| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 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) | |
| X | g.154368021T>A | CA415250613 | FLNA | c.443A>T (p.Tyr148Phe) c.362A>T (p.Tyr121Phe) c.401A>T (p.Tyr134Phe) | |
| X | g.154368021T>C | CA415250619 | FLNA | c.443A>G (p.Tyr148Cys) c.362A>G (p.Tyr121Cys) c.401A>G (p.Tyr134Cys) | |
| X | g.154368021T>G | CA415250628 | FLNA | c.443A>C (p.Tyr148Ser) c.362A>C (p.Tyr121Ser) c.401A>C (p.Tyr134Ser) | |
| X | g.154368022A>C | CA415250631 | FLNA | c.442T>G (p.Tyr148Asp) c.361T>G (p.Tyr121Asp) c.400T>G (p.Tyr134Asp) | |
| X | g.154368022A>G | CA415250633 | FLNA | c.442T>C (p.Tyr148His) c.361T>C (p.Tyr121His) c.400T>C (p.Tyr134His) | |
| X | g.154368022A>T | CA415250638 | FLNA | c.442T>A (p.Tyr148Asn) c.361T>A (p.Tyr121Asn) c.400T>A (p.Tyr134Asn) | |
| X | g.154368023G>A | CA10561409 | FLNA | c.441C>T (p.His147=) c.360C>T (p.His120=) c.399C>T (p.His133=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.154368023G>C | CA415250649 | FLNA | c.441C>G (p.His147Gln) c.360C>G (p.His120Gln) c.399C>G (p.His133Gln) | |
| X | g.154368023G= | CA2466659090 | FLNA | c.441C= (p.His147=) c.360C= (p.His120=) c.399C= (p.His133=) | |
| X | g.154368023G>T | CA415250652 | FLNA | c.441C>A (p.His147Gln) c.360C>A (p.His120Gln) c.399C>A (p.His133Gln) | gnomAD v4 |
| X | g.154368024T>A | CA415250655 | FLNA | c.440A>T (p.His147Leu) c.359A>T (p.His120Leu) c.398A>T (p.His133Leu) | |
| X | g.154368024T>C | CA415250660 | FLNA | c.440A>G (p.His147Arg) c.359A>G (p.His120Arg) c.398A>G (p.His133Arg) | |
| X | g.154368024T>G | CA415250657 | FLNA | c.440A>C (p.His147Pro) c.359A>C (p.His120Pro) c.398A>C (p.His133Pro) | |
| X | g.154368025G>A | CA415250664 | FLNA | c.439C>T (p.His147Tyr) c.358C>T (p.His120Tyr) c.397C>T (p.His133Tyr) | gnomAD v4 COSMIC COSMIC |
| X | g.154368025G>C | CA415250666 | FLNA | c.439C>G (p.His147Asp) c.358C>G (p.His120Asp) c.397C>G (p.His133Asp) | |
| X | g.154368025G>T | CA415250675 | FLNA | c.439C>A (p.His147Asn) c.358C>A (p.His120Asn) c.397C>A (p.His133Asn) | |
| X | g.154368026C>A | CA519277156 | FLNA | c.438G>T (p.Leu146=) c.357G>T (p.Leu119=) c.396G>T (p.Leu132=) | |
| X | g.154368026C>G | CA519277158 | FLNA | c.438G>C (p.Leu146=) c.357G>C (p.Leu119=) c.396G>C (p.Leu132=) | |
| X | g.154368026C>T | CA519277157 | FLNA | c.438G>A (p.Leu146=) c.357G>A (p.Leu119=) c.396G>A (p.Leu132=) | gnomAD v4 |
| X | g.154368027A>C | CA415250680 | FLNA | c.437T>G (p.Leu146Arg) c.356T>G (p.Leu119Arg) c.395T>G (p.Leu132Arg) | |
| X | g.154368027A>G | CA415250683 | FLNA | c.437T>C (p.Leu146Pro) c.356T>C (p.Leu119Pro) c.395T>C (p.Leu132Pro) | |
| X | g.154368027A>T | CA415250685 | FLNA | c.437T>A (p.Leu146Gln) c.356T>A (p.Leu119Gln) c.395T>A (p.Leu132Gln) | |
| X | g.154368028G>A | CA519277159 | FLNA | c.436C>T (p.Leu146=) c.355C>T (p.Leu119=) c.394C>T (p.Leu132=) | |
| X | g.154368028G>C | CA415250689 | FLNA | c.436C>G (p.Leu146Val) c.355C>G (p.Leu119Val) c.394C>G (p.Leu132Val) | |
| X | g.154368028G>T | CA415250692 | FLNA | c.436C>A (p.Leu146Met) c.355C>A (p.Leu119Met) c.394C>A (p.Leu132Met) | |
| X | g.154368029G>A | CA519277160 | FLNA | c.435C>T (p.Ile145=) c.354C>T (p.Ile118=) c.393C>T (p.Ile131=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.154368029G>C | CA415250695 | FLNA | c.435C>G (p.Ile145Met) c.354C>G (p.Ile118Met) c.393C>G (p.Ile131Met) | |
| X | g.154368029G= | CA2466659091 | FLNA | c.435C= (p.Ile145=) c.354C= (p.Ile118=) c.393C= (p.Ile131=) | |
| X | g.154368029G>T | CA519277162 | FLNA | c.435C>A (p.Ile145=) c.354C>A (p.Ile118=) c.393C>A (p.Ile131=) | ClinVar gnomAD v4 |
| X | g.154368030A>C | CA415250699 | FLNA | c.434T>G (p.Ile145Ser) c.353T>G (p.Ile118Ser) c.392T>G (p.Ile131Ser) | |
| X | g.154368030A>G | CA415250702 | FLNA | c.434T>C (p.Ile145Thr) c.353T>C (p.Ile118Thr) c.392T>C (p.Ile131Thr) | |
| X | g.154368030A>T | CA415250705 | FLNA | c.434T>A (p.Ile145Asn) c.353T>A (p.Ile118Asn) c.392T>A (p.Ile131Asn) | |
| X | g.154368031T>A | CA415250710 | FLNA | c.433A>T (p.Ile145Phe) c.352A>T (p.Ile118Phe) c.391A>T (p.Ile131Phe) | |
| X | g.154368031T>C | CA415250716 | FLNA | c.433A>G (p.Ile145Val) c.352A>G (p.Ile118Val) c.391A>G (p.Ile131Val) | |
| X | g.154368031T>G | CA415250714 | FLNA | c.433A>C (p.Ile145Leu) c.352A>C (p.Ile118Leu) c.391A>C (p.Ile131Leu) | |
| X | g.154368032C>A | CA519277163 | FLNA | c.432G>T (p.Leu144=) c.351G>T (p.Leu117=) c.390G>T (p.Leu130=) | |
| X | g.154368032C>G | CA519277165 | FLNA | c.432G>C (p.Leu144=) c.351G>C (p.Leu117=) c.390G>C (p.Leu130=) | gnomAD v4 |
| X | g.154368032C>T | CA519277164 | FLNA | c.432G>A (p.Leu144=) c.351G>A (p.Leu117=) c.390G>A (p.Leu130=) | gnomAD v4 |
| X | g.154368033A>C | CA415250730 | FLNA | c.431T>G (p.Leu144Arg) c.350T>G (p.Leu117Arg) c.389T>G (p.Leu130Arg) | |
| X | g.154368033A>G | CA415250732 | FLNA | c.431T>C (p.Leu144Pro) c.350T>C (p.Leu117Pro) c.389T>C (p.Leu130Pro) | |
| X | g.154368033A>T | CA415250734 | FLNA | c.431T>A (p.Leu144Gln) c.350T>A (p.Leu117Gln) c.389T>A (p.Leu130Gln) | |
| X | g.154368034G>A | CA519277166 | FLNA | c.430C>T (p.Leu144=) c.349C>T (p.Leu117=) c.388C>T (p.Leu130=) | |
| X | g.154368034G>C | CA415250738 | FLNA | c.430C>G (p.Leu144Val) c.349C>G (p.Leu117Val) c.388C>G (p.Leu130Val) | |
| X | g.154368034G>T | CA415250740 | FLNA | c.430C>A (p.Leu144Met) c.349C>A (p.Leu117Met) c.388C>A (p.Leu130Met) | |
| X | g.154368035G>A | CA519277167 | FLNA | c.429C>T (p.Thr143=) c.348C>T (p.Thr116=) c.387C>T (p.Thr129=) | |
| X | g.154368035G>C | CA519277168 | FLNA | c.429C>G (p.Thr143=) c.348C>G (p.Thr116=) c.387C>G (p.Thr129=) | |
| X | g.154368035G>T | CA519277169 | FLNA | c.429C>A (p.Thr143=) c.348C>A (p.Thr116=) c.387C>A (p.Thr129=) | COSMIC COSMIC |
| X | g.154368036G>A | CA415250744 | FLNA | c.428C>T (p.Thr143Ile) c.347C>T (p.Thr116Ile) c.386C>T (p.Thr129Ile) | ClinVar dbSNP |
| X | g.154368036G>C | CA415250751 | FLNA | c.428C>G (p.Thr143Ser) c.347C>G (p.Thr116Ser) c.386C>G (p.Thr129Ser) | |
| X | g.154368036G= | CA2466659092 | FLNA | c.428C= (p.Thr143=) c.347C= (p.Thr116=) c.386C= (p.Thr129=) | |
| X | g.154368036G>T | CA415250754 | FLNA | c.428C>A (p.Thr143Asn) c.347C>A (p.Thr116Asn) c.386C>A (p.Thr129Asn) | |
| X | g.154368037T>A | CA415250774 | FLNA | c.427A>T (p.Thr143Ser) c.346A>T (p.Thr116Ser) c.385A>T (p.Thr129Ser) | |
| X | g.154368037T>C | CA415250771 | FLNA | c.427A>G (p.Thr143Ala) c.346A>G (p.Thr116Ala) c.385A>G (p.Thr129Ala) | |
| X | g.154368037T>G | CA415250769 | FLNA | c.427A>C (p.Thr143Pro) c.346A>C (p.Thr116Pro) c.385A>C (p.Thr129Pro) | |
| X | g.154368038C>A | CA415250775 | FLNA | c.426G>T (p.Trp142Cys) c.345G>T (p.Trp115Cys) c.384G>T (p.Trp128Cys) | |
| X | g.154368038C>G | CA415250779 | FLNA | c.426G>C (p.Trp142Cys) c.345G>C (p.Trp115Cys) c.384G>C (p.Trp128Cys) | |
| X | g.154368038C>T | CA415250777 | FLNA | c.426G>A (p.Trp142Ter) c.345G>A (p.Trp115Ter) c.384G>A (p.Trp128Ter) | |
| X | g.154368039del | CA2579738372 | FLNA | c.426del (p.Trp142Ter) c.345del (p.Trp115Ter) c.384del (p.Trp128Ter) | |
| X | g.154368039C>A | CA16608824 | FLNA | c.425G>T (p.Trp142Leu) c.344G>T (p.Trp115Leu) c.383G>T (p.Trp128Leu) | ClinVar dbSNP |
| X | g.154368039C= | CA2466659093 | FLNA | c.425G= (p.Trp142=) c.344G= (p.Trp115=) c.383G= (p.Trp128=) | |
| X | g.154368039C>G | CA415250789 | FLNA | c.425G>C (p.Trp142Ser) c.344G>C (p.Trp115Ser) c.383G>C (p.Trp128Ser) | |
| X | g.154368039C>T | CA415250783 | FLNA | c.425G>A (p.Trp142Ter) c.344G>A (p.Trp115Ter) c.383G>A (p.Trp128Ter) | |
| X | g.154368040A>C | CA415250793 | FLNA | c.424T>G (p.Trp142Gly) c.343T>G (p.Trp115Gly) c.382T>G (p.Trp128Gly) | |
| X | g.154368040A>G | CA415250795 | FLNA | c.424T>C (p.Trp142Arg) c.343T>C (p.Trp115Arg) c.382T>C (p.Trp128Arg) | COSMIC COSMIC |
| X | g.154368040A>T | CA415250797 | FLNA | c.424T>A (p.Trp142Arg) c.343T>A (p.Trp115Arg) c.382T>A (p.Trp128Arg) | |
| X | g.154368041G>A | CA10561410 | FLNA | c.423C>T (p.Ile141=) c.342C>T (p.Ile114=) c.381C>T (p.Ile127=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.154368041G>C | CA415250801 | FLNA | c.423C>G (p.Ile141Met) c.342C>G (p.Ile114Met) c.381C>G (p.Ile127Met) | |
| X | g.154368041G= | CA2466659094 | FLNA | c.423C= (p.Ile141=) c.342C= (p.Ile114=) c.381C= (p.Ile127=) | |
| X | g.154368041G>T | CA519277170 | FLNA | c.423C>A (p.Ile141=) c.342C>A (p.Ile114=) c.381C>A (p.Ile127=) | ClinVar |
| X | g.154368042A>C | CA415250805 | FLNA | c.422T>G (p.Ile141Ser) c.341T>G (p.Ile114Ser) c.380T>G (p.Ile127Ser) | |
| X | g.154368042A>G | CA415250809 | FLNA | c.422T>C (p.Ile141Thr) c.341T>C (p.Ile114Thr) c.380T>C (p.Ile127Thr) | |
| X | g.154368042A>T | CA415250810 | FLNA | c.422T>A (p.Ile141Asn) c.341T>A (p.Ile114Asn) c.380T>A (p.Ile127Asn) | |
| X | g.154368043T>A | CA415250811 | FLNA | c.421A>T (p.Ile141Phe) c.340A>T (p.Ile114Phe) c.379A>T (p.Ile127Phe) | |
| X | g.154368043T>C | CA415250812 | FLNA | c.421A>G (p.Ile141Val) c.340A>G (p.Ile114Val) c.379A>G (p.Ile127Val) | |
| X | g.154368043T>G | CA415250813 | FLNA | c.421A>C (p.Ile141Leu) c.340A>C (p.Ile114Leu) c.379A>C (p.Ile127Leu) | |
| X | g.154368044G>A | CA519277171 | FLNA | c.420C>T (p.Leu140=) c.339C>T (p.Leu113=) c.378C>T (p.Leu126=) | gnomAD v4 |
| X | g.154368044G>C | CA519277172 | FLNA | c.420C>G (p.Leu140=) c.339C>G (p.Leu113=) c.378C>G (p.Leu126=) | |
| X | g.154368044G>T | CA519277173 | FLNA | c.420C>A (p.Leu140=) c.339C>A (p.Leu113=) c.378C>A (p.Leu126=) | |
| X | g.154368045A>C | CA415250816 | FLNA | c.419T>G (p.Leu140Arg) c.338T>G (p.Leu113Arg) c.377T>G (p.Leu126Arg) | |
| X | g.154368045A>G | CA415250814 | FLNA | c.419T>C (p.Leu140Pro) c.338T>C (p.Leu113Pro) c.377T>C (p.Leu126Pro) | |
| X | g.154368045A>T | CA415250815 | FLNA | c.419T>A (p.Leu140His) c.338T>A (p.Leu113His) c.377T>A (p.Leu126His) | |
| X | g.154368046G>A | CA415250818 | FLNA | c.418C>T (p.Leu140Phe) c.337C>T (p.Leu113Phe) c.376C>T (p.Leu126Phe) | ClinVar dbSNP |
| X | g.154368046G>C | CA415250820 | FLNA | c.418C>G (p.Leu140Val) c.337C>G (p.Leu113Val) c.376C>G (p.Leu126Val) | |
| X | g.154368046G>T | CA415250821 | FLNA | c.418C>A (p.Leu140Ile) c.337C>A (p.Leu113Ile) c.376C>A (p.Leu126Ile) | |
| X | g.154368047G>A | CA519277174 | FLNA | c.417C>T (p.Gly139=) c.336C>T (p.Gly112=) c.375C>T (p.Gly125=) | ClinVar |
| X | g.154368047G>C | CA519277176 | FLNA | c.417C>G (p.Gly139=) c.336C>G (p.Gly112=) c.375C>G (p.Gly125=) | |
| X | g.154368047G>T | CA519277175 | FLNA | c.417C>A (p.Gly139=) c.336C>A (p.Gly112=) c.375C>A (p.Gly125=) | |
| X | g.154368048C>A | CA415250823 | FLNA | c.416G>T (p.Gly139Val) c.335G>T (p.Gly112Val) c.374G>T (p.Gly125Val) | |
| X | g.154368048C>G | CA415250826 | FLNA | c.416G>C (p.Gly139Ala) c.335G>C (p.Gly112Ala) c.374G>C (p.Gly125Ala) | |
| X | g.154368048C>T | CA415250828 | FLNA | c.416G>A (p.Gly139Asp) c.335G>A (p.Gly112Asp) c.374G>A (p.Gly125Asp) | |
| X | g.154368049C>A | CA415250834 | FLNA | c.415G>T (p.Gly139Cys) c.334G>T (p.Gly112Cys) c.373G>T (p.Gly125Cys) | |
| X | g.154368049C= | CA2466659095 | FLNA | c.415G= (p.Gly139=) c.334G= (p.Gly112=) c.373G= (p.Gly125=) | |
| X | g.154368049C>G | CA415250836 | FLNA | c.415G>C (p.Gly139Arg) c.334G>C (p.Gly112Arg) c.373G>C (p.Gly125Arg) | ClinVar dbSNP |
| X | g.154368049C>T | CA415250839 | FLNA | c.415G>A (p.Gly139Ser) c.334G>A (p.Gly112Ser) c.373G>A (p.Gly125Ser) | |
| X | g.154368050C>A | CA519277177 | FLNA | c.414G>T (p.Leu138=) c.333G>T (p.Leu111=) c.372G>T (p.Leu124=) | COSMIC COSMIC |
| X | g.154368050C>G | CA519277179 | FLNA | c.414G>C (p.Leu138=) c.333G>C (p.Leu111=) c.372G>C (p.Leu124=) | |
| X | g.154368050C>T | CA519277178 | FLNA | c.414G>A (p.Leu138=) c.333G>A (p.Leu111=) c.372G>A (p.Leu124=) | gnomAD v4 |
| X | g.154368051A>C | CA415250846 | FLNA | c.413T>G (p.Leu138Arg) c.332T>G (p.Leu111Arg) c.371T>G (p.Leu124Arg) | |
| X | g.154368051A>G | CA415250844 | FLNA | c.413T>C (p.Leu138Pro) c.332T>C (p.Leu111Pro) c.371T>C (p.Leu124Pro) | |
| X | g.154368051A>T | CA415250842 | FLNA | c.413T>A (p.Leu138Gln) c.332T>A (p.Leu111Gln) c.371T>A (p.Leu124Gln) | |
| X | g.154368052G>A | CA519277180 | FLNA | c.412C>T (p.Leu138=) c.331C>T (p.Leu111=) c.370C>T (p.Leu124=) | |
| X | g.154368052G>C | CA415250847 | FLNA | c.412C>G (p.Leu138Val) c.331C>G (p.Leu111Val) c.370C>G (p.Leu124Val) | |
| X | g.154368052G>T | CA415250849 | FLNA | c.412C>A (p.Leu138Met) c.331C>A (p.Leu111Met) c.370C>A (p.Leu124Met) | |
| X | g.154368053G>A | CA519277181 | FLNA | c.411C>T (p.Ile137=) c.330C>T (p.Ile110=) c.369C>T (p.Ile123=) | COSMIC COSMIC |
| X | g.154368053G>C | CA415250855 | FLNA | c.411C>G (p.Ile137Met) c.330C>G (p.Ile110Met) c.369C>G (p.Ile123Met) | |
| X | g.154368053G>T | CA519277182 | FLNA | c.411C>A (p.Ile137=) c.330C>A (p.Ile110=) c.369C>A (p.Ile123=) | |
| X | g.154368054A= | CA2466659096 | FLNA | c.410T= (p.Ile137=) c.329T= (p.Ile110=) c.368T= (p.Ile123=) | |
| X | g.154368054A>C | CA415250857 | FLNA | c.410T>G (p.Ile137Ser) c.329T>G (p.Ile110Ser) c.368T>G (p.Ile123Ser) | |
| X | g.154368054A>G | CA415250860 | FLNA | c.410T>C (p.Ile137Thr) c.329T>C (p.Ile110Thr) c.368T>C (p.Ile123Thr) | |
| X | g.154368054A>T | CA415250863 | FLNA | c.410T>A (p.Ile137Asn) c.329T>A (p.Ile110Asn) c.368T>A (p.Ile123Asn) | ClinVar dbSNP |
| X | g.154368055T>A | CA415250867 | FLNA | c.409A>T (p.Ile137Phe) c.328A>T (p.Ile110Phe) c.367A>T (p.Ile123Phe) | |
| X | g.154368055T>C | CA415250873 | FLNA | c.409A>G (p.Ile137Val) c.328A>G (p.Ile110Val) c.367A>G (p.Ile123Val) | |
| X | g.154368055T>G | CA415250876 | FLNA | c.409A>C (p.Ile137Leu) c.328A>C (p.Ile110Leu) c.367A>C (p.Ile123Leu) | |
| X | g.154368056C>A | CA519277183 | FLNA | c.408G>T (p.Leu136=) c.327G>T (p.Leu109=) c.366G>T (p.Leu122=) | |
| X | g.154368056C>G | CA519277184 | FLNA | c.408G>C (p.Leu136=) c.327G>C (p.Leu109=) c.366G>C (p.Leu122=) | gnomAD v4 |
| X | g.154368056C>T | CA519277185 | FLNA | c.408G>A (p.Leu136=) c.327G>A (p.Leu109=) c.366G>A (p.Leu122=) | |
| X | g.154368057A>C | CA415250882 | FLNA | c.407T>G (p.Leu136Arg) c.326T>G (p.Leu109Arg) c.365T>G (p.Leu122Arg) | |
| X | g.154368057A>G | CA415250888 | FLNA | c.407T>C (p.Leu136Pro) c.326T>C (p.Leu109Pro) c.365T>C (p.Leu122Pro) | |
| X | g.154368057A>T | CA415250904 | FLNA | c.407T>A (p.Leu136Gln) c.326T>A (p.Leu109Gln) c.365T>A (p.Leu122Gln) | |
| X | g.154368058G>A | CA519277186 | FLNA | c.406C>T (p.Leu136=) c.325C>T (p.Leu109=) c.364C>T (p.Leu122=) | ClinVar gnomAD v4 |
| X | g.154368058G>C | CA415250910 | FLNA | c.406C>G (p.Leu136Val) c.325C>G (p.Leu109Val) c.364C>G (p.Leu122Val) | |
| X | g.154368058G>T | CA415250912 | FLNA | c.406C>A (p.Leu136Met) c.325C>A (p.Leu109Met) c.364C>A (p.Leu122Met) | |
| X | g.154368059C>A | CA415250914 | FLNA | c.405G>T (p.Lys135Asn) c.324G>T (p.Lys108Asn) c.363G>T (p.Lys121Asn) | |
| X | g.154368059C>G | CA415250919 | FLNA | c.405G>C (p.Lys135Asn) c.324G>C (p.Lys108Asn) c.363G>C (p.Lys121Asn) | |
| X | g.154368059C>T | CA519277187 | FLNA | c.405G>A (p.Lys135=) c.324G>A (p.Lys108=) c.363G>A (p.Lys121=) | |
| X | g.154368060T>A | CA415250922 | FLNA | c.404A>T (p.Lys135Met) c.323A>T (p.Lys108Met) c.362A>T (p.Lys121Met) | |
| X | g.154368060T>C | CA415250923 | FLNA | c.404A>G (p.Lys135Arg) c.323A>G (p.Lys108Arg) c.362A>G (p.Lys121Arg) | |
| X | g.154368060T>G | CA415250924 | FLNA | c.404A>C (p.Lys135Thr) c.323A>C (p.Lys108Thr) c.362A>C (p.Lys121Thr) | |
| X | g.154368061T>A | CA415250926 | FLNA | c.403A>T (p.Lys135Ter) c.322A>T (p.Lys108Ter) c.361A>T (p.Lys121Ter) | |
| X | g.154368061T>C | CA415250927 | FLNA | c.403A>G (p.Lys135Glu) c.322A>G (p.Lys108Glu) c.361A>G (p.Lys121Glu) | |
| X | g.154368061T>G | CA415250928 | FLNA | c.403A>C (p.Lys135Gln) c.322A>C (p.Lys108Gln) c.361A>C (p.Lys121Gln) | |
| X | g.154368062C>A | CA519277188 | FLNA | c.402G>T (p.Leu134=) c.321G>T (p.Leu107=) c.360G>T (p.Leu120=) | |
| X | g.154368062C>G | CA519277190 | FLNA | c.402G>C (p.Leu134=) c.321G>C (p.Leu107=) c.360G>C (p.Leu120=) | |
| X | g.154368062C>T | CA519277189 | FLNA | c.402G>A (p.Leu134=) c.321G>A (p.Leu107=) c.360G>A (p.Leu120=) | ClinVar COSMIC COSMIC |
| X | g.154368063A>C | CA415250933 | FLNA | c.401T>G (p.Leu134Arg) c.320T>G (p.Leu107Arg) c.359T>G (p.Leu120Arg) | |
| X | g.154368063A>G | CA415250937 | FLNA | c.401T>C (p.Leu134Pro) c.320T>C (p.Leu107Pro) c.359T>C (p.Leu120Pro) | |
| X | g.154368063A>T | CA415250938 | FLNA | c.401T>A (p.Leu134Gln) c.320T>A (p.Leu107Gln) c.359T>A (p.Leu120Gln) | |
| X | g.154368064G>A | CA519277191 | FLNA | c.400C>T (p.Leu134=) c.319C>T (p.Leu107=) c.358C>T (p.Leu120=) | |
| X | g.154368064G>C | CA415250940 | FLNA | c.400C>G (p.Leu134Val) c.319C>G (p.Leu107Val) c.358C>G (p.Leu120Val) | |
| X | g.154368064G>T | CA415250939 | FLNA | c.400C>A (p.Leu134Met) c.319C>A (p.Leu107Met) c.358C>A (p.Leu120Met) | |
| X | g.154368065G>A | CA519277192 | FLNA | c.399C>T (p.Asn133=) c.318C>T (p.Asn106=) c.357C>T (p.Asn119=) | |
| X | g.154368065G>C | CA415250942 | FLNA | c.399C>G (p.Asn133Lys) c.318C>G (p.Asn106Lys) c.357C>G (p.Asn119Lys) | |
| X | g.154368065G= | CA2466659097 | FLNA | c.399C= (p.Asn133=) c.318C= (p.Asn106=) c.357C= (p.Asn119=) | |
| X | g.154368065G>T | CA415250944 | FLNA | c.399C>A (p.Asn133Lys) c.318C>A (p.Asn106Lys) c.357C>A (p.Asn119Lys) | dbSNP gnomAD v2 gnomAD v4 |
| X | g.154368066T>A | CA415250949 | FLNA | c.398A>T (p.Asn133Ile) c.317A>T (p.Asn106Ile) c.356A>T (p.Asn119Ile) | |
| X | g.154368066T>C | CA415250950 | FLNA | c.398A>G (p.Asn133Ser) c.317A>G (p.Asn106Ser) c.356A>G (p.Asn119Ser) | |
| X | g.154368066T>G | CA415250951 | FLNA | c.398A>C (p.Asn133Thr) c.317A>C (p.Asn106Thr) c.356A>C (p.Asn119Thr) | |
| X | g.154368067T>A | CA415250954 | FLNA | c.397A>T (p.Asn133Tyr) c.316A>T (p.Asn106Tyr) c.355A>T (p.Asn119Tyr) | |
| X | g.154368067T>C | CA415250968 | FLNA | c.397A>G (p.Asn133Asp) c.316A>G (p.Asn106Asp) c.355A>G (p.Asn119Asp) | |
| X | g.154368067T>G | CA415250972 | FLNA | c.397A>C (p.Asn133His) c.316A>C (p.Asn106His) c.355A>C (p.Asn119His) | |
| X | g.154368068C>A | CA519277193 | FLNA | c.396G>T (p.Gly132=) c.315G>T (p.Gly105=) c.354G>T (p.Gly118=) | ClinVar dbSNP |
| X | g.154368068C= | CA2466659098 | FLNA | c.396G= (p.Gly132=) c.315G= (p.Gly105=) c.354G= (p.Gly118=) | |
| X | g.154368068C>G | CA519277194 | FLNA | c.396G>C (p.Gly132=) c.315G>C (p.Gly105=) c.354G>C (p.Gly118=) | |
| X | g.154368068C>T | CA519277195 | FLNA | c.396G>A (p.Gly132=) c.315G>A (p.Gly105=) c.354G>A (p.Gly118=) | |
| X | g.154368070dup | CA2695236984 | FLNA | c.396dup (p.Asn133GlufsTer29) c.315dup (p.Asn106GlufsTer29) c.354dup (p.Asn119GlufsTer29) | |
| X | g.154368069C>A | CA415250979 | FLNA | c.395G>T (p.Gly132Val) c.314G>T (p.Gly105Val) c.353G>T (p.Gly118Val) | |
| X | g.154368069C>G | CA415250983 | FLNA | c.395G>C (p.Gly132Ala) c.314G>C (p.Gly105Ala) c.353G>C (p.Gly118Ala) | |
| X | g.154368069C>T | CA415250985 | FLNA | c.395G>A (p.Gly132Glu) c.314G>A (p.Gly105Glu) c.353G>A (p.Gly118Glu) |