UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.41136888_41136890del | CA16043269 | USP9X | c.520_522del (p.Leu174del) | ClinVar dbSNP |
| 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) | |
| X | g.41136931A>C | CA412763324 | USP9X | c.563A>C (p.Asn188Thr) | |
| X | g.41136931A>G | CA412763326 | USP9X | c.563A>G (p.Asn188Ser) | gnomAD v4 |
| X | g.41136931A>T | CA412763328 | USP9X | c.563A>T (p.Asn188Ile) | |
| X | g.41136932T>A | CA412763332 | USP9X | c.564T>A (p.Asn188Lys) | |
| X | g.41136932T>C | CA515966524 | USP9X | c.564T>C (p.Asn188=) | gnomAD v4 COSMIC COSMIC |
| X | g.41136932T>G | CA412763333 | USP9X | c.564T>G (p.Asn188Lys) | |
| X | g.41136933G>A | CA412763334 | USP9X | c.565G>A (p.Gly189Ser) | ClinVar dbSNP |
| X | g.41136933G>C | CA412763335 | USP9X | c.565G>C (p.Gly189Arg) | |
| X | g.41136933G>T | CA412763336 | USP9X | c.565G>T (p.Gly189Cys) | |
| X | g.41136934G>A | CA412763338 | USP9X | c.566G>A (p.Gly189Asp) | |
| X | g.41136934G>C | CA412763339 | USP9X | c.566G>C (p.Gly189Ala) | |
| X | g.41136934G>T | CA412763337 | USP9X | c.566G>T (p.Gly189Val) | |
| X | g.41136935T>A | CA515966539 | USP9X | c.567T>A (p.Gly189=) | COSMIC COSMIC |
| X | g.41136935T>C | CA515966535 | USP9X | c.567T>C (p.Gly189=) | gnomAD v4 |
| X | g.41136935T>G | CA515966532 | USP9X | c.567T>G (p.Gly189=) | |
| X | g.41136936A>C | CA412763340 | USP9X | c.568A>C (p.Thr190Pro) | |
| X | g.41136936A>G | CA412763341 | USP9X | c.568A>G (p.Thr190Ala) | |
| X | g.41136936A>T | CA412763342 | USP9X | c.568A>T (p.Thr190Ser) | |
| X | g.41136937C>A | CA412763343 | USP9X | c.569C>A (p.Thr190Lys) | |
| X | g.41136937C>G | CA412763344 | USP9X | c.569C>G (p.Thr190Arg) | |
| X | g.41136937C>T | CA412763345 | USP9X | c.569C>T (p.Thr190Ile) | gnomAD v4 |
| X | g.41136938A= | CA2425806614 | USP9X | c.570A= (p.Thr190=) | |
| X | g.41136938A>C | CA515966544 | USP9X | c.570A>C (p.Thr190=) | |
| X | g.41136938A>G | CA515966546 | USP9X | c.570A>G (p.Thr190=) | dbSNP gnomAD v4 |
| X | g.41136938A>T | CA515966547 | USP9X | c.570A>T (p.Thr190=) | |
| X | g.41136939C>A | CA412763346 | USP9X | c.571C>A (p.Arg191Ser) | |
| X | g.41136939C>G | CA412763347 | USP9X | c.571C>G (p.Arg191Gly) | |
| X | g.41136939C>T | CA412763348 | USP9X | c.571C>T (p.Arg191Cys) | ClinVar gnomAD v4 COSMIC |
| X | g.41136940G>A | CA412763349 | USP9X | c.572G>A (p.Arg191His) | gnomAD v4 |
| X | g.41136940G>C | CA412763350 | USP9X | c.572G>C (p.Arg191Pro) | |
| X | g.41136940G>T | CA412763351 | USP9X | c.572G>T (p.Arg191Leu) | |
| X | g.41136941T>A | CA515966552 | USP9X | c.573T>A (p.Arg191=) | gnomAD v4 |
| X | g.41136941T>C | CA515966553 | USP9X | c.573T>C (p.Arg191=) | |
| X | g.41136941T>G | CA515966555 | USP9X | c.573T>G (p.Arg191=) | |
| X | g.41136942C>A | CA412763354 | USP9X | c.574C>A (p.Pro192Thr) | |
| X | g.41136942C>G | CA412763352 | USP9X | c.574C>G (p.Pro192Ala) | |
| X | g.41136942C>T | CA412763353 | USP9X | c.574C>T (p.Pro192Ser) | gnomAD v4 |
| X | g.41136943C>A | CA412763355 | USP9X | c.575C>A (p.Pro192Gln) | |
| X | g.41136943C>G | CA412763356 | USP9X | c.575C>G (p.Pro192Arg) | |
| X | g.41136943C>T | CA412763357 | USP9X | c.575C>T (p.Pro192Leu) | |
| X | g.41136944A= | CA2425806615 | USP9X | c.576A= (p.Pro192=) | |
| X | g.41136944A>C | CA515966557 | USP9X | c.576A>C (p.Pro192=) | |
| X | g.41136944A>G | CA10388327 | USP9X | c.576A>G (p.Pro192=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.41136944A>T | CA329012353 | USP9X | c.576A>T (p.Pro192=) | dbSNP |
| X | g.41136945T>A | CA412763358 | USP9X | c.577T>A (p.Cys193Ser) | |
| X | g.41136945T>C | CA412763359 | USP9X | c.577T>C (p.Cys193Arg) | |
| X | g.41136945T>G | CA412763360 | USP9X | c.577T>G (p.Cys193Gly) | |
| X | g.41136946G>A | CA412763361 | USP9X | c.578G>A (p.Cys193Tyr) | |
| X | g.41136946G>C | CA412763362 | USP9X | c.578G>C (p.Cys193Ser) | |
| X | g.41136946G>T | CA412763363 | USP9X | c.578G>T (p.Cys193Phe) | |
| X | g.41136947T>A | CA412763365 | USP9X | c.579T>A (p.Cys193Ter) | |
| X | g.41136947T>C | CA515966566 | USP9X | c.579T>C (p.Cys193=) | ClinVar |
| X | g.41136947T>G | CA412763364 | USP9X | c.579T>G (p.Cys193Trp) | |
| X | g.41136948G>A | CA412763366 | USP9X | c.580G>A (p.Glu194Lys) | |
| X | g.41136948G>C | CA412763368 | USP9X | c.580G>C (p.Glu194Gln) | |
| X | g.41136948G>T | CA412763367 | USP9X | c.580G>T (p.Glu194Ter) | |
| X | g.41136949A>C | CA412763369 | USP9X | c.581A>C (p.Glu194Ala) | |
| X | g.41136949A>G | CA412763370 | USP9X | c.581A>G (p.Glu194Gly) | |
| X | g.41136949A>T | CA412763371 | USP9X | c.581A>T (p.Glu194Val) | |
| X | g.41136950A>C | CA412763372 | USP9X | c.582A>C (p.Glu194Asp) | gnomAD v4 |
| X | g.41136950A>G | CA515966568 | USP9X | c.582A>G (p.Glu194=) | ClinVar |
| X | g.41136950A>T | CA412763373 | USP9X | c.582A>T (p.Glu194Asp) | |
| X | g.41136951T>A | CA412763374 | USP9X | c.583T>A (p.Ser195Thr) | |
| X | g.41136951T>C | CA412763375 | USP9X | c.583T>C (p.Ser195Pro) | |
| X | g.41136951T>G | CA412763376 | USP9X | c.583T>G (p.Ser195Ala) | |
| X | g.41136952C>A | CA412763377 | USP9X | c.584C>A (p.Ser195Ter) | |
| X | g.41136952C>G | CA412763378 | USP9X | c.584C>G (p.Ser195Ter) | |
| X | g.41136952C>T | CA412763379 | USP9X | c.584C>T (p.Ser195Leu) | |
| X | g.41136953A>C | CA515966572 | USP9X | c.585A>C (p.Ser195=) | |
| X | g.41136953A>G | CA515966573 | USP9X | c.585A>G (p.Ser195=) | |
| X | g.41136953A>T | CA515966575 | USP9X | c.585A>T (p.Ser195=) | |
| X | g.41136954G>A | CA412763384 | USP9X | c.586G>A (p.Val196Ile) | |
| X | g.41136954G>C | CA412763382 | USP9X | c.586G>C (p.Val196Leu) | |
| X | g.41136954G>T | CA412763380 | USP9X | c.586G>T (p.Val196Phe) | |
| X | g.41136955T>A | CA412763386 | USP9X | c.587T>A (p.Val196Asp) | |
| X | g.41136955T>C | CA412763387 | USP9X | c.587T>C (p.Val196Ala) | |
| X | g.41136955T>G | CA412763390 | USP9X | c.587T>G (p.Val196Gly) | |
| X | g.41136956T>A | CA515966582 | USP9X | c.588T>A (p.Val196=) | |
| X | g.41136956T>C | CA515966584 | USP9X | c.588T>C (p.Val196=) | |
| X | g.41136956T>G | CA515966581 | USP9X | c.588T>G (p.Val196=) | |
| X | g.41136957T>A | CA412763392 | USP9X | c.589T>A (p.Ser197Thr) | |
| X | g.41136957T>C | CA412763393 | USP9X | c.589T>C (p.Ser197Pro) | dbSNP |
| X | g.41136957T>G | CA412763394 | USP9X | c.589T>G (p.Ser197Ala) | |
| X | g.41136957T= | CA2425806616 | USP9X | c.589T= (p.Ser197=) | |
| X | g.41136958C>A | CA412763397 | USP9X | c.590C>A (p.Ser197Tyr) | |
| X | g.41136958C>G | CA412763398 | USP9X | c.590C>G (p.Ser197Cys) | |
| X | g.41136958C>T | CA412763399 | USP9X | c.590C>T (p.Ser197Phe) | |
| X | g.41136959C>A | CA515966590 | USP9X | c.591C>A (p.Ser197=) | |
| X | g.41136959C>G | CA515966588 | USP9X | c.591C>G (p.Ser197=) | |
| X | g.41136959C>T | CA515966589 | USP9X | c.591C>T (p.Ser197=) | gnomAD v4 |
| X | g.41136960T>A | CA412763401 | USP9X | c.592T>A (p.Ser198Thr) | |
| X | g.41136960T>C | CA412763403 | USP9X | c.592T>C (p.Ser198Pro) | |
| X | g.41136960T>G | CA412763405 | USP9X | c.592T>G (p.Ser198Ala) | |
| X | g.41136961C>A | CA412763410 | USP9X | c.593C>A (p.Ser198Ter) | |
| X | g.41136961C>G | CA412763409 | USP9X | c.593C>G (p.Ser198Ter) | |
| X | g.41136961C>T | CA412763407 | USP9X | c.593C>T (p.Ser198Leu) | |
| X | g.41136962A= | CA2425806617 | USP9X | c.594A= (p.Ser198=) | |
| X | g.41136962A>C | CA515966602 | USP9X | c.594A>C (p.Ser198=) | |
| X | g.41136962A>G | CA515966605 | USP9X | c.594A>G (p.Ser198=) | COSMIC COSMIC |
| X | g.41136962A>T | CA515966604 | USP9X | c.594A>T (p.Ser198=) | dbSNP gnomAD v2 gnomAD v4 |
| X | g.41136963A= | CA2425806618 | USP9X | c.595A= (p.Ser199=) | |
| X | g.41136963A>C | CA412763416 | USP9X | c.595A>C (p.Ser199Arg) | |
| X | g.41136963A>G | CA10388328 | USP9X | c.595A>G (p.Ser199Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.41136963A>T | CA412763414 | USP9X | c.595A>T (p.Ser199Cys) | |
| X | g.41136964G>A | CA412763418 | USP9X | c.596G>A (p.Ser199Asn) | |
| X | g.41136964G>C | CA412763419 | USP9X | c.596G>C (p.Ser199Thr) | |
| X | g.41136964G>T | CA412763421 | USP9X | c.596G>T (p.Ser199Ile) | |
| X | g.41136965T>A | CA412763423 | USP9X | c.597T>A (p.Ser199Arg) | |
| X | g.41136965T>C | CA515966611 | USP9X | c.597T>C (p.Ser199=) | dbSNP gnomAD v2 gnomAD v4 |
| X | g.41136965T>G | CA412763425 | USP9X | c.597T>G (p.Ser199Arg) | |
| X | g.41136965T= | CA2425806619 | USP9X | c.597T= (p.Ser199=) | |
| X | g.41136966G>A | CA412763427 | USP9X | c.598G>A (p.Val200Ile) | |
| X | g.41136966G>C | CA412763431 | USP9X | c.598G>C (p.Val200Leu) | |
| X | g.41136966G>T | CA412763429 | USP9X | c.598G>T (p.Val200Phe) | |
| X | g.41136967T>A | CA412763433 | USP9X | c.599T>A (p.Val200Asp) | |
| X | g.41136967T>C | CA412763435 | USP9X | c.599T>C (p.Val200Ala) | |
| X | g.41136967T>G | CA412763437 | USP9X | c.599T>G (p.Val200Gly) | |
| X | g.41136968T>A | CA515966612 | USP9X | c.600T>A (p.Val200=) | |
| X | g.41136968T>C | CA515966614 | USP9X | c.600T>C (p.Val200=) | |
| X | g.41136968T>G | CA10388329 | USP9X | c.600T>G (p.Val200=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.41136968T= | CA2425806620 | USP9X | c.600T= (p.Val200=) | |
| X | g.41136969C>A | CA412763440 | USP9X | c.601C>A (p.Gln201Lys) | |
| X | g.41136969C>G | CA412763443 | USP9X | c.601C>G (p.Gln201Glu) | |
| X | g.41136969C>T | CA412763441 | USP9X | c.601C>T (p.Gln201Ter) | |
| X | g.41136970A>C | CA412763446 | USP9X | c.602A>C (p.Gln201Pro) | |
| X | g.41136970A>G | CA412763447 | USP9X | c.602A>G (p.Gln201Arg) | |
| X | g.41136970A>T | CA412763450 | USP9X | c.602A>T (p.Gln201Leu) | gnomAD v4 |
| X | g.41136971G>A | CA515966618 | USP9X | c.603G>A (p.Gln201=) | |
| X | g.41136971G>C | CA412763452 | USP9X | c.603G>C (p.Gln201His) | |
| X | g.41136971G= | CA2425806621 | USP9X | c.603G= (p.Gln201=) | |
| X | g.41136971G>T | CA329012367 | USP9X | c.603G>T (p.Gln201His) | dbSNP gnomAD v4 |
| X | g.41136972T>A | CA412763454 | USP9X | c.604T>A (p.Leu202Met) | |
| X | g.41136972T>C | CA515966621 | USP9X | c.604T>C (p.Leu202=) | |
| X | g.41136972T>G | CA412763456 | USP9X | c.604T>G (p.Leu202Val) | |
| X | g.41136973T>A | CA412763459 | USP9X | c.605T>A (p.Leu202Ter) | |
| X | g.41136973T>C | CA412763460 | USP9X | c.605T>C (p.Leu202Ser) | |
| X | g.41136973T>G | CA412763463 | USP9X | c.605T>G (p.Leu202Trp) | |
| X | g.41136974G>A | CA515966622 | USP9X | c.606G>A (p.Leu202=) | |
| X | g.41136974G>C | CA412763465 | USP9X | c.606G>C (p.Leu202Phe) | dbSNP gnomAD v2 |
| X | g.41136974G= | CA2425806622 | USP9X | c.606G= (p.Leu202=) | |
| X | g.41136974G>T | CA412763467 | USP9X | c.606G>T (p.Leu202Phe) | |
| X | g.41136975C>A | CA412763470 | USP9X | c.607C>A (p.Pro203Thr) | |
| X | g.41136975C>G | CA412763473 | USP9X | c.607C>G (p.Pro203Ala) | |
| X | g.41136975C>T | CA412763469 | USP9X | c.607C>T (p.Pro203Ser) | |
| X | g.41136976C>A | CA412763475 | USP9X | c.608C>A (p.Pro203His) | |
| X | g.41136976C>G | CA412763479 | USP9X | c.608C>G (p.Pro203Arg) | |
| X | g.41136976C>T | CA412763477 | USP9X | c.608C>T (p.Pro203Leu) | |
| X | g.41136977T>A | CA515966624 | USP9X | c.609T>A (p.Pro203=) | |
| X | g.41136977T>C | CA515966627 | USP9X | c.609T>C (p.Pro203=) | |
| X | g.41136977T>G | CA515966626 | USP9X | c.609T>G (p.Pro203=) | |
| X | g.41136978G>A | CA412763482 | USP9X | c.610G>A (p.Glu204Lys) | dbSNP gnomAD v2 gnomAD v4 |
| X | g.41136978G>C | CA412763483 | USP9X | c.610G>C (p.Glu204Gln) | |
| X | g.41136978G= | CA2425806623 | USP9X | c.610G= (p.Glu204=) | |
| X | g.41136978G>T | CA412763485 | USP9X | c.610G>T (p.Glu204Ter) | |
| X | g.41136979A>C | CA412763487 | USP9X | c.611A>C (p.Glu204Ala) | |
| X | g.41136979A>G | CA412763489 | USP9X | c.611A>G (p.Glu204Gly) | |
| X | g.41136979A>T | CA412763491 | USP9X | c.611A>T (p.Glu204Val) | |
| X | g.41136980A>C | CA412763493 | USP9X | c.612A>C (p.Glu204Asp) | |
| X | g.41136980A>G | CA515966628 | USP9X | c.612A>G (p.Glu204=) | |
| X | g.41136980A>T | CA412763494 | USP9X | c.612A>T (p.Glu204Asp) | |
| X | g.41136981G>A | CA412763497 | USP9X | c.613G>A (p.Asp205Asn) | |
| X | g.41136981G>C | CA412763498 | USP9X | c.613G>C (p.Asp205His) | |
| X | g.41136981G>T | CA412763500 | USP9X | c.613G>T (p.Asp205Tyr) | |
| X | g.41136982A>C | CA412763506 | USP9X | c.614A>C (p.Asp205Ala) | |
| X | g.41136982A>G | CA412763503 | USP9X | c.614A>G (p.Asp205Gly) | gnomAD v4 COSMIC COSMIC |
| X | g.41136982A>T | CA412763504 | USP9X | c.614A>T (p.Asp205Val) | |
| X | g.41136983T>A | CA412763509 | USP9X | c.615T>A (p.Asp205Glu) | |
| X | g.41136983T>C | CA515966630 | USP9X | c.615T>C (p.Asp205=) | |
| X | g.41136983T>G | CA412763510 | USP9X | c.615T>G (p.Asp205Glu) | |
| X | g.41136984G>A | CA412763513 | USP9X | c.616G>A (p.Glu206Lys) | |
| X | g.41136984G>C | CA412763515 | USP9X | c.616G>C (p.Glu206Gln) | |
| X | g.41136984G>T | CA412763518 | USP9X | c.616G>T (p.Glu206Ter) | |
| X | g.41136985A>C | CA412763520 | USP9X | c.617A>C (p.Glu206Ala) | |
| X | g.41136985A>G | CA412763523 | USP9X | c.617A>G (p.Glu206Gly) | |
| X | g.41136985A>T | CA412763524 | USP9X | c.617A>T (p.Glu206Val) | |
| X | g.41136986A>C | CA412763527 | USP9X | c.618A>C (p.Glu206Asp) | |
| X | g.41136986A>G | CA515966632 | USP9X | c.618A>G (p.Glu206=) | |
| X | g.41136986A>T | CA412763529 | USP9X | c.618A>T (p.Glu206Asp) | |
| X | g.41136987C>A | CA412763534 | USP9X | c.619C>A (p.Leu207Ile) | |
| X | g.41136987C>G | CA412763535 | USP9X | c.619C>G (p.Leu207Val) | |
| X | g.41136987C>T | CA412763531 | USP9X | c.619C>T (p.Leu207Phe) | gnomAD v4 |
| X | g.41136988T>A | CA412763537 | USP9X | c.620T>A (p.Leu207His) | |
| X | g.41136988T>C | CA412763539 | USP9X | c.620T>C (p.Leu207Pro) | |
| X | g.41136988T>G | CA412763541 | USP9X | c.620T>G (p.Leu207Arg) |