Asn115Lys) c.404T>A c.602T>A n.481T>A | |
| 22 | g.20242789T>A | CA410713240 | RTN4R | c.344A>T (p.Asn115Ile) c.403A>T c.601A>T n.480A>T | |
| 22 | g.20242789T>C | CA410713243 | RTN4R | c.344A>G (p.Asn115Ser) c.403A>G c.601A>G n.480A>G | |
| 22 | g.20242789T>G | CA410713242 | RTN4R | c.344A>C (p.Asn115Thr) c.403A>C c.601A>C n.480A>C | |
| 22 | g.20242790T>A | CA410713245 | RTN4R | c.343A>T (p.Asn115Tyr) c.402A>T c.600A>T n.479A>T | |
| 22 | g.20242790T>C | CA410713246 | RTN4R | c.343A>G (p.Asn115Asp) c.402A>G c.600A>G n.479A>G | |
| 22 | g.20242790T>G | CA410713248 | RTN4R | c.343A>C (p.Asn115His) c.402A>C c.600A>C n.479A>C | |
| 22 | g.20242791A>C | CA410713249 | RTN4R | c.342T>G (p.Asp114Glu) c.401T>G c.599T>G n.478T>G | |
| 22 | g.20242791A>G | CA513693181 | RTN4R | c.342T>C (p.Asp114=) c.401T>C c.599T>C n.478T>C | |
| 22 | g.20242791A>T | CA410713250 | RTN4R | c.342T>A (p.Asp114Glu) c.401T>A c.599T>A n.478T>A | |
| 22 | g.20242792T>A | CA410713251 | RTN4R | c.341A>T (p.Asp114Val) c.400A>T c.598A>T n.477A>T | |
| 22 | g.20242792T>C | CA410713253 | RTN4R | c.341A>G (p.Asp114Gly) c.400A>G c.598A>G n.477A>G | |
| 22 | g.20242792T>G | CA410713254 | RTN4R | c.341A>C (p.Asp114Ala) c.400A>C c.598A>C n.477A>C |