| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.78969056A= | CA1557703756 | ARSB | c.449T= (p.Met150=) n.520T= | |
| 5 | g.78969056A>C | CA360194002 | ARSB | c.449T>G (p.Met150Arg) n.520T>G | dbSNP |
| 5 | g.78969056A>G | CA360194000 | ARSB | c.449T>C (p.Met150Thr) n.520T>C | gnomAD v4 |
| 5 | g.78969056A>T | CA360193998 | ARSB | c.449T>A (p.Met150Lys) n.520T>A | |
| 5 | g.78969057T>A | CA360194003 | ARSB | c.448A>T (p.Met150Leu) n.519A>T | COSMIC |
| 5 | g.78969057T>C | CA121107818 | ARSB | c.448A>G (p.Met150Val) n.519A>G | ClinVar dbSNP |
| 5 | g.78969057T>G | CA360194005 | ARSB | c.448A>C (p.Met150Leu) n.519A>C | |
| 5 | g.78969057T= | CA1557703757 | ARSB | c.448A= (p.Met150=) n.519A= | |
| 5 | g.78969058T>A | CA445103375 | ARSB | c.447A>T (p.Gly149=) n.518A>T | |
| 5 | g.78969058T>C | CA445103376 | ARSB | c.447A>G (p.Gly149=) n.518A>G | |
| 5 | g.78969058T>G | CA445103377 | ARSB | c.447A>C (p.Gly149=) n.518A>C | |
| 5 | g.78969059C>A | CA360194007 | ARSB | c.446G>T (p.Gly149Val) n.517G>T | gnomAD v4 |
| 5 | g.78969059C>G | CA360194008 | ARSB | c.446G>C (p.Gly149Ala) n.517G>C | |
| 5 | g.78969059C>T | CA360194010 | ARSB | c.446G>A (p.Gly149Glu) n.517G>A | gnomAD v4 |
| 5 | g.78969060C>A | CA360194012 | ARSB | c.445G>T (p.Gly149Ter) n.516G>T | |
| 5 | g.78969060C= | CA1557703758 | ARSB | c.445G= (p.Gly149=) n.516G= | |
| 5 | g.78969060C>G | CA360194013 | ARSB | c.445G>C (p.Gly149Arg) n.516G>C | dbSNP gnomAD v2 |
| 5 | g.78969060C>T | CA360194015 | ARSB | c.445G>A (p.Gly149Arg) n.516G>A | |
| 5 | g.78969061C>A | CA445103384 | ARSB | c.444G>T (p.Leu148=) n.515G>T | |
| 5 | g.78969061C>G | CA445103388 | ARSB | c.444G>C (p.Leu148=) n.515G>C | |
| 5 | g.78969061C>T | CA445103390 | ARSB | c.444G>A (p.Leu148=) n.515G>A | |
| 5 | g.78969062A>C | CA360194017 | ARSB | c.443T>G (p.Leu148Arg) n.514T>G | |
| 5 | g.78969062A>G | CA360194018 | ARSB | c.443T>C (p.Leu148Pro) n.514T>C | |
| 5 | g.78969062A>T | CA360194020 | ARSB | c.443T>A (p.Leu148Gln) n.514T>A | |
| 5 | g.78969063G>A | CA445103396 | ARSB | c.442C>T (p.Leu148=) n.513C>T | |
| 5 | g.78969063G>C | CA360194024 | ARSB | c.442C>G (p.Leu148Val) n.513C>G | |
| 5 | g.78969063G>T | CA360194022 | ARSB | c.442C>A (p.Leu148Met) n.513C>A | |
| 5 | g.78969064G>A | CA445103400 | ARSB | c.441C>T (p.His147=) n.512C>T | dbSNP gnomAD v4 |
| 5 | g.78969064G>C | CA360194025 | ARSB | c.441C>G (p.His147Gln) n.512C>G | ClinVar dbSNP gnomAD v4 |
| 5 | g.78969064G= | CA1557703759 | ARSB | c.441C= (p.His147=) n.512C= | |
| 5 | g.78969064G>T | CA360194027 | ARSB | c.441C>A (p.His147Gln) n.512C>A | |
| 5 | g.78969065T>A | CA360194029 | ARSB | c.440A>T (p.His147Leu) n.511A>T | gnomAD v4 |
| 5 | g.78969065T>C | CA360194030 | ARSB | c.440A>G (p.His147Arg) n.511A>G | |
| 5 | g.78969065T>G | CA360194032 | ARSB | c.440A>C (p.His147Pro) n.511A>C | ClinVar dbSNP |
| 5 | g.78969065T= | CA1557703760 | ARSB | c.440A= (p.His147=) n.511A= | |
| 5 | g.78969066G>A | CA360194036 | ARSB | c.439C>T (p.His147Tyr) n.510C>T | gnomAD v4 |
| 5 | g.78969066G>C | CA360194034 | ARSB | c.439C>G (p.His147Asp) n.510C>G | |
| 5 | g.78969066G>T | CA360194033 | ARSB | c.439C>A (p.His147Asn) n.510C>A | |
| 5 | g.78969067C>A | CA360194038 | ARSB | c.438G>T (p.Trp146Cys) n.509G>T | gnomAD v4 |
| 5 | g.78969067C= | CA1557703761 | ARSB | c.438G= (p.Trp146=) n.509G= | |
| 5 | g.78969067C>G | CA360194040 | ARSB | c.438G>C (p.Trp146Cys) n.509G>C | |
| 5 | g.78969067C>T | CA121107823 | ARSB | c.438G>A (p.Trp146Ter) n.509G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.78969068del | CA2580073473 | ARSB | c.438del (p.Trp146CysfsTer?) n.509del | ClinVar |
| 5 | g.78969068C>A | CA360194041 | ARSB | c.437G>T (p.Trp146Leu) n.508G>T | ClinVar dbSNP |
| 5 | g.78969068C= | CA1557703762 | ARSB | c.437G= (p.Trp146=) n.508G= | |
| 5 | g.78969068C>G | CA360194043 | ARSB | c.437G>C (p.Trp146Ser) n.508G>C | ClinVar dbSNP |
| 5 | g.78969068C>T | CA360194044 | ARSB | c.437G>A (p.Trp146Ter) n.508G>A | |
| 5 | g.78969069A= | CA1557703763 | ARSB | c.436T= (p.Trp146=) n.507T= | |
| 5 | g.78969069A>C | CA360194045 | ARSB | c.436T>G (p.Trp146Gly) n.507T>G | |
| 5 | g.78969069A>G | CA360194048 | ARSB | c.436T>C (p.Trp146Arg) n.507T>C | ClinVar dbSNP |