| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.89282672A>C | CA397158816 | ANKRD11 | c.3870T>G (p.His1290Gln) c.*3673T>G (n.*3673T>G) c.744+5856T>G (n.744+5856T>G) c.151+5856T>G c.3768T>G (p.His1256Gln) c.3573T>G (p.His1191Gln) c.3741T>G (p.His1247Gln) | |
| 16 | g.89282672A>G | CA497374443 | ANKRD11 | c.3870T>C (p.His1290=) c.*3673T>C (n.*3673T>C) c.744+5856T>C (n.744+5856T>C) c.151+5856T>C c.3768T>C (p.His1256=) c.3573T>C (p.His1191=) c.3741T>C (p.His1247=) | |
| 16 | g.89282672A>T | CA397158817 | ANKRD11 | c.3870T>A (p.His1290Gln) c.*3673T>A (n.*3673T>A) c.744+5856T>A (n.744+5856T>A) c.151+5856T>A c.3768T>A (p.His1256Gln) c.3573T>A (p.His1191Gln) c.3741T>A (p.His1247Gln) | |
| 16 | g.89282673T>A | CA397158818 | ANKRD11 | c.3869A>T (p.His1290Leu) c.*3672A>T (n.*3672A>T) c.744+5855A>T (n.744+5855A>T) c.151+5855A>T c.3767A>T (p.His1256Leu) c.3572A>T (p.His1191Leu) c.3740A>T (p.His1247Leu) | |
| 16 | g.89282673T>C | CA8242273 | ANKRD11 | c.3869A>G (p.His1290Arg) c.*3672A>G (n.*3672A>G) c.744+5855A>G (n.744+5855A>G) c.151+5855A>G c.3767A>G (p.His1256Arg) c.3572A>G (p.His1191Arg) c.3740A>G (p.His1247Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 16 | g.89282673T>G | CA397158819 | ANKRD11 | c.3869A>C (p.His1290Pro) c.*3672A>C (n.*3672A>C) c.744+5855A>C (n.744+5855A>C) c.151+5855A>C c.3767A>C (p.His1256Pro) c.3572A>C (p.His1191Pro) c.3740A>C (p.His1247Pro) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 16 | g.89282673T= | CA2241603395 | ANKRD11 | c.3869A= (p.His1290=) c.*3672A= (n.*3672A=) c.744+5855A= (n.744+5855A=) c.151+5855A= c.3767A= (p.His1256=) c.3572A= (p.His1191=) c.3740A= (p.His1247=) | |
| 16 | g.89282674G>A | CA286516870 | ANKRD11 | c.3868C>T (p.His1290Tyr) c.*3671C>T (n.*3671C>T) c.744+5854C>T (n.744+5854C>T) c.151+5854C>T c.3766C>T (p.His1256Tyr) c.3571C>T (p.His1191Tyr) c.3739C>T (p.His1247Tyr) | ClinVar dbSNP gnomAD v4 |
| 16 | g.89282674G>C | CA397158821 | ANKRD11 | c.3868C>G (p.His1290Asp) c.*3671C>G (n.*3671C>G) c.744+5854C>G (n.744+5854C>G) c.151+5854C>G c.3766C>G (p.His1256Asp) c.3571C>G (p.His1191Asp) c.3739C>G (p.His1247Asp) | |
| 16 | g.89282674G= | CA2241603399 | ANKRD11 | c.3868C= (p.His1290=) c.*3671C= (n.*3671C=) c.744+5854C= (n.744+5854C=) c.151+5854C= c.3766C= (p.His1256=) c.3571C= (p.His1191=) c.3739C= (p.His1247=) | |
| 16 | g.89282674G>T | CA397158820 | ANKRD11 | c.3868C>A (p.His1290Asn) c.*3671C>A (n.*3671C>A) c.744+5854C>A (n.744+5854C>A) c.151+5854C>A c.3766C>A (p.His1256Asn) c.3571C>A (p.His1191Asn) c.3739C>A (p.His1247Asn) | gnomAD v4 |
| 16 | g.89282675G>A | CA497374451 | ANKRD11 | c.3867C>T (p.Leu1289=) c.*3670C>T (n.*3670C>T) c.744+5853C>T (n.744+5853C>T) c.151+5853C>T c.3765C>T (p.Leu1255=) c.3570C>T (p.Leu1190=) c.3738C>T (p.Leu1246=) | |
| 16 | g.89282675G>C | CA497374455 | ANKRD11 | c.3867C>G (p.Leu1289=) c.*3670C>G (n.*3670C>G) c.744+5853C>G (n.744+5853C>G) c.151+5853C>G c.3765C>G (p.Leu1255=) c.3570C>G (p.Leu1190=) c.3738C>G (p.Leu1246=) | |
| 16 | g.89282675G>T | CA497374454 | ANKRD11 | c.3867C>A (p.Leu1289=) c.*3670C>A (n.*3670C>A) c.744+5853C>A (n.744+5853C>A) c.151+5853C>A c.3765C>A (p.Leu1255=) c.3570C>A (p.Leu1190=) c.3738C>A (p.Leu1246=) | |
| 16 | g.89282676A= | CA2241603401 | ANKRD11 | c.3866T= (p.Leu1289=) c.*3669T= (n.*3669T=) c.744+5852T= (n.744+5852T=) c.151+5852T= c.3764T= (p.Leu1255=) c.3569T= (p.Leu1190=) c.3737T= (p.Leu1246=) | |
| 16 | g.89282676A>C | CA397158822 | ANKRD11 | c.3866T>G (p.Leu1289Arg) c.*3669T>G (n.*3669T>G) c.744+5852T>G (n.744+5852T>G) c.151+5852T>G c.3764T>G (p.Leu1255Arg) c.3569T>G (p.Leu1190Arg) c.3737T>G (p.Leu1246Arg) | |
| 16 | g.89282676A>G | CA397158823 | ANKRD11 | c.3866T>C (p.Leu1289Pro) c.*3669T>C (n.*3669T>C) c.744+5852T>C (n.744+5852T>C) c.151+5852T>C c.3764T>C (p.Leu1255Pro) c.3569T>C (p.Leu1190Pro) c.3737T>C (p.Leu1246Pro) | |
| 16 | g.89282676A>T | CA397158824 | ANKRD11 | c.3866T>A (p.Leu1289His) c.*3669T>A (n.*3669T>A) c.744+5852T>A (n.744+5852T>A) c.151+5852T>A c.3764T>A (p.Leu1255His) c.3569T>A (p.Leu1190His) c.3737T>A (p.Leu1246His) | dbSNP |
| 16 | g.89282677G>A | CA8242274 | ANKRD11 | c.3865C>T (p.Leu1289Phe) c.*3668C>T (n.*3668C>T) c.744+5851C>T (n.744+5851C>T) c.151+5851C>T c.3763C>T (p.Leu1255Phe) c.3568C>T (p.Leu1190Phe) c.3736C>T (p.Leu1246Phe) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89282677G>C | CA397158825 | ANKRD11 | c.3865C>G (p.Leu1289Val) c.*3668C>G (n.*3668C>G) c.744+5851C>G (n.744+5851C>G) c.151+5851C>G c.3763C>G (p.Leu1255Val) c.3568C>G (p.Leu1190Val) c.3736C>G (p.Leu1246Val) | |
| 16 | g.89282677G= | CA2241603402 | ANKRD11 | c.3865C= (p.Leu1289=) c.*3668C= (n.*3668C=) c.744+5851C= (n.744+5851C=) c.151+5851C= c.3763C= (p.Leu1255=) c.3568C= (p.Leu1190=) c.3736C= (p.Leu1246=) | |
| 16 | g.89282677G>T | CA397158826 | ANKRD11 | c.3865C>A (p.Leu1289Ile) c.*3668C>A (n.*3668C>A) c.744+5851C>A (n.744+5851C>A) c.151+5851C>A c.3763C>A (p.Leu1255Ile) c.3568C>A (p.Leu1190Ile) c.3736C>A (p.Leu1246Ile) | |
| 16 | g.89282677_89282682dup | CA2634942517 | ANKRD11 | c.3860_3865dup (p.Ala1288_Leu1289insGlnAla) c.*3663_*3668dup (n.*3663_*3668dup) c.744+5846_744+5851dup (n.744+5846_744+5851dup) c.151+5846_151+5851dup c.3758_3763dup (p.Ala1254_Leu1255insGlnAla) c.3563_3568dup (p.Ala1189_Leu1190insGlnAla) c.3731_3736dup (p.Ala1245_Leu1246insGlnAla) | gnomAD v4 |
| 16 | g.89282678A>C | CA497374460 | ANKRD11 | c.3864T>G (p.Ala1288=) c.*3667T>G (n.*3667T>G) c.744+5850T>G (n.744+5850T>G) c.151+5850T>G c.3762T>G (p.Ala1254=) c.3567T>G (p.Ala1189=) c.3735T>G (p.Ala1245=) | |
| 16 | g.89282678A>G | CA497374461 | ANKRD11 | c.3864T>C (p.Ala1288=) c.*3667T>C (n.*3667T>C) c.744+5850T>C (n.744+5850T>C) c.151+5850T>C c.3762T>C (p.Ala1254=) c.3567T>C (p.Ala1189=) c.3735T>C (p.Ala1245=) | gnomAD v4 |
| 16 | g.89282678A>T | CA497374462 | ANKRD11 | c.3864T>A (p.Ala1288=) c.*3667T>A (n.*3667T>A) c.744+5850T>A (n.744+5850T>A) c.151+5850T>A c.3762T>A (p.Ala1254=) c.3567T>A (p.Ala1189=) c.3735T>A (p.Ala1245=) | |
| 16 | g.89282679G>A | CA397158827 | ANKRD11 | c.3863C>T (p.Ala1288Val) c.*3666C>T (n.*3666C>T) c.744+5849C>T (n.744+5849C>T) c.151+5849C>T c.3761C>T (p.Ala1254Val) c.3566C>T (p.Ala1189Val) c.3734C>T (p.Ala1245Val) | dbSNP |
| 16 | g.89282679G>C | CA397158828 | ANKRD11 | c.3863C>G (p.Ala1288Gly) c.*3666C>G (n.*3666C>G) c.744+5849C>G (n.744+5849C>G) c.151+5849C>G c.3761C>G (p.Ala1254Gly) c.3566C>G (p.Ala1189Gly) c.3734C>G (p.Ala1245Gly) | |
| 16 | g.89282679G= | CA2241603404 | ANKRD11 | c.3863C= (p.Ala1288=) c.*3666C= (n.*3666C=) c.744+5849C= (n.744+5849C=) c.151+5849C= c.3761C= (p.Ala1254=) c.3566C= (p.Ala1189=) c.3734C= (p.Ala1245=) | |
| 16 | g.89282679G>T | CA397158829 | ANKRD11 | c.3863C>A (p.Ala1288Asp) c.*3666C>A (n.*3666C>A) c.744+5849C>A (n.744+5849C>A) c.151+5849C>A c.3761C>A (p.Ala1254Asp) c.3566C>A (p.Ala1189Asp) c.3734C>A (p.Ala1245Asp) | |
| 16 | g.89282680C>A | CA397158830 | ANKRD11 | c.3862G>T (p.Ala1288Ser) c.*3665G>T (n.*3665G>T) c.744+5848G>T (n.744+5848G>T) c.151+5848G>T c.3760G>T (p.Ala1254Ser) c.3565G>T (p.Ala1189Ser) c.3733G>T (p.Ala1245Ser) | |
| 16 | g.89282680C>G | CA397158831 | ANKRD11 | c.3862G>C (p.Ala1288Pro) c.*3665G>C (n.*3665G>C) c.744+5848G>C (n.744+5848G>C) c.151+5848G>C c.3760G>C (p.Ala1254Pro) c.3565G>C (p.Ala1189Pro) c.3733G>C (p.Ala1245Pro) | |
| 16 | g.89282680C>T | CA397158832 | ANKRD11 | c.3862G>A (p.Ala1288Thr) c.*3665G>A (n.*3665G>A) c.744+5848G>A (n.744+5848G>A) c.151+5848G>A c.3760G>A (p.Ala1254Thr) c.3565G>A (p.Ala1189Thr) c.3733G>A (p.Ala1245Thr) | COSMIC |
| 16 | g.89282681C>A | CA397158833 | ANKRD11 | c.3861G>T (p.Glu1287Asp) c.*3664G>T (n.*3664G>T) c.744+5847G>T (n.744+5847G>T) c.151+5847G>T c.3759G>T (p.Glu1253Asp) c.3564G>T (p.Glu1188Asp) c.3732G>T (p.Glu1244Asp) | |
| 16 | g.89282681C= | CA2241603406 | ANKRD11 | c.3861G= (p.Glu1287=) c.*3664G= (n.*3664G=) c.744+5847G= (n.744+5847G=) c.151+5847G= c.3759G= (p.Glu1253=) c.3564G= (p.Glu1188=) c.3732G= (p.Glu1244=) | |
| 16 | g.89282681C>G | CA397158834 | ANKRD11 | c.3861G>C (p.Glu1287Asp) c.*3664G>C (n.*3664G>C) c.744+5847G>C (n.744+5847G>C) c.151+5847G>C c.3759G>C (p.Glu1253Asp) c.3564G>C (p.Glu1188Asp) c.3732G>C (p.Glu1244Asp) | |
| 16 | g.89282681C>T | CA497374473 | ANKRD11 | c.3861G>A (p.Glu1287=) c.*3664G>A (n.*3664G>A) c.744+5847G>A (n.744+5847G>A) c.151+5847G>A c.3759G>A (p.Glu1253=) c.3564G>A (p.Glu1188=) c.3732G>A (p.Glu1244=) | dbSNP gnomAD v2 gnomAD v4 |
| 16 | g.89282682T>A | CA397158835 | ANKRD11 | c.3860A>T (p.Glu1287Val) c.*3663A>T (n.*3663A>T) c.744+5846A>T (n.744+5846A>T) c.151+5846A>T c.3758A>T (p.Glu1253Val) c.3563A>T (p.Glu1188Val) c.3731A>T (p.Glu1244Val) | |
| 16 | g.89282682T>C | CA397158837 | ANKRD11 | c.3860A>G (p.Glu1287Gly) c.*3663A>G (n.*3663A>G) c.744+5846A>G (n.744+5846A>G) c.151+5846A>G c.3758A>G (p.Glu1253Gly) c.3563A>G (p.Glu1188Gly) c.3731A>G (p.Glu1244Gly) | |
| 16 | g.89282682T>G | CA397158836 | ANKRD11 | c.3860A>C (p.Glu1287Ala) c.*3663A>C (n.*3663A>C) c.744+5846A>C (n.744+5846A>C) c.151+5846A>C c.3758A>C (p.Glu1253Ala) c.3563A>C (p.Glu1188Ala) c.3731A>C (p.Glu1244Ala) | gnomAD v4 |
| 16 | g.89282683C>A | CA397158838 | ANKRD11 | c.3859G>T (p.Glu1287Ter) c.*3662G>T (n.*3662G>T) c.744+5845G>T (n.744+5845G>T) c.151+5845G>T c.3757G>T (p.Glu1253Ter) c.3562G>T (p.Glu1188Ter) c.3730G>T (p.Glu1244Ter) | |
| 16 | g.89282683C= | CA2241603408 | ANKRD11 | c.3859G= (p.Glu1287=) c.*3662G= (n.*3662G=) c.744+5845G= (n.744+5845G=) c.151+5845G= c.3757G= (p.Glu1253=) c.3562G= (p.Glu1188=) c.3730G= (p.Glu1244=) | |
| 16 | g.89282683C>G | CA397158839 | ANKRD11 | c.3859G>C (p.Glu1287Gln) c.*3662G>C (n.*3662G>C) c.744+5845G>C (n.744+5845G>C) c.151+5845G>C c.3757G>C (p.Glu1253Gln) c.3562G>C (p.Glu1188Gln) c.3730G>C (p.Glu1244Gln) | COSMIC |
| 16 | g.89282683C>T | CA8242275 | ANKRD11 | c.3859G>A (p.Glu1287Lys) c.*3662G>A (n.*3662G>A) c.744+5845G>A (n.744+5845G>A) c.151+5845G>A c.3757G>A (p.Glu1253Lys) c.3562G>A (p.Glu1188Lys) c.3730G>A (p.Glu1244Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89282684T>A | CA397158840 | ANKRD11 | c.3858A>T (p.Glu1286Asp) c.*3661A>T (n.*3661A>T) c.744+5844A>T (n.744+5844A>T) c.151+5844A>T c.3756A>T (p.Glu1252Asp) c.3561A>T (p.Glu1187Asp) c.3729A>T (p.Glu1243Asp) | dbSNP gnomAD v2 gnomAD v4 |
| 16 | g.89282684T>C | CA497374597 | ANKRD11 | c.3858A>G (p.Glu1286=) c.*3661A>G (n.*3661A>G) c.744+5844A>G (n.744+5844A>G) c.151+5844A>G c.3756A>G (p.Glu1252=) c.3561A>G (p.Glu1187=) c.3729A>G (p.Glu1243=) | gnomAD v4 |
| 16 | g.89282684T>G | CA397158841 | ANKRD11 | c.3858A>C (p.Glu1286Asp) c.*3661A>C (n.*3661A>C) c.744+5844A>C (n.744+5844A>C) c.151+5844A>C c.3756A>C (p.Glu1252Asp) c.3561A>C (p.Glu1187Asp) c.3729A>C (p.Glu1243Asp) | |
| 16 | g.89282684T= | CA2241603411 | ANKRD11 | c.3858A= (p.Glu1286=) c.*3661A= (n.*3661A=) c.744+5844A= (n.744+5844A=) c.151+5844A= c.3756A= (p.Glu1252=) c.3561A= (p.Glu1187=) c.3729A= (p.Glu1243=) | |
| 16 | g.89282685T>A | CA397158842 | ANKRD11 | c.3857A>T (p.Glu1286Val) c.*3660A>T (n.*3660A>T) c.744+5843A>T (n.744+5843A>T) c.151+5843A>T c.3755A>T (p.Glu1252Val) c.3560A>T (p.Glu1187Val) c.3728A>T (p.Glu1243Val) | |
| 16 | g.89282685T>C | CA397158843 | ANKRD11 | c.3857A>G (p.Glu1286Gly) c.*3660A>G (n.*3660A>G) c.744+5843A>G (n.744+5843A>G) c.151+5843A>G c.3755A>G (p.Glu1252Gly) c.3560A>G (p.Glu1187Gly) c.3728A>G (p.Glu1243Gly) |