| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 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=) | |
| X | g.154367982T>A | CA415250137 | FLNA | c.482A>T (p.Glu161Val) c.401A>T (p.Glu134Val) c.440A>T (p.Glu147Val) | |
| X | g.154367982T>C | CA415250142 | FLNA | c.482A>G (p.Glu161Gly) c.401A>G (p.Glu134Gly) c.440A>G (p.Glu147Gly) | |
| X | g.154367982T>G | CA415250143 | FLNA | c.482A>C (p.Glu161Ala) c.401A>C (p.Glu134Ala) c.440A>C (p.Glu147Ala) | |
| X | g.154367983C>A | CA415250144 | FLNA | c.481G>T (p.Glu161Ter) c.400G>T (p.Glu134Ter) c.439G>T (p.Glu147Ter) | |
| X | g.154367983C>G | CA415250145 | FLNA | c.481G>C (p.Glu161Gln) c.400G>C (p.Glu134Gln) c.439G>C (p.Glu147Gln) | |
| X | g.154367983C>T | CA415250146 | FLNA | c.481G>A (p.Glu161Lys) c.400G>A (p.Glu134Lys) c.439G>A (p.Glu147Lys) | |
| X | g.154367984A>C | CA415250150 | FLNA | c.480T>G (p.Asp160Glu) c.399T>G (p.Asp133Glu) c.438T>G (p.Asp146Glu) | |
| X | g.154367984A>G | CA519277141 | FLNA | c.480T>C (p.Asp160=) c.399T>C (p.Asp133=) c.438T>C (p.Asp146=) | ClinVar |
| X | g.154367984A>T | CA415250152 | FLNA | c.480T>A (p.Asp160Glu) c.399T>A (p.Asp133Glu) c.438T>A (p.Asp146Glu) | |
| X | g.154367984_154367987delinsATCC | CA2466659079 | FLNA | c.477_480delinsGGAT (p.Glu159=) c.396_399delinsGGAT (p.Glu132=) c.435_438delinsGGAT (p.Glu145=) | |
| X | g.154367985T>A | CA415250163 | FLNA | c.479A>T (p.Asp160Val) c.398A>T (p.Asp133Val) c.437A>T (p.Asp146Val) | |
| X | g.154367985T>C | CA415250161 | FLNA | c.479A>G (p.Asp160Gly) c.398A>G (p.Asp133Gly) c.437A>G (p.Asp146Gly) | |
| X | g.154367985T>G | CA415250159 | FLNA | c.479A>C (p.Asp160Ala) c.398A>C (p.Asp133Ala) c.437A>C (p.Asp146Ala) | |
| X | g.154367993_154367995del | CA2466659080 | FLNA | c.477_479del (p.Glu159del) c.396_398del (p.Glu132del) c.435_437del (p.Glu145del) | ClinVar dbSNP |
| X | g.154367986C>A | CA415250167 | FLNA | c.478G>T (p.Asp160Tyr) c.397G>T (p.Asp133Tyr) c.436G>T (p.Asp146Tyr) | |
| X | g.154367986C>G | CA415250171 | FLNA | c.478G>C (p.Asp160His) c.397G>C (p.Asp133His) c.436G>C (p.Asp146His) | |
| X | g.154367986C>T | CA415250176 | FLNA | c.478G>A (p.Asp160Asn) c.397G>A (p.Asp133Asn) c.436G>A (p.Asp146Asn) | |
| X | g.154367987C>A | CA415250182 | FLNA | c.477G>T (p.Glu159Asp) c.396G>T (p.Glu132Asp) c.435G>T (p.Glu145Asp) | |
| X | g.154367987C= | CA2466659081 | FLNA | c.477G= (p.Glu159=) c.396G= (p.Glu132=) c.435G= (p.Glu145=) | |
| X | g.154367987C>G | CA415250186 | FLNA | c.477G>C (p.Glu159Asp) c.396G>C (p.Glu132Asp) c.435G>C (p.Glu145Asp) | ClinVar dbSNP COSMIC |
| X | g.154367987C>T | CA519277142 | FLNA | c.477G>A (p.Glu159=) c.396G>A (p.Glu132=) c.435G>A (p.Glu145=) | |
| X | g.154367988T>A | CA415250191 | FLNA | c.476A>T (p.Glu159Val) c.395A>T (p.Glu132Val) c.434A>T (p.Glu145Val) | |
| X | g.154367988T>C | CA415250197 | FLNA | c.476A>G (p.Glu159Gly) c.395A>G (p.Glu132Gly) c.434A>G (p.Glu145Gly) | |
| X | g.154367988T>G | CA415250205 | FLNA | c.476A>C (p.Glu159Ala) c.395A>C (p.Glu132Ala) c.434A>C (p.Glu145Ala) | |
| X | g.154367989C>A | CA415250212 | FLNA | c.475G>T (p.Glu159Ter) c.394G>T (p.Glu132Ter) c.433G>T (p.Glu145Ter) | |
| X | g.154367989C>G | CA415250216 | FLNA | c.475G>C (p.Glu159Gln) c.394G>C (p.Glu132Gln) c.433G>C (p.Glu145Gln) | |
| X | g.154367989C>T | CA415250221 | FLNA | c.475G>A (p.Glu159Lys) c.394G>A (p.Glu132Lys) c.433G>A (p.Glu145Lys) | |
| X | g.154367990C>A | CA415250231 | FLNA | c.474G>T (p.Glu158Asp) c.393G>T (p.Glu131Asp) c.432G>T (p.Glu144Asp) | |
| X | g.154367990C>G | CA415250245 | FLNA | c.474G>C (p.Glu158Asp) c.393G>C (p.Glu131Asp) c.432G>C (p.Glu144Asp) | |
| X | g.154367990C>T | CA519277143 | FLNA | c.474G>A (p.Glu158=) c.393G>A (p.Glu131=) c.432G>A (p.Glu144=) | |
| X | g.154367991T>A | CA415250251 | FLNA | c.473A>T (p.Glu158Val) c.392A>T (p.Glu131Val) c.431A>T (p.Glu144Val) | |
| X | g.154367991T>C | CA415250253 | FLNA | c.473A>G (p.Glu158Gly) c.392A>G (p.Glu131Gly) c.431A>G (p.Glu144Gly) | ClinVar dbSNP |
| X | g.154367991T>G | CA415250254 | FLNA | c.473A>C (p.Glu158Ala) c.392A>C (p.Glu131Ala) c.431A>C (p.Glu144Ala) | |
| X | g.154367992C>A | CA415250260 | FLNA | c.472G>T (p.Glu158Ter) c.391G>T (p.Glu131Ter) c.430G>T (p.Glu144Ter) | |
| X | g.154367992C>G | CA415250265 | FLNA | c.472G>C (p.Glu158Gln) c.391G>C (p.Glu131Gln) c.430G>C (p.Glu144Gln) | |
| X | g.154367992C>T | CA415250272 | FLNA | c.472G>A (p.Glu158Lys) c.391G>A (p.Glu131Lys) c.430G>A (p.Glu144Lys) | |
| X | g.154367993C>A | CA415250276 | FLNA | c.471G>T (p.Glu157Asp) c.390G>T (p.Glu130Asp) c.429G>T (p.Glu143Asp) | |
| X | g.154367993C>G | CA415250275 | FLNA | c.471G>C (p.Glu157Asp) c.390G>C (p.Glu130Asp) c.429G>C (p.Glu143Asp) | |
| X | g.154367993C>T | CA519277144 | FLNA | c.471G>A (p.Glu157=) c.390G>A (p.Glu130=) c.429G>A (p.Glu143=) | |
| X | g.154367994T>A | CA415250282 | FLNA | c.470A>T (p.Glu157Val) c.389A>T (p.Glu130Val) c.428A>T (p.Glu143Val) | |
| X | g.154367994T>C | CA415250304 | FLNA | c.470A>G (p.Glu157Gly) c.389A>G (p.Glu130Gly) c.428A>G (p.Glu143Gly) | |
| X | g.154367994T>G | CA415250308 | FLNA | c.470A>C (p.Glu157Ala) c.389A>C (p.Glu130Ala) c.428A>C (p.Glu143Ala) | |
| X | g.154367995C>A | CA415250320 | FLNA | c.469G>T (p.Glu157Ter) c.388G>T (p.Glu130Ter) c.427G>T (p.Glu143Ter) | |
| X | g.154367995C= | CA2466659082 | FLNA | c.469G= (p.Glu157=) c.388G= (p.Glu130=) c.427G= (p.Glu143=) | |
| X | g.154367995C>G | CA415250329 | FLNA | c.469G>C (p.Glu157Gln) c.388G>C (p.Glu130Gln) c.427G>C (p.Glu143Gln) | |
| X | g.154367995C>T | CA415250338 | FLNA | c.469G>A (p.Glu157Lys) c.388G>A (p.Glu130Lys) c.427G>A (p.Glu143Lys) | dbSNP |
| X | g.154367996G>A | CA10561406 | FLNA | c.468C>T (p.Asp156=) c.387C>T (p.Asp129=) c.426C>T (p.Asp142=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| X | g.154367996G>C | CA415250341 | FLNA | c.468C>G (p.Asp156Glu) c.387C>G (p.Asp129Glu) c.426C>G (p.Asp142Glu) | dbSNP gnomAD v3 gnomAD v4 |
| X | g.154367996G= | CA2466659083 | FLNA | c.468C= (p.Asp156=) c.387C= (p.Asp129=) c.426C= (p.Asp142=) | |
| X | g.154367996G>T | CA415250345 | FLNA | c.468C>A (p.Asp156Glu) c.387C>A (p.Asp129Glu) c.426C>A (p.Asp142Glu) | |
| X | g.154367997T>A | CA415250358 | FLNA | c.467A>T (p.Asp156Val) c.386A>T (p.Asp129Val) c.425A>T (p.Asp142Val) | |
| X | g.154367997T>C | CA415250364 | FLNA | c.467A>G (p.Asp156Gly) c.386A>G (p.Asp129Gly) c.425A>G (p.Asp142Gly) | |
| X | g.154367997T>G | CA415250365 | FLNA | c.467A>C (p.Asp156Ala) c.386A>C (p.Asp129Ala) c.425A>C (p.Asp142Ala) | |
| X | g.154367998C>A | CA415250366 | FLNA | c.466G>T (p.Asp156Tyr) c.385G>T (p.Asp129Tyr) c.424G>T (p.Asp142Tyr) | |
| X | g.154367998C>G | CA415250367 | FLNA | c.466G>C (p.Asp156His) c.385G>C (p.Asp129His) c.424G>C (p.Asp142His) | |
| X | g.154367998C>T | CA415250371 | FLNA | c.466G>A (p.Asp156Asn) c.385G>A (p.Asp129Asn) c.424G>A (p.Asp142Asn) | |
| X | g.154367999C>A | CA415250376 | FLNA | c.465G>T (p.Trp155Cys) c.384G>T (p.Trp128Cys) c.423G>T (p.Trp141Cys) | |
| X | g.154367999C>G | CA415250381 | FLNA | c.465G>C (p.Trp155Cys) c.384G>C (p.Trp128Cys) c.423G>C (p.Trp141Cys) | |
| X | g.154367999C>T | CA415250384 | FLNA | c.465G>A (p.Trp155Ter) c.384G>A (p.Trp128Ter) c.423G>A (p.Trp141Ter) | |
| X | g.154368000C>A | CA415250393 | FLNA | c.464G>T (p.Trp155Leu) c.383G>T (p.Trp128Leu) c.422G>T (p.Trp141Leu) | |
| X | g.154368000C= | CA2466659084 | FLNA | c.464G= (p.Trp155=) c.383G= (p.Trp128=) c.422G= (p.Trp141=) | |
| X | g.154368000C>G | CA415250398 | FLNA | c.464G>C (p.Trp155Ser) c.383G>C (p.Trp128Ser) c.422G>C (p.Trp141Ser) | ClinVar dbSNP gnomAD v4 |
| X | g.154368000C>T | CA415250399 | FLNA | c.464G>A (p.Trp155Ter) c.383G>A (p.Trp128Ter) c.422G>A (p.Trp141Ter) | |
| X | g.154368001A>C | CA415250400 | FLNA | c.463T>G (p.Trp155Gly) c.382T>G (p.Trp128Gly) c.421T>G (p.Trp141Gly) | ClinVar dbSNP |
| X | g.154368001A>G | CA415250419 | FLNA | c.463T>C (p.Trp155Arg) c.382T>C (p.Trp128Arg) c.421T>C (p.Trp141Arg) | |
| X | g.154368001A>T | CA415250403 | FLNA | c.463T>A (p.Trp155Arg) c.382T>A (p.Trp128Arg) c.421T>A (p.Trp141Arg) | |
| X | g.154368002C>A | CA324452 | FLNA | c.462G>T (p.Met154Ile) c.381G>T (p.Met127Ile) c.420G>T (p.Met140Ile) | ClinVar dbSNP |
| X | g.154368002C= | CA2466659085 | FLNA | c.462G= (p.Met154=) c.381G= (p.Met127=) c.420G= (p.Met140=) | |
| X | g.154368002C>G | CA415250424 | FLNA | c.462G>C (p.Met154Ile) c.381G>C (p.Met127Ile) c.420G>C (p.Met140Ile) | |
| X | g.154368002C>T | CA415250429 | FLNA | c.462G>A (p.Met154Ile) c.381G>A (p.Met127Ile) c.420G>A (p.Met140Ile) | dbSNP gnomAD v2 gnomAD v4 |
| X | g.154368003A= | CA2466659086 | FLNA | c.461T= (p.Met154=) c.380T= (p.Met127=) c.419T= (p.Met140=) | |
| X | g.154368003A>C | CA415250439 | FLNA | c.461T>G (p.Met154Arg) c.380T>G (p.Met127Arg) c.419T>G (p.Met140Arg) | ClinVar |
| X | g.154368003A>G | CA10561407 | FLNA | c.461T>C (p.Met154Thr) c.380T>C (p.Met127Thr) c.419T>C (p.Met140Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.154368003A>T | CA415250440 | FLNA | c.461T>A (p.Met154Lys) c.380T>A (p.Met127Lys) c.419T>A (p.Met140Lys) | |
| X | g.154368004T>A | CA415250446 | FLNA | c.460A>T (p.Met154Leu) c.379A>T (p.Met127Leu) c.418A>T (p.Met140Leu) | |
| X | g.154368004T>C | CA415250452 | FLNA | c.460A>G (p.Met154Val) c.379A>G (p.Met127Val) c.418A>G (p.Met140Val) | |
| X | g.154368004T>G | CA415250457 | FLNA | c.460A>C (p.Met154Leu) c.379A>C (p.Met127Leu) c.418A>C (p.Met140Leu) | |
| X | g.154368005G>A | CA519277146 | FLNA | c.459C>T (p.Pro153=) c.378C>T (p.Pro126=) c.417C>T (p.Pro139=) | |
| X | g.154368005G>C | CA519277147 | FLNA | c.459C>G (p.Pro153=) c.378C>G (p.Pro126=) c.417C>G (p.Pro139=) | |
| X | g.154368005G>T | CA519277145 | FLNA | c.459C>A (p.Pro153=) c.378C>A (p.Pro126=) c.417C>A (p.Pro139=) | |
| X | g.154368006G>A | CA415250462 | FLNA | c.458C>T (p.Pro153Leu) c.377C>T (p.Pro126Leu) c.416C>T (p.Pro139Leu) | |
| X | g.154368006G>C | CA415250466 | FLNA | c.458C>G (p.Pro153Arg) c.377C>G (p.Pro126Arg) c.416C>G (p.Pro139Arg) | |
| X | g.154368006G>T | CA415250467 | FLNA | c.458C>A (p.Pro153His) c.377C>A (p.Pro126His) c.416C>A (p.Pro139His) | |
| X | g.154368007G>A | CA415250477 | FLNA | c.457C>T (p.Pro153Ser) c.376C>T (p.Pro126Ser) c.415C>T (p.Pro139Ser) | |
| X | g.154368007G>C | CA415250471 | FLNA | c.457C>G (p.Pro153Ala) c.376C>G (p.Pro126Ala) c.415C>G (p.Pro139Ala) | |
| X | g.154368007G>T | CA415250474 | FLNA | c.457C>A (p.Pro153Thr) c.376C>A (p.Pro126Thr) c.415C>A (p.Pro139Thr) | gnomAD v4 |
| X | g.154368008C>A | CA415250481 | FLNA | c.456G>T (p.Met152Ile) c.375G>T (p.Met125Ile) c.414G>T (p.Met138Ile) | |
| X | g.154368008C>G | CA415250486 | FLNA | c.456G>C (p.Met152Ile) c.375G>C (p.Met125Ile) c.414G>C (p.Met138Ile) | |
| X | g.154368008C>T | CA415250487 | FLNA | c.456G>A (p.Met152Ile) c.375G>A (p.Met125Ile) c.414G>A (p.Met138Ile) | |
| X | g.154368009A= | CA2466659087 | FLNA | c.455T= (p.Met152=) c.374T= (p.Met125=) c.413T= (p.Met138=) | |
| X | g.154368009A>C | CA415250491 | FLNA | c.455T>G (p.Met152Arg) c.374T>G (p.Met125Arg) c.413T>G (p.Met138Arg) | |
| X | g.154368009A>G | CA415250495 | FLNA | c.455T>C (p.Met152Thr) c.374T>C (p.Met125Thr) c.413T>C (p.Met138Thr) | dbSNP |
| X | g.154368009A>T | CA415250497 | FLNA | c.455T>A (p.Met152Lys) c.374T>A (p.Met125Lys) c.413T>A (p.Met138Lys) | |
| X | g.154368010T>A | CA415250500 | FLNA | c.454A>T (p.Met152Leu) c.373A>T (p.Met125Leu) c.412A>T (p.Met138Leu) | |
| X | g.154368010T>C | CA415250503 | FLNA | c.454A>G (p.Met152Val) c.373A>G (p.Met125Val) c.412A>G (p.Met138Val) | |
| X | g.154368010T>G | CA415250505 | FLNA | c.454A>C (p.Met152Leu) c.373A>C (p.Met125Leu) c.412A>C (p.Met138Leu) | dbSNP gnomAD v4 |
| X | g.154368011G>A | CA10561408 | FLNA | c.453C>T (p.Ser151=) c.372C>T (p.Ser124=) c.411C>T (p.Ser137=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.154368011G>C | CA519277149 | FLNA | c.453C>G (p.Ser151=) c.372C>G (p.Ser124=) c.411C>G (p.Ser137=) | |
| X | g.154368011G= | CA2466659088 | FLNA | c.453C= (p.Ser151=) c.372C= (p.Ser124=) c.411C= (p.Ser137=) | |
| X | g.154368011G>T | CA519277148 | FLNA | c.453C>A (p.Ser151=) c.372C>A (p.Ser124=) c.411C>A (p.Ser137=) | |
| X | g.154368012G>A | CA415250513 | FLNA | c.452C>T (p.Ser151Phe) c.371C>T (p.Ser124Phe) c.410C>T (p.Ser137Phe) | |
| X | g.154368012G>C | CA415250519 | FLNA | c.452C>G (p.Ser151Cys) c.371C>G (p.Ser124Cys) c.410C>G (p.Ser137Cys) | dbSNP |
| X | g.154368012G>T | CA415250517 | FLNA | c.452C>A (p.Ser151Tyr) c.371C>A (p.Ser124Tyr) c.410C>A (p.Ser137Tyr) | |
| X | g.154368013A>C | CA415250520 | FLNA | c.451T>G (p.Ser151Ala) c.370T>G (p.Ser124Ala) c.409T>G (p.Ser137Ala) | |
| X | g.154368013A>G | CA415250522 | FLNA | c.451T>C (p.Ser151Pro) c.370T>C (p.Ser124Pro) c.409T>C (p.Ser137Pro) | |
| X | g.154368013A>T | CA415250526 | FLNA | c.451T>A (p.Ser151Thr) c.370T>A (p.Ser124Thr) c.409T>A (p.Ser137Thr) | |
| X | g.154368014G>A | CA519277150 | FLNA | c.450C>T (p.Ile150=) c.369C>T (p.Ile123=) c.408C>T (p.Ile136=) | |
| X | g.154368014G>C | CA415250529 | FLNA | c.450C>G (p.Ile150Met) c.369C>G (p.Ile123Met) c.408C>G (p.Ile136Met) | |
| X | g.154368014G>T | CA519277151 | FLNA | c.450C>A (p.Ile150=) c.369C>A (p.Ile123=) c.408C>A (p.Ile136=) | |
| X | g.154368015A>C | CA415250530 | FLNA | c.449T>G (p.Ile150Ser) c.368T>G (p.Ile123Ser) c.407T>G (p.Ile136Ser) | |
| X | g.154368015A>G | CA415250531 | FLNA | c.449T>C (p.Ile150Thr) c.368T>C (p.Ile123Thr) c.407T>C (p.Ile136Thr) | |
| X | g.154368015A>T | CA415250532 | FLNA | c.449T>A (p.Ile150Asn) c.368T>A (p.Ile123Asn) c.407T>A (p.Ile136Asn) | |
| X | g.154368016T>A | CA415250536 | FLNA | c.448A>T (p.Ile150Phe) c.367A>T (p.Ile123Phe) c.406A>T (p.Ile136Phe) | |
| X | g.154368016T>C | CA415250539 | FLNA | c.448A>G (p.Ile150Val) c.367A>G (p.Ile123Val) c.406A>G (p.Ile136Val) | |
| X | g.154368016T>G | CA415250543 | FLNA | c.448A>C (p.Ile150Leu) c.367A>C (p.Ile123Leu) c.406A>C (p.Ile136Leu) | |
| X | g.154368017G>A | CA519277152 | FLNA | c.447C>T (p.Ser149=) c.366C>T (p.Ser122=) c.405C>T (p.Ser135=) | gnomAD v4 |
| X | g.154368017G>C | CA519277153 | FLNA | c.447C>G (p.Ser149=) c.366C>G (p.Ser122=) c.405C>G (p.Ser135=) | |
| X | g.154368017G>T | CA519277154 | FLNA | c.447C>A (p.Ser149=) c.366C>A (p.Ser122=) c.405C>A (p.Ser135=) | |
| X | g.154368018G>A | CA415250551 | FLNA | c.446C>T (p.Ser149Phe) c.365C>T (p.Ser122Phe) c.404C>T (p.Ser135Phe) | |
| X | g.154368018G>C | CA415250569 | FLNA | c.446C>G (p.Ser149Cys) c.365C>G (p.Ser122Cys) c.404C>G (p.Ser135Cys) | |
| X | g.154368018G>T | CA415250573 | FLNA | c.446C>A (p.Ser149Tyr) c.365C>A (p.Ser122Tyr) c.404C>A (p.Ser135Tyr) | |
| X | g.154368019A>C | CA415250593 | FLNA | c.445T>G (p.Ser149Ala) c.364T>G (p.Ser122Ala) c.403T>G (p.Ser135Ala) | gnomAD v4 |
| X | g.154368019A>G | CA415250583 | FLNA | c.445T>C (p.Ser149Pro) c.364T>C (p.Ser122Pro) c.403T>C (p.Ser135Pro) | |
| X | g.154368019A>T | CA415250588 | FLNA | c.445T>A (p.Ser149Thr) c.364T>A (p.Ser122Thr) c.403T>A (p.Ser135Thr) | |
| X | g.154368020G>A | CA337284437 | FLNA | c.444C>T (p.Tyr148=) c.363C>T (p.Tyr121=) c.402C>T (p.Tyr134=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| X | g.154368020G>C | CA415250598 | FLNA | c.444C>G (p.Tyr148Ter) c.363C>G (p.Tyr121Ter) c.402C>G (p.Tyr134Ter) | |
| X | g.154368020G= | CA2466659089 | FLNA | c.444C= (p.Tyr148=) c.363C= (p.Tyr121=) c.402C= (p.Tyr134=) | |
| X | g.154368020G>T | CA415250602 | FLNA | c.444C>A (p.Tyr148Ter) c.363C>A (p.Tyr121Ter) c.402C>A (p.Tyr134Ter) |