| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.44907842_44907857delinsGCGCTGGGAACTGGCA | CA2338167349 | APOE | c.126_141delinsGCGCTGGGAACTGGCA (p.Gln42=) c.204_219delinsGCGCTGGGAACTGGCA (p.Gln68=) | |
| 19 | g.44907844_44907858del | CA9505982 | APOE | c.128_142del (p.Arg43_Ala47del) c.206_220del (p.Arg69_Ala73del) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 19 | g.44907844G>A | CA9505983 | APOE | c.128G>A (p.Arg43His) c.206G>A (p.Arg69His) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.44907844G>C | CA406303313 | APOE | c.128G>C (p.Arg43Pro) c.206G>C (p.Arg69Pro) | dbSNP |
| 19 | g.44907844G= | CA2338167352 | APOE | c.128G= (p.Arg43=) c.206G= (p.Arg69=) | |
| 19 | g.44907844G>T | CA406303315 | APOE | c.128G>T (p.Arg43Leu) c.206G>T (p.Arg69Leu) | dbSNP COSMIC |
| 19 | g.44907845C>A | CA507799007 | APOE | c.129C>A (p.Arg43=) c.207C>A (p.Arg69=) | |
| 19 | g.44907845C= | CA2338167353 | APOE | c.129C= (p.Arg43=) c.207C= (p.Arg69=) | |
| 19 | g.44907845C>G | CA507799008 | APOE | c.129C>G (p.Arg43=) c.207C>G (p.Arg69=) | |
| 19 | g.44907845C>T | CA9505984 | APOE | c.129C>T (p.Arg43=) c.207C>T (p.Arg69=) | dbSNP ExAC gnomAD v2 |
| 19 | g.44907846T>A | CA406303321 | APOE | c.130T>A (p.Trp44Arg) c.208T>A (p.Trp70Arg) | |
| 19 | g.44907846T>C | CA406303323 | APOE | c.130T>C (p.Trp44Arg) c.208T>C (p.Trp70Arg) | gnomAD v4 |
| 19 | g.44907846T>G | CA406303325 | APOE | c.130T>G (p.Trp44Gly) c.208T>G (p.Trp70Gly) | |
| 19 | g.44907847G>A | CA406303329 | APOE | c.131G>A (p.Trp44Ter) c.209G>A (p.Trp70Ter) | |
| 19 | g.44907847G>C | CA406303331 | APOE | c.131G>C (p.Trp44Ser) c.209G>C (p.Trp70Ser) | |
| 19 | g.44907847G>T | CA406303327 | APOE | c.131G>T (p.Trp44Leu) c.209G>T (p.Trp70Leu) | |
| 19 | g.44907848G>A | CA9505985 | APOE | c.132G>A (p.Trp44Ter) c.210G>A (p.Trp70Ter) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 19 | g.44907848G>C | CA406303334 | APOE | c.132G>C (p.Trp44Cys) c.210G>C (p.Trp70Cys) | |
| 19 | g.44907848G= | CA2338167354 | APOE | c.132G= (p.Trp44=) c.210G= (p.Trp70=) | |
| 19 | g.44907848G>T | CA406303336 | APOE | c.132G>T (p.Trp44Cys) c.210G>T (p.Trp70Cys) | |
| 19 | g.44907849G>A | CA406303338 | APOE | c.133G>A (p.Glu45Lys) c.211G>A (p.Glu71Lys) | |
| 19 | g.44907849G>C | CA406303340 | APOE | c.133G>C (p.Glu45Gln) c.211G>C (p.Glu71Gln) | |
| 19 | g.44907849G>T | CA406303342 | APOE | c.133G>T (p.Glu45Ter) c.211G>T (p.Glu71Ter) | |
| 19 | g.44907850A= | CA2338167355 | APOE | c.134A= (p.Glu45=) c.212A= (p.Glu71=) | |
| 19 | g.44907850A>C | CA406303344 | APOE | c.134A>C (p.Glu45Ala) c.212A>C (p.Glu71Ala) | |
| 19 | g.44907850A>G | CA406303348 | APOE | c.134A>G (p.Glu45Gly) c.212A>G (p.Glu71Gly) | dbSNP |
| 19 | g.44907850A>T | CA406303346 | APOE | c.134A>T (p.Glu45Val) c.212A>T (p.Glu71Val) | |
| 19 | g.44907851A= | CA2338167356 | APOE | c.135A= (p.Glu45=) c.213A= (p.Glu71=) | |
| 19 | g.44907851A>C | CA406303350 | APOE | c.135A>C (p.Glu45Asp) c.213A>C (p.Glu71Asp) | |
| 19 | g.44907851A>G | CA308884513 | APOE | c.135A>G (p.Glu45=) c.213A>G (p.Glu71=) | dbSNP |
| 19 | g.44907851A>T | CA406303353 | APOE | c.135A>T (p.Glu45Asp) c.213A>T (p.Glu71Asp) | |
| 19 | g.44907852C>A | CA406303355 | APOE | c.136C>A (p.Leu46Met) c.214C>A (p.Leu72Met) | |
| 19 | g.44907852C>G | CA406303358 | APOE | c.136C>G (p.Leu46Val) c.214C>G (p.Leu72Val) | |
| 19 | g.44907852C>T | CA507799009 | APOE | c.136C>T (p.Leu46=) c.214C>T (p.Leu72=) | |
| 19 | g.44907853T>A | CA406303362 | APOE | c.137T>A (p.Leu46Gln) c.215T>A (p.Leu72Gln) | dbSNP |
| 19 | g.44907853T>C | CA041808 | APOE | c.137T>C (p.Leu46Pro) c.215T>C (p.Leu72Pro) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.[44907853T>C;44908684T>C] | CA041979 | APOE | c.[137T>C;388T>C] (p.[Leu46Pro;Cys130Arg]) c.[215T>C;466T>C] (p.[Leu72Pro;Cys156Arg]) | ClinVar |
| 19 | g.44907853T>G | CA406303360 | APOE | c.137T>G (p.Leu46Arg) c.215T>G (p.Leu72Arg) | |
| 19 | g.44907853T= | CA2338167357 | APOE | c.137T= (p.Leu46=) c.215T= (p.Leu72=) | |
| 19 | g.44907854G>A | CA9505986 | APOE | c.138G>A (p.Leu46=) c.216G>A (p.Leu72=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.44907854G>C | CA507799010 | APOE | c.138G>C (p.Leu46=) c.216G>C (p.Leu72=) | |
| 19 | g.44907854G= | CA2338167358 | APOE | c.138G= (p.Leu46=) c.216G= (p.Leu72=) | |
| 19 | g.44907854G>T | CA507799011 | APOE | c.138G>T (p.Leu46=) c.216G>T (p.Leu72=) | |
| 19 | g.44907855del | CA2585715223 | APOE | c.139del (p.Ala47HisfsTer?) c.217del (p.Ala73HisfsTer?) | gnomAD v4 |
| 19 | g.44907855G>A | CA406303369 | APOE | c.139G>A (p.Ala47Thr) c.217G>A (p.Ala73Thr) | COSMIC |
| 19 | g.44907855G>C | CA406303365 | APOE | c.139G>C (p.Ala47Pro) c.217G>C (p.Ala73Pro) | |
| 19 | g.44907855G>T | CA406303367 | APOE | c.139G>T (p.Ala47Ser) c.217G>T (p.Ala73Ser) | |
| 19 | g.44907856C>A | CA406303371 | APOE | c.140C>A (p.Ala47Glu) c.218C>A (p.Ala73Glu) | |
| 19 | g.44907856C>G | CA406303372 | APOE | c.140C>G (p.Ala47Gly) c.218C>G (p.Ala73Gly) | |
| 19 | g.44907856C>T | CA406303374 | APOE | c.140C>T (p.Ala47Val) c.218C>T (p.Ala73Val) | gnomAD v4 |