SUSPENSION NOTICE:2024-08-07T19:00:00-0500 — 2024-09-25T08:00:00-0500
New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.41136830T>A | CA515966297 | USP9X | c.462T>A (p.Arg154=) | |
| X | g.41136830T>C | CA515966300 | USP9X | c.462T>C (p.Arg154=) | |
| X | g.41136830T>G | CA515966299 | USP9X | c.462T>G (p.Arg154=) | |
| X | g.41136831C>A | CA412762730 | USP9X | c.463C>A (p.Leu155Met) | |
| X | g.41136831C= | CA2425806592 | USP9X | c.463C= (p.Leu155=) | |
| X | g.41136831C>G | CA412762732 | USP9X | c.463C>G (p.Leu155Val) | gnomAD v4 |
| X | g.41136831C>T | CA329012326 | USP9X | c.463C>T (p.Leu155=) | dbSNP gnomAD v2 gnomAD v4 |
| X | g.41136832T>A | CA412762737 | USP9X | c.464T>A (p.Leu155Gln) | |
| X | g.41136832T>C | CA412762735 | USP9X | c.464T>C (p.Leu155Pro) | |
| X | g.41136832T>G | CA412762734 | USP9X | c.464T>G (p.Leu155Arg) | |
| X | g.41136833G>A | CA515966307 | USP9X | c.465G>A (p.Leu155=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| X | g.41136833G>C | CA515966305 | USP9X | c.465G>C (p.Leu155=) | |
| X | g.41136833G= | CA2425806593 | USP9X | c.465G= (p.Leu155=) | |
| X | g.41136833G>T | CA515966303 | USP9X | c.465G>T (p.Leu155=) | |
| X | g.41136834del | CA2548185416 | USP9X | c.466del (p.Val156TrpfsTer16) | |
| X | g.41136834G>A | CA412762740 | USP9X | c.466G>A (p.Val156Met) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.41136834G>C | CA412762742 | USP9X | c.466G>C (p.Val156Leu) | |
| X | g.41136834G= | CA2425806594 | USP9X | c.466G= (p.Val156=) | |
| X | g.41136834G>T | CA412762743 | USP9X | c.466G>T (p.Val156Leu) | gnomAD v4 |
| X | g.41136835T>A | CA412762746 | USP9X | c.467T>A (p.Val156Glu) | |
| X | g.41136835T>C | CA412762747 | USP9X | c.467T>C (p.Val156Ala) | |
| X | g.41136835T>G | CA412762749 | USP9X | c.467T>G (p.Val156Gly) | gnomAD v4 |
| X | g.41136836G>A | CA515966310 | USP9X | c.468G>A (p.Val156=) | |
| X | g.41136836G>C | CA515966313 | USP9X | c.468G>C (p.Val156=) | |
| X | g.41136836G>T | CA515966312 | USP9X | c.468G>T (p.Val156=) | |
| X | g.41136837G>A | CA412762751 | USP9X | c.469G>A (p.Glu157Lys) | |
| X | g.41136837G>C | CA412762755 | USP9X | c.469G>C (p.Glu157Gln) | |
| X | g.41136837G>T | CA412762752 | USP9X | c.469G>T (p.Glu157Ter) | |
| X | g.41136838A>C | CA412762757 | USP9X | c.470A>C (p.Glu157Ala) | |
| X | g.41136838A>G | CA412762759 | USP9X | c.470A>G (p.Glu157Gly) | |
| X | g.41136838A>T | CA412762761 | USP9X | c.470A>T (p.Glu157Val) | |
| X | g.41136839G>A | CA515966319 | USP9X | c.471G>A (p.Glu157=) | |
| X | g.41136839G>C | CA412762763 | USP9X | c.471G>C (p.Glu157Asp) | |
| X | g.41136839G>T | CA412762765 | USP9X | c.471G>T (p.Glu157Asp) | |
| X | g.41136840C>A | CA412762767 | USP9X | c.472C>A (p.Leu158Ile) | |
| X | g.41136840C>G | CA412762769 | USP9X | c.472C>G (p.Leu158Val) | |
| X | g.41136840C>T | CA515966321 | USP9X | c.472C>T (p.Leu158=) | |
| X | g.41136841T>A | CA412762771 | USP9X | c.473T>A (p.Leu158Gln) | |
| X | g.41136841T>C | CA412762772 | USP9X | c.473T>C (p.Leu158Pro) | |
| X | g.41136841T>G | CA412762775 | USP9X | c.473T>G (p.Leu158Arg) | |
| X | g.41136842A= | CA2425806595 | USP9X | c.474A= (p.Leu158=) | |
| X | g.41136842A>C | CA515966323 | USP9X | c.474A>C (p.Leu158=) | |
| X | g.41136842A>G | CA10388319 | USP9X | c.474A>G (p.Leu158=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.41136842A>T | CA515966325 | USP9X | c.474A>T (p.Leu158=) | |
| X | g.41136843T>A | CA412762778 | USP9X | c.475T>A (p.Cys159Ser) | |
| X | g.41136843T>C | CA412762782 | USP9X | c.475T>C (p.Cys159Arg) | |
| X | g.41136843T>G | CA412762780 | USP9X | c.475T>G (p.Cys159Gly) | |
| X | g.41136844G>A | CA412762784 | USP9X | c.476G>A (p.Cys159Tyr) | |
| X | g.41136844G>C | CA412762787 | USP9X | c.476G>C (p.Cys159Ser) | |
| X | g.41136844G>T | CA412762786 | USP9X | c.476G>T (p.Cys159Phe) | |
| X | g.41136845T>A | CA412762788 | USP9X | c.477T>A (p.Cys159Ter) | |
| X | g.41136845T>C | CA515966327 | USP9X | c.477T>C (p.Cys159=) | |
| X | g.41136845T>G | CA412762790 | USP9X | c.477T>G (p.Cys159Trp) | |
| X | g.41136846G>A | CA412762793 | USP9X | c.478G>A (p.Val160Met) | |
| X | g.41136846G>C | CA10388320 | USP9X | c.478G>C (p.Val160Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.41136846G= | CA2425806596 | USP9X | c.478G= (p.Val160=) | |
| X | g.41136846G>T | CA412762795 | USP9X | c.478G>T (p.Val160Leu) | |
| X | g.41136847T>A | CA412762802 | USP9X | c.479T>A (p.Val160Glu) | |
| X | g.41136847T>C | CA412762800 | USP9X | c.479T>C (p.Val160Ala) | |
| X | g.41136847T>G | CA412762798 | USP9X | c.479T>G (p.Val160Gly) | |
| X | g.41136848G>A | CA515966332 | USP9X | c.480G>A (p.Val160=) | |
| X | g.41136848G>C | CA515966333 | USP9X | c.480G>C (p.Val160=) | |
| X | g.41136848G>T | CA515966335 | USP9X | c.480G>T (p.Val160=) | |
| X | g.41136849G>A | CA10388321 | USP9X | c.481G>A (p.Ala161Thr) | dbSNP ExAC gnomAD v4 |
| X | g.41136849G>C | CA412762806 | USP9X | c.481G>C (p.Ala161Pro) | |
| X | g.41136849G= | CA2425806597 | USP9X | c.481G= (p.Ala161=) | |
| X | g.41136849G>T | CA412762808 | USP9X | c.481G>T (p.Ala161Ser) | |
| X | g.41136850C>A | CA412762811 | USP9X | c.482C>A (p.Ala161Asp) | |
| X | g.41136850C>G | CA412762814 | USP9X | c.482C>G (p.Ala161Gly) | |
| X | g.41136850C>T | CA412762815 | USP9X | c.482C>T (p.Ala161Val) | |
| X | g.41136851C>A | CA515966342 | USP9X | c.483C>A (p.Ala161=) | dbSNP gnomAD v3 gnomAD v4 |
| X | g.41136851C= | CA2425806598 | USP9X | c.483C= (p.Ala161=) | |
| X | g.41136851C>G | CA515966345 | USP9X | c.483C>G (p.Ala161=) | dbSNP gnomAD v2 gnomAD v4 |
| X | g.41136851C>T | CA515966344 | USP9X | c.483C>T (p.Ala161=) | |
| X | g.41136852A>C | CA412762820 | USP9X | c.484A>C (p.Lys162Gln) | |
| X | g.41136852A>G | CA412762824 | USP9X | c.484A>G (p.Lys162Glu) | |
| X | g.41136852A>T | CA412762821 | USP9X | c.484A>T (p.Lys162Ter) | |
| X | g.41136853A>C | CA412762827 | USP9X | c.485A>C (p.Lys162Thr) | |
| X | g.41136853A>G | CA412762830 | USP9X | c.485A>G (p.Lys162Arg) | |
| X | g.41136853A>T | CA412762833 | USP9X | c.485A>T (p.Lys162Met) | |
| X | g.41136854G>A | CA515966350 | USP9X | c.486G>A (p.Lys162=) | gnomAD v4 |
| X | g.41136854G>C | CA412762836 | USP9X | c.486G>C (p.Lys162Asn) | |
| X | g.41136854G>T | CA412762838 | USP9X | c.486G>T (p.Lys162Asn) | |
| X | g.41136855T>A | CA412762842 | USP9X | c.487T>A (p.Leu163Met) | |
| X | g.41136855T>C | CA10388322 | USP9X | c.487T>C (p.Leu163=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.41136855T>G | CA412762846 | USP9X | c.487T>G (p.Leu163Val) | |
| X | g.41136855T= | CA2425806599 | USP9X | c.487T= (p.Leu163=) | |
| X | g.41136856T>A | CA412762850 | USP9X | c.488T>A (p.Leu163Ter) | |
| X | g.41136856T>C | CA412762853 | USP9X | c.488T>C (p.Leu163Ser) | |
| X | g.41136856T>G | CA412762854 | USP9X | c.488T>G (p.Leu163Trp) | |
| X | g.41136857G>A | CA515966358 | USP9X | c.489G>A (p.Leu163=) | |
| X | g.41136857G>C | CA412762858 | USP9X | c.489G>C (p.Leu163Phe) | |
| X | g.41136857G>T | CA412762860 | USP9X | c.489G>T (p.Leu163Phe) | |
| X | g.41136858T>A | CA412762863 | USP9X | c.490T>A (p.Ser164Thr) | |
| X | g.41136858T>C | CA412762866 | USP9X | c.490T>C (p.Ser164Pro) | |
| X | g.41136858T>G | CA412762869 | USP9X | c.490T>G (p.Ser164Ala) | |
| X | g.41136859C>A | CA412762873 | USP9X | c.491C>A (p.Ser164Tyr) | |
| X | g.41136859C>G | CA412762876 | USP9X | c.491C>G (p.Ser164Cys) | |
| X | g.41136859C>T | CA412762879 | USP9X | c.491C>T (p.Ser164Phe) | |
| X | g.41136860C>A | CA515966363 | USP9X | c.492C>A (p.Ser164=) | |
| X | g.41136860C>G | CA515966364 | USP9X | c.492C>G (p.Ser164=) | |
| X | g.41136860C>T | CA515966365 | USP9X | c.492C>T (p.Ser164=) | gnomAD v4 |
| X | g.41136861C>A | CA412762892 | USP9X | c.493C>A (p.Gln165Lys) | |
| X | g.41136861C>G | CA412762891 | USP9X | c.493C>G (p.Gln165Glu) | |
| X | g.41136861C>T | CA412762883 | USP9X | c.493C>T (p.Gln165Ter) | |
| X | g.41136862A>C | CA412762894 | USP9X | c.494A>C (p.Gln165Pro) | |
| X | g.41136862A>G | CA412762898 | USP9X | c.494A>G (p.Gln165Arg) | |
| X | g.41136862A>T | CA412762900 | USP9X | c.494A>T (p.Gln165Leu) | |
| X | g.41136863A= | CA2425806600 | USP9X | c.495A= (p.Gln165=) | |
| X | g.41136863A>C | CA412762903 | USP9X | c.495A>C (p.Gln165His) | gnomAD v4 |
| X | g.41136863A>G | CA10388323 | USP9X | c.495A>G (p.Gln165=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.41136863A>T | CA412762907 | USP9X | c.495A>T (p.Gln165His) | |
| X | g.41136864G>A | CA412762911 | USP9X | c.496G>A (p.Asp166Asn) | |
| X | g.41136864G>C | CA412762916 | USP9X | c.496G>C (p.Asp166His) | |
| X | g.41136864G>T | CA412762913 | USP9X | c.496G>T (p.Asp166Tyr) | |
| X | g.41136865A>C | CA412762920 | USP9X | c.497A>C (p.Asp166Ala) | |
| X | g.41136865A>G | CA412762923 | USP9X | c.497A>G (p.Asp166Gly) | |
| X | g.41136865A>T | CA412762924 | USP9X | c.497A>T (p.Asp166Val) | |
| X | g.41136866C>A | CA412762927 | USP9X | c.498C>A (p.Asp166Glu) | |
| X | g.41136866C>G | CA412762930 | USP9X | c.498C>G (p.Asp166Glu) | |
| X | g.41136866C>T | CA515966375 | USP9X | c.498C>T (p.Asp166=) | |
| X | g.41136867T>A | CA412762933 | USP9X | c.499T>A (p.Trp167Arg) | |
| X | g.41136867T>C | CA412762936 | USP9X | c.499T>C (p.Trp167Arg) | dbSNP |
| X | g.41136867T>G | CA412762938 | USP9X | c.499T>G (p.Trp167Gly) | |
| X | g.41136867T= | CA2425806601 | USP9X | c.499T= (p.Trp167=) | |
| X | g.41136868G>A | CA412762941 | USP9X | c.500G>A (p.Trp167Ter) | |
| X | g.41136868G>C | CA412762944 | USP9X | c.500G>C (p.Trp167Ser) | |
| X | g.41136868G>T | CA412762947 | USP9X | c.500G>T (p.Trp167Leu) | |
| X | g.41136869G>A | CA412762950 | USP9X | c.501G>A (p.Trp167Ter) | |
| X | g.41136869G>C | CA412762955 | USP9X | c.501G>C (p.Trp167Cys) | |
| X | g.41136869G>T | CA412762952 | USP9X | c.501G>T (p.Trp167Cys) | |
| X | g.41136870T>A | CA412762958 | USP9X | c.502T>A (p.Phe168Ile) | |
| X | g.41136870T>C | CA412762962 | USP9X | c.502T>C (p.Phe168Leu) | |
| X | g.41136870T>G | CA412762959 | USP9X | c.502T>G (p.Phe168Val) | |
| X | g.41136871T>A | CA412762966 | USP9X | c.503T>A (p.Phe168Tyr) | |
| X | g.41136871T>C | CA412762968 | USP9X | c.503T>C (p.Phe168Ser) | gnomAD v4 |
| X | g.41136871T>G | CA412762971 | USP9X | c.503T>G (p.Phe168Cys) | |
| X | g.41136872T>A | CA412762974 | USP9X | c.504T>A (p.Phe168Leu) | gnomAD v4 |
| X | g.41136872T>C | CA515966383 | USP9X | c.504T>C (p.Phe168=) | |
| X | g.41136872T>G | CA412762977 | USP9X | c.504T>G (p.Phe168Leu) | |
| X | g.41136873C>A | CA412762981 | USP9X | c.505C>A (p.Pro169Thr) | |
| X | g.41136873C>G | CA412762983 | USP9X | c.505C>G (p.Pro169Ala) | |
| X | g.41136873C>T | CA412762984 | USP9X | c.505C>T (p.Pro169Ser) | |
| X | g.41136874C>A | CA412762989 | USP9X | c.506C>A (p.Pro169Gln) | |
| X | g.41136874C>G | CA412762991 | USP9X | c.506C>G (p.Pro169Arg) | |
| X | g.41136874C>T | CA412762993 | USP9X | c.506C>T (p.Pro169Leu) | |
| X | g.41136875A>C | CA515966390 | USP9X | c.507A>C (p.Pro169=) | |
| X | g.41136875A>G | CA515966388 | USP9X | c.507A>G (p.Pro169=) | |
| X | g.41136875A>T | CA515966389 | USP9X | c.507A>T (p.Pro169=) | |
| X | g.41136876C>A | CA412763002 | USP9X | c.508C>A (p.Leu170Ile) | |
| X | g.41136876C= | CA2425806602 | USP9X | c.508C= (p.Leu170=) | |
| X | g.41136876C>G | CA412762997 | USP9X | c.508C>G (p.Leu170Val) | dbSNP |
| X | g.41136876C>T | CA412763000 | USP9X | c.508C>T (p.Leu170Phe) | |
| X | g.41136877T>A | CA412763005 | USP9X | c.509T>A (p.Leu170His) | |
| X | g.41136877T>C | CA412763008 | USP9X | c.509T>C (p.Leu170Pro) | |
| X | g.41136877T>G | CA412763011 | USP9X | c.509T>G (p.Leu170Arg) | |
| X | g.41136878T>A | CA515966396 | USP9X | c.510T>A (p.Leu170=) | |
| X | g.41136878T>C | CA515966399 | USP9X | c.510T>C (p.Leu170=) | |
| X | g.41136878T>G | CA515966398 | USP9X | c.510T>G (p.Leu170=) | |
| X | g.41136879T>A | CA412763014 | USP9X | c.511T>A (p.Leu171Ile) | |
| X | g.41136879T>C | CA515966401 | USP9X | c.511T>C (p.Leu171=) | ClinVar dbSNP |
| X | g.41136879T>G | CA412763017 | USP9X | c.511T>G (p.Leu171Val) | |
| X | g.41136880T>A | CA412763018 | USP9X | c.512T>A (p.Leu171Ter) | |
| X | g.41136880T>C | CA412763019 | USP9X | c.512T>C (p.Leu171Ser) | |
| X | g.41136880T>G | CA412763020 | USP9X | c.512T>G (p.Leu171Ter) | |
| X | g.41136881A>C | CA412763021 | USP9X | c.513A>C (p.Leu171Phe) | |
| X | g.41136881A>G | CA515966405 | USP9X | c.513A>G (p.Leu171=) | |
| X | g.41136881A>T | CA412763023 | USP9X | c.513A>T (p.Leu171Phe) | |
| X | g.41136882G>A | CA412763027 | USP9X | c.514G>A (p.Glu172Lys) | |
| X | g.41136882G>C | CA412763030 | USP9X | c.514G>C (p.Glu172Gln) | |
| X | g.41136882G>T | CA412763026 | USP9X | c.514G>T (p.Glu172Ter) | |
| X | g.41136883A>C | CA412763033 | USP9X | c.515A>C (p.Glu172Ala) | |
| X | g.41136883A>G | CA412763036 | USP9X | c.515A>G (p.Glu172Gly) | |
| X | g.41136883A>T | CA412763038 | USP9X | c.515A>T (p.Glu172Val) | |
| X | g.41136884A= | CA2425806603 | USP9X | c.516A= (p.Glu172=) | |
| X | g.41136884A>C | CA329012338 | USP9X | c.516A>C (p.Glu172Asp) | dbSNP |
| X | g.41136884A>G | CA515966409 | USP9X | c.516A>G (p.Glu172=) | |
| X | g.41136884A>T | CA412763044 | USP9X | c.516A>T (p.Glu172Asp) | |
| X | g.41136884_41136887delinsACTT | CA2425806604 | USP9X | c.516_519delinsACTT (p.Glu172=) | |
| X | g.41136885C>A | CA412763053 | USP9X | c.517C>A (p.Leu173Ile) | |
| X | g.41136885C>G | CA412763055 | USP9X | c.517C>G (p.Leu173Val) | |
| X | g.41136885C>T | CA412763050 | USP9X | c.517C>T (p.Leu173Phe) | |
| X | g.41136888_41136890del | CA16043269 | USP9X | c.520_522del (p.Leu174del) | ClinVar dbSNP |
| X | g.41136886T>A | CA412763057 | USP9X | c.518T>A (p.Leu173His) | |
| X | g.41136886T>C | CA412763058 | USP9X | c.518T>C (p.Leu173Pro) | |
| X | g.41136886T>G | CA412763059 | USP9X | c.518T>G (p.Leu173Arg) | |
| X | g.41136887T>A | CA515966413 | USP9X | c.519T>A (p.Leu173=) | |
| X | g.41136887T>C | CA515966414 | USP9X | c.519T>C (p.Leu173=) | |
| X | g.41136887T>G | CA515966415 | USP9X | c.519T>G (p.Leu173=) | |
| X | g.41136888C>A | CA412763060 | USP9X | c.520C>A (p.Leu174Ile) | |
| X | g.41136888C>G | CA412763062 | USP9X | c.520C>G (p.Leu174Val) | |
| X | g.41136888C>T | CA412763064 | USP9X | c.520C>T (p.Leu174Phe) | |
| X | g.41136889T>A | CA412763066 | USP9X | c.521T>A (p.Leu174His) | |
| X | g.41136889T>C | CA412763068 | USP9X | c.521T>C (p.Leu174Pro) | |
| X | g.41136889T>G | CA412763071 | USP9X | c.521T>G (p.Leu174Arg) | |
| X | g.41136890T>A | CA515966416 | USP9X | c.522T>A (p.Leu174=) | |
| X | g.41136890T>C | CA515966417 | USP9X | c.522T>C (p.Leu174=) | |
| X | g.41136890T>G | CA515966418 | USP9X | c.522T>G (p.Leu174=) | |
| X | g.41136891G>A | CA412763074 | USP9X | c.523G>A (p.Ala175Thr) | |
| X | g.41136891G>C | CA412763081 | USP9X | c.523G>C (p.Ala175Pro) | |
| X | g.41136891G>T | CA412763077 | USP9X | c.523G>T (p.Ala175Ser) | gnomAD v4 |
| X | g.41136892C>A | CA412763085 | USP9X | c.524C>A (p.Ala175Asp) | |
| X | g.41136892C>G | CA412763087 | USP9X | c.524C>G (p.Ala175Gly) | |
| X | g.41136892C>T | CA412763091 | USP9X | c.524C>T (p.Ala175Val) | |
| X | g.41136893C>A | CA515966423 | USP9X | c.525C>A (p.Ala175=) | ClinVar |
| X | g.41136893C= | CA2425806605 | USP9X | c.525C= (p.Ala175=) | |
| X | g.41136893C>G | CA10388324 | USP9X | c.525C>G (p.Ala175=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.41136893C>T | CA515966424 | USP9X | c.525C>T (p.Ala175=) | |
| X | g.41136894A= | CA2425806606 | USP9X | c.526A= (p.Met176=) | |
| X | g.41136894A>C | CA412763094 | USP9X | c.526A>C (p.Met176Leu) | |
| X | g.41136894A>G | CA412763098 | USP9X | c.526A>G (p.Met176Val) | |
| X | g.41136894A>T | CA412763100 | USP9X | c.526A>T (p.Met176Leu) | dbSNP gnomAD v4 |
| X | g.41136895T>A | CA412763110 | USP9X | c.527T>A (p.Met176Lys) | |
| X | g.41136895T>C | CA412763104 | USP9X | c.527T>C (p.Met176Thr) | dbSNP gnomAD v2 gnomAD v4 |
| X | g.41136895T>G | CA412763108 | USP9X | c.527T>G (p.Met176Arg) | |
| X | g.41136895T= | CA2425806607 | USP9X | c.527T= (p.Met176=) | |
| X | g.41136896G>A | CA412763115 | USP9X | c.528G>A (p.Met176Ile) | |
| X | g.41136896G>C | CA412763119 | USP9X | c.528G>C (p.Met176Ile) | |
| X | g.41136896G>T | CA412763116 | USP9X | c.528G>T (p.Met176Ile) | |
| X | g.41136897G>A | CA412763124 | USP9X | c.529G>A (p.Ala177Thr) | gnomAD v4 |
| X | g.41136897G>C | CA412763128 | USP9X | c.529G>C (p.Ala177Pro) | |
| X | g.41136897G>T | CA412763126 | USP9X | c.529G>T (p.Ala177Ser) | |
| X | g.41136898C>A | CA412763131 | USP9X | c.530C>A (p.Ala177Asp) | |
| X | g.41136898C>G | CA412763137 | USP9X | c.530C>G (p.Ala177Gly) | |
| X | g.41136898C>T | CA412763134 | USP9X | c.530C>T (p.Ala177Val) | gnomAD v4 |
| X | g.41136899C>A | CA515966436 | USP9X | c.531C>A (p.Ala177=) | |
| X | g.41136899C>G | CA515966437 | USP9X | c.531C>G (p.Ala177=) | |
| X | g.41136899C>T | CA515966438 | USP9X | c.531C>T (p.Ala177=) | gnomAD v4 |
| X | g.41136900T>A | CA412763139 | USP9X | c.532T>A (p.Leu178Ile) | |
| X | g.41136900T>C | CA515966439 | USP9X | c.532T>C (p.Leu178=) | |
| X | g.41136900T>G | CA412763142 | USP9X | c.532T>G (p.Leu178Val) | |
| X | g.41136901T>A | CA412763145 | USP9X | c.533T>A (p.Leu178Ter) | |
| X | g.41136901T>C | CA412763148 | USP9X | c.533T>C (p.Leu178Ser) | |
| X | g.41136901T>G | CA412763151 | USP9X | c.533T>G (p.Leu178Ter) | |
| X | g.41136902A>C | CA412763154 | USP9X | c.534A>C (p.Leu178Phe) | |
| X | g.41136902A>G | CA515966442 | USP9X | c.534A>G (p.Leu178=) | |
| X | g.41136902A>T | CA412763156 | USP9X | c.534A>T (p.Leu178Phe) | |
| X | g.41136903A>C | CA412763160 | USP9X | c.535A>C (p.Asn179His) | COSMIC |
| X | g.41136903A>G | CA412763163 | USP9X | c.535A>G (p.Asn179Asp) | |
| X | g.41136903A>T | CA412763165 | USP9X | c.535A>T (p.Asn179Tyr) | |
| X | g.41136904A= | CA2425806608 | USP9X | c.536A= (p.Asn179=) | |
| X | g.41136904A>C | CA412763167 | USP9X | c.536A>C (p.Asn179Thr) | |
| X | g.41136904A>G | CA412763169 | USP9X | c.536A>G (p.Asn179Ser) | dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |
| X | g.41136904A>T | CA412763171 | USP9X | c.536A>T (p.Asn179Ile) | |
| X | g.41136905T>A | CA412763173 | USP9X | c.537T>A (p.Asn179Lys) | |
| X | g.41136905T>C | CA515966455 | USP9X | c.537T>C (p.Asn179=) | |
| X | g.41136905T>G | CA412763175 | USP9X | c.537T>G (p.Asn179Lys) | |
| X | g.41136906C>A | CA412763177 | USP9X | c.538C>A (p.Pro180Thr) | ClinVar dbSNP |
| X | g.41136906C>G | CA412763178 | USP9X | c.538C>G (p.Pro180Ala) | |
| X | g.41136906C>T | CA412763179 | USP9X | c.538C>T (p.Pro180Ser) | |
| X | g.41136907C>A | CA412763180 | USP9X | c.539C>A (p.Pro180His) | |
| X | g.41136907C>G | CA412763183 | USP9X | c.539C>G (p.Pro180Arg) | |
| X | g.41136907C>T | CA412763184 | USP9X | c.539C>T (p.Pro180Leu) | |
| X | g.41136908T>A | CA515966460 | USP9X | c.540T>A (p.Pro180=) | |
| X | g.41136908T>C | CA515966465 | USP9X | c.540T>C (p.Pro180=) | |
| X | g.41136908T>G | CA515966467 | USP9X | c.540T>G (p.Pro180=) | |
| X | g.41136909C>A | CA412763187 | USP9X | c.541C>A (p.His181Asn) | |
| X | g.41136909C>G | CA412763188 | USP9X | c.541C>G (p.His181Asp) | |
| X | g.41136909C>T | CA412763190 | USP9X | c.541C>T (p.His181Tyr) | gnomAD v4 |
| X | g.41136910A= | CA2425806609 | USP9X | c.542A= (p.His181=) | |
| X | g.41136910A>C | CA412763192 | USP9X | c.542A>C (p.His181Pro) | |
| X | g.41136910A>G | CA412763193 | USP9X | c.542A>G (p.His181Arg) | |
| X | g.41136910A>T | CA412763194 | USP9X | c.542A>T (p.His181Leu) | ClinVar dbSNP |
| X | g.41136911T>A | CA412763197 | USP9X | c.543T>A (p.His181Gln) | |
| X | g.41136911T>C | CA515966470 | USP9X | c.543T>C (p.His181=) | dbSNP |
| X | g.41136911T>G | CA412763199 | USP9X | c.543T>G (p.His181Gln) | |
| X | g.41136912T>A | CA412763202 | USP9X | c.544T>A (p.Cys182Ser) | |
| X | g.41136912T>C | CA412763203 | USP9X | c.544T>C (p.Cys182Arg) | |
| X | g.41136912T>G | CA412763206 | USP9X | c.544T>G (p.Cys182Gly) | |
| X | g.41136913G>A | CA412763209 | USP9X | c.545G>A (p.Cys182Tyr) | COSMIC COSMIC |
| X | g.41136913G>C | CA412763211 | USP9X | c.545G>C (p.Cys182Ser) | |
| X | g.41136913G>T | CA412763213 | USP9X | c.545G>T (p.Cys182Phe) | |
| X | g.41136914C>A | CA412763218 | USP9X | c.546C>A (p.Cys182Ter) | |
| X | g.41136914C>G | CA412763216 | USP9X | c.546C>G (p.Cys182Trp) | gnomAD v4 |
| X | g.41136914C>T | CA515966479 | USP9X | c.546C>T (p.Cys182=) | |
| X | g.41136915A>C | CA412763220 | USP9X | c.547A>C (p.Lys183Gln) | |
| X | g.41136915A>G | CA412763222 | USP9X | c.547A>G (p.Lys183Glu) | ClinVar dbSNP |
| X | g.41136915A>T | CA412763224 | USP9X | c.547A>T (p.Lys183Ter) | |
| X | g.41136916A= | CA2425806610 | USP9X | c.548A= (p.Lys183=) | |
| X | g.41136916A>C | CA412763226 | USP9X | c.548A>C (p.Lys183Thr) | |
| X | g.41136916A>G | CA412763227 | USP9X | c.548A>G (p.Lys183Arg) | dbSNP gnomAD v2 gnomAD v4 |
| X | g.41136916A>T | CA412763229 | USP9X | c.548A>T (p.Lys183Ile) | |
| X | g.41136917A= | CA2425806611 | USP9X | c.549A= (p.Lys183=) | |
| X | g.41136917A>C | CA412763231 | USP9X | c.549A>C (p.Lys183Asn) | |
| X | g.41136917A>G | CA10388325 | USP9X | c.549A>G (p.Lys183=) | dbSNP ExAC |
| X | g.41136917A>T | CA412763234 | USP9X | c.549A>T (p.Lys183Asn) | |
| X | g.41136918T>A | CA412763238 | USP9X | c.550T>A (p.Phe184Ile) | |
| X | g.41136918T>C | CA412763240 | USP9X | c.550T>C (p.Phe184Leu) | |
| X | g.41136918T>G | CA412763243 | USP9X | c.550T>G (p.Phe184Val) | |
| X | g.41136919T>A | CA412763247 | USP9X | c.551T>A (p.Phe184Tyr) | |
| X | g.41136919T>C | CA412763249 | USP9X | c.551T>C (p.Phe184Ser) | |
| X | g.41136919T>G | CA412763252 | USP9X | c.551T>G (p.Phe184Cys) | COSMIC COSMIC |
| X | g.41136920C>A | CA412763255 | USP9X | c.552C>A (p.Phe184Leu) | COSMIC COSMIC |
| X | g.41136920C>G | CA412763257 | USP9X | c.552C>G (p.Phe184Leu) | |
| X | g.41136920C>T | CA515966495 | USP9X | c.552C>T (p.Phe184=) | |
| X | g.41136920_41136921insAAA | CA515966498 | USP9X | c.552_553insAAA (p.Phe184_His185insLys) | |
| X | g.41136921C>A | CA412763261 | USP9X | c.553C>A (p.His185Asn) | |
| X | g.41136921C>G | CA412763264 | USP9X | c.553C>G (p.His185Asp) | |
| X | g.41136921C>T | CA412763266 | USP9X | c.553C>T (p.His185Tyr) | |
| X | g.41136922A>C | CA412763269 | USP9X | c.554A>C (p.His185Pro) | |
| X | g.41136922A>G | CA412763274 | USP9X | c.554A>G (p.His185Arg) | |
| X | g.41136922A>T | CA412763271 | USP9X | c.554A>T (p.His185Leu) | |
| X | g.41136922_41136923insGAAA | CA515966499 | USP9X | c.554_555insGAAA (p.His185GlnfsTer11) | |
| X | g.41136923T>A | CA412763277 | USP9X | c.555T>A (p.His185Gln) | |
| X | g.41136923T>C | CA515966506 | USP9X | c.555T>C (p.His185=) | |
| X | g.41136923T>G | CA412763279 | USP9X | c.555T>G (p.His185Gln) | |
| X | g.41136924A>C | CA412763282 | USP9X | c.556A>C (p.Ile186Leu) | |
| X | g.41136924A>G | CA412763283 | USP9X | c.556A>G (p.Ile186Val) | gnomAD v4 |
| X | g.41136924A>T | CA412763285 | USP9X | c.556A>T (p.Ile186Phe) | |
| X | g.41136925T>A | CA412763287 | USP9X | c.557T>A (p.Ile186Asn) | |
| X | g.41136925T>C | CA412763289 | USP9X | c.557T>C (p.Ile186Thr) | |
| X | g.41136925T>G | CA412763292 | USP9X | c.557T>G (p.Ile186Ser) | |
| X | g.41136926C>A | CA515966508 | USP9X | c.558C>A (p.Ile186=) | |
| X | g.41136926C= | CA2425806612 | USP9X | c.558C= (p.Ile186=) | |
| X | g.41136926C>G | CA412763294 | USP9X | c.558C>G (p.Ile186Met) | |
| X | g.41136926C>T | CA515966509 | USP9X | c.558C>T (p.Ile186=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| X | g.41136927T>A | CA412763297 | USP9X | c.559T>A (p.Tyr187Asn) | |
| X | g.41136927T>C | CA412763299 | USP9X | c.559T>C (p.Tyr187His) | |
| X | g.41136927T>G | CA412763302 | USP9X | c.559T>G (p.Tyr187Asp) | |
| X | g.41136928A>C | CA412763309 | USP9X | c.560A>C (p.Tyr187Ser) | |
| X | g.41136928A>G | CA412763306 | USP9X | c.560A>G (p.Tyr187Cys) | gnomAD v4 |
| X | g.41136928A>T | CA412763304 | USP9X | c.560A>T (p.Tyr187Phe) | |
| X | g.41136929C>A | CA412763313 | USP9X | c.561C>A (p.Tyr187Ter) | |
| X | g.41136929C>G | CA412763314 | USP9X | c.561C>G (p.Tyr187Ter) | |
| X | g.41136929C>T | CA515966519 | USP9X | c.561C>T (p.Tyr187=) | gnomAD v4 |
| X | g.41136930A= | CA2425806613 | USP9X | c.562A= (p.Asn188=) | |
| X | g.41136930A>C | CA412763317 | USP9X | c.562A>C (p.Asn188His) | |
| X | g.41136930A>G | CA10388326 | USP9X | c.562A>G (p.Asn188Asp) | ClinVar dbSNP ExAC |
| X | g.41136930A>T | CA412763321 | USP9X | c.562A>T (p.Asn188Tyr) |