| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154367881C>A | CA415249138 | FLNA | c.583G>T (p.Gly195Cys) c.502G>T (p.Gly168Cys) c.541G>T (p.Gly181Cys) | |
| X | g.154367881C>G | CA415249143 | FLNA | c.583G>C (p.Gly195Arg) c.502G>C (p.Gly168Arg) c.541G>C (p.Gly181Arg) | |
| X | g.154367881C>T | CA415249140 | FLNA | c.583G>A (p.Gly195Ser) c.502G>A (p.Gly168Ser) c.541G>A (p.Gly181Ser) | |
| X | g.154367882G>A | CA519709942 | FLNA | c.582C>T (p.Ser194=) c.501C>T (p.Ser167=) c.540C>T (p.Ser180=) | ClinVar dbSNP gnomAD v4 |
| X | g.154367882G>C | CA415249145 | FLNA | c.582C>G (p.Ser194Arg) c.501C>G (p.Ser167Arg) c.540C>G (p.Ser180Arg) | |
| X | g.154367882G= | CA2466659056 | FLNA | c.582C= (p.Ser194=) c.501C= (p.Ser167=) c.540C= (p.Ser180=) | |
| X | g.154367882G>T | CA415249146 | FLNA | c.582C>A (p.Ser194Arg) c.501C>A (p.Ser167Arg) c.540C>A (p.Ser180Arg) | |
| X | g.154367883C>A | CA415249148 | FLNA | c.581G>T (p.Ser194Ile) c.500G>T (p.Ser167Ile) c.539G>T (p.Ser180Ile) | |
| X | g.154367883C= | CA2466659057 | FLNA | c.581G= (p.Ser194=) c.500G= (p.Ser167=) c.539G= (p.Ser180=) | |
| X | g.154367883C>G | CA415249151 | FLNA | c.581G>C (p.Ser194Thr) c.500G>C (p.Ser167Thr) c.539G>C (p.Ser180Thr) | |
| X | g.154367883C>T | CA415249154 | FLNA | c.581G>A (p.Ser194Asn) c.500G>A (p.Ser167Asn) c.539G>A (p.Ser180Asn) | dbSNP gnomAD v2 gnomAD v4 |
| X | g.154367884T>A | CA415249159 | FLNA | c.580A>T (p.Ser194Cys) c.499A>T (p.Ser167Cys) c.538A>T (p.Ser180Cys) | |
| X | g.154367884T>C | CA415249161 | FLNA | c.580A>G (p.Ser194Gly) c.499A>G (p.Ser167Gly) c.538A>G (p.Ser180Gly) | |
| X | g.154367884T>G | CA415249163 | FLNA | c.580A>C (p.Ser194Arg) c.499A>C (p.Ser167Arg) c.538A>C (p.Ser180Arg) | |
| X | g.154367885C>A | CA415249166 | FLNA | c.579G>T (p.Gln193His) c.498G>T (p.Gln166His) c.537G>T (p.Gln179His) | |
| X | g.154367885C>G | CA415249168 | FLNA | c.579G>C (p.Gln193His) c.498G>C (p.Gln166His) c.537G>C (p.Gln179His) | |
| X | g.154367885C>T | CA519709945 | FLNA | c.579G>A (p.Gln193=) c.498G>A (p.Gln166=) c.537G>A (p.Gln179=) | gnomAD v4 |
| X | g.154367886T>A | CA415249175 | FLNA | c.578A>T (p.Gln193Leu) c.497A>T (p.Gln166Leu) c.536A>T (p.Gln179Leu) | |
| X | g.154367886T>C | CA415249173 | FLNA | c.578A>G (p.Gln193Arg) c.497A>G (p.Gln166Arg) c.536A>G (p.Gln179Arg) | |
| X | g.154367886T>G | CA415249172 | FLNA | c.578A>C (p.Gln193Pro) c.497A>C (p.Gln166Pro) c.536A>C (p.Gln179Pro) | |
| X | g.154367887G>A | CA415249180 | FLNA | c.577C>T (p.Gln193Ter) c.496C>T (p.Gln166Ter) c.535C>T (p.Gln179Ter) | ClinVar dbSNP |
| X | g.154367887G>C | CA415249182 | FLNA | c.577C>G (p.Gln193Glu) c.496C>G (p.Gln166Glu) c.535C>G (p.Gln179Glu) | |
| X | g.154367887G>T | CA415249183 | FLNA | c.577C>A (p.Gln193Lys) c.496C>A (p.Gln166Lys) c.535C>A (p.Gln179Lys) | |
| X | g.154367888C>A | CA415249185 | FLNA | c.576G>T (p.Trp192Cys) c.495G>T (p.Trp165Cys) c.534G>T (p.Trp178Cys) | |
| X | g.154367888C= | CA2466659058 | FLNA | c.576G= (p.Trp192=) c.495G= (p.Trp165=) c.534G= (p.Trp178=) | |
| X | g.154367888C>G | CA415249187 | FLNA | c.576G>C (p.Trp192Cys) c.495G>C (p.Trp165Cys) c.534G>C (p.Trp178Cys) | |
| X | g.154367888C>T | CA337284394 | FLNA | c.576G>A (p.Trp192Ter) c.495G>A (p.Trp165Ter) c.534G>A (p.Trp178Ter) | dbSNP |
| X | g.154367889C>A | CA415249191 | FLNA | c.575G>T (p.Trp192Leu) c.494G>T (p.Trp165Leu) c.533G>T (p.Trp178Leu) | |
| X | g.154367889C>G | CA415249194 | FLNA | c.575G>C (p.Trp192Ser) c.494G>C (p.Trp165Ser) c.533G>C (p.Trp178Ser) | |
| X | g.154367889C>T | CA415249196 | FLNA | c.575G>A (p.Trp192Ter) c.494G>A (p.Trp165Ter) c.533G>A (p.Trp178Ter) | |
| X | g.154367890A>C | CA415249199 | FLNA | c.574T>G (p.Trp192Gly) c.493T>G (p.Trp165Gly) c.532T>G (p.Trp178Gly) | |
| X | g.154367890A>G | CA415249201 | FLNA | c.574T>C (p.Trp192Arg) c.493T>C (p.Trp165Arg) c.532T>C (p.Trp178Arg) | |
| X | g.154367890A>T | CA415249204 | FLNA | c.574T>A (p.Trp192Arg) c.493T>A (p.Trp165Arg) c.532T>A (p.Trp178Arg) | |
| X | g.154367891G>A | CA519709949 | FLNA | c.573C>T (p.Asp191=) c.492C>T (p.Asp164=) c.531C>T (p.Asp177=) | |
| X | g.154367891G>C | CA415249207 | FLNA | c.573C>G (p.Asp191Glu) c.492C>G (p.Asp164Glu) c.531C>G (p.Asp177Glu) | |
| X | g.154367891G>T | CA415249217 | FLNA | c.573C>A (p.Asp191Glu) c.492C>A (p.Asp164Glu) c.531C>A (p.Asp177Glu) | |
| X | g.154367892T>A | CA415249221 | FLNA | c.572A>T (p.Asp191Val) c.491A>T (p.Asp164Val) c.530A>T (p.Asp177Val) | |
| X | g.154367892T>C | CA415249228 | FLNA | c.572A>G (p.Asp191Gly) c.491A>G (p.Asp164Gly) c.530A>G (p.Asp177Gly) | |
| X | g.154367892T>G | CA415249224 | FLNA | c.572A>C (p.Asp191Ala) c.491A>C (p.Asp164Ala) c.530A>C (p.Asp177Ala) | |
| X | g.154367893C>A | CA415249231 | FLNA | c.571G>T (p.Asp191Tyr) c.490G>T (p.Asp164Tyr) c.529G>T (p.Asp177Tyr) | ClinVar dbSNP |
| X | g.154367893C>G | CA415249233 | FLNA | c.571G>C (p.Asp191His) c.490G>C (p.Asp164His) c.529G>C (p.Asp177His) | |
| X | g.154367893C>T | CA415249232 | FLNA | c.571G>A (p.Asp191Asn) c.490G>A (p.Asp164Asn) c.529G>A (p.Asp177Asn) | |
| X | g.154367894C>A | CA519709950 | FLNA | c.570G>T (p.Arg190=) c.489G>T (p.Arg163=) c.528G>T (p.Arg176=) | |
| X | g.154367894C>G | CA519709951 | FLNA | c.570G>C (p.Arg190=) c.489G>C (p.Arg163=) c.528G>C (p.Arg176=) | |
| X | g.154367894C>T | CA519709952 | FLNA | c.570G>A (p.Arg190=) c.489G>A (p.Arg163=) c.528G>A (p.Arg176=) | |
| X | g.154367895C>A | CA415249235 | FLNA | c.569G>T (p.Arg190Leu) c.488G>T (p.Arg163Leu) c.527G>T (p.Arg176Leu) | |
| X | g.154367895C= | CA2466659059 | FLNA | c.569G= (p.Arg190=) c.488G= (p.Arg163=) c.527G= (p.Arg176=) | |
| X | g.154367895C>G | CA415249237 | FLNA | c.569G>C (p.Arg190Pro) c.488G>C (p.Arg163Pro) c.527G>C (p.Arg176Pro) | |
| X | g.154367895C>T | CA322045 | FLNA | c.569G>A (p.Arg190Gln) c.488G>A (p.Arg163Gln) c.527G>A (p.Arg176Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.154367896G>A | CA415249239 | FLNA | c.568C>T (p.Arg190Trp) c.487C>T (p.Arg163Trp) c.526C>T (p.Arg176Trp) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.154367896G>C | CA415249250 | FLNA | c.568C>G (p.Arg190Gly) c.487C>G (p.Arg163Gly) c.526C>G (p.Arg176Gly) | |
| X | g.154367896G= | CA2466659060 | FLNA | c.568C= (p.Arg190=) c.487C= (p.Arg163=) c.526C= (p.Arg176=) | |
| X | g.154367896G>T | CA519709953 | FLNA | c.568C>A (p.Arg190=) c.487C>A (p.Arg163=) c.526C>A (p.Arg176=) | |
| X | g.154367897G>A | CA519709954 | FLNA | c.567C>T (p.Ser189=) c.486C>T (p.Ser162=) c.525C>T (p.Ser175=) | |
| X | g.154367897G>C | CA415249254 | FLNA | c.567C>G (p.Ser189Arg) c.486C>G (p.Ser162Arg) c.525C>G (p.Ser175Arg) | |
| X | g.154367897G>T | CA415249261 | FLNA | c.567C>A (p.Ser189Arg) c.486C>A (p.Ser162Arg) c.525C>A (p.Ser175Arg) | |
| X | g.154367898C>A | CA415249267 | FLNA | c.566G>T (p.Ser189Ile) c.485G>T (p.Ser162Ile) c.524G>T (p.Ser175Ile) | |
| X | g.154367898C= | CA2466659061 | FLNA | c.566G= (p.Ser189=) c.485G= (p.Ser162=) c.524G= (p.Ser175=) | |
| X | g.154367898C>G | CA415249270 | FLNA | c.566G>C (p.Ser189Thr) c.485G>C (p.Ser162Thr) c.524G>C (p.Ser175Thr) | |
| X | g.154367898C>T | CA415249273 | FLNA | c.566G>A (p.Ser189Asn) c.485G>A (p.Ser162Asn) c.524G>A (p.Ser175Asn) | dbSNP gnomAD v3 gnomAD v4 |
| X | g.154367899T>A | CA415249283 | FLNA | c.565A>T (p.Ser189Cys) c.484A>T (p.Ser162Cys) c.523A>T (p.Ser175Cys) | |
| X | g.154367899T>C | CA415249279 | FLNA | c.565A>G (p.Ser189Gly) c.484A>G (p.Ser162Gly) c.523A>G (p.Ser175Gly) | |
| X | g.154367899T>G | CA415249277 | FLNA | c.565A>C (p.Ser189Arg) c.484A>C (p.Ser162Arg) c.523A>C (p.Ser175Arg) | |
| X | g.154367900G>A | CA519709957 | FLNA | c.564C>T (p.Phe188=) c.483C>T (p.Phe161=) c.522C>T (p.Phe174=) | ClinVar dbSNP |
| X | g.154367900G>C | CA415249286 | FLNA | c.564C>G (p.Phe188Leu) c.483C>G (p.Phe161Leu) c.522C>G (p.Phe174Leu) | |
| X | g.154367900G>T | CA415249287 | FLNA | c.564C>A (p.Phe188Leu) c.483C>A (p.Phe161Leu) c.522C>A (p.Phe174Leu) | |
| X | g.154367901A>C | CA415249291 | FLNA | c.563T>G (p.Phe188Cys) c.482T>G (p.Phe161Cys) c.521T>G (p.Phe174Cys) | |
| X | g.154367901A>G | CA415249294 | FLNA | c.563T>C (p.Phe188Ser) c.482T>C (p.Phe161Ser) c.521T>C (p.Phe174Ser) | |
| X | g.154367901A>T | CA415249296 | FLNA | c.563T>A (p.Phe188Tyr) c.482T>A (p.Phe161Tyr) c.521T>A (p.Phe174Tyr) | |
| X | g.154367902A>C | CA415249299 | FLNA | c.562T>G (p.Phe188Val) c.481T>G (p.Phe161Val) c.520T>G (p.Phe174Val) | |
| X | g.154367902A>G | CA415249303 | FLNA | c.562T>C (p.Phe188Leu) c.481T>C (p.Phe161Leu) c.520T>C (p.Phe174Leu) | |
| X | g.154367902A>T | CA415249304 | FLNA | c.562T>A (p.Phe188Ile) c.481T>A (p.Phe161Ile) c.520T>A (p.Phe174Ile) | |
| X | g.154367903G>A | CA519709960 | FLNA | c.561C>T (p.Asn187=) c.480C>T (p.Asn160=) c.519C>T (p.Asn173=) | |
| X | g.154367903G>C | CA415249305 | FLNA | c.561C>G (p.Asn187Lys) c.480C>G (p.Asn160Lys) c.519C>G (p.Asn173Lys) | |
| X | g.154367903G>T | CA415249306 | FLNA | c.561C>A (p.Asn187Lys) c.480C>A (p.Asn160Lys) c.519C>A (p.Asn173Lys) | COSMIC COSMIC |
| X | g.154367904T>A | CA415249312 | FLNA | c.560A>T (p.Asn187Ile) c.479A>T (p.Asn160Ile) c.518A>T (p.Asn173Ile) | |
| X | g.154367904T>C | CA415249310 | FLNA | c.560A>G (p.Asn187Ser) c.479A>G (p.Asn160Ser) c.518A>G (p.Asn173Ser) | |
| X | g.154367904T>G | CA415249308 | FLNA | c.560A>C (p.Asn187Thr) c.479A>C (p.Asn160Thr) c.518A>C (p.Asn173Thr) | |
| X | g.154367905T>A | CA415249316 | FLNA | c.559A>T (p.Asn187Tyr) c.478A>T (p.Asn160Tyr) c.517A>T (p.Asn173Tyr) | |
| X | g.154367905T>C | CA415249318 | FLNA | c.559A>G (p.Asn187Asp) c.478A>G (p.Asn160Asp) c.517A>G (p.Asn173Asp) | |
| X | g.154367905T>G | CA415249326 | FLNA | c.559A>C (p.Asn187His) c.478A>C (p.Asn160His) c.517A>C (p.Asn173His) | |
| X | g.154367906G>A | CA519709962 | FLNA | c.558C>T (p.Thr186=) c.477C>T (p.Thr159=) c.516C>T (p.Thr172=) | ClinVar gnomAD v4 |
| X | g.154367906G>C | CA519709963 | FLNA | c.558C>G (p.Thr186=) c.477C>G (p.Thr159=) c.516C>G (p.Thr172=) | |
| X | g.154367906G>T | CA519709964 | FLNA | c.558C>A (p.Thr186=) c.477C>A (p.Thr159=) c.516C>A (p.Thr172=) | |
| X | g.154367907G>A | CA415249328 | FLNA | c.557C>T (p.Thr186Ile) c.476C>T (p.Thr159Ile) c.515C>T (p.Thr172Ile) | |
| X | g.154367907G>C | CA415249331 | FLNA | c.557C>G (p.Thr186Ser) c.476C>G (p.Thr159Ser) c.515C>G (p.Thr172Ser) | |
| X | g.154367907G>T | CA415249335 | FLNA | c.557C>A (p.Thr186Asn) c.476C>A (p.Thr159Asn) c.515C>A (p.Thr172Asn) | |
| X | g.154367908T>A | CA415249340 | FLNA | c.556A>T (p.Thr186Ser) c.475A>T (p.Thr159Ser) c.514A>T (p.Thr172Ser) | |
| X | g.154367908T>C | CA415249342 | FLNA | c.556A>G (p.Thr186Ala) c.475A>G (p.Thr159Ala) c.514A>G (p.Thr172Ala) | |
| X | g.154367908T>G | CA415249346 | FLNA | c.556A>C (p.Thr186Pro) c.475A>C (p.Thr159Pro) c.514A>C (p.Thr172Pro) | |
| X | g.154367909G>A | CA519709966 | FLNA | c.555C>T (p.Ile185=) c.474C>T (p.Ile158=) c.513C>T (p.Ile171=) | |
| X | g.154367909G>C | CA415249350 | FLNA | c.555C>G (p.Ile185Met) c.474C>G (p.Ile158Met) c.513C>G (p.Ile171Met) | |
| X | g.154367909G>T | CA519709968 | FLNA | c.555C>A (p.Ile185=) c.474C>A (p.Ile158=) c.513C>A (p.Ile171=) | |
| X | g.154367910A>C | CA415249365 | FLNA | c.554T>G (p.Ile185Ser) c.473T>G (p.Ile158Ser) c.512T>G (p.Ile171Ser) | |
| X | g.154367910A>G | CA415249362 | FLNA | c.554T>C (p.Ile185Thr) c.473T>C (p.Ile158Thr) c.512T>C (p.Ile171Thr) | |
| X | g.154367910A>T | CA415249359 | FLNA | c.554T>A (p.Ile185Asn) c.473T>A (p.Ile158Asn) c.512T>A (p.Ile171Asn) | |
| X | g.154367911T>A | CA415249371 | FLNA | c.553A>T (p.Ile185Phe) c.472A>T (p.Ile158Phe) c.511A>T (p.Ile171Phe) | |
| X | g.154367911T>C | CA415249375 | FLNA | c.553A>G (p.Ile185Val) c.472A>G (p.Ile158Val) c.511A>G (p.Ile171Val) | dbSNP COSMIC COSMIC |
| X | g.154367911T>G | CA415249380 | FLNA | c.553A>C (p.Ile185Leu) c.472A>C (p.Ile158Leu) c.511A>C (p.Ile171Leu) | |
| X | g.154367911T= | CA2466659062 | FLNA | c.553A= (p.Ile185=) c.472A= (p.Ile158=) c.511A= (p.Ile171=) | |
| X | g.154367912G>A | CA519709971 | FLNA | c.552C>T (p.Pro184=) c.471C>T (p.Pro157=) c.510C>T (p.Pro170=) | gnomAD v4 |
| X | g.154367912G>C | CA519709972 | FLNA | c.552C>G (p.Pro184=) c.471C>G (p.Pro157=) c.510C>G (p.Pro170=) | |
| X | g.154367912G= | CA2466659063 | FLNA | c.552C= (p.Pro184=) c.471C= (p.Pro157=) c.510C= (p.Pro170=) | |
| X | g.154367912G>T | CA519709973 | FLNA | c.552C>A (p.Pro184=) c.471C>A (p.Pro157=) c.510C>A (p.Pro170=) | dbSNP |
| X | g.154367913G>A | CA415249381 | FLNA | c.551C>T (p.Pro184Leu) c.470C>T (p.Pro157Leu) c.509C>T (p.Pro170Leu) | |
| X | g.154367913G>C | CA415249383 | FLNA | c.551C>G (p.Pro184Arg) c.470C>G (p.Pro157Arg) c.509C>G (p.Pro170Arg) | dbSNP |
| X | g.154367913G= | CA2466659064 | FLNA | c.551C= (p.Pro184=) c.470C= (p.Pro157=) c.509C= (p.Pro170=) | |
| X | g.154367913G>T | CA415249385 | FLNA | c.551C>A (p.Pro184His) c.470C>A (p.Pro157His) c.509C>A (p.Pro170His) | |
| X | g.154367914G>A | CA415249387 | FLNA | c.550C>T (p.Pro184Ser) c.469C>T (p.Pro157Ser) c.508C>T (p.Pro170Ser) | |
| X | g.154367914G>C | CA415249391 | FLNA | c.550C>G (p.Pro184Ala) c.469C>G (p.Pro157Ala) c.508C>G (p.Pro170Ala) | |
| X | g.154367914G>T | CA415249394 | FLNA | c.550C>A (p.Pro184Thr) c.469C>A (p.Pro157Thr) c.508C>A (p.Pro170Thr) | |
| X | g.154367915C>A | CA519709977 | FLNA | c.549G>T (p.Leu183=) c.468G>T (p.Leu156=) c.507G>T (p.Leu169=) | |
| X | g.154367915C>G | CA519709978 | FLNA | c.549G>C (p.Leu183=) c.468G>C (p.Leu156=) c.507G>C (p.Leu169=) | |
| X | g.154367915C>T | CA519709979 | FLNA | c.549G>A (p.Leu183=) c.468G>A (p.Leu156=) c.507G>A (p.Leu169=) | |
| X | g.154367916A>C | CA415249400 | FLNA | c.548T>G (p.Leu183Arg) c.467T>G (p.Leu156Arg) c.506T>G (p.Leu169Arg) | |
| X | g.154367916A>G | CA415249408 | FLNA | c.548T>C (p.Leu183Pro) c.467T>C (p.Leu156Pro) c.506T>C (p.Leu169Pro) | |
| X | g.154367916A>T | CA415249410 | FLNA | c.548T>A (p.Leu183Gln) c.467T>A (p.Leu156Gln) c.506T>A (p.Leu169Gln) | |
| X | g.154367917G>A | CA519709983 | FLNA | c.547C>T (p.Leu183=) c.466C>T (p.Leu156=) c.505C>T (p.Leu169=) | |
| X | g.154367917G>C | CA415249414 | FLNA | c.547C>G (p.Leu183Val) c.466C>G (p.Leu156Val) c.505C>G (p.Leu169Val) | |
| X | g.154367917G>T | CA415249416 | FLNA | c.547C>A (p.Leu183Met) c.466C>A (p.Leu156Met) c.505C>A (p.Leu169Met) | |
| X | g.154367918C>A | CA415249425 | FLNA | c.546G>T (p.Gln182His) c.465G>T (p.Gln155His) c.504G>T (p.Gln168His) | |
| X | g.154367918C= | CA2466659065 | FLNA | c.546G= (p.Gln182=) c.465G= (p.Gln155=) c.504G= (p.Gln168=) | |
| X | g.154367918C>G | CA415249427 | FLNA | c.546G>C (p.Gln182His) c.465G>C (p.Gln155His) c.504G>C (p.Gln168His) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| X | g.154367918C>T | CA519709984 | FLNA | c.546G>A (p.Gln182=) c.465G>A (p.Gln155=) c.504G>A (p.Gln168=) | |
| X | g.154367919T>A | CA415249431 | FLNA | c.545A>T (p.Gln182Leu) c.464A>T (p.Gln155Leu) c.503A>T (p.Gln168Leu) | |
| X | g.154367919T>C | CA415249434 | FLNA | c.545A>G (p.Gln182Arg) c.464A>G (p.Gln155Arg) c.503A>G (p.Gln168Arg) | ClinVar |
| X | g.154367919T>G | CA415249437 | FLNA | c.545A>C (p.Gln182Pro) c.464A>C (p.Gln155Pro) c.503A>C (p.Gln168Pro) | |
| X | g.154367920G>A | CA256051 | FLNA | c.544C>T (p.Gln182Ter) c.463C>T (p.Gln155Ter) c.502C>T (p.Gln168Ter) | ClinVar dbSNP |
| X | g.154367920G>C | CA415249444 | FLNA | c.544C>G (p.Gln182Glu) c.463C>G (p.Gln155Glu) c.502C>G (p.Gln168Glu) | |
| X | g.154367920G= | CA2466659066 | FLNA | c.544C= (p.Gln182=) c.463C= (p.Gln155=) c.502C= (p.Gln168=) | |
| X | g.154367920G>T | CA415249446 | FLNA | c.544C>A (p.Gln182Lys) c.463C>A (p.Gln155Lys) c.502C>A (p.Gln168Lys) | |
| X | g.154367921C>A | CA519709988 | FLNA | c.543G>T (p.Pro181=) c.462G>T (p.Pro154=) c.501G>T (p.Pro167=) | |
| X | g.154367921C= | CA2466659067 | FLNA | c.543G= (p.Pro181=) c.462G= (p.Pro154=) c.501G= (p.Pro167=) | |
| X | g.154367921C>G | CA10561403 | FLNA | c.543G>C (p.Pro181=) c.462G>C (p.Pro154=) c.501G>C (p.Pro167=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.154367921C>T | CA10561404 | FLNA | c.543G>A (p.Pro181=) c.462G>A (p.Pro154=) c.501G>A (p.Pro167=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| X | g.154367922G>A | CA320493 | FLNA | c.542C>T (p.Pro181Leu) c.461C>T (p.Pro154Leu) c.500C>T (p.Pro167Leu) | ClinVar dbSNP |
| X | g.154367922G>C | CA415249456 | FLNA | c.542C>G (p.Pro181Arg) c.461C>G (p.Pro154Arg) c.500C>G (p.Pro167Arg) | |
| X | g.154367922G= | CA2466659068 | FLNA | c.542C= (p.Pro181=) c.461C= (p.Pro154=) c.500C= (p.Pro167=) | |
| X | g.154367922G>T | CA415249457 | FLNA | c.542C>A (p.Pro181Gln) c.461C>A (p.Pro154Gln) c.500C>A (p.Pro167Gln) | |
| X | g.154367923G>A | CA415249464 | FLNA | c.541C>T (p.Pro181Ser) c.460C>T (p.Pro154Ser) c.499C>T (p.Pro167Ser) | |
| X | g.154367923G>C | CA415249459 | FLNA | c.541C>G (p.Pro181Ala) c.460C>G (p.Pro154Ala) c.499C>G (p.Pro167Ala) | |
| X | g.154367923G>T | CA415249461 | FLNA | c.541C>A (p.Pro181Thr) c.460C>A (p.Pro154Thr) c.499C>A (p.Pro167Thr) | |
| X | g.154367924C>A | CA519709992 | FLNA | c.540G>T (p.Leu180=) c.459G>T (p.Leu153=) c.498G>T (p.Leu166=) | |
| X | g.154367924C>G | CA519709993 | FLNA | c.540G>C (p.Leu180=) c.459G>C (p.Leu153=) c.498G>C (p.Leu166=) | gnomAD v4 |
| X | g.154367924C>T | CA519709994 | FLNA | c.540G>A (p.Leu180=) c.459G>A (p.Leu153=) c.498G>A (p.Leu166=) | |
| X | g.154367925A>C | CA415249479 | FLNA | c.539T>G (p.Leu180Arg) c.458T>G (p.Leu153Arg) c.497T>G (p.Leu166Arg) | |
| X | g.154367925A>G | CA415249481 | FLNA | c.539T>C (p.Leu180Pro) c.458T>C (p.Leu153Pro) c.497T>C (p.Leu166Pro) | |
| X | g.154367925A>T | CA415249483 | FLNA | c.539T>A (p.Leu180Gln) c.458T>A (p.Leu153Gln) c.497T>A (p.Leu166Gln) | |
| X | g.154367926G>A | CA519709998 | FLNA | c.538C>T (p.Leu180=) c.457C>T (p.Leu153=) c.496C>T (p.Leu166=) | |
| X | g.154367926G>C | CA415249487 | FLNA | c.538C>G (p.Leu180Val) c.457C>G (p.Leu153Val) c.496C>G (p.Leu166Val) | |
| X | g.154367926G>T | CA415249490 | FLNA | c.538C>A (p.Leu180Met) c.457C>A (p.Leu153Met) c.496C>A (p.Leu166Met) | |
| X | g.154367927C>A | CA415249494 | FLNA | c.537G>T (p.Lys179Asn) c.456G>T (p.Lys152Asn) c.495G>T (p.Lys165Asn) | |
| X | g.154367927C= | CA2466659069 | FLNA | c.537G= (p.Lys179=) c.456G= (p.Lys152=) c.495G= (p.Lys165=) | |
| X | g.154367927C>G | CA415249497 | FLNA | c.537G>C (p.Lys179Asn) c.456G>C (p.Lys152Asn) c.495G>C (p.Lys165Asn) | ClinVar dbSNP |
| X | g.154367927C>T | CA519710000 | FLNA | c.537G>A (p.Lys179=) c.456G>A (p.Lys152=) c.495G>A (p.Lys165=) | |
| X | g.154367928T>A | CA415249504 | FLNA | c.536A>T (p.Lys179Met) c.455A>T (p.Lys152Met) c.494A>T (p.Lys165Met) | |
| X | g.154367928T>C | CA415249508 | FLNA | c.536A>G (p.Lys179Arg) c.455A>G (p.Lys152Arg) c.494A>G (p.Lys165Arg) | gnomAD v4 |
| X | g.154367928T>G | CA415249510 | FLNA | c.536A>C (p.Lys179Thr) c.455A>C (p.Lys152Thr) c.494A>C (p.Lys165Thr) | |
| X | g.154367929T>A | CA415249516 | FLNA | c.535A>T (p.Lys179Ter) c.454A>T (p.Lys152Ter) c.493A>T (p.Lys165Ter) | |
| X | g.154367929T>C | CA415249518 | FLNA | c.535A>G (p.Lys179Glu) c.454A>G (p.Lys152Glu) c.493A>G (p.Lys165Glu) | |
| X | g.154367929T>G | CA415249514 | FLNA | c.535A>C (p.Lys179Gln) c.454A>C (p.Lys152Gln) c.493A>C (p.Lys165Gln) | gnomAD v4 |
| X | g.154367930G>A | CA519710001 | FLNA | c.534C>T (p.Asn178=) c.453C>T (p.Asn151=) c.492C>T (p.Asn164=) | |
| X | g.154367930G>C | CA415249519 | FLNA | c.534C>G (p.Asn178Lys) c.453C>G (p.Asn151Lys) c.492C>G (p.Asn164Lys) | |
| X | g.154367930G>T | CA415249520 | FLNA | c.534C>A (p.Asn178Lys) c.453C>A (p.Asn151Lys) c.492C>A (p.Asn164Lys) | |
| X | g.154367931T>A | CA415249525 | FLNA | c.533A>T (p.Asn178Ile) c.452A>T (p.Asn151Ile) c.491A>T (p.Asn164Ile) | |
| X | g.154367931T>C | CA415249527 | FLNA | c.533A>G (p.Asn178Ser) c.452A>G (p.Asn151Ser) c.491A>G (p.Asn164Ser) | |
| X | g.154367931T>G | CA415249537 | FLNA | c.533A>C (p.Asn178Thr) c.452A>C (p.Asn151Thr) c.491A>C (p.Asn164Thr) | |
| X | g.154367932T>A | CA415249549 | FLNA | c.532A>T (p.Asn178Tyr) c.451A>T (p.Asn151Tyr) c.490A>T (p.Asn164Tyr) | |
| X | g.154367932T>C | CA415249541 | FLNA | c.532A>G (p.Asn178Asp) c.451A>G (p.Asn151Asp) c.490A>G (p.Asn164Asp) | |
| X | g.154367932T>G | CA415249546 | FLNA | c.532A>C (p.Asn178His) c.451A>C (p.Asn151His) c.490A>C (p.Asn164His) | |
| X | g.154367933C>A | CA415249563 | FLNA | c.531G>T (p.Gln177His) c.450G>T (p.Gln150His) c.489G>T (p.Gln163His) | |
| X | g.154367933C>G | CA415249566 | FLNA | c.531G>C (p.Gln177His) c.450G>C (p.Gln150His) c.489G>C (p.Gln163His) | |
| X | g.154367933C>T | CA519710002 | FLNA | c.531G>A (p.Gln177=) c.450G>A (p.Gln150=) c.489G>A (p.Gln163=) | |
| X | g.154367934T>A | CA415249567 | FLNA | c.530A>T (p.Gln177Leu) c.449A>T (p.Gln150Leu) c.488A>T (p.Gln163Leu) | |
| X | g.154367934T>C | CA415249568 | FLNA | c.530A>G (p.Gln177Arg) c.449A>G (p.Gln150Arg) c.488A>G (p.Gln163Arg) | |
| X | g.154367934T>G | CA415249570 | FLNA | c.530A>C (p.Gln177Pro) c.449A>C (p.Gln150Pro) c.488A>C (p.Gln163Pro) | |
| X | g.154367935G>A | CA415249574 | FLNA | c.529C>T (p.Gln177Ter) c.448C>T (p.Gln150Ter) c.487C>T (p.Gln163Ter) | |
| X | g.154367935G>C | CA415249579 | FLNA | c.529C>G (p.Gln177Glu) c.448C>G (p.Gln150Glu) c.487C>G (p.Gln163Glu) | |
| X | g.154367935G>T | CA415249576 | FLNA | c.529C>A (p.Gln177Lys) c.448C>A (p.Gln150Lys) c.487C>A (p.Gln163Lys) | |
| X | g.154367936G>A | CA519710007 | FLNA | c.528C>T (p.Ile176=) c.447C>T (p.Ile149=) c.486C>T (p.Ile162=) | |
| X | g.154367936G>C | CA415249580 | FLNA | c.528C>G (p.Ile176Met) c.447C>G (p.Ile149Met) c.486C>G (p.Ile162Met) | |
| X | g.154367936G>T | CA519710009 | FLNA | c.528C>A (p.Ile176=) c.447C>A (p.Ile149=) c.486C>A (p.Ile162=) | |
| X | g.154367937A>C | CA415249584 | FLNA | c.527T>G (p.Ile176Ser) c.446T>G (p.Ile149Ser) c.485T>G (p.Ile162Ser) | |
| X | g.154367937A>G | CA415249587 | FLNA | c.527T>C (p.Ile176Thr) c.446T>C (p.Ile149Thr) c.485T>C (p.Ile162Thr) | |
| X | g.154367937A>T | CA415249589 | FLNA | c.527T>A (p.Ile176Asn) c.446T>A (p.Ile149Asn) c.485T>A (p.Ile162Asn) | |
| X | g.154367938T>A | CA415249591 | FLNA | c.526A>T (p.Ile176Phe) c.445A>T (p.Ile149Phe) c.484A>T (p.Ile162Phe) | |
| X | g.154367938T>C | CA415249595 | FLNA | c.526A>G (p.Ile176Val) c.445A>G (p.Ile149Val) c.484A>G (p.Ile162Val) | |
| X | g.154367938T>G | CA415249599 | FLNA | c.526A>C (p.Ile176Leu) c.445A>C (p.Ile149Leu) c.484A>C (p.Ile162Leu) | |
| X | g.154367939C>A | CA415249602 | FLNA | c.525G>T (p.Trp175Cys) c.444G>T (p.Trp148Cys) c.483G>T (p.Trp161Cys) | |
| X | g.154367939C>G | CA415249604 | FLNA | c.525G>C (p.Trp175Cys) c.444G>C (p.Trp148Cys) c.483G>C (p.Trp161Cys) | gnomAD v4 |
| X | g.154367939C>T | CA415249609 | FLNA | c.525G>A (p.Trp175Ter) c.444G>A (p.Trp148Ter) c.483G>A (p.Trp161Ter) | |
| X | g.154367940C>A | CA415249619 | FLNA | c.524G>T (p.Trp175Leu) c.443G>T (p.Trp148Leu) c.482G>T (p.Trp161Leu) | |
| X | g.154367940C>G | CA415249625 | FLNA | c.524G>C (p.Trp175Ser) c.443G>C (p.Trp148Ser) c.482G>C (p.Trp161Ser) | gnomAD v4 |
| X | g.154367940C>T | CA415249622 | FLNA | c.524G>A (p.Trp175Ter) c.443G>A (p.Trp148Ter) c.482G>A (p.Trp161Ter) | ClinVar |
| X | g.154367941A>C | CA415249635 | FLNA | c.523T>G (p.Trp175Gly) c.442T>G (p.Trp148Gly) c.481T>G (p.Trp161Gly) | |
| X | g.154367941A>G | CA415249637 | FLNA | c.523T>C (p.Trp175Arg) c.442T>C (p.Trp148Arg) c.481T>C (p.Trp161Arg) | |
| X | g.154367941A>T | CA415249636 | FLNA | c.523T>A (p.Trp175Arg) c.442T>A (p.Trp148Arg) c.481T>A (p.Trp161Arg) | |
| X | g.154367942G>A | CA519710015 | FLNA | c.522C>T (p.Gly174=) c.441C>T (p.Gly147=) c.480C>T (p.Gly160=) | |
| X | g.154367942G>C | CA519710017 | FLNA | c.522C>G (p.Gly174=) c.441C>G (p.Gly147=) c.480C>G (p.Gly160=) | |
| X | g.154367942G>T | CA519710014 | FLNA | c.522C>A (p.Gly174=) c.441C>A (p.Gly147=) c.480C>A (p.Gly160=) | gnomAD v4 |
| X | g.154367943C>A | CA415249642 | FLNA | c.521G>T (p.Gly174Val) c.440G>T (p.Gly147Val) c.479G>T (p.Gly160Val) | |
| X | g.154367943C= | CA2466659070 | FLNA | c.521G= (p.Gly174=) c.440G= (p.Gly147=) c.479G= (p.Gly160=) | |
| X | g.154367943C>G | CA415249650 | FLNA | c.521G>C (p.Gly174Ala) c.440G>C (p.Gly147Ala) c.479G>C (p.Gly160Ala) | |
| X | g.154367943C>T | CA415249644 | FLNA | c.521G>A (p.Gly174Asp) c.440G>A (p.Gly147Asp) c.479G>A (p.Gly160Asp) | ClinVar dbSNP |
| X | g.154367944C>A | CA415249655 | FLNA | c.520G>T (p.Gly174Cys) c.439G>T (p.Gly147Cys) c.478G>T (p.Gly160Cys) | |
| X | g.154367944C>G | CA415249662 | FLNA | c.520G>C (p.Gly174Arg) c.439G>C (p.Gly147Arg) c.478G>C (p.Gly160Arg) | |
| X | g.154367944C>T | CA415249660 | FLNA | c.520G>A (p.Gly174Ser) c.439G>A (p.Gly147Ser) c.478G>A (p.Gly160Ser) | |
| X | g.154367945C>A | CA519710020 | FLNA | c.519G>T (p.Leu173=) c.438G>T (p.Leu146=) c.477G>T (p.Leu159=) | |
| X | g.154367945C>G | CA519710022 | FLNA | c.519G>C (p.Leu173=) c.438G>C (p.Leu146=) c.477G>C (p.Leu159=) | |
| X | g.154367945C>T | CA519710024 | FLNA | c.519G>A (p.Leu173=) c.438G>A (p.Leu146=) c.477G>A (p.Leu159=) | |
| X | g.154367946del | CA2824282242 | FLNA | c.518del (p.Leu173ArgfsTer?) c.437del (p.Leu146ArgfsTer?) c.476del (p.Leu159ArgfsTer?) | |
| X | g.154367946A>C | CA415249665 | FLNA | c.518T>G (p.Leu173Arg) c.437T>G (p.Leu146Arg) c.476T>G (p.Leu159Arg) | |
| X | g.154367946A>G | CA415249677 | FLNA | c.518T>C (p.Leu173Pro) c.437T>C (p.Leu146Pro) c.476T>C (p.Leu159Pro) | |
| X | g.154367946A>T | CA415249669 | FLNA | c.518T>A (p.Leu173Gln) c.437T>A (p.Leu146Gln) c.476T>A (p.Leu159Gln) | |
| X | g.154367947G>A | CA519710025 | FLNA | c.517C>T (p.Leu173=) c.436C>T (p.Leu146=) c.475C>T (p.Leu159=) | |
| X | g.154367947G>C | CA415249680 | FLNA | c.517C>G (p.Leu173Val) c.436C>G (p.Leu146Val) c.475C>G (p.Leu159Val) | |
| X | g.154367947G= | CA2466659071 | FLNA | c.517C= (p.Leu173=) c.436C= (p.Leu146=) c.475C= (p.Leu159=) | |
| X | g.154367947G>T | CA415249681 | FLNA | c.517C>A (p.Leu173Met) c.436C>A (p.Leu146Met) c.475C>A (p.Leu159Met) | dbSNP gnomAD v3 gnomAD v4 |
| X | g.154367948G>A | CA519710027 | FLNA | c.516C>T (p.Leu172=) c.435C>T (p.Leu145=) c.474C>T (p.Leu158=) | ClinVar dbSNP gnomAD v4 |
| X | g.154367948G>C | CA519710028 | FLNA | c.516C>G (p.Leu172=) c.435C>G (p.Leu145=) c.474C>G (p.Leu158=) | |
| X | g.154367948G>T | CA519710029 | FLNA | c.516C>A (p.Leu172=) c.435C>A (p.Leu145=) c.474C>A (p.Leu158=) | |
| X | g.154367949A>C | CA415249682 | FLNA | c.515T>G (p.Leu172Arg) c.434T>G (p.Leu145Arg) c.473T>G (p.Leu158Arg) | |
| X | g.154367949A>G | CA415249685 | FLNA | c.515T>C (p.Leu172Pro) c.434T>C (p.Leu145Pro) c.473T>C (p.Leu158Pro) | |
| X | g.154367949A>T | CA415249688 | FLNA | c.515T>A (p.Leu172His) c.434T>A (p.Leu145His) c.473T>A (p.Leu158His) | |
| X | g.154367950G>A | CA415249694 | FLNA | c.514C>T (p.Leu172Phe) c.433C>T (p.Leu145Phe) c.472C>T (p.Leu158Phe) | ClinVar dbSNP |
| X | g.154367950G>C | CA415249704 | FLNA | c.514C>G (p.Leu172Val) c.433C>G (p.Leu145Val) c.472C>G (p.Leu158Val) | |
| X | g.154367950G>T | CA415249706 | FLNA | c.514C>A (p.Leu172Ile) c.433C>A (p.Leu145Ile) c.472C>A (p.Leu158Ile) | |
| X | g.154367951C>A | CA415249719 | FLNA | c.513G>T (p.Arg171Ser) c.432G>T (p.Arg144Ser) c.471G>T (p.Arg157Ser) | |
| X | g.154367951C= | CA2466659072 | FLNA | c.513G= (p.Arg171=) c.432G= (p.Arg144=) c.471G= (p.Arg157=) | |
| X | g.154367951C>G | CA415249717 | FLNA | c.513G>C (p.Arg171Ser) c.432G>C (p.Arg144Ser) c.471G>C (p.Arg157Ser) | |
| X | g.154367951C>T | CA10561405 | FLNA | c.513G>A (p.Arg171=) c.432G>A (p.Arg144=) c.471G>A (p.Arg157=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.154367952C>A | CA415249726 | FLNA | c.512G>T (p.Arg171Met) c.431G>T (p.Arg144Met) c.470G>T (p.Arg157Met) | |
| X | g.154367952C>G | CA415249728 | FLNA | c.512G>C (p.Arg171Thr) c.431G>C (p.Arg144Thr) c.470G>C (p.Arg157Thr) | COSMIC COSMIC |
| X | g.154367952C>T | CA415249732 | FLNA | c.512G>A (p.Arg171Lys) c.431G>A (p.Arg144Lys) c.470G>A (p.Arg157Lys) | ClinVar dbSNP |
| X | g.154367953T>A | CA415249737 | FLNA | c.511A>T (p.Arg171Trp) c.430A>T (p.Arg144Trp) c.469A>T (p.Arg157Trp) | |
| X | g.154367953T>C | CA415249738 | FLNA | c.511A>G (p.Arg171Gly) c.430A>G (p.Arg144Gly) c.469A>G (p.Arg157Gly) | |
| X | g.154367953T>G | CA519277109 | FLNA | c.511A>C (p.Arg171=) c.430A>C (p.Arg144=) c.469A>C (p.Arg157=) | |
| X | g.154367954C>A | CA415249742 | FLNA | c.510G>T (p.Gln170His) c.429G>T (p.Gln143His) c.468G>T (p.Gln156His) | |
| X | g.154367954C>G | CA415249748 | FLNA | c.510G>C (p.Gln170His) c.429G>C (p.Gln143His) c.468G>C (p.Gln156His) | ClinVar |
| X | g.154367954C>T | CA519277111 | FLNA | c.510G>A (p.Gln170=) c.429G>A (p.Gln143=) c.468G>A (p.Gln156=) | |
| X | g.154367955T>A | CA415249757 | FLNA | c.509A>T (p.Gln170Leu) c.428A>T (p.Gln143Leu) c.467A>T (p.Gln156Leu) | |
| X | g.154367955T>C | CA415249764 | FLNA | c.509A>G (p.Gln170Arg) c.428A>G (p.Gln143Arg) c.467A>G (p.Gln156Arg) | |
| X | g.154367955T>G | CA323849 | FLNA | c.509A>C (p.Gln170Pro) c.428A>C (p.Gln143Pro) c.467A>C (p.Gln156Pro) | dbSNP |
| X | g.154367955T= | CA2466659073 | FLNA | c.509A= (p.Gln170=) c.428A= (p.Gln143=) c.467A= (p.Gln156=) | |
| X | g.154367956G>A | CA415249794 | FLNA | c.508C>T (p.Gln170Ter) c.427C>T (p.Gln143Ter) c.466C>T (p.Gln156Ter) | |
| X | g.154367956G>C | CA415249797 | FLNA | c.508C>G (p.Gln170Glu) c.427C>G (p.Gln143Glu) c.466C>G (p.Gln156Glu) | |
| X | g.154367956G>T | CA415249791 | FLNA | c.508C>A (p.Gln170Lys) c.427C>A (p.Gln143Lys) c.466C>A (p.Gln156Lys) | |
| X | g.154367957C>A | CA415249802 | FLNA | c.507G>T (p.Lys169Asn) c.426G>T (p.Lys142Asn) c.465G>T (p.Lys155Asn) | |
| X | g.154367957C>G | CA415249818 | FLNA | c.507G>C (p.Lys169Asn) c.426G>C (p.Lys142Asn) c.465G>C (p.Lys155Asn) | |
| X | g.154367957C>T | CA519277116 | FLNA | c.507G>A (p.Lys169=) c.426G>A (p.Lys142=) c.465G>A (p.Lys155=) | gnomAD v4 |
| X | g.154367958T>A | CA415249819 | FLNA | c.506A>T (p.Lys169Met) c.425A>T (p.Lys142Met) c.464A>T (p.Lys155Met) | |
| X | g.154367958T>C | CA415249820 | FLNA | c.506A>G (p.Lys169Arg) c.425A>G (p.Lys142Arg) c.464A>G (p.Lys155Arg) | gnomAD v4 |
| X | g.154367958T>G | CA415249826 | FLNA | c.506A>C (p.Lys169Thr) c.425A>C (p.Lys142Thr) c.464A>C (p.Lys155Thr) | COSMIC COSMIC |
| X | g.154367959T>A | CA415249835 | FLNA | c.505A>T (p.Lys169Ter) c.424A>T (p.Lys142Ter) c.463A>T (p.Lys155Ter) | |
| X | g.154367959T>C | CA415249848 | FLNA | c.505A>G (p.Lys169Glu) c.424A>G (p.Lys142Glu) c.463A>G (p.Lys155Glu) | |
| X | g.154367959T>G | CA415249854 | FLNA | c.505A>C (p.Lys169Gln) c.424A>C (p.Lys142Gln) c.463A>C (p.Lys155Gln) | |
| X | g.154367960G>A | CA519277123 | FLNA | c.504C>T (p.Pro168=) c.423C>T (p.Pro141=) c.462C>T (p.Pro154=) | |
| X | g.154367960G>C | CA519277120 | FLNA | c.504C>G (p.Pro168=) c.423C>G (p.Pro141=) c.462C>G (p.Pro154=) | |
| X | g.154367960G>T | CA519277122 | FLNA | c.504C>A (p.Pro168=) c.423C>A (p.Pro141=) c.462C>A (p.Pro154=) | |
| X | g.154367964dup | CA2824282247 | FLNA | c.504dup (p.Lys169GlnfsTer?) c.423dup (p.Lys142GlnfsTer?) c.462dup (p.Lys155GlnfsTer?) | |
| X | g.154367964del | CA645602600 | FLNA | c.504del (p.Lys169SerfsTer?) c.423del (p.Lys142SerfsTer?) c.462del (p.Lys155SerfsTer?) | COSMIC COSMIC |
| X | g.154367963_154367964del | CA2579738371 | FLNA | c.503_504del (p.Pro168GlnfsTer?) c.422_423del (p.Pro141GlnfsTer?) c.461_462del (p.Pro154GlnfsTer?) | |
| X | g.154367961G>A | CA415249858 | FLNA | c.503C>T (p.Pro168Leu) c.422C>T (p.Pro141Leu) c.461C>T (p.Pro154Leu) | ClinVar dbSNP |
| X | g.154367961G>C | CA415249861 | FLNA | c.503C>G (p.Pro168Arg) c.422C>G (p.Pro141Arg) c.461C>G (p.Pro154Arg) | |
| X | g.154367961G>T | CA415249872 | FLNA | c.503C>A (p.Pro168His) c.422C>A (p.Pro141His) c.461C>A (p.Pro154His) | |
| X | g.154367962G>A | CA415249910 | FLNA | c.502C>T (p.Pro168Ser) c.421C>T (p.Pro141Ser) c.460C>T (p.Pro154Ser) | |
| X | g.154367962G>C | CA415249877 | FLNA | c.502C>G (p.Pro168Ala) c.421C>G (p.Pro141Ala) c.460C>G (p.Pro154Ala) | |
| X | g.154367962G>T | CA415249882 | FLNA | c.502C>A (p.Pro168Thr) c.421C>A (p.Pro141Thr) c.460C>A (p.Pro154Thr) | |
| X | g.154367963G>A | CA519277128 | FLNA | c.501C>T (p.Thr167=) c.420C>T (p.Thr140=) c.459C>T (p.Thr153=) | |
| X | g.154367963G>C | CA519277129 | FLNA | c.501C>G (p.Thr167=) c.420C>G (p.Thr140=) c.459C>G (p.Thr153=) | |
| X | g.154367963G>T | CA519277126 | FLNA | c.501C>A (p.Thr167=) c.420C>A (p.Thr140=) c.459C>A (p.Thr153=) | |
| X | g.154367964G>A | CA415249915 | FLNA | c.500C>T (p.Thr167Ile) c.419C>T (p.Thr140Ile) c.458C>T (p.Thr153Ile) | |
| X | g.154367964G>C | CA415249919 | FLNA | c.500C>G (p.Thr167Ser) c.419C>G (p.Thr140Ser) c.458C>G (p.Thr153Ser) | |
| X | g.154367964G= | CA2466659074 | FLNA | c.500C= (p.Thr167=) c.419C= (p.Thr140=) c.458C= (p.Thr153=) | |
| X | g.154367964G>T | CA321035 | FLNA | c.500C>A (p.Thr167Asn) c.419C>A (p.Thr140Asn) c.458C>A (p.Thr153Asn) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| X | g.154367965T>A | CA415249928 | FLNA | c.499A>T (p.Thr167Ser) c.418A>T (p.Thr140Ser) c.457A>T (p.Thr153Ser) | |
| X | g.154367965T>C | CA415249931 | FLNA | c.499A>G (p.Thr167Ala) c.418A>G (p.Thr140Ala) c.457A>G (p.Thr153Ala) | |
| X | g.154367965T>G | CA415249935 | FLNA | c.499A>C (p.Thr167Pro) c.418A>C (p.Thr140Pro) c.457A>C (p.Thr153Pro) | |
| X | g.154367966C>A | CA415249938 | FLNA | c.498G>T (p.Gln166His) c.417G>T (p.Gln139His) c.456G>T (p.Gln152His) | |
| X | g.154367966C>G | CA415249942 | FLNA | c.498G>C (p.Gln166His) c.417G>C (p.Gln139His) c.456G>C (p.Gln152His) | |
| X | g.154367966C>T | CA519277133 | FLNA | c.498G>A (p.Gln166=) c.417G>A (p.Gln139=) c.456G>A (p.Gln152=) | |
| X | g.154367967T>A | CA415249949 | FLNA | c.497A>T (p.Gln166Leu) c.416A>T (p.Gln139Leu) c.455A>T (p.Gln152Leu) | |
| X | g.154367967T>C | CA415249951 | FLNA | c.497A>G (p.Gln166Arg) c.416A>G (p.Gln139Arg) c.455A>G (p.Gln152Arg) | |
| X | g.154367967T>G | CA415249959 | FLNA | c.497A>C (p.Gln166Pro) c.416A>C (p.Gln139Pro) c.455A>C (p.Gln152Pro) | |
| X | g.154367968G>A | CA415249982 | FLNA | c.496C>T (p.Gln166Ter) c.415C>T (p.Gln139Ter) c.454C>T (p.Gln152Ter) | |
| X | g.154367968G>C | CA415249979 | FLNA | c.496C>G (p.Gln166Glu) c.415C>G (p.Gln139Glu) c.454C>G (p.Gln152Glu) | |
| X | g.154367968G>T | CA415249970 | FLNA | c.496C>A (p.Gln166Lys) c.415C>A (p.Gln139Lys) c.454C>A (p.Gln152Lys) | |
| X | g.154367969C>A | CA415249987 | FLNA | c.495G>T (p.Lys165Asn) c.414G>T (p.Lys138Asn) c.453G>T (p.Lys151Asn) | |
| X | g.154367969C= | CA2466659075 | FLNA | c.495G= (p.Lys165=) c.414G= (p.Lys138=) c.453G= (p.Lys151=) | |
| X | g.154367969C>G | CA415249991 | FLNA | c.495G>C (p.Lys165Asn) c.414G>C (p.Lys138Asn) c.453G>C (p.Lys151Asn) | |
| X | g.154367969C>T | CA519277134 | FLNA | c.495G>A (p.Lys165=) c.414G>A (p.Lys138=) c.453G>A (p.Lys151=) | ClinVar dbSNP gnomAD v4 |
| X | g.154367970T>A | CA415250004 | FLNA | c.494A>T (p.Lys165Met) c.413A>T (p.Lys138Met) c.452A>T (p.Lys151Met) | |
| X | g.154367970T>C | CA415250007 | FLNA | c.494A>G (p.Lys165Arg) c.413A>G (p.Lys138Arg) c.452A>G (p.Lys151Arg) | ClinVar dbSNP |
| X | g.154367970T>G | CA415250011 | FLNA | c.494A>C (p.Lys165Thr) c.413A>C (p.Lys138Thr) c.452A>C (p.Lys151Thr) | |
| X | g.154367970T= | CA2466659076 | FLNA | c.494A= (p.Lys165=) c.413A= (p.Lys138=) c.452A= (p.Lys151=) | |
| X | g.154367971T>A | CA415250012 | FLNA | c.493A>T (p.Lys165Ter) c.412A>T (p.Lys138Ter) c.451A>T (p.Lys151Ter) | |
| X | g.154367971T>C | CA415250013 | FLNA | c.493A>G (p.Lys165Glu) c.412A>G (p.Lys138Glu) c.451A>G (p.Lys151Glu) | |
| X | g.154367971T>G | CA415250015 | FLNA | c.493A>C (p.Lys165Gln) c.412A>C (p.Lys138Gln) c.451A>C (p.Lys151Gln) | |
| X | g.154367972C>A | CA415250019 | FLNA | c.492G>T (p.Lys164Asn) c.411G>T (p.Lys137Asn) c.450G>T (p.Lys150Asn) | |
| X | g.154367972C>G | CA415250020 | FLNA | c.492G>C (p.Lys164Asn) c.411G>C (p.Lys137Asn) c.450G>C (p.Lys150Asn) | |
| X | g.154367972C>T | CA519277135 | FLNA | c.492G>A (p.Lys164=) c.411G>A (p.Lys137=) c.450G>A (p.Lys150=) | |
| X | g.154367973T>A | CA415250031 | FLNA | c.491A>T (p.Lys164Met) c.410A>T (p.Lys137Met) c.449A>T (p.Lys150Met) | |
| X | g.154367973T>C | CA415250033 | FLNA | c.491A>G (p.Lys164Arg) c.410A>G (p.Lys137Arg) c.449A>G (p.Lys150Arg) | |
| X | g.154367973T>G | CA415250035 | FLNA | c.491A>C (p.Lys164Thr) c.410A>C (p.Lys137Thr) c.449A>C (p.Lys150Thr) | |
| X | g.154367974T>A | CA415250046 | FLNA | c.490A>T (p.Lys164Ter) c.409A>T (p.Lys137Ter) c.448A>T (p.Lys150Ter) | |
| X | g.154367974T>C | CA415250039 | FLNA | c.490A>G (p.Lys164Glu) c.409A>G (p.Lys137Glu) c.448A>G (p.Lys150Glu) | |
| X | g.154367974T>G | CA415250042 | FLNA | c.490A>C (p.Lys164Gln) c.409A>C (p.Lys137Gln) c.448A>C (p.Lys150Gln) | |
| X | g.154367975G>A | CA519277136 | FLNA | c.489C>T (p.Ala163=) c.408C>T (p.Ala136=) c.447C>T (p.Ala149=) | COSMIC COSMIC |
| X | g.154367975G>C | CA519277137 | FLNA | c.489C>G (p.Ala163=) c.408C>G (p.Ala136=) c.447C>G (p.Ala149=) | |
| X | g.154367975G>T | CA519277138 | FLNA | c.489C>A (p.Ala163=) c.408C>A (p.Ala136=) c.447C>A (p.Ala149=) | |
| X | g.154367976G>A | CA415250052 | FLNA | c.488C>T (p.Ala163Val) c.407C>T (p.Ala136Val) c.446C>T (p.Ala149Val) | |
| X | g.154367976G>C | CA415250053 | FLNA | c.488C>G (p.Ala163Gly) c.407C>G (p.Ala136Gly) c.446C>G (p.Ala149Gly) | |
| X | g.154367976G>T | CA415250055 | FLNA | c.488C>A (p.Ala163Asp) c.407C>A (p.Ala136Asp) c.446C>A (p.Ala149Asp) | |
| X | g.154367977C>A | CA415250060 | FLNA | c.487G>T (p.Ala163Ser) c.406G>T (p.Ala136Ser) c.445G>T (p.Ala149Ser) | |
| X | g.154367977C= | CA2466659077 | FLNA | c.487G= (p.Ala163=) c.406G= (p.Ala136=) c.445G= (p.Ala149=) | |
| X | g.154367977C>G | CA415250063 | FLNA | c.487G>C (p.Ala163Pro) c.406G>C (p.Ala136Pro) c.445G>C (p.Ala149Pro) | |
| X | g.154367977C>T | CA415250066 | FLNA | c.487G>A (p.Ala163Thr) c.406G>A (p.Ala136Thr) c.445G>A (p.Ala149Thr) | ClinVar dbSNP |
| X | g.154367981_154367983del | CA645602602 | FLNA | c.485_487del (p.Glu162del) c.404_406del (p.Glu135del) c.443_445del (p.Glu148del) | gnomAD v4 COSMIC COSMIC |
| X | g.154367978C>A | CA415250080 | FLNA | c.486G>T (p.Glu162Asp) c.405G>T (p.Glu135Asp) c.444G>T (p.Glu148Asp) | |
| X | g.154367978C>G | CA415250091 | FLNA | c.486G>C (p.Glu162Asp) c.405G>C (p.Glu135Asp) c.444G>C (p.Glu148Asp) | |
| X | g.154367978C>T | CA519277139 | FLNA | c.486G>A (p.Glu162=) c.405G>A (p.Glu135=) c.444G>A (p.Glu148=) | ClinVar |
| X | g.154367979T>A | CA415250096 | FLNA | c.485A>T (p.Glu162Val) c.404A>T (p.Glu135Val) c.443A>T (p.Glu148Val) | COSMIC |
| X | g.154367979T>C | CA415250097 | FLNA | c.485A>G (p.Glu162Gly) c.404A>G (p.Glu135Gly) c.443A>G (p.Glu148Gly) | |
| X | g.154367979T>G | CA415250098 | FLNA | c.485A>C (p.Glu162Ala) c.404A>C (p.Glu135Ala) c.443A>C (p.Glu148Ala) | |
| X | g.154367980C>A | CA415250103 | FLNA | c.484G>T (p.Glu162Ter) c.403G>T (p.Glu135Ter) c.442G>T (p.Glu148Ter) | |
| X | g.154367980C= | CA2466659078 | FLNA | c.484G= (p.Glu162=) c.403G= (p.Glu135=) c.442G= (p.Glu148=) | |
| X | g.154367980C>G | CA415250121 | FLNA | c.484G>C (p.Glu162Gln) c.403G>C (p.Glu135Gln) c.442G>C (p.Glu148Gln) | |
| X | g.154367980C>T | CA415250106 | FLNA | c.484G>A (p.Glu162Lys) c.403G>A (p.Glu135Lys) c.442G>A (p.Glu148Lys) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| X | g.154367981C>A | CA415250126 | FLNA | c.483G>T (p.Glu161Asp) c.402G>T (p.Glu134Asp) c.441G>T (p.Glu147Asp) | |
| X | g.154367981C>G | CA415250129 | FLNA | c.483G>C (p.Glu161Asp) c.402G>C (p.Glu134Asp) c.441G>C (p.Glu147Asp) | |
| X | g.154367981C>T | CA519277140 | FLNA | c.483G>A (p.Glu161=) c.402G>A (p.Glu134=) c.441G>A (p.Glu147=) |