Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.154361812_154363756delinsCA | CA341137 | FLNA | c.2280+266_2827-25delinsTG c.2199+266_2746-25delinsTG c.2337+266_2884-25delinsTG c.279+1680_279+3624delinsTG c.2559+266_3106-25delinsTG c.2236+266_2783-25delinsTG c.2079+266_2626-25delinsTG | ClinVar |
X | g.154362679A>C | CA415237201 | FLNA | c.2386T>G (p.Cys796Gly) c.2305T>G (p.Cys769Gly) c.2443T>G (n.2443T>G) c.279+2757T>G c.2665T>G (n.2665T>G) c.2342T>G (n.2342T>G) c.2185T>G (p.Cys729Gly) | |
X | g.154362679A>G | CA415237203 | FLNA | c.2386T>C (p.Cys796Arg) c.2305T>C (p.Cys769Arg) c.2443T>C (n.2443T>C) c.279+2757T>C c.2665T>C (n.2665T>C) c.2342T>C (n.2342T>C) c.2185T>C (p.Cys729Arg) | |
X | g.154362679A>T | CA415237205 | FLNA | c.2386T>A (p.Cys796Ser) c.2305T>A (p.Cys769Ser) c.2443T>A (n.2443T>A) c.279+2757T>A c.2665T>A (n.2665T>A) c.2342T>A (n.2342T>A) c.2185T>A (p.Cys729Ser) | |
X | g.154362680del | CA2695237775 | FLNA | c.2385del (p.Cys796AlafsTer20) c.2304del (p.Cys769AlafsTer20) c.2442del (n.2442del) c.279+2756del c.2664del (n.2664del) c.2341del (n.2341del) c.2184del (p.Cys729AlafsTer20) | |
X | g.154362680G>A | CA519708904 | FLNA | c.2385C>T (p.Asp795=) c.2304C>T (p.Asp768=) c.2442C>T (n.2442C>T) c.279+2756C>T c.2664C>T (n.2664C>T) c.2341C>T (n.2341C>T) c.2184C>T (p.Asp728=) | |
X | g.154362680G>C | CA415237208 | FLNA | c.2385C>G (p.Asp795Glu) c.2304C>G (p.Asp768Glu) c.2442C>G (n.2442C>G) c.279+2756C>G c.2664C>G (n.2664C>G) c.2341C>G (n.2341C>G) c.2184C>G (p.Asp728Glu) | gnomAD v4 |
X | g.154362680G>T | CA415237209 | FLNA | c.2385C>A (p.Asp795Glu) c.2304C>A (p.Asp768Glu) c.2442C>A (n.2442C>A) c.279+2756C>A c.2664C>A (n.2664C>A) c.2341C>A (n.2341C>A) c.2184C>A (p.Asp728Glu) | |
X | g.154362681T>A | CA415237213 | FLNA | c.2384A>T (p.Asp795Val) c.2303A>T (p.Asp768Val) c.2441A>T (n.2441A>T) c.279+2755A>T c.2663A>T (n.2663A>T) c.2340A>T (n.2340A>T) c.2183A>T (p.Asp728Val) | |
X | g.154362681T>C | CA415237218 | FLNA | c.2384A>G (p.Asp795Gly) c.2303A>G (p.Asp768Gly) c.2441A>G (n.2441A>G) c.279+2755A>G c.2663A>G (n.2663A>G) c.2340A>G (n.2340A>G) c.2183A>G (p.Asp728Gly) | |
X | g.154362681T>G | CA415237215 | FLNA | c.2384A>C (p.Asp795Ala) c.2303A>C (p.Asp768Ala) c.2441A>C (n.2441A>C) c.279+2755A>C c.2663A>C (n.2663A>C) c.2340A>C (n.2340A>C) c.2183A>C (p.Asp728Ala) | |
X | g.154362682C>A | CA415237221 | FLNA | c.2383G>T (p.Asp795Tyr) c.2302G>T (p.Asp768Tyr) c.2440G>T (n.2440G>T) c.279+2754G>T c.2662G>T (n.2662G>T) c.2339G>T (n.2339G>T) c.2182G>T (p.Asp728Tyr) | |
X | g.154362682C>G | CA415237223 | FLNA | c.2383G>C (p.Asp795His) c.2302G>C (p.Asp768His) c.2440G>C (n.2440G>C) c.279+2754G>C c.2662G>C (n.2662G>C) c.2339G>C (n.2339G>C) c.2182G>C (p.Asp728His) | |
X | g.154362682C>T | CA415237225 | FLNA | c.2383G>A (p.Asp795Asn) c.2302G>A (p.Asp768Asn) c.2440G>A (n.2440G>A) c.279+2754G>A c.2662G>A (n.2662G>A) c.2339G>A (n.2339G>A) c.2182G>A (p.Asp728Asn) | gnomAD v4 |
X | g.154362683C>A | CA519708908 | FLNA | c.2382G>T (p.Val794=) c.2301G>T (p.Val767=) c.2439G>T (n.2439G>T) c.279+2753G>T c.2661G>T (n.2661G>T) c.2338G>T (n.2338G>T) c.2181G>T (p.Val727=) | |
X | g.154362683C= | CA2466656937 | FLNA | c.2382G= (p.Val794=) c.2301G= (p.Val767=) c.2439G= (n.2439G=) c.279+2753G= c.2661G= (n.2661G=) c.2338G= (n.2338G=) c.2181G= (p.Val727=) | |
X | g.154362683C>G | CA519708907 | FLNA | c.2382G>C (p.Val794=) c.2301G>C (p.Val767=) c.2439G>C (n.2439G>C) c.279+2753G>C c.2661G>C (n.2661G>C) c.2338G>C (n.2338G>C) c.2181G>C (p.Val727=) | |
X | g.154362683C>T | CA337281840 | FLNA | c.2382G>A (p.Val794=) c.2301G>A (p.Val767=) c.2439G>A (n.2439G>A) c.279+2753G>A c.2661G>A (n.2661G>A) c.2338G>A (n.2338G>A) c.2181G>A (p.Val727=) | dbSNP |
X | g.154362685_154362686del | CA2824295657 | FLNA | c.2381_2382del (p.Val794GlyfsTer27) c.2300_2301del (p.Val767GlyfsTer27) c.2438_2439del (n.2438_2439del) c.279+2752_279+2753del c.2660_2661del (n.2660_2661del) c.2337_2338del (n.2337_2338del) c.2180_2181del (p.Val727GlyfsTer27) | |
X | g.154362684A>C | CA415237228 | FLNA | c.2381T>G (p.Val794Gly) c.2300T>G (p.Val767Gly) c.2438T>G (n.2438T>G) c.279+2752T>G c.2660T>G (n.2660T>G) c.2337T>G (n.2337T>G) c.2180T>G (p.Val727Gly) | |
X | g.154362684A>G | CA415237230 | FLNA | c.2381T>C (p.Val794Ala) c.2300T>C (p.Val767Ala) c.2438T>C (n.2438T>C) c.279+2752T>C c.2660T>C (n.2660T>C) c.2337T>C (n.2337T>C) c.2180T>C (p.Val727Ala) | |
X | g.154362684A>T | CA415237232 | FLNA | c.2381T>A (p.Val794Glu) c.2300T>A (p.Val767Glu) c.2438T>A (n.2438T>A) c.279+2752T>A c.2660T>A (n.2660T>A) c.2337T>A (n.2337T>A) c.2180T>A (p.Val727Glu) | |
X | g.154362685C>A | CA415237236 | FLNA | c.2380G>T (p.Val794Leu) c.2299G>T (p.Val767Leu) c.2437G>T (n.2437G>T) c.279+2751G>T c.2659G>T (n.2659G>T) c.2336G>T (n.2336G>T) c.2179G>T (p.Val727Leu) | |
X | g.154362685C>G | CA415237238 | FLNA | c.2380G>C (p.Val794Leu) c.2299G>C (p.Val767Leu) c.2437G>C (n.2437G>C) c.279+2751G>C c.2659G>C (n.2659G>C) c.2336G>C (n.2336G>C) c.2179G>C (p.Val727Leu) | |
X | g.154362685C>T | CA415237240 | FLNA | c.2380G>A (p.Val794Met) c.2299G>A (p.Val767Met) c.2437G>A (n.2437G>A) c.279+2751G>A c.2659G>A (n.2659G>A) c.2336G>A (n.2336G>A) c.2179G>A (p.Val727Met) | |
X | g.154362686A= | CA2466656938 | FLNA | c.2379T= (p.Thr793=) c.2298T= (p.Thr766=) c.2436T= (n.2436T=) c.279+2750T= c.2658T= (n.2658T=) c.2335T= (n.2335T=) c.2178T= (p.Thr726=) | |
X | g.154362686A>C | CA519708911 | FLNA | c.2379T>G (p.Thr793=) c.2298T>G (p.Thr766=) c.2436T>G (n.2436T>G) c.279+2750T>G c.2658T>G (n.2658T>G) c.2335T>G (n.2335T>G) c.2178T>G (p.Thr726=) | dbSNP |
X | g.154362686A>G | CA10560949 | FLNA | c.2379T>C (p.Thr793=) c.2298T>C (p.Thr766=) c.2436T>C (n.2436T>C) c.279+2750T>C c.2658T>C (n.2658T>C) c.2335T>C (n.2335T>C) c.2178T>C (p.Thr726=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154362686A>T | CA519708912 | FLNA | c.2379T>A (p.Thr793=) c.2298T>A (p.Thr766=) c.2436T>A (n.2436T>A) c.279+2750T>A c.2658T>A (n.2658T>A) c.2335T>A (n.2335T>A) c.2178T>A (p.Thr726=) | |
X | g.154362687G>A | CA415237250 | FLNA | c.2378C>T (p.Thr793Ile) c.2297C>T (p.Thr766Ile) c.2435C>T (n.2435C>T) c.279+2749C>T c.2657C>T (n.2657C>T) c.2334C>T (n.2334C>T) c.2177C>T (p.Thr726Ile) | |
X | g.154362687G>C | CA415237247 | FLNA | c.2378C>G (p.Thr793Ser) c.2297C>G (p.Thr766Ser) c.2435C>G (n.2435C>G) c.279+2749C>G c.2657C>G (n.2657C>G) c.2334C>G (n.2334C>G) c.2177C>G (p.Thr726Ser) | |
X | g.154362687G>T | CA415237245 | FLNA | c.2378C>A (p.Thr793Asn) c.2297C>A (p.Thr766Asn) c.2435C>A (n.2435C>A) c.279+2749C>A c.2657C>A (n.2657C>A) c.2334C>A (n.2334C>A) c.2177C>A (p.Thr726Asn) | |
X | g.154362688T>A | CA415237253 | FLNA | c.2377A>T (p.Thr793Ser) c.2296A>T (p.Thr766Ser) c.2434A>T (n.2434A>T) c.279+2748A>T c.2656A>T (n.2656A>T) c.2333A>T (n.2333A>T) c.2176A>T (p.Thr726Ser) | |
X | g.154362688T>C | CA415237257 | FLNA | c.2377A>G (p.Thr793Ala) c.2296A>G (p.Thr766Ala) c.2434A>G (n.2434A>G) c.279+2748A>G c.2656A>G (n.2656A>G) c.2333A>G (n.2333A>G) c.2176A>G (p.Thr726Ala) | |
X | g.154362688T>G | CA415237255 | FLNA | c.2377A>C (p.Thr793Pro) c.2296A>C (p.Thr766Pro) c.2434A>C (n.2434A>C) c.279+2748A>C c.2656A>C (n.2656A>C) c.2333A>C (n.2333A>C) c.2176A>C (p.Thr726Pro) | |
X | g.154362689G>A | CA519708919 | FLNA | c.2376C>T (p.Phe792=) c.2295C>T (p.Phe765=) c.2433C>T (n.2433C>T) c.279+2747C>T c.2655C>T (n.2655C>T) c.2332C>T (n.2332C>T) c.2175C>T (p.Phe725=) | |
X | g.154362689G>C | CA415237260 | FLNA | c.2376C>G (p.Phe792Leu) c.2295C>G (p.Phe765Leu) c.2433C>G (n.2433C>G) c.279+2747C>G c.2655C>G (n.2655C>G) c.2332C>G (n.2332C>G) c.2175C>G (p.Phe725Leu) | |
X | g.154362689G>T | CA415237265 | FLNA | c.2376C>A (p.Phe792Leu) c.2295C>A (p.Phe765Leu) c.2433C>A (n.2433C>A) c.279+2747C>A c.2655C>A (n.2655C>A) c.2332C>A (n.2332C>A) c.2175C>A (p.Phe725Leu) | |
X | g.154362690A>C | CA415237268 | FLNA | c.2375T>G (p.Phe792Cys) c.2294T>G (p.Phe765Cys) c.2432T>G (n.2432T>G) c.279+2746T>G c.2654T>G (n.2654T>G) c.2331T>G (n.2331T>G) c.2174T>G (p.Phe725Cys) | |
X | g.154362690A>G | CA415237270 | FLNA | c.2375T>C (p.Phe792Ser) c.2294T>C (p.Phe765Ser) c.2432T>C (n.2432T>C) c.279+2746T>C c.2654T>C (n.2654T>C) c.2331T>C (n.2331T>C) c.2174T>C (p.Phe725Ser) | |
X | g.154362690A>T | CA415237272 | FLNA | c.2375T>A (p.Phe792Tyr) c.2294T>A (p.Phe765Tyr) c.2432T>A (n.2432T>A) c.279+2746T>A c.2654T>A (n.2654T>A) c.2331T>A (n.2331T>A) c.2174T>A (p.Phe725Tyr) | |
X | g.154362691A>C | CA415237273 | FLNA | c.2374T>G (p.Phe792Val) c.2293T>G (p.Phe765Val) c.2431T>G (n.2431T>G) c.279+2745T>G c.2653T>G (n.2653T>G) c.2330T>G (n.2330T>G) c.2173T>G (p.Phe725Val) | |
X | g.154362691A>G | CA415237274 | FLNA | c.2374T>C (p.Phe792Leu) c.2293T>C (p.Phe765Leu) c.2431T>C (n.2431T>C) c.279+2745T>C c.2653T>C (n.2653T>C) c.2330T>C (n.2330T>C) c.2173T>C (p.Phe725Leu) | |
X | g.154362691A>T | CA415237276 | FLNA | c.2374T>A (p.Phe792Ile) c.2293T>A (p.Phe765Ile) c.2431T>A (n.2431T>A) c.279+2745T>A c.2653T>A (n.2653T>A) c.2330T>A (n.2330T>A) c.2173T>A (p.Phe725Ile) | |
X | g.154362692G>A | CA519708924 | FLNA | c.2373C>T (p.Tyr791=) c.2292C>T (p.Tyr764=) c.2430C>T (n.2430C>T) c.279+2744C>T c.2652C>T (n.2652C>T) c.2329C>T (n.2329C>T) c.2172C>T (p.Tyr724=) | |
X | g.154362692G>C | CA415237278 | FLNA | c.2373C>G (p.Tyr791Ter) c.2292C>G (p.Tyr764Ter) c.2430C>G (n.2430C>G) c.279+2744C>G c.2652C>G (n.2652C>G) c.2329C>G (n.2329C>G) c.2172C>G (p.Tyr724Ter) | |
X | g.154362692G>T | CA415237280 | FLNA | c.2373C>A (p.Tyr791Ter) c.2292C>A (p.Tyr764Ter) c.2430C>A (n.2430C>A) c.279+2744C>A c.2652C>A (n.2652C>A) c.2329C>A (n.2329C>A) c.2172C>A (p.Tyr724Ter) | |
X | g.154362693T>A | CA415237283 | FLNA | c.2372A>T (p.Tyr791Phe) c.2291A>T (p.Tyr764Phe) c.2429A>T (n.2429A>T) c.279+2743A>T c.2651A>T (n.2651A>T) c.2328A>T (n.2328A>T) c.2171A>T (p.Tyr724Phe) | |
X | g.154362693T>C | CA415237285 | FLNA | c.2372A>G (p.Tyr791Cys) c.2291A>G (p.Tyr764Cys) c.2429A>G (n.2429A>G) c.279+2743A>G c.2651A>G (n.2651A>G) c.2328A>G (n.2328A>G) c.2171A>G (p.Tyr724Cys) | |
X | g.154362693T>G | CA415237287 | FLNA | c.2372A>C (p.Tyr791Ser) c.2291A>C (p.Tyr764Ser) c.2429A>C (n.2429A>C) c.279+2743A>C c.2651A>C (n.2651A>C) c.2328A>C (n.2328A>C) c.2171A>C (p.Tyr724Ser) | |
X | g.154362694A>C | CA415237291 | FLNA | c.2371T>G (p.Tyr791Asp) c.2290T>G (p.Tyr764Asp) c.2428T>G (n.2428T>G) c.279+2742T>G c.2650T>G (n.2650T>G) c.2327T>G (n.2327T>G) c.2170T>G (p.Tyr724Asp) | |
X | g.154362694A>G | CA415237297 | FLNA | c.2371T>C (p.Tyr791His) c.2290T>C (p.Tyr764His) c.2428T>C (n.2428T>C) c.279+2742T>C c.2650T>C (n.2650T>C) c.2327T>C (n.2327T>C) c.2170T>C (p.Tyr724His) | |
X | g.154362694A>T | CA415237294 | FLNA | c.2371T>A (p.Tyr791Asn) c.2290T>A (p.Tyr764Asn) c.2428T>A (n.2428T>A) c.279+2742T>A c.2650T>A (n.2650T>A) c.2327T>A (n.2327T>A) c.2170T>A (p.Tyr724Asn) | |
X | g.154362695G>A | CA519708936 | FLNA | c.2370C>T (p.Thr790=) c.2289C>T (p.Thr763=) c.2427C>T (n.2427C>T) c.279+2741C>T c.2649C>T (n.2649C>T) c.2326C>T (n.2326C>T) c.2169C>T (p.Thr723=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
X | g.154362695G>C | CA519708938 | FLNA | c.2370C>G (p.Thr790=) c.2289C>G (p.Thr763=) c.2427C>G (n.2427C>G) c.279+2741C>G c.2649C>G (n.2649C>G) c.2326C>G (n.2326C>G) c.2169C>G (p.Thr723=) | |
X | g.154362695G= | CA2466656939 | FLNA | c.2370C= (p.Thr790=) c.2289C= (p.Thr763=) c.2427C= (n.2427C=) c.279+2741C= c.2649C= (n.2649C=) c.2326C= (n.2326C=) c.2169C= (p.Thr723=) | |
X | g.154362695G>T | CA519708940 | FLNA | c.2370C>A (p.Thr790=) c.2289C>A (p.Thr763=) c.2427C>A (n.2427C>A) c.279+2741C>A c.2649C>A (n.2649C>A) c.2326C>A (n.2326C>A) c.2169C>A (p.Thr723=) | |
X | g.154362696G>A | CA415237300 | FLNA | c.2369C>T (p.Thr790Ile) c.2288C>T (p.Thr763Ile) c.2426C>T (n.2426C>T) c.279+2740C>T c.2648C>T (n.2648C>T) c.2325C>T (n.2325C>T) c.2168C>T (p.Thr723Ile) | ClinVar dbSNP |
X | g.154362696G>C | CA415237302 | FLNA | c.2369C>G (p.Thr790Ser) c.2288C>G (p.Thr763Ser) c.2426C>G (n.2426C>G) c.279+2740C>G c.2648C>G (n.2648C>G) c.2325C>G (n.2325C>G) c.2168C>G (p.Thr723Ser) | |
X | g.154362696G>T | CA415237305 | FLNA | c.2369C>A (p.Thr790Asn) c.2288C>A (p.Thr763Asn) c.2426C>A (n.2426C>A) c.279+2740C>A c.2648C>A (n.2648C>A) c.2325C>A (n.2325C>A) c.2168C>A (p.Thr723Asn) | |
X | g.154362697T>A | CA415237307 | FLNA | c.2368A>T (p.Thr790Ser) c.2287A>T (p.Thr763Ser) c.2425A>T (n.2425A>T) c.279+2739A>T c.2647A>T (n.2647A>T) c.2324A>T (n.2324A>T) c.2167A>T (p.Thr723Ser) | |
X | g.154362697T>C | CA415237309 | FLNA | c.2368A>G (p.Thr790Ala) c.2287A>G (p.Thr763Ala) c.2425A>G (n.2425A>G) c.279+2739A>G c.2647A>G (n.2647A>G) c.2324A>G (n.2324A>G) c.2167A>G (p.Thr723Ala) | gnomAD v4 |
X | g.154362697T>G | CA415237311 | FLNA | c.2368A>C (p.Thr790Pro) c.2287A>C (p.Thr763Pro) c.2425A>C (n.2425A>C) c.279+2739A>C c.2647A>C (n.2647A>C) c.2324A>C (n.2324A>C) c.2167A>C (p.Thr723Pro) | |
X | g.154362698G>A | CA519708944 | FLNA | c.2367C>T (p.Pro789=) c.2286C>T (p.Pro762=) c.2424C>T (n.2424C>T) c.279+2738C>T c.2646C>T (n.2646C>T) c.2323C>T (n.2323C>T) c.2166C>T (p.Pro722=) | ClinVar dbSNP |
X | g.154362698G>C | CA519708945 | FLNA | c.2367C>G (p.Pro789=) c.2286C>G (p.Pro762=) c.2424C>G (n.2424C>G) c.279+2738C>G c.2646C>G (n.2646C>G) c.2323C>G (n.2323C>G) c.2166C>G (p.Pro722=) | |
X | g.154362698G= | CA2466656940 | FLNA | c.2367C= (p.Pro789=) c.2286C= (p.Pro762=) c.2424C= (n.2424C=) c.279+2738C= c.2646C= (n.2646C=) c.2323C= (n.2323C=) c.2166C= (p.Pro722=) | |
X | g.154362698G>T | CA519708946 | FLNA | c.2367C>A (p.Pro789=) c.2286C>A (p.Pro762=) c.2424C>A (n.2424C>A) c.279+2738C>A c.2646C>A (n.2646C>A) c.2323C>A (n.2323C>A) c.2166C>A (p.Pro722=) | |
X | g.154362700del | CA2579738104 | FLNA | c.2367del (p.Thr790ProfsTer26) c.2286del (p.Thr763ProfsTer26) c.2424del (n.2424del) c.279+2738del c.2646del (n.2646del) c.2323del (n.2323del) c.2166del (p.Thr723ProfsTer26) | |
X | g.154362698_154362699insA | CA16621254 | FLNA | c.2366_2367insT (p.Thr790HisfsTer?) c.2285_2286insT (p.Thr763HisfsTer?) c.2423_2424insT (n.2423_2424insT) c.279+2737_279+2738insT c.2645_2646insT (n.2645_2646insT) c.2322_2323insT (n.2322_2323insT) c.2165_2166insT (p.Thr723HisfsTer?) | ClinVar dbSNP |
X | g.154362699G>A | CA415237314 | FLNA | c.2366C>T (p.Pro789Leu) c.2285C>T (p.Pro762Leu) c.2423C>T (n.2423C>T) c.279+2737C>T c.2645C>T (n.2645C>T) c.2322C>T (n.2322C>T) c.2165C>T (p.Pro722Leu) | ClinVar |
X | g.154362699G>C | CA415237315 | FLNA | c.2366C>G (p.Pro789Arg) c.2285C>G (p.Pro762Arg) c.2423C>G (n.2423C>G) c.279+2737C>G c.2645C>G (n.2645C>G) c.2322C>G (n.2322C>G) c.2165C>G (p.Pro722Arg) | |
X | g.154362699G>T | CA415237317 | FLNA | c.2366C>A (p.Pro789His) c.2285C>A (p.Pro762His) c.2423C>A (n.2423C>A) c.279+2737C>A c.2645C>A (n.2645C>A) c.2322C>A (n.2322C>A) c.2165C>A (p.Pro722His) | |
X | g.154362700G>A | CA10560950 | FLNA | c.2365C>T (p.Pro789Ser) c.2284C>T (p.Pro762Ser) c.2422C>T (n.2422C>T) c.279+2736C>T c.2644C>T (n.2644C>T) c.2321C>T (n.2321C>T) c.2164C>T (p.Pro722Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154362700G>C | CA415237322 | FLNA | c.2365C>G (p.Pro789Ala) c.2284C>G (p.Pro762Ala) c.2422C>G (n.2422C>G) c.279+2736C>G c.2644C>G (n.2644C>G) c.2321C>G (n.2321C>G) c.2164C>G (p.Pro722Ala) | |
X | g.154362700G= | CA2466656941 | FLNA | c.2365C= (p.Pro789=) c.2284C= (p.Pro762=) c.2422C= (n.2422C=) c.279+2736C= c.2644C= (n.2644C=) c.2321C= (n.2321C=) c.2164C= (p.Pro722=) | |
X | g.154362700G>T | CA415237318 | FLNA | c.2365C>A (p.Pro789Thr) c.2284C>A (p.Pro762Thr) c.2422C>A (n.2422C>A) c.279+2736C>A c.2644C>A (n.2644C>A) c.2321C>A (n.2321C>A) c.2164C>A (p.Pro722Thr) | |
X | g.154362701C>A | CA415237325 | FLNA | c.2364G>T (p.Glu788Asp) c.2283G>T (p.Glu761Asp) c.2421G>T (n.2421G>T) c.279+2735G>T c.2643G>T (n.2643G>T) c.2320G>T (n.2320G>T) c.2163G>T (p.Glu721Asp) | gnomAD v4 |
X | g.154362701C= | CA2466656942 | FLNA | c.2364G= (p.Glu788=) c.2283G= (p.Glu761=) c.2421G= (n.2421G=) c.279+2735G= c.2643G= (n.2643G=) c.2320G= (n.2320G=) c.2163G= (p.Glu721=) | |
X | g.154362701C>G | CA415237327 | FLNA | c.2364G>C (p.Glu788Asp) c.2283G>C (p.Glu761Asp) c.2421G>C (n.2421G>C) c.279+2735G>C c.2643G>C (n.2643G>C) c.2320G>C (n.2320G>C) c.2163G>C (p.Glu721Asp) | |
X | g.154362701C>T | CA519708960 | FLNA | c.2364G>A (p.Glu788=) c.2283G>A (p.Glu761=) c.2421G>A (n.2421G>A) c.279+2735G>A c.2643G>A (n.2643G>A) c.2320G>A (n.2320G>A) c.2163G>A (p.Glu721=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154362702T>A | CA415237330 | FLNA | c.2363A>T (p.Glu788Val) c.2282A>T (p.Glu761Val) c.2420A>T (n.2420A>T) c.279+2734A>T c.2642A>T (n.2642A>T) c.2319A>T (n.2319A>T) c.2162A>T (p.Glu721Val) | |
X | g.154362702T>C | CA415237332 | FLNA | c.2363A>G (p.Glu788Gly) c.2282A>G (p.Glu761Gly) c.2420A>G (n.2420A>G) c.279+2734A>G c.2642A>G (n.2642A>G) c.2319A>G (n.2319A>G) c.2162A>G (p.Glu721Gly) | |
X | g.154362702T>G | CA415237334 | FLNA | c.2363A>C (p.Glu788Ala) c.2282A>C (p.Glu761Ala) c.2420A>C (n.2420A>C) c.279+2734A>C c.2642A>C (n.2642A>C) c.2319A>C (n.2319A>C) c.2162A>C (p.Glu721Ala) | |
X | g.154362703C>A | CA415237338 | FLNA | c.2362G>T (p.Glu788Ter) c.2281G>T (p.Glu761Ter) c.2419G>T (n.2419G>T) c.279+2733G>T c.2641G>T (n.2641G>T) c.2318G>T (n.2318G>T) c.2161G>T (p.Glu721Ter) | |
X | g.154362703C= | CA2466656943 | FLNA | c.2362G= (p.Glu788=) c.2281G= (p.Glu761=) c.2419G= (n.2419G=) c.279+2733G= c.2641G= (n.2641G=) c.2318G= (n.2318G=) c.2161G= (p.Glu721=) | |
X | g.154362703C>G | CA415237340 | FLNA | c.2362G>C (p.Glu788Gln) c.2281G>C (p.Glu761Gln) c.2419G>C (n.2419G>C) c.279+2733G>C c.2641G>C (n.2641G>C) c.2318G>C (n.2318G>C) c.2161G>C (p.Glu721Gln) | |
X | g.154362703C>T | CA337281848 | FLNA | c.2362G>A (p.Glu788Lys) c.2281G>A (p.Glu761Lys) c.2419G>A (n.2419G>A) c.279+2733G>A c.2641G>A (n.2641G>A) c.2318G>A (n.2318G>A) c.2161G>A (p.Glu721Lys) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
X | g.154362704G>A | CA519708965 | FLNA | c.2361C>T (p.His787=) c.2280C>T (p.His760=) c.2418C>T (n.2418C>T) c.279+2732C>T c.2640C>T (n.2640C>T) c.2317C>T (n.2317C>T) c.2160C>T (p.His720=) | ClinVar dbSNP gnomAD v4 |
X | g.154362704G>C | CA321022 | FLNA | c.2361C>G (p.His787Gln) c.2280C>G (p.His760Gln) c.2418C>G (n.2418C>G) c.279+2732C>G c.2640C>G (n.2640C>G) c.2317C>G (n.2317C>G) c.2160C>G (p.His720Gln) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154362704G= | CA2466656944 | FLNA | c.2361C= (p.His787=) c.2280C= (p.His760=) c.2418C= (n.2418C=) c.279+2732C= c.2640C= (n.2640C=) c.2317C= (n.2317C=) c.2160C= (p.His720=) | |
X | g.154362704G>T | CA415237345 | FLNA | c.2361C>A (p.His787Gln) c.2280C>A (p.His760Gln) c.2418C>A (n.2418C>A) c.279+2732C>A c.2640C>A (n.2640C>A) c.2317C>A (n.2317C>A) c.2160C>A (p.His720Gln) | |
X | g.154362705T>A | CA415237352 | FLNA | c.2360A>T (p.His787Leu) c.2279A>T (p.His760Leu) c.2417A>T (n.2417A>T) c.279+2731A>T c.2639A>T (n.2639A>T) c.2316A>T (n.2316A>T) c.2159A>T (p.His720Leu) | |
X | g.154362705T>C | CA415237350 | FLNA | c.2360A>G (p.His787Arg) c.2279A>G (p.His760Arg) c.2417A>G (n.2417A>G) c.279+2731A>G c.2639A>G (n.2639A>G) c.2316A>G (n.2316A>G) c.2159A>G (p.His720Arg) | ClinVar |
X | g.154362705T>G | CA415237348 | FLNA | c.2360A>C (p.His787Pro) c.2279A>C (p.His760Pro) c.2417A>C (n.2417A>C) c.279+2731A>C c.2639A>C (n.2639A>C) c.2316A>C (n.2316A>C) c.2159A>C (p.His720Pro) | |
X | g.154362706G>A | CA415237356 | FLNA | c.2359C>T (p.His787Tyr) c.2278C>T (p.His760Tyr) c.2416C>T (n.2416C>T) c.279+2730C>T c.2638C>T (n.2638C>T) c.2315C>T (n.2315C>T) c.2158C>T (p.His720Tyr) | dbSNP |
X | g.154362706G>C | CA415237359 | FLNA | c.2359C>G (p.His787Asp) c.2278C>G (p.His760Asp) c.2416C>G (n.2416C>G) c.279+2730C>G c.2638C>G (n.2638C>G) c.2315C>G (n.2315C>G) c.2158C>G (p.His720Asp) | gnomAD v4 |
X | g.154362706G= | CA2466656945 | FLNA | c.2359C= (p.His787=) c.2278C= (p.His760=) c.2416C= (n.2416C=) c.279+2730C= c.2638C= (n.2638C=) c.2315C= (n.2315C=) c.2158C= (p.His720=) | |
X | g.154362706G>T | CA415237361 | FLNA | c.2359C>A (p.His787Asn) c.2278C>A (p.His760Asn) c.2416C>A (n.2416C>A) c.279+2730C>A c.2638C>A (n.2638C>A) c.2315C>A (n.2315C>A) c.2158C>A (p.His720Asn) | dbSNP |
X | g.154362707G>A | CA10560951 | FLNA | c.2358C>T (p.Ala786=) c.2277C>T (p.Ala759=) c.2415C>T (n.2415C>T) c.279+2729C>T c.2637C>T (n.2637C>T) c.2314C>T (n.2314C>T) c.2157C>T (p.Ala719=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
X | g.154362707G>C | CA519708980 | FLNA | c.2358C>G (p.Ala786=) c.2277C>G (p.Ala759=) c.2415C>G (n.2415C>G) c.279+2729C>G c.2637C>G (n.2637C>G) c.2314C>G (n.2314C>G) c.2157C>G (p.Ala719=) | |
X | g.154362707G= | CA2466656946 | FLNA | c.2358C= (p.Ala786=) c.2277C= (p.Ala759=) c.2415C= (n.2415C=) c.279+2729C= c.2637C= (n.2637C=) c.2314C= (n.2314C=) c.2157C= (p.Ala719=) | |
X | g.154362707G>T | CA519708981 | FLNA | c.2358C>A (p.Ala786=) c.2277C>A (p.Ala759=) c.2415C>A (n.2415C>A) c.279+2729C>A c.2637C>A (n.2637C>A) c.2314C>A (n.2314C>A) c.2157C>A (p.Ala719=) | |
X | g.154362708G>A | CA415237366 | FLNA | c.2357C>T (p.Ala786Val) c.2276C>T (p.Ala759Val) c.2414C>T (n.2414C>T) c.279+2728C>T c.2636C>T (n.2636C>T) c.2313C>T (n.2313C>T) c.2156C>T (p.Ala719Val) | |
X | g.154362708G>C | CA415237367 | FLNA | c.2357C>G (p.Ala786Gly) c.2276C>G (p.Ala759Gly) c.2414C>G (n.2414C>G) c.279+2728C>G c.2636C>G (n.2636C>G) c.2313C>G (n.2313C>G) c.2156C>G (p.Ala719Gly) | ClinVar dbSNP gnomAD v4 |
X | g.154362708G= | CA2466656947 | FLNA | c.2357C= (p.Ala786=) c.2276C= (p.Ala759=) c.2414C= (n.2414C=) c.279+2728C= c.2636C= (n.2636C=) c.2313C= (n.2313C=) c.2156C= (p.Ala719=) | |
X | g.154362708G>T | CA415237369 | FLNA | c.2357C>A (p.Ala786Asp) c.2276C>A (p.Ala759Asp) c.2414C>A (n.2414C>A) c.279+2728C>A c.2636C>A (n.2636C>A) c.2313C>A (n.2313C>A) c.2156C>A (p.Ala719Asp) | |
X | g.154362709C>A | CA415237372 | FLNA | c.2356G>T (p.Ala786Ser) c.2275G>T (p.Ala759Ser) c.2413G>T (n.2413G>T) c.279+2727G>T c.2635G>T (n.2635G>T) c.2312G>T (n.2312G>T) c.2155G>T (p.Ala719Ser) | |
X | g.154362709C= | CA2466656948 | FLNA | c.2356G= (p.Ala786=) c.2275G= (p.Ala759=) c.2413G= (n.2413G=) c.279+2727G= c.2635G= (n.2635G=) c.2312G= (n.2312G=) c.2155G= (p.Ala719=) | |
X | g.154362709C>G | CA415237374 | FLNA | c.2356G>C (p.Ala786Pro) c.2275G>C (p.Ala759Pro) c.2413G>C (n.2413G>C) c.279+2727G>C c.2635G>C (n.2635G>C) c.2312G>C (n.2312G>C) c.2155G>C (p.Ala719Pro) | |
X | g.154362709C>T | CA415237377 | FLNA | c.2356G>A (p.Ala786Thr) c.2275G>A (p.Ala759Thr) c.2413G>A (n.2413G>A) c.279+2727G>A c.2635G>A (n.2635G>A) c.2312G>A (n.2312G>A) c.2155G>A (p.Ala719Thr) | ClinVar dbSNP |
X | g.154362710_154362718del | CA645603465 | FLNA | c.2348_2356del (p.Gly783_Lys785del) c.2267_2275del (p.Gly756_Lys758del) c.2405_2413del (n.2405_2413del) c.279+2719_279+2727del c.2627_2635del (n.2627_2635del) c.2304_2312del (n.2304_2312del) c.2147_2155del (p.Gly716_Lys718del) | COSMIC COSMIC |
X | g.154362710C>A | CA415237379 | FLNA | c.2355G>T (p.Lys785Asn) c.2274G>T (p.Lys758Asn) c.2412G>T (n.2412G>T) c.279+2726G>T c.2634G>T (n.2634G>T) c.2311G>T (n.2311G>T) c.2154G>T (p.Lys718Asn) | |
X | g.154362710C>G | CA415237381 | FLNA | c.2355G>C (p.Lys785Asn) c.2274G>C (p.Lys758Asn) c.2412G>C (n.2412G>C) c.279+2726G>C c.2634G>C (n.2634G>C) c.2311G>C (n.2311G>C) c.2154G>C (p.Lys718Asn) | gnomAD v4 |
X | g.154362710C>T | CA519708984 | FLNA | c.2355G>A (p.Lys785=) c.2274G>A (p.Lys758=) c.2412G>A (n.2412G>A) c.279+2726G>A c.2634G>A (n.2634G>A) c.2311G>A (n.2311G>A) c.2154G>A (p.Lys718=) | |
X | g.154362711T>A | CA415237390 | FLNA | c.2354A>T (p.Lys785Met) c.2273A>T (p.Lys758Met) c.2411A>T (n.2411A>T) c.279+2725A>T c.2633A>T (n.2633A>T) c.2310A>T (n.2310A>T) c.2153A>T (p.Lys718Met) | |
X | g.154362711T>C | CA415237387 | FLNA | c.2354A>G (p.Lys785Arg) c.2273A>G (p.Lys758Arg) c.2411A>G (n.2411A>G) c.279+2725A>G c.2633A>G (n.2633A>G) c.2310A>G (n.2310A>G) c.2153A>G (p.Lys718Arg) | |
X | g.154362711T>G | CA415237385 | FLNA | c.2354A>C (p.Lys785Thr) c.2273A>C (p.Lys758Thr) c.2411A>C (n.2411A>C) c.279+2725A>C c.2633A>C (n.2633A>C) c.2310A>C (n.2310A>C) c.2153A>C (p.Lys718Thr) | |
X | g.154362712T>A | CA415237394 | FLNA | c.2353A>T (p.Lys785Ter) c.2272A>T (p.Lys758Ter) c.2410A>T (n.2410A>T) c.279+2724A>T c.2632A>T (n.2632A>T) c.2309A>T (n.2309A>T) c.2152A>T (p.Lys718Ter) | |
X | g.154362712T>C | CA415237398 | FLNA | c.2353A>G (p.Lys785Glu) c.2272A>G (p.Lys758Glu) c.2410A>G (n.2410A>G) c.279+2724A>G c.2632A>G (n.2632A>G) c.2309A>G (n.2309A>G) c.2152A>G (p.Lys718Glu) | |
X | g.154362712T>G | CA415237395 | FLNA | c.2353A>C (p.Lys785Gln) c.2272A>C (p.Lys758Gln) c.2410A>C (n.2410A>C) c.279+2724A>C c.2632A>C (n.2632A>C) c.2309A>C (n.2309A>C) c.2152A>C (p.Lys718Gln) | |
X | g.154362713G>A | CA519708995 | FLNA | c.2352C>T (p.Leu784=) c.2271C>T (p.Leu757=) c.2409C>T (n.2409C>T) c.279+2723C>T c.2631C>T (n.2631C>T) c.2308C>T (n.2308C>T) c.2151C>T (p.Leu717=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154362713G>C | CA519708996 | FLNA | c.2352C>G (p.Leu784=) c.2271C>G (p.Leu757=) c.2409C>G (n.2409C>G) c.279+2723C>G c.2631C>G (n.2631C>G) c.2308C>G (n.2308C>G) c.2151C>G (p.Leu717=) | gnomAD v4 |
X | g.154362713G= | CA2466656949 | FLNA | c.2352C= (p.Leu784=) c.2271C= (p.Leu757=) c.2409C= (n.2409C=) c.279+2723C= c.2631C= (n.2631C=) c.2308C= (n.2308C=) c.2151C= (p.Leu717=) | |
X | g.154362713G>T | CA519708997 | FLNA | c.2352C>A (p.Leu784=) c.2271C>A (p.Leu757=) c.2409C>A (n.2409C>A) c.279+2723C>A c.2631C>A (n.2631C>A) c.2308C>A (n.2308C>A) c.2151C>A (p.Leu717=) | |
X | g.154362714A>C | CA415237402 | FLNA | c.2351T>G (p.Leu784Arg) c.2270T>G (p.Leu757Arg) c.2408T>G (n.2408T>G) c.279+2722T>G c.2630T>G (n.2630T>G) c.2307T>G (n.2307T>G) c.2150T>G (p.Leu717Arg) | |
X | g.154362714A>G | CA415237404 | FLNA | c.2351T>C (p.Leu784Pro) c.2270T>C (p.Leu757Pro) c.2408T>C (n.2408T>C) c.279+2722T>C c.2630T>C (n.2630T>C) c.2307T>C (n.2307T>C) c.2150T>C (p.Leu717Pro) | |
X | g.154362714A>T | CA415237405 | FLNA | c.2351T>A (p.Leu784His) c.2270T>A (p.Leu757His) c.2408T>A (n.2408T>A) c.279+2722T>A c.2630T>A (n.2630T>A) c.2307T>A (n.2307T>A) c.2150T>A (p.Leu717His) | |
X | g.154362715G>A | CA10560952 | FLNA | c.2350C>T (p.Leu784Phe) c.2269C>T (p.Leu757Phe) c.2407C>T (n.2407C>T) c.279+2721C>T c.2629C>T (n.2629C>T) c.2306C>T (n.2306C>T) c.2149C>T (p.Leu717Phe) | dbSNP ExAC |
X | g.154362715G>C | CA415237410 | FLNA | c.2350C>G (p.Leu784Val) c.2269C>G (p.Leu757Val) c.2407C>G (n.2407C>G) c.279+2721C>G c.2629C>G (n.2629C>G) c.2306C>G (n.2306C>G) c.2149C>G (p.Leu717Val) | |
X | g.154362715G= | CA2466656950 | FLNA | c.2350C= (p.Leu784=) c.2269C= (p.Leu757=) c.2407C= (n.2407C=) c.279+2721C= c.2629C= (n.2629C=) c.2306C= (n.2306C=) c.2149C= (p.Leu717=) | |
X | g.154362715G>T | CA415237412 | FLNA | c.2350C>A (p.Leu784Ile) c.2269C>A (p.Leu757Ile) c.2407C>A (n.2407C>A) c.279+2721C>A c.2629C>A (n.2629C>A) c.2306C>A (n.2306C>A) c.2149C>A (p.Leu717Ile) | |
X | g.154362716C>A | CA519709007 | FLNA | c.2349G>T (p.Gly783=) c.2268G>T (p.Gly756=) c.2406G>T (n.2406G>T) c.279+2720G>T c.2628G>T (n.2628G>T) c.2305G>T (n.2305G>T) c.2148G>T (p.Gly716=) | dbSNP gnomAD v2 gnomAD v4 |
X | g.154362716C= | CA2466656951 | FLNA | c.2349G= (p.Gly783=) c.2268G= (p.Gly756=) c.2406G= (n.2406G=) c.279+2720G= c.2628G= (n.2628G=) c.2305G= (n.2305G=) c.2148G= (p.Gly716=) | |
X | g.154362716C>G | CA519709008 | FLNA | c.2349G>C (p.Gly783=) c.2268G>C (p.Gly756=) c.2406G>C (n.2406G>C) c.279+2720G>C c.2628G>C (n.2628G>C) c.2305G>C (n.2305G>C) c.2148G>C (p.Gly716=) | |
X | g.154362716C>T | CA519709012 | FLNA | c.2349G>A (p.Gly783=) c.2268G>A (p.Gly756=) c.2406G>A (n.2406G>A) c.279+2720G>A c.2628G>A (n.2628G>A) c.2305G>A (n.2305G>A) c.2148G>A (p.Gly716=) | |
X | g.154362717C>A | CA415237415 | FLNA | c.2348G>T (p.Gly783Val) c.2267G>T (p.Gly756Val) c.2405G>T (n.2405G>T) c.279+2719G>T c.2627G>T (n.2627G>T) c.2304G>T (n.2304G>T) c.2147G>T (p.Gly716Val) | |
X | g.154362717C>G | CA415237417 | FLNA | c.2348G>C (p.Gly783Ala) c.2267G>C (p.Gly756Ala) c.2405G>C (n.2405G>C) c.279+2719G>C c.2627G>C (n.2627G>C) c.2304G>C (n.2304G>C) c.2147G>C (p.Gly716Ala) | |
X | g.154362717C>T | CA415237420 | FLNA | c.2348G>A (p.Gly783Glu) c.2267G>A (p.Gly756Glu) c.2405G>A (n.2405G>A) c.279+2719G>A c.2627G>A (n.2627G>A) c.2304G>A (n.2304G>A) c.2147G>A (p.Gly716Glu) | |
X | g.154362718C>A | CA415237427 | FLNA | c.2347G>T (p.Gly783Trp) c.2266G>T (p.Gly756Trp) c.2404G>T (n.2404G>T) c.279+2718G>T c.2626G>T (n.2626G>T) c.2303G>T (n.2303G>T) c.2146G>T (p.Gly716Trp) | |
X | g.154362718C= | CA2466656952 | FLNA | c.2347G= (p.Gly783=) c.2266G= (p.Gly756=) c.2404G= (n.2404G=) c.279+2718G= c.2626G= (n.2626G=) c.2303G= (n.2303G=) c.2146G= (p.Gly716=) | |
X | g.154362718C>G | CA415237425 | FLNA | c.2347G>C (p.Gly783Arg) c.2266G>C (p.Gly756Arg) c.2404G>C (n.2404G>C) c.279+2718G>C c.2626G>C (n.2626G>C) c.2303G>C (n.2303G>C) c.2146G>C (p.Gly716Arg) | |
X | g.154362718C>T | CA415237423 | FLNA | c.2347G>A (p.Gly783Arg) c.2266G>A (p.Gly756Arg) c.2404G>A (n.2404G>A) c.279+2718G>A c.2626G>A (n.2626G>A) c.2303G>A (n.2303G>A) c.2146G>A (p.Gly716Arg) | dbSNP |
X | g.154362719T>A | CA519709023 | FLNA | c.2346A>T (p.Thr782=) c.2265A>T (p.Thr755=) c.2403A>T (n.2403A>T) c.279+2717A>T c.2625A>T (n.2625A>T) c.2302A>T (n.2302A>T) c.2145A>T (p.Thr715=) | |
X | g.154362719T>C | CA519709027 | FLNA | c.2346A>G (p.Thr782=) c.2265A>G (p.Thr755=) c.2403A>G (n.2403A>G) c.279+2717A>G c.2625A>G (n.2625A>G) c.2302A>G (n.2302A>G) c.2145A>G (p.Thr715=) | dbSNP gnomAD v4 |
X | g.154362719T>G | CA519709020 | FLNA | c.2346A>C (p.Thr782=) c.2265A>C (p.Thr755=) c.2403A>C (n.2403A>C) c.279+2717A>C c.2625A>C (n.2625A>C) c.2302A>C (n.2302A>C) c.2145A>C (p.Thr715=) | |
X | g.154362719T= | CA2466656953 | FLNA | c.2346A= (p.Thr782=) c.2265A= (p.Thr755=) c.2403A= (n.2403A=) c.279+2717A= c.2625A= (n.2625A=) c.2302A= (n.2302A=) c.2145A= (p.Thr715=) | |
X | g.154362720G>A | CA415237431 | FLNA | c.2345C>T (p.Thr782Ile) c.2264C>T (p.Thr755Ile) c.2402C>T (n.2402C>T) c.279+2716C>T c.2624C>T (n.2624C>T) c.2301C>T (n.2301C>T) c.2144C>T (p.Thr715Ile) | |
X | g.154362720G>C | CA415237434 | FLNA | c.2345C>G (p.Thr782Arg) c.2264C>G (p.Thr755Arg) c.2402C>G (n.2402C>G) c.279+2716C>G c.2624C>G (n.2624C>G) c.2301C>G (n.2301C>G) c.2144C>G (p.Thr715Arg) | |
X | g.154362720G>T | CA415237436 | FLNA | c.2345C>A (p.Thr782Lys) c.2264C>A (p.Thr755Lys) c.2402C>A (n.2402C>A) c.279+2716C>A c.2624C>A (n.2624C>A) c.2301C>A (n.2301C>A) c.2144C>A (p.Thr715Lys) | gnomAD v4 |
X | g.154362721T>A | CA415237439 | FLNA | c.2344A>T (p.Thr782Ser) c.2263A>T (p.Thr755Ser) c.2401A>T (n.2401A>T) c.279+2715A>T c.2623A>T (n.2623A>T) c.2300A>T (n.2300A>T) c.2143A>T (p.Thr715Ser) | |
X | g.154362721T>C | CA415237440 | FLNA | c.2344A>G (p.Thr782Ala) c.2263A>G (p.Thr755Ala) c.2401A>G (n.2401A>G) c.279+2715A>G c.2623A>G (n.2623A>G) c.2300A>G (n.2300A>G) c.2143A>G (p.Thr715Ala) | |
X | g.154362721T>G | CA415237442 | FLNA | c.2344A>C (p.Thr782Pro) c.2263A>C (p.Thr755Pro) c.2401A>C (n.2401A>C) c.279+2715A>C c.2623A>C (n.2623A>C) c.2300A>C (n.2300A>C) c.2143A>C (p.Thr715Pro) | |
X | g.154362722C>A | CA415237447 | FLNA | c.2343G>T (p.Lys781Asn) c.2262G>T (p.Lys754Asn) c.2400G>T (n.2400G>T) c.279+2714G>T c.2622G>T (n.2622G>T) c.2299G>T (n.2299G>T) c.2142G>T (p.Lys714Asn) | |
X | g.154362722C>G | CA415237449 | FLNA | c.2343G>C (p.Lys781Asn) c.2262G>C (p.Lys754Asn) c.2400G>C (n.2400G>C) c.279+2714G>C c.2622G>C (n.2622G>C) c.2299G>C (n.2299G>C) c.2142G>C (p.Lys714Asn) | |
X | g.154362722C>T | CA519709029 | FLNA | c.2343G>A (p.Lys781=) c.2262G>A (p.Lys754=) c.2400G>A (n.2400G>A) c.279+2714G>A c.2622G>A (n.2622G>A) c.2299G>A (n.2299G>A) c.2142G>A (p.Lys714=) | |
X | g.154362723T>A | CA415237452 | FLNA | c.2342A>T (p.Lys781Met) c.2261A>T (p.Lys754Met) c.2399A>T (n.2399A>T) c.279+2713A>T c.2621A>T (n.2621A>T) c.2298A>T (n.2298A>T) c.2141A>T (p.Lys714Met) | |
X | g.154362723T>C | CA415237454 | FLNA | c.2342A>G (p.Lys781Arg) c.2261A>G (p.Lys754Arg) c.2399A>G (n.2399A>G) c.279+2713A>G c.2621A>G (n.2621A>G) c.2298A>G (n.2298A>G) c.2141A>G (p.Lys714Arg) | |
X | g.154362723T>G | CA415237456 | FLNA | c.2342A>C (p.Lys781Thr) c.2261A>C (p.Lys754Thr) c.2399A>C (n.2399A>C) c.279+2713A>C c.2621A>C (n.2621A>C) c.2298A>C (n.2298A>C) c.2141A>C (p.Lys714Thr) | |
X | g.154362724T>A | CA415237460 | FLNA | c.2341A>T (p.Lys781Ter) c.2260A>T (p.Lys754Ter) c.2398A>T (n.2398A>T) c.279+2712A>T c.2620A>T (n.2620A>T) c.2297A>T (n.2297A>T) c.2140A>T (p.Lys714Ter) | |
X | g.154362724T>C | CA415237461 | FLNA | c.2341A>G (p.Lys781Glu) c.2260A>G (p.Lys754Glu) c.2398A>G (n.2398A>G) c.279+2712A>G c.2620A>G (n.2620A>G) c.2297A>G (n.2297A>G) c.2140A>G (p.Lys714Glu) | |
X | g.154362724T>G | CA415237459 | FLNA | c.2341A>C (p.Lys781Gln) c.2260A>C (p.Lys754Gln) c.2398A>C (n.2398A>C) c.279+2712A>C c.2620A>C (n.2620A>C) c.2297A>C (n.2297A>C) c.2140A>C (p.Lys714Gln) | |
X | g.154362725G>A | CA519709035 | FLNA | c.2340C>T (p.Ala780=) c.2259C>T (p.Ala753=) c.2397C>T (n.2397C>T) c.279+2711C>T c.2619C>T (n.2619C>T) c.2296C>T (n.2296C>T) c.2139C>T (p.Ala713=) | |
X | g.154362725G>C | CA519709036 | FLNA | c.2340C>G (p.Ala780=) c.2259C>G (p.Ala753=) c.2397C>G (n.2397C>G) c.279+2711C>G c.2619C>G (n.2619C>G) c.2296C>G (n.2296C>G) c.2139C>G (p.Ala713=) | |
X | g.154362725G= | CA2466656954 | FLNA | c.2340C= (p.Ala780=) c.2259C= (p.Ala753=) c.2397C= (n.2397C=) c.279+2711C= c.2619C= (n.2619C=) c.2296C= (n.2296C=) c.2139C= (p.Ala713=) | |
X | g.154362725G>T | CA519709037 | FLNA | c.2340C>A (p.Ala780=) c.2259C>A (p.Ala753=) c.2397C>A (n.2397C>A) c.279+2711C>A c.2619C>A (n.2619C>A) c.2296C>A (n.2296C>A) c.2139C>A (p.Ala713=) | |
X | g.154362725_154362726insTT | CA10605292 | FLNA | c.2339_2340insAA (p.Lys781ThrfsTer?) c.2258_2259insAA (p.Lys754ThrfsTer?) c.2396_2397insAA (n.2396_2397insAA) c.279+2710_279+2711insAA c.2618_2619insAA (n.2618_2619insAA) c.2295_2296insAA (n.2295_2296insAA) c.2138_2139insAA (p.Lys714ThrfsTer?) | ClinVar dbSNP |
X | g.154362726G>A | CA415237466 | FLNA | c.2339C>T (p.Ala780Val) c.2258C>T (p.Ala753Val) c.2396C>T (n.2396C>T) c.279+2710C>T c.2618C>T (n.2618C>T) c.2295C>T (n.2295C>T) c.2138C>T (p.Ala713Val) | |
X | g.154362726G>C | CA415237468 | FLNA | c.2339C>G (p.Ala780Gly) c.2258C>G (p.Ala753Gly) c.2396C>G (n.2396C>G) c.279+2710C>G c.2618C>G (n.2618C>G) c.2295C>G (n.2295C>G) c.2138C>G (p.Ala713Gly) | |
X | g.154362726G>T | CA415237470 | FLNA | c.2339C>A (p.Ala780Asp) c.2258C>A (p.Ala753Asp) c.2396C>A (n.2396C>A) c.279+2710C>A c.2618C>A (n.2618C>A) c.2295C>A (n.2295C>A) c.2138C>A (p.Ala713Asp) | |
X | g.154362727C>A | CA415237477 | FLNA | c.2338G>T (p.Ala780Ser) c.2257G>T (p.Ala753Ser) c.2395G>T (n.2395G>T) c.279+2709G>T c.2617G>T (n.2617G>T) c.2294G>T (n.2294G>T) c.2137G>T (p.Ala713Ser) | |
X | g.154362727C>G | CA415237475 | FLNA | c.2338G>C (p.Ala780Pro) c.2257G>C (p.Ala753Pro) c.2395G>C (n.2395G>C) c.279+2709G>C c.2617G>C (n.2617G>C) c.2294G>C (n.2294G>C) c.2137G>C (p.Ala713Pro) | |
X | g.154362727C>T | CA415237473 | FLNA | c.2338G>A (p.Ala780Thr) c.2257G>A (p.Ala753Thr) c.2395G>A (n.2395G>A) c.279+2709G>A c.2617G>A (n.2617G>A) c.2294G>A (n.2294G>A) c.2137G>A (p.Ala713Thr) | |
X | g.154362728T>A | CA519709039 | FLNA | c.2337A>T (p.Val779=) c.2256A>T (p.Val752=) c.2394A>T (n.2394A>T) c.279+2708A>T c.2616A>T (n.2616A>T) c.2293A>T (n.2293A>T) c.2136A>T (p.Val712=) | |
X | g.154362728T>C | CA519709040 | FLNA | c.2337A>G (p.Val779=) c.2256A>G (p.Val752=) c.2394A>G (n.2394A>G) c.279+2708A>G c.2616A>G (n.2616A>G) c.2293A>G (n.2293A>G) c.2136A>G (p.Val712=) | |
X | g.154362728T>G | CA519709041 | FLNA | c.2337A>C (p.Val779=) c.2256A>C (p.Val752=) c.2394A>C (n.2394A>C) c.279+2708A>C c.2616A>C (n.2616A>C) c.2293A>C (n.2293A>C) c.2136A>C (p.Val712=) | |
X | g.154362729A>C | CA415237479 | FLNA | c.2336T>G (p.Val779Gly) c.2255T>G (p.Val752Gly) c.2393T>G (n.2393T>G) c.279+2707T>G c.2615T>G (n.2615T>G) c.2292T>G (n.2292T>G) c.2135T>G (p.Val712Gly) | |
X | g.154362729A>G | CA415237480 | FLNA | c.2336T>C (p.Val779Ala) c.2255T>C (p.Val752Ala) c.2393T>C (n.2393T>C) c.279+2707T>C c.2615T>C (n.2615T>C) c.2292T>C (n.2292T>C) c.2135T>C (p.Val712Ala) | |
X | g.154362729A>T | CA415237481 | FLNA | c.2336T>A (p.Val779Glu) c.2255T>A (p.Val752Glu) c.2393T>A (n.2393T>A) c.279+2707T>A c.2615T>A (n.2615T>A) c.2292T>A (n.2292T>A) c.2135T>A (p.Val712Glu) | |
X | g.154362730C>A | CA415237482 | FLNA | c.2335G>T (p.Val779Leu) c.2254G>T (p.Val752Leu) c.2392G>T (n.2392G>T) c.279+2706G>T c.2614G>T (n.2614G>T) c.2291G>T (n.2291G>T) c.2134G>T (p.Val712Leu) | dbSNP gnomAD v2 |
X | g.154362730C= | CA2466656955 | FLNA | c.2335G= (p.Val779=) c.2254G= (p.Val752=) c.2392G= (n.2392G=) c.279+2706G= c.2614G= (n.2614G=) c.2291G= (n.2291G=) c.2134G= (p.Val712=) | |
X | g.154362730C>G | CA415237483 | FLNA | c.2335G>C (p.Val779Leu) c.2254G>C (p.Val752Leu) c.2392G>C (n.2392G>C) c.279+2706G>C c.2614G>C (n.2614G>C) c.2291G>C (n.2291G>C) c.2134G>C (p.Val712Leu) | |
X | g.154362730C>T | CA337281863 | FLNA | c.2335G>A (p.Val779Ile) c.2254G>A (p.Val752Ile) c.2392G>A (n.2392G>A) c.279+2706G>A c.2614G>A (n.2614G>A) c.2291G>A (n.2291G>A) c.2134G>A (p.Val712Ile) | dbSNP |
X | g.154362731T>A | CA519709048 | FLNA | c.2334A>T (p.Gly778=) c.2253A>T (p.Gly751=) c.2391A>T (n.2391A>T) c.279+2705A>T c.2613A>T (n.2613A>T) c.2290A>T (n.2290A>T) c.2133A>T (p.Gly711=) | |
X | g.154362731T>C | CA519709050 | FLNA | c.2334A>G (p.Gly778=) c.2253A>G (p.Gly751=) c.2391A>G (n.2391A>G) c.279+2705A>G c.2613A>G (n.2613A>G) c.2290A>G (n.2290A>G) c.2133A>G (p.Gly711=) | |
X | g.154362731T>G | CA519709052 | FLNA | c.2334A>C (p.Gly778=) c.2253A>C (p.Gly751=) c.2391A>C (n.2391A>C) c.279+2705A>C c.2613A>C (n.2613A>C) c.2290A>C (n.2290A>C) c.2133A>C (p.Gly711=) | |
X | g.154362732C>A | CA415237484 | FLNA | c.2333G>T (p.Gly778Val) c.2252G>T (p.Gly751Val) c.2390G>T (n.2390G>T) c.279+2704G>T c.2612G>T (n.2612G>T) c.2289G>T (n.2289G>T) c.2132G>T (p.Gly711Val) | COSMIC COSMIC |
X | g.154362732C>G | CA415237486 | FLNA | c.2333G>C (p.Gly778Ala) c.2252G>C (p.Gly751Ala) c.2390G>C (n.2390G>C) c.279+2704G>C c.2612G>C (n.2612G>C) c.2289G>C (n.2289G>C) c.2132G>C (p.Gly711Ala) | |
X | g.154362732C>T | CA415237485 | FLNA | c.2333G>A (p.Gly778Glu) c.2252G>A (p.Gly751Glu) c.2390G>A (n.2390G>A) c.279+2704G>A c.2612G>A (n.2612G>A) c.2289G>A (n.2289G>A) c.2132G>A (p.Gly711Glu) | |
X | g.154362733C>A | CA415237487 | FLNA | c.2332G>T (p.Gly778Ter) c.2251G>T (p.Gly751Ter) c.2389G>T (n.2389G>T) c.279+2703G>T c.2611G>T (n.2611G>T) c.2288G>T (n.2288G>T) c.2131G>T (p.Gly711Ter) | |
X | g.154362733C>G | CA415237488 | FLNA | c.2332G>C (p.Gly778Arg) c.2251G>C (p.Gly751Arg) c.2389G>C (n.2389G>C) c.279+2703G>C c.2611G>C (n.2611G>C) c.2288G>C (n.2288G>C) c.2131G>C (p.Gly711Arg) | |
X | g.154362733C>T | CA415237489 | FLNA | c.2332G>A (p.Gly778Arg) c.2251G>A (p.Gly751Arg) c.2389G>A (n.2389G>A) c.279+2703G>A c.2611G>A (n.2611G>A) c.2288G>A (n.2288G>A) c.2131G>A (p.Gly711Arg) | ClinVar dbSNP |
X | g.154362734G>A | CA10560953 | FLNA | c.2331C>T (p.Pro777=) c.2250C>T (p.Pro750=) c.2388C>T (n.2388C>T) c.279+2702C>T c.2610C>T (n.2610C>T) c.2287C>T (n.2287C>T) c.2130C>T (p.Pro710=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154362734G>C | CA519709058 | FLNA | c.2331C>G (p.Pro777=) c.2250C>G (p.Pro750=) c.2388C>G (n.2388C>G) c.279+2702C>G c.2610C>G (n.2610C>G) c.2287C>G (n.2287C>G) c.2130C>G (p.Pro710=) | |
X | g.154362734G= | CA2466656956 | FLNA | c.2331C= (p.Pro777=) c.2250C= (p.Pro750=) c.2388C= (n.2388C=) c.279+2702C= c.2610C= (n.2610C=) c.2287C= (n.2287C=) c.2130C= (p.Pro710=) | |
X | g.154362734G>T | CA519709059 | FLNA | c.2331C>A (p.Pro777=) c.2250C>A (p.Pro750=) c.2388C>A (n.2388C>A) c.279+2702C>A c.2610C>A (n.2610C>A) c.2287C>A (n.2287C>A) c.2130C>A (p.Pro710=) | gnomAD v4 |
X | g.154362735G>A | CA415237490 | FLNA | c.2330C>T (p.Pro777Leu) c.2249C>T (p.Pro750Leu) c.2387C>T (n.2387C>T) c.279+2701C>T c.2609C>T (n.2609C>T) c.2286C>T (n.2286C>T) c.2129C>T (p.Pro710Leu) | dbSNP gnomAD v2 gnomAD v4 |
X | g.154362735G>C | CA322832 | FLNA | c.2330C>G (p.Pro777Arg) c.2249C>G (p.Pro750Arg) c.2387C>G (n.2387C>G) c.279+2701C>G c.2609C>G (n.2609C>G) c.2286C>G (n.2286C>G) c.2129C>G (p.Pro710Arg) | ClinVar dbSNP |
X | g.154362735G= | CA2466656957 | FLNA | c.2330C= (p.Pro777=) c.2249C= (p.Pro750=) c.2387C= (n.2387C=) c.279+2701C= c.2609C= (n.2609C=) c.2286C= (n.2286C=) c.2129C= (p.Pro710=) | |
X | g.154362735G>T | CA415237491 | FLNA | c.2330C>A (p.Pro777His) c.2249C>A (p.Pro750His) c.2387C>A (n.2387C>A) c.279+2701C>A c.2609C>A (n.2609C>A) c.2286C>A (n.2286C>A) c.2129C>A (p.Pro710His) | |
X | g.154362735_154362736insTGTCATTGTCATTGCGGATGATGTCGAAGTCGATGTCAGCTTC | CA2824295658 | FLNA | c.2329_2330insGAAGCTGACATCGACTTCGACATCATCCGCAATGACAATGACA (p.Pro777ArgfsTer3) c.2248_2249insGAAGCTGACATCGACTTCGACATCATCCGCAATGACAATGACA (p.Pro750ArgfsTer3) c.2386_2387insGAAGCTGACATCGACTTCGACATCATCCGCAATGACAATGACA (n.2386_2387insGAAGCTGACATCGACTTCGACATCATCCGCAATGACAATGACA) c.279+2700_279+2701insGAAGCTGACATCGACTTCGACATCATCCGCAATGACAATGACA c.2608_2609insGAAGCTGACATCGACTTCGACATCATCCGCAATGACAATGACA (n.2608_2609insGAAGCTGACATCGACTTCGACATCATCCGCAATGACAATGACA) c.2285_2286insGAAGCTGACATCGACTTCGACATCATCCGCAATGACAATGACA (n.2285_2286insGAAGCTGACATCGACTTCGACATCATCCGCAATGACAATGACA) c.2128_2129insGAAGCTGACATCGACTTCGACATCATCCGCAATGACAATGACA (p.Pro710ArgfsTer3) | |
X | g.154362736G>A | CA415237492 | FLNA | c.2329C>T (p.Pro777Ser) c.2248C>T (p.Pro750Ser) c.2386C>T (n.2386C>T) c.279+2700C>T c.2608C>T (n.2608C>T) c.2285C>T (n.2285C>T) c.2128C>T (p.Pro710Ser) | |
X | g.154362736G>C | CA415237493 | FLNA | c.2329C>G (p.Pro777Ala) c.2248C>G (p.Pro750Ala) c.2386C>G (n.2386C>G) c.279+2700C>G c.2608C>G (n.2608C>G) c.2285C>G (n.2285C>G) c.2128C>G (p.Pro710Ala) | |
X | g.154362736G>T | CA415237494 | FLNA | c.2329C>A (p.Pro777Thr) c.2248C>A (p.Pro750Thr) c.2386C>A (n.2386C>A) c.279+2700C>A c.2608C>A (n.2608C>A) c.2285C>A (n.2285C>A) c.2128C>A (p.Pro710Thr) | |
X | g.154362737G>A | CA519709064 | FLNA | c.2328C>T (p.Gly776=) c.2247C>T (p.Gly749=) c.2385C>T (n.2385C>T) c.279+2699C>T c.2607C>T (n.2607C>T) c.2284C>T (n.2284C>T) c.2127C>T (p.Gly709=) | |
X | g.154362737G>C | CA519709066 | FLNA | c.2328C>G (p.Gly776=) c.2247C>G (p.Gly749=) c.2385C>G (n.2385C>G) c.279+2699C>G c.2607C>G (n.2607C>G) c.2284C>G (n.2284C>G) c.2127C>G (p.Gly709=) | |
X | g.154362737G>T | CA519709068 | FLNA | c.2328C>A (p.Gly776=) c.2247C>A (p.Gly749=) c.2385C>A (n.2385C>A) c.279+2699C>A c.2607C>A (n.2607C>A) c.2284C>A (n.2284C>A) c.2127C>A (p.Gly709=) | gnomAD v4 |
X | g.154362738C>A | CA415237497 | FLNA | c.2327G>T (p.Gly776Val) c.2246G>T (p.Gly749Val) c.2384G>T (n.2384G>T) c.279+2698G>T c.2606G>T (n.2606G>T) c.2283G>T (n.2283G>T) c.2126G>T (p.Gly709Val) | COSMIC COSMIC |
X | g.154362738C>G | CA415237496 | FLNA | c.2327G>C (p.Gly776Ala) c.2246G>C (p.Gly749Ala) c.2384G>C (n.2384G>C) c.279+2698G>C c.2606G>C (n.2606G>C) c.2283G>C (n.2283G>C) c.2126G>C (p.Gly709Ala) | |
X | g.154362738C>T | CA415237495 | FLNA | c.2327G>A (p.Gly776Asp) c.2246G>A (p.Gly749Asp) c.2384G>A (n.2384G>A) c.279+2698G>A c.2606G>A (n.2606G>A) c.2283G>A (n.2283G>A) c.2126G>A (p.Gly709Asp) | |
X | g.154362739C>A | CA415237498 | FLNA | c.2326G>T (p.Gly776Cys) c.2245G>T (p.Gly749Cys) c.2383G>T (n.2383G>T) c.279+2697G>T c.2605G>T (n.2605G>T) c.2282G>T (n.2282G>T) c.2125G>T (p.Gly709Cys) | |
X | g.154362739C= | CA2466656958 | FLNA | c.2326G= (p.Gly776=) c.2245G= (p.Gly749=) c.2383G= (n.2383G=) c.279+2697G= c.2605G= (n.2605G=) c.2282G= (n.2282G=) c.2125G= (p.Gly709=) | |
X | g.154362739C>G | CA415237500 | FLNA | c.2326G>C (p.Gly776Arg) c.2245G>C (p.Gly749Arg) c.2383G>C (n.2383G>C) c.279+2697G>C c.2605G>C (n.2605G>C) c.2282G>C (n.2282G>C) c.2125G>C (p.Gly709Arg) | |
X | g.154362739C>T | CA415237499 | FLNA | c.2326G>A (p.Gly776Ser) c.2245G>A (p.Gly749Ser) c.2383G>A (n.2383G>A) c.279+2697G>A c.2605G>A (n.2605G>A) c.2282G>A (n.2282G>A) c.2125G>A (p.Gly709Ser) | dbSNP gnomAD v4 |
X | g.154362740G>A | CA10560954 | FLNA | c.2325C>T (p.Tyr775=) c.2244C>T (p.Tyr748=) c.2382C>T (n.2382C>T) c.279+2696C>T c.2604C>T (n.2604C>T) c.2281C>T (n.2281C>T) c.2124C>T (p.Tyr708=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154362740G>C | CA415237501 | FLNA | c.2325C>G (p.Tyr775Ter) c.2244C>G (p.Tyr748Ter) c.2382C>G (n.2382C>G) c.279+2696C>G c.2604C>G (n.2604C>G) c.2281C>G (n.2281C>G) c.2124C>G (p.Tyr708Ter) | |
X | g.154362740G= | CA2466656959 | FLNA | c.2325C= (p.Tyr775=) c.2244C= (p.Tyr748=) c.2382C= (n.2382C=) c.279+2696C= c.2604C= (n.2604C=) c.2281C= (n.2281C=) c.2124C= (p.Tyr708=) | |
X | g.154362740G>T | CA415237502 | FLNA | c.2325C>A (p.Tyr775Ter) c.2244C>A (p.Tyr748Ter) c.2382C>A (n.2382C>A) c.279+2696C>A c.2604C>A (n.2604C>A) c.2281C>A (n.2281C>A) c.2124C>A (p.Tyr708Ter) | |
X | g.154362741T>A | CA415237503 | FLNA | c.2324A>T (p.Tyr775Phe) c.2243A>T (p.Tyr748Phe) c.2381A>T (n.2381A>T) c.279+2695A>T c.2603A>T (n.2603A>T) c.2280A>T (n.2280A>T) c.2123A>T (p.Tyr708Phe) | |
X | g.154362741T>C | CA415237504 | FLNA | c.2324A>G (p.Tyr775Cys) c.2243A>G (p.Tyr748Cys) c.2381A>G (n.2381A>G) c.279+2695A>G c.2603A>G (n.2603A>G) c.2280A>G (n.2280A>G) c.2123A>G (p.Tyr708Cys) | |
X | g.154362741T>G | CA415237505 | FLNA | c.2324A>C (p.Tyr775Ser) c.2243A>C (p.Tyr748Ser) c.2381A>C (n.2381A>C) c.279+2695A>C c.2603A>C (n.2603A>C) c.2280A>C (n.2280A>C) c.2123A>C (p.Tyr708Ser) | |
X | g.154362742A= | CA2466656960 | FLNA | c.2323T= (p.Tyr775=) c.2242T= (p.Tyr748=) c.2380T= (n.2380T=) c.279+2694T= c.2602T= (n.2602T=) c.2279T= (n.2279T=) c.2122T= (p.Tyr708=) | |
X | g.154362742A>C | CA415237506 | FLNA | c.2323T>G (p.Tyr775Asp) c.2242T>G (p.Tyr748Asp) c.2380T>G (n.2380T>G) c.279+2694T>G c.2602T>G (n.2602T>G) c.2279T>G (n.2279T>G) c.2122T>G (p.Tyr708Asp) | ClinVar dbSNP |
X | g.154362742A>G | CA10560955 | FLNA | c.2323T>C (p.Tyr775His) c.2242T>C (p.Tyr748His) c.2380T>C (n.2380T>C) c.279+2694T>C c.2602T>C (n.2602T>C) c.2279T>C (n.2279T>C) c.2122T>C (p.Tyr708His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154362742A>T | CA415237507 | FLNA | c.2323T>A (p.Tyr775Asn) c.2242T>A (p.Tyr748Asn) c.2380T>A (n.2380T>A) c.279+2694T>A c.2602T>A (n.2602T>A) c.2279T>A (n.2279T>A) c.2122T>A (p.Tyr708Asn) | |
X | g.154362743T>A | CA519709087 | FLNA | c.2322A>T (p.Val774=) c.2241A>T (p.Val747=) c.2379A>T (n.2379A>T) c.279+2693A>T c.2601A>T (n.2601A>T) c.2278A>T (n.2278A>T) c.2121A>T (p.Val707=) | dbSNP |
X | g.154362743T>C | CA519709088 | FLNA | c.2322A>G (p.Val774=) c.2241A>G (p.Val747=) c.2379A>G (n.2379A>G) c.279+2693A>G c.2601A>G (n.2601A>G) c.2278A>G (n.2278A>G) c.2121A>G (p.Val707=) | |
X | g.154362743T>G | CA519709090 | FLNA | c.2322A>C (p.Val774=) c.2241A>C (p.Val747=) c.2379A>C (n.2379A>C) c.279+2693A>C c.2601A>C (n.2601A>C) c.2278A>C (n.2278A>C) c.2121A>C (p.Val707=) | |
X | g.154362743T= | CA2466656961 | FLNA | c.2322A= (p.Val774=) c.2241A= (p.Val747=) c.2379A= (n.2379A=) c.279+2693A= c.2601A= (n.2601A=) c.2278A= (n.2278A=) c.2121A= (p.Val707=) | |
X | g.154362744A>C | CA415237508 | FLNA | c.2321T>G (p.Val774Gly) c.2240T>G (p.Val747Gly) c.2378T>G (n.2378T>G) c.279+2692T>G c.2600T>G (n.2600T>G) c.2277T>G (n.2277T>G) c.2120T>G (p.Val707Gly) | |
X | g.154362744A>G | CA415237509 | FLNA | c.2321T>C (p.Val774Ala) c.2240T>C (p.Val747Ala) c.2378T>C (n.2378T>C) c.279+2692T>C c.2600T>C (n.2600T>C) c.2277T>C (n.2277T>C) c.2120T>C (p.Val707Ala) | gnomAD v4 |
X | g.154362744A>T | CA415237510 | FLNA | c.2321T>A (p.Val774Glu) c.2240T>A (p.Val747Glu) c.2378T>A (n.2378T>A) c.279+2692T>A c.2600T>A (n.2600T>A) c.2277T>A (n.2277T>A) c.2120T>A (p.Val707Glu) | |
X | g.154362745C>A | CA415237513 | FLNA | c.2320G>T (p.Val774Leu) c.2239G>T (p.Val747Leu) c.2377G>T (n.2377G>T) c.279+2691G>T c.2599G>T (n.2599G>T) c.2276G>T (n.2276G>T) c.2119G>T (p.Val707Leu) | |
X | g.154362745C= | CA2466656962 | FLNA | c.2320G= (p.Val774=) c.2239G= (p.Val747=) c.2377G= (n.2377G=) c.279+2691G= c.2599G= (n.2599G=) c.2276G= (n.2276G=) c.2119G= (p.Val707=) | |
X | g.154362745C>G | CA415237512 | FLNA | c.2320G>C (p.Val774Leu) c.2239G>C (p.Val747Leu) c.2377G>C (n.2377G>C) c.279+2691G>C c.2599G>C (n.2599G>C) c.2276G>C (n.2276G>C) c.2119G>C (p.Val707Leu) | |
X | g.154362745C>T | CA415237511 | FLNA | c.2320G>A (p.Val774Ile) c.2239G>A (p.Val747Ile) c.2377G>A (n.2377G>A) c.279+2691G>A c.2599G>A (n.2599G>A) c.2276G>A (n.2276G>A) c.2119G>A (p.Val707Ile) | |
X | g.154362746T>A | CA16616653 | FLNA | c.2319A>T (p.Lys773Asn) c.2238A>T (p.Lys746Asn) c.2376A>T (n.2376A>T) c.279+2690A>T c.2598A>T (n.2598A>T) c.2275A>T (n.2275A>T) c.2118A>T (p.Lys706Asn) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
X | g.154362746T>C | CA519709098 | FLNA | c.2319A>G (p.Lys773=) c.2238A>G (p.Lys746=) c.2376A>G (n.2376A>G) c.279+2690A>G c.2598A>G (n.2598A>G) c.2275A>G (n.2275A>G) c.2118A>G (p.Lys706=) | ClinVar dbSNP |
X | g.154362746T>G | CA415237514 | FLNA | c.2319A>C (p.Lys773Asn) c.2238A>C (p.Lys746Asn) c.2376A>C (n.2376A>C) c.279+2690A>C c.2598A>C (n.2598A>C) c.2275A>C (n.2275A>C) c.2118A>C (p.Lys706Asn) | ClinVar dbSNP gnomAD v4 |
X | g.154362746T= | CA2466656963 | FLNA | c.2319A= (p.Lys773=) c.2238A= (p.Lys746=) c.2376A= (n.2376A=) c.279+2690A= c.2598A= (n.2598A=) c.2275A= (n.2275A=) c.2118A= (p.Lys706=) | |
X | g.154362747_154362748dup | CA10605374 | FLNA | c.2318_2319dup (p.Val774LysfsTer7) c.2237_2238dup (p.Val747LysfsTer7) c.2375_2376dup (n.2375_2376dup) c.279+2689_279+2690dup c.2597_2598dup (n.2597_2598dup) c.2274_2275dup (n.2274_2275dup) c.2117_2118dup (p.Val707LysfsTer7) | ClinVar dbSNP |
X | g.154362747T>A | CA415237515 | FLNA | c.2318A>T (p.Lys773Ile) c.2237A>T (p.Lys746Ile) c.2375A>T (n.2375A>T) c.279+2689A>T c.2597A>T (n.2597A>T) c.2274A>T (n.2274A>T) c.2117A>T (p.Lys706Ile) | |
X | g.154362747T>C | CA415237516 | FLNA | c.2318A>G (p.Lys773Arg) c.2237A>G (p.Lys746Arg) c.2375A>G (n.2375A>G) c.279+2689A>G c.2597A>G (n.2597A>G) c.2274A>G (n.2274A>G) c.2117A>G (p.Lys706Arg) | |
X | g.154362747T>G | CA415237517 | FLNA | c.2318A>C (p.Lys773Thr) c.2237A>C (p.Lys746Thr) c.2375A>C (n.2375A>C) c.279+2689A>C c.2597A>C (n.2597A>C) c.2274A>C (n.2274A>C) c.2117A>C (p.Lys706Thr) | |
X | g.154362748T>A | CA415237518 | FLNA | c.2317A>T (p.Lys773Ter) c.2236A>T (p.Lys746Ter) c.2374A>T (n.2374A>T) c.279+2688A>T c.2596A>T (n.2596A>T) c.2273A>T (n.2273A>T) c.2116A>T (p.Lys706Ter) | |
X | g.154362748T>C | CA415237519 | FLNA | c.2317A>G (p.Lys773Glu) c.2236A>G (p.Lys746Glu) c.2374A>G (n.2374A>G) c.279+2688A>G c.2596A>G (n.2596A>G) c.2273A>G (n.2273A>G) c.2116A>G (p.Lys706Glu) | ClinVar |
X | g.154362748T>G | CA415237520 | FLNA | c.2317A>C (p.Lys773Gln) c.2236A>C (p.Lys746Gln) c.2374A>C (n.2374A>C) c.279+2688A>C c.2596A>C (n.2596A>C) c.2273A>C (n.2273A>C) c.2116A>C (p.Lys706Gln) | |
X | g.154362749G>A | CA519709109 | FLNA | c.2316C>T (p.Val772=) c.2235C>T (p.Val745=) c.2373C>T (n.2373C>T) c.279+2687C>T c.2595C>T (n.2595C>T) c.2272C>T (n.2272C>T) c.2115C>T (p.Val705=) | |
X | g.154362749G>C | CA519709110 | FLNA | c.2316C>G (p.Val772=) c.2235C>G (p.Val745=) c.2373C>G (n.2373C>G) c.279+2687C>G c.2595C>G (n.2595C>G) c.2272C>G (n.2272C>G) c.2115C>G (p.Val705=) | |
X | g.154362749G= | CA2466656964 | FLNA | c.2316C= (p.Val772=) c.2235C= (p.Val745=) c.2373C= (n.2373C=) c.279+2687C= c.2595C= (n.2595C=) c.2272C= (n.2272C=) c.2115C= (p.Val705=) | |
X | g.154362749G>T | CA519709111 | FLNA | c.2316C>A (p.Val772=) c.2235C>A (p.Val745=) c.2373C>A (n.2373C>A) c.279+2687C>A c.2595C>A (n.2595C>A) c.2272C>A (n.2272C>A) c.2115C>A (p.Val705=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
X | g.154362750A>C | CA415237521 | FLNA | c.2315T>G (p.Val772Gly) c.2234T>G (p.Val745Gly) c.2372T>G (n.2372T>G) c.279+2686T>G c.2594T>G (n.2594T>G) c.2271T>G (n.2271T>G) c.2114T>G (p.Val705Gly) | |
X | g.154362750A>G | CA415237522 | FLNA | c.2315T>C (p.Val772Ala) c.2234T>C (p.Val745Ala) c.2372T>C (n.2372T>C) c.279+2686T>C c.2594T>C (n.2594T>C) c.2271T>C (n.2271T>C) c.2114T>C (p.Val705Ala) | |
X | g.154362750A>T | CA415237523 | FLNA | c.2315T>A (p.Val772Asp) c.2234T>A (p.Val745Asp) c.2372T>A (n.2372T>A) c.279+2686T>A c.2594T>A (n.2594T>A) c.2271T>A (n.2271T>A) c.2114T>A (p.Val705Asp) | |
X | g.154362751C>A | CA415237524 | FLNA | c.2314G>T (p.Val772Phe) c.2233G>T (p.Val745Phe) c.2371G>T (n.2371G>T) c.279+2685G>T c.2593G>T (n.2593G>T) c.2270G>T (n.2270G>T) c.2113G>T (p.Val705Phe) | |
X | g.154362751C= | CA2466656965 | FLNA | c.2314G= (p.Val772=) c.2233G= (p.Val745=) c.2371G= (n.2371G=) c.279+2685G= c.2593G= (n.2593G=) c.2270G= (n.2270G=) c.2113G= (p.Val705=) | |
X | g.154362751C>G | CA415237526 | FLNA | c.2314G>C (p.Val772Leu) c.2233G>C (p.Val745Leu) c.2371G>C (n.2371G>C) c.279+2685G>C c.2593G>C (n.2593G>C) c.2270G>C (n.2270G>C) c.2113G>C (p.Val705Leu) | |
X | g.154362751C>T | CA415237525 | FLNA | c.2314G>A (p.Val772Ile) c.2233G>A (p.Val745Ile) c.2371G>A (n.2371G>A) c.279+2685G>A c.2593G>A (n.2593G>A) c.2270G>A (n.2270G>A) c.2113G>A (p.Val705Ile) | dbSNP |
X | g.154362752C>A | CA415237527 | FLNA | c.2313G>T (p.Lys771Asn) c.2232G>T (p.Lys744Asn) c.2370G>T (n.2370G>T) c.279+2684G>T c.2592G>T (n.2592G>T) c.2269G>T (n.2269G>T) c.2112G>T (p.Lys704Asn) | COSMIC COSMIC |
X | g.154362752C= | CA2466656966 | FLNA | c.2313G= (p.Lys771=) c.2232G= (p.Lys744=) c.2370G= (n.2370G=) c.279+2684G= c.2592G= (n.2592G=) c.2269G= (n.2269G=) c.2112G= (p.Lys704=) | |
X | g.154362752C>G | CA415237528 | FLNA | c.2313G>C (p.Lys771Asn) c.2232G>C (p.Lys744Asn) c.2370G>C (n.2370G>C) c.279+2684G>C c.2592G>C (n.2592G>C) c.2269G>C (n.2269G>C) c.2112G>C (p.Lys704Asn) | |
X | g.154362752C>T | CA10560956 | FLNA | c.2313G>A (p.Lys771=) c.2232G>A (p.Lys744=) c.2370G>A (n.2370G>A) c.279+2684G>A c.2592G>A (n.2592G>A) c.2269G>A (n.2269G>A) c.2112G>A (p.Lys704=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154362753T>A | CA415237529 | FLNA | c.2312A>T (p.Lys771Met) c.2231A>T (p.Lys744Met) c.2369A>T (n.2369A>T) c.279+2683A>T c.2591A>T (n.2591A>T) c.2268A>T (n.2268A>T) c.2111A>T (p.Lys704Met) | |
X | g.154362753T>C | CA415237530 | FLNA | c.2312A>G (p.Lys771Arg) c.2231A>G (p.Lys744Arg) c.2369A>G (n.2369A>G) c.279+2683A>G c.2591A>G (n.2591A>G) c.2268A>G (n.2268A>G) c.2111A>G (p.Lys704Arg) | gnomAD v4 |
X | g.154362753T>G | CA415237531 | FLNA | c.2312A>C (p.Lys771Thr) c.2231A>C (p.Lys744Thr) c.2369A>C (n.2369A>C) c.279+2683A>C c.2591A>C (n.2591A>C) c.2268A>C (n.2268A>C) c.2111A>C (p.Lys704Thr) | |
X | g.154362754T>A | CA415237532 | FLNA | c.2311A>T (p.Lys771Ter) c.2230A>T (p.Lys744Ter) c.2368A>T (n.2368A>T) c.279+2682A>T c.2590A>T (n.2590A>T) c.2267A>T (n.2267A>T) c.2110A>T (p.Lys704Ter) | |
X | g.154362754T>C | CA415237533 | FLNA | c.2311A>G (p.Lys771Glu) c.2230A>G (p.Lys744Glu) c.2368A>G (n.2368A>G) c.279+2682A>G c.2590A>G (n.2590A>G) c.2267A>G (n.2267A>G) c.2110A>G (p.Lys704Glu) | |
X | g.154362754T>G | CA415237534 | FLNA | c.2311A>C (p.Lys771Gln) c.2230A>C (p.Lys744Gln) c.2368A>C (n.2368A>C) c.279+2682A>C c.2590A>C (n.2590A>C) c.2267A>C (n.2267A>C) c.2110A>C (p.Lys704Gln) | |
X | g.154362755G>A | CA10560958 | FLNA | c.2310C>T (p.Asn770=) c.2229C>T (p.Asn743=) c.2367C>T (n.2367C>T) c.279+2681C>T c.2589C>T (n.2589C>T) c.2266C>T (n.2266C>T) c.2109C>T (p.Asn703=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154362755G>C | CA415237535 | FLNA | c.2310C>G (p.Asn770Lys) c.2229C>G (p.Asn743Lys) c.2367C>G (n.2367C>G) c.279+2681C>G c.2589C>G (n.2589C>G) c.2266C>G (n.2266C>G) c.2109C>G (p.Asn703Lys) | |
X | g.154362755G= | CA2466656967 | FLNA | c.2310C= (p.Asn770=) c.2229C= (p.Asn743=) c.2367C= (n.2367C=) c.279+2681C= c.2589C= (n.2589C=) c.2266C= (n.2266C=) c.2109C= (p.Asn703=) | |
X | g.154362755G>T | CA10560957 | FLNA | c.2310C>A (p.Asn770Lys) c.2229C>A (p.Asn743Lys) c.2367C>A (n.2367C>A) c.279+2681C>A c.2589C>A (n.2589C>A) c.2266C>A (n.2266C>A) c.2109C>A (p.Asn703Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154362756T>A | CA415237536 | FLNA | c.2309A>T (p.Asn770Ile) c.2228A>T (p.Asn743Ile) c.2366A>T (n.2366A>T) c.279+2680A>T c.2588A>T (n.2588A>T) c.2265A>T (n.2265A>T) c.2108A>T (p.Asn703Ile) | |
X | g.154362756T>C | CA415237538 | FLNA | c.2309A>G (p.Asn770Ser) c.2228A>G (p.Asn743Ser) c.2366A>G (n.2366A>G) c.279+2680A>G c.2588A>G (n.2588A>G) c.2265A>G (n.2265A>G) c.2108A>G (p.Asn703Ser) | ClinVar dbSNP gnomAD v4 |
X | g.154362756T>G | CA415237537 | FLNA | c.2309A>C (p.Asn770Thr) c.2228A>C (p.Asn743Thr) c.2366A>C (n.2366A>C) c.279+2680A>C c.2588A>C (n.2588A>C) c.2265A>C (n.2265A>C) c.2108A>C (p.Asn703Thr) | |
X | g.154362756T= | CA2466656968 | FLNA | c.2309A= (p.Asn770=) c.2228A= (p.Asn743=) c.2366A= (n.2366A=) c.279+2680A= c.2588A= (n.2588A=) c.2265A= (n.2265A=) c.2108A= (p.Asn703=) | |
X | g.154362757T>A | CA415237539 | FLNA | c.2308A>T (p.Asn770Tyr) c.2227A>T (p.Asn743Tyr) c.2365A>T (n.2365A>T) c.279+2679A>T c.2587A>T (n.2587A>T) c.2264A>T (n.2264A>T) c.2107A>T (p.Asn703Tyr) | |
X | g.154362757T>C | CA415237540 | FLNA | c.2308A>G (p.Asn770Asp) c.2227A>G (p.Asn743Asp) c.2365A>G (n.2365A>G) c.279+2679A>G c.2587A>G (n.2587A>G) c.2264A>G (n.2264A>G) c.2107A>G (p.Asn703Asp) | |
X | g.154362757T>G | CA415237541 | FLNA | c.2308A>C (p.Asn770His) c.2227A>C (p.Asn743His) c.2365A>C (n.2365A>C) c.279+2679A>C c.2587A>C (n.2587A>C) c.2264A>C (n.2264A>C) c.2107A>C (p.Asn703His) | |
X | g.154362758G>A | CA519709132 | FLNA | c.2307C>T (p.Pro769=) c.2226C>T (p.Pro742=) c.2364C>T (n.2364C>T) c.279+2678C>T c.2586C>T (n.2586C>T) c.2263C>T (n.2263C>T) c.2106C>T (p.Pro702=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154362758G>C | CA519709135 | FLNA | c.2307C>G (p.Pro769=) c.2226C>G (p.Pro742=) c.2364C>G (n.2364C>G) c.279+2678C>G c.2586C>G (n.2586C>G) c.2263C>G (n.2263C>G) c.2106C>G (p.Pro702=) | |
X | g.154362758G= | CA2466656969 | FLNA | c.2307C= (p.Pro769=) c.2226C= (p.Pro742=) c.2364C= (n.2364C=) c.279+2678C= c.2586C= (n.2586C=) c.2263C= (n.2263C=) c.2106C= (p.Pro702=) | |
X | g.154362758G>T | CA519709138 | FLNA | c.2307C>A (p.Pro769=) c.2226C>A (p.Pro742=) c.2364C>A (n.2364C>A) c.279+2678C>A c.2586C>A (n.2586C>A) c.2263C>A (n.2263C>A) c.2106C>A (p.Pro702=) | dbSNP |
X | g.154362759G>A | CA415237542 | FLNA | c.2306C>T (p.Pro769Leu) c.2225C>T (p.Pro742Leu) c.2363C>T (n.2363C>T) c.279+2677C>T c.2585C>T (n.2585C>T) c.2262C>T (n.2262C>T) c.2105C>T (p.Pro702Leu) | |
X | g.154362759G>C | CA415237543 | FLNA | c.2306C>G (p.Pro769Arg) c.2225C>G (p.Pro742Arg) c.2363C>G (n.2363C>G) c.279+2677C>G c.2585C>G (n.2585C>G) c.2262C>G (n.2262C>G) c.2105C>G (p.Pro702Arg) | |
X | g.154362759G= | CA2466656970 | FLNA | c.2306C= (p.Pro769=) c.2225C= (p.Pro742=) c.2363C= (n.2363C=) c.279+2677C= c.2585C= (n.2585C=) c.2262C= (n.2262C=) c.2105C= (p.Pro702=) | |
X | g.154362759G>T | CA10560959 | FLNA | c.2306C>A (p.Pro769His) c.2225C>A (p.Pro742His) c.2363C>A (n.2363C>A) c.279+2677C>A c.2585C>A (n.2585C>A) c.2262C>A (n.2262C>A) c.2105C>A (p.Pro702His) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.154362760G>A | CA415237544 | FLNA | c.2305C>T (p.Pro769Ser) c.2224C>T (p.Pro742Ser) c.2362C>T (n.2362C>T) c.279+2676C>T c.2584C>T (n.2584C>T) c.2261C>T (n.2261C>T) c.2104C>T (p.Pro702Ser) | |
X | g.154362760G>C | CA415237545 | FLNA | c.2305C>G (p.Pro769Ala) c.2224C>G (p.Pro742Ala) c.2362C>G (n.2362C>G) c.279+2676C>G c.2584C>G (n.2584C>G) c.2261C>G (n.2261C>G) c.2104C>G (p.Pro702Ala) | |
X | g.154362760G>T | CA415237546 | FLNA | c.2305C>A (p.Pro769Thr) c.2224C>A (p.Pro742Thr) c.2362C>A (n.2362C>A) c.279+2676C>A c.2584C>A (n.2584C>A) c.2261C>A (n.2261C>A) c.2104C>A (p.Pro702Thr) | |
X | g.154362761G>A | CA519709147 | FLNA | c.2304C>T (p.His768=) c.2223C>T (p.His741=) c.2361C>T (n.2361C>T) c.279+2675C>T c.2583C>T (n.2583C>T) c.2260C>T (n.2260C>T) c.2103C>T (p.His701=) | |
X | g.154362761G>C | CA415237548 | FLNA | c.2304C>G (p.His768Gln) c.2223C>G (p.His741Gln) c.2361C>G (n.2361C>G) c.279+2675C>G c.2583C>G (n.2583C>G) c.2260C>G (n.2260C>G) c.2103C>G (p.His701Gln) | |
X | g.154362761G>T | CA415237547 | FLNA | c.2304C>A (p.His768Gln) c.2223C>A (p.His741Gln) c.2361C>A (n.2361C>A) c.279+2675C>A c.2583C>A (n.2583C>A) c.2260C>A (n.2260C>A) c.2103C>A (p.His701Gln) | |
X | g.154362762T>A | CA415237549 | FLNA | c.2303A>T (p.His768Leu) c.2222A>T (p.His741Leu) c.2360A>T (n.2360A>T) c.279+2674A>T c.2582A>T (n.2582A>T) c.2259A>T (n.2259A>T) c.2102A>T (p.His701Leu) | |
X | g.154362762T>C | CA415237550 | FLNA | c.2303A>G (p.His768Arg) c.2222A>G (p.His741Arg) c.2360A>G (n.2360A>G) c.279+2674A>G c.2582A>G (n.2582A>G) c.2259A>G (n.2259A>G) c.2102A>G (p.His701Arg) | |
X | g.154362762T>G | CA415237551 | FLNA | c.2303A>C (p.His768Pro) c.2222A>C (p.His741Pro) c.2360A>C (n.2360A>C) c.279+2674A>C c.2582A>C (n.2582A>C) c.2259A>C (n.2259A>C) c.2102A>C (p.His701Pro) | |
X | g.154362763G>A | CA415237552 | FLNA | c.2302C>T (p.His768Tyr) c.2221C>T (p.His741Tyr) c.2359C>T (n.2359C>T) c.279+2673C>T c.2581C>T (n.2581C>T) c.2258C>T (n.2258C>T) c.2101C>T (p.His701Tyr) | |
X | g.154362763G>C | CA415237553 | FLNA | c.2302C>G (p.His768Asp) c.2221C>G (p.His741Asp) c.2359C>G (n.2359C>G) c.279+2673C>G c.2581C>G (n.2581C>G) c.2258C>G (n.2258C>G) c.2101C>G (p.His701Asp) | |
X | g.154362763G>T | CA415237554 | FLNA | c.2302C>A (p.His768Asn) c.2221C>A (p.His741Asn) c.2359C>A (n.2359C>A) c.279+2673C>A c.2581C>A (n.2581C>A) c.2258C>A (n.2258C>A) c.2101C>A (p.His701Asn) | ClinVar dbSNP gnomAD v4 |
X | g.154362764del | CA2842895844 | FLNA | c.2302del (p.His768ThrfsTer12) c.2221del (p.His741ThrfsTer12) c.2359del (n.2359del) c.279+2673del c.2581del (n.2581del) c.2258del (n.2258del) c.2101del (p.His701ThrfsTer12) | |
X | g.154362764G>A | CA519709157 | FLNA | c.2301C>T (p.Ser767=) c.2220C>T (p.Ser740=) c.2358C>T (n.2358C>T) c.279+2672C>T c.2580C>T (n.2580C>T) c.2257C>T (n.2257C>T) c.2100C>T (p.Ser700=) | |
X | g.154362764G>C | CA415237556 | FLNA | c.2301C>G (p.Ser767Arg) c.2220C>G (p.Ser740Arg) c.2358C>G (n.2358C>G) c.279+2672C>G c.2580C>G (n.2580C>G) c.2257C>G (n.2257C>G) c.2100C>G (p.Ser700Arg) | |
X | g.154362764G>T | CA415237555 | FLNA | c.2301C>A (p.Ser767Arg) c.2220C>A (p.Ser740Arg) c.2358C>A (n.2358C>A) c.279+2672C>A c.2580C>A (n.2580C>A) c.2257C>A (n.2257C>A) c.2100C>A (p.Ser700Arg) | |
X | g.154362765C>A | CA415237557 | FLNA | c.2300G>T (p.Ser767Ile) c.2219G>T (p.Ser740Ile) c.2357G>T (n.2357G>T) c.279+2671G>T c.2579G>T (n.2579G>T) c.2256G>T (n.2256G>T) c.2099G>T (p.Ser700Ile) | dbSNP gnomAD v2 gnomAD v4 |
X | g.154362765C= | CA2466656971 | FLNA | c.2300G= (p.Ser767=) c.2219G= (p.Ser740=) c.2357G= (n.2357G=) c.279+2671G= c.2579G= (n.2579G=) c.2256G= (n.2256G=) c.2099G= (p.Ser700=) | |
X | g.154362765C>G | CA415237558 | FLNA | c.2300G>C (p.Ser767Thr) c.2219G>C (p.Ser740Thr) c.2357G>C (n.2357G>C) c.279+2671G>C c.2579G>C (n.2579G>C) c.2256G>C (n.2256G>C) c.2099G>C (p.Ser700Thr) | |
X | g.154362765C>T | CA415237559 | FLNA | c.2300G>A (p.Ser767Asn) c.2219G>A (p.Ser740Asn) c.2357G>A (n.2357G>A) c.279+2671G>A c.2579G>A (n.2579G>A) c.2256G>A (n.2256G>A) c.2099G>A (p.Ser700Asn) | |
X | g.154362766T>A | CA415237560 | FLNA | c.2299A>T (p.Ser767Cys) c.2218A>T (p.Ser740Cys) c.2356A>T (n.2356A>T) c.279+2670A>T c.2578A>T (n.2578A>T) c.2255A>T (n.2255A>T) c.2098A>T (p.Ser700Cys) | |
X | g.154362766T>C | CA415237561 | FLNA | c.2299A>G (p.Ser767Gly) c.2218A>G (p.Ser740Gly) c.2356A>G (n.2356A>G) c.279+2670A>G c.2578A>G (n.2578A>G) c.2255A>G (n.2255A>G) c.2098A>G (p.Ser700Gly) | |
X | g.154362766T>G | CA415237562 | FLNA | c.2299A>C (p.Ser767Arg) c.2218A>C (p.Ser740Arg) c.2356A>C (n.2356A>C) c.279+2670A>C c.2578A>C (n.2578A>C) c.2255A>C (n.2255A>C) c.2098A>C (p.Ser700Arg) | |
X | g.154362767G>A | CA519709167 | FLNA | c.2298C>T (p.Gly766=) c.2217C>T (p.Gly739=) c.2355C>T (n.2355C>T) c.279+2669C>T c.2577C>T (n.2577C>T) c.2254C>T (n.2254C>T) c.2097C>T (p.Gly699=) | gnomAD v4 |
X | g.154362767G>C | CA519709170 | FLNA | c.2298C>G (p.Gly766=) c.2217C>G (p.Gly739=) c.2355C>G (n.2355C>G) c.279+2669C>G c.2577C>G (n.2577C>G) c.2254C>G (n.2254C>G) c.2097C>G (p.Gly699=) | |
X | g.154362767G>T | CA519709173 | FLNA | c.2298C>A (p.Gly766=) c.2217C>A (p.Gly739=) c.2355C>A (n.2355C>A) c.279+2669C>A c.2577C>A (n.2577C>A) c.2254C>A (n.2254C>A) c.2097C>A (p.Gly699=) | |
X | g.154362768C>A | CA415237563 | FLNA | c.2297G>T (p.Gly766Val) c.2216G>T (p.Gly739Val) c.2354G>T (n.2354G>T) c.279+2668G>T c.2576G>T (n.2576G>T) c.2253G>T (n.2253G>T) c.2096G>T (p.Gly699Val) | |
X | g.154362768C>G | CA415237565 | FLNA | c.2297G>C (p.Gly766Ala) c.2216G>C (p.Gly739Ala) c.2354G>C (n.2354G>C) c.279+2668G>C c.2576G>C (n.2576G>C) c.2253G>C (n.2253G>C) c.2096G>C (p.Gly699Ala) | |
X | g.154362768C>T | CA415237564 | FLNA | c.2297G>A (p.Gly766Asp) c.2216G>A (p.Gly739Asp) c.2354G>A (n.2354G>A) c.279+2668G>A c.2576G>A (n.2576G>A) c.2253G>A (n.2253G>A) c.2096G>A (p.Gly699Asp) | |
X | g.154362769C>A | CA415237566 | FLNA | c.2296G>T (p.Gly766Cys) c.2215G>T (p.Gly739Cys) c.2353G>T (n.2353G>T) c.279+2667G>T c.2575G>T (n.2575G>T) c.2252G>T (n.2252G>T) c.2095G>T (p.Gly699Cys) | |
X | g.154362769C>G | CA415237567 | FLNA | c.2296G>C (p.Gly766Arg) c.2215G>C (p.Gly739Arg) c.2353G>C (n.2353G>C) c.279+2667G>C c.2575G>C (n.2575G>C) c.2252G>C (n.2252G>C) c.2095G>C (p.Gly699Arg) | |
X | g.154362769C>T | CA415237568 | FLNA | c.2296G>A (p.Gly766Ser) c.2215G>A (p.Gly739Ser) c.2353G>A (n.2353G>A) c.279+2667G>A c.2575G>A (n.2575G>A) c.2252G>A (n.2252G>A) c.2095G>A (p.Gly699Ser) | gnomAD v4 |
X | g.154362770A>C | CA519709177 | FLNA | c.2295T>G (p.Ala765=) c.2214T>G (p.Ala738=) c.2352T>G (n.2352T>G) c.279+2666T>G c.2574T>G (n.2574T>G) c.2251T>G (n.2251T>G) c.2094T>G (p.Ala698=) | |
X | g.154362770A>G | CA519709180 | FLNA | c.2295T>C (p.Ala765=) c.2214T>C (p.Ala738=) c.2352T>C (n.2352T>C) c.279+2666T>C c.2574T>C (n.2574T>C) c.2251T>C (n.2251T>C) c.2094T>C (p.Ala698=) | |
X | g.154362770A>T | CA519709181 | FLNA | c.2295T>A (p.Ala765=) c.2214T>A (p.Ala738=) c.2352T>A (n.2352T>A) c.279+2666T>A c.2574T>A (n.2574T>A) c.2251T>A (n.2251T>A) c.2094T>A (p.Ala698=) | |
X | g.154362771G>A | CA415237569 | FLNA | c.2294C>T (p.Ala765Val) c.2213C>T (p.Ala738Val) c.2351C>T (n.2351C>T) c.279+2665C>T c.2573C>T (n.2573C>T) c.2250C>T (n.2250C>T) c.2093C>T (p.Ala698Val) | dbSNP gnomAD v2 gnomAD v4 |
X | g.154362771G>C | CA415237570 | FLNA | c.2294C>G (p.Ala765Gly) c.2213C>G (p.Ala738Gly) c.2351C>G (n.2351C>G) c.279+2665C>G c.2573C>G (n.2573C>G) c.2250C>G (n.2250C>G) c.2093C>G (p.Ala698Gly) | |
X | g.154362771G= | CA2466656972 | FLNA | c.2294C= (p.Ala765=) c.2213C= (p.Ala738=) c.2351C= (n.2351C=) c.279+2665C= c.2573C= (n.2573C=) c.2250C= (n.2250C=) c.2093C= (p.Ala698=) | |
X | g.154362771G>T | CA415237571 | FLNA | c.2294C>A (p.Ala765Asp) c.2213C>A (p.Ala738Asp) c.2351C>A (n.2351C>A) c.279+2665C>A c.2573C>A (n.2573C>A) c.2250C>A (n.2250C>A) c.2093C>A (p.Ala698Asp) | gnomAD v4 |
X | g.154362772C>A | CA415237572 | FLNA | c.2293G>T (p.Ala765Ser) c.2212G>T (p.Ala738Ser) c.2350G>T (n.2350G>T) c.279+2664G>T c.2572G>T (n.2572G>T) c.2249G>T (n.2249G>T) c.2092G>T (p.Ala698Ser) | gnomAD v4 |
X | g.154362772C= | CA2466656973 | FLNA | c.2293G= (p.Ala765=) c.2212G= (p.Ala738=) c.2350G= (n.2350G=) c.279+2664G= c.2572G= (n.2572G=) c.2249G= (n.2249G=) c.2092G= (p.Ala698=) | |
X | g.154362772C>G | CA415237573 | FLNA | c.2293G>C (p.Ala765Pro) c.2212G>C (p.Ala738Pro) c.2350G>C (n.2350G>C) c.279+2664G>C c.2572G>C (n.2572G>C) c.2249G>C (n.2249G>C) c.2092G>C (p.Ala698Pro) | |
X | g.154362772C>T | CA415237574 | FLNA | c.2293G>A (p.Ala765Thr) c.2212G>A (p.Ala738Thr) c.2350G>A (n.2350G>A) c.279+2664G>A c.2572G>A (n.2572G>A) c.2249G>A (n.2249G>A) c.2092G>A (p.Ala698Thr) | dbSNP gnomAD v2 COSMIC COSMIC |
X | g.154362773T>A | CA519709186 | FLNA | c.2292A>T (p.Gly764=) c.2211A>T (p.Gly737=) c.2349A>T (n.2349A>T) c.279+2663A>T c.2571A>T (n.2571A>T) c.2248A>T (n.2248A>T) c.2091A>T (p.Gly697=) | |
X | g.154362773T>C | CA519709189 | FLNA | c.2292A>G (p.Gly764=) c.2211A>G (p.Gly737=) c.2349A>G (n.2349A>G) c.279+2663A>G c.2571A>G (n.2571A>G) c.2248A>G (n.2248A>G) c.2091A>G (p.Gly697=) | |
X | g.154362773T>G | CA10560960 | FLNA | c.2292A>C (p.Gly764=) c.2211A>C (p.Gly737=) c.2349A>C (n.2349A>C) c.279+2663A>C c.2571A>C (n.2571A>C) c.2248A>C (n.2248A>C) c.2091A>C (p.Gly697=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.154362773T= | CA2466656974 | FLNA | c.2292A= (p.Gly764=) c.2211A= (p.Gly737=) c.2349A= (n.2349A=) c.279+2663A= c.2571A= (n.2571A=) c.2248A= (n.2248A=) c.2091A= (p.Gly697=) | |
X | g.154362774C>A | CA415237575 | FLNA | c.2291G>T (p.Gly764Val) c.2210G>T (p.Gly737Val) c.2348G>T (n.2348G>T) c.279+2662G>T c.2570G>T (n.2570G>T) c.2247G>T (n.2247G>T) c.2090G>T (p.Gly697Val) | |
X | g.154362774C= | CA2466656975 | FLNA | c.2291G= (p.Gly764=) c.2210G= (p.Gly737=) c.2348G= (n.2348G=) c.279+2662G= c.2570G= (n.2570G=) c.2247G= (n.2247G=) c.2090G= (p.Gly697=) | |
X | g.154362774C>G | CA10560961 | FLNA | c.2291G>C (p.Gly764Ala) c.2210G>C (p.Gly737Ala) c.2348G>C (n.2348G>C) c.279+2662G>C c.2570G>C (n.2570G>C) c.2247G>C (n.2247G>C) c.2090G>C (p.Gly697Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154362774C>T | CA337281882 | FLNA | c.2291G>A (p.Gly764Glu) c.2210G>A (p.Gly737Glu) c.2348G>A (n.2348G>A) c.279+2662G>A c.2570G>A (n.2570G>A) c.2247G>A (n.2247G>A) c.2090G>A (p.Gly697Glu) | dbSNP gnomAD v4 |
X | g.154362775C>A | CA415237576 | FLNA | c.2290G>T (p.Gly764Ter) c.2209G>T (p.Gly737Ter) c.2347G>T (n.2347G>T) c.279+2661G>T c.2569G>T (n.2569G>T) c.2246G>T (n.2246G>T) c.2089G>T (p.Gly697Ter) | gnomAD v4 |
X | g.154362775C>G | CA415237577 | FLNA | c.2290G>C (p.Gly764Arg) c.2209G>C (p.Gly737Arg) c.2347G>C (n.2347G>C) c.279+2661G>C c.2569G>C (n.2569G>C) c.2246G>C (n.2246G>C) c.2089G>C (p.Gly697Arg) | |
X | g.154362775C>T | CA415237578 | FLNA | c.2290G>A (p.Gly764Arg) c.2209G>A (p.Gly737Arg) c.2347G>A (n.2347G>A) c.279+2661G>A c.2569G>A (n.2569G>A) c.2246G>A (n.2246G>A) c.2089G>A (p.Gly697Arg) | gnomAD v4 |
X | g.154362776C>A | CA519709193 | FLNA | c.2289G>T (p.Val763=) c.2208G>T (p.Val736=) c.2346G>T (n.2346G>T) c.279+2660G>T c.2568G>T (n.2568G>T) c.2245G>T (n.2245G>T) c.2088G>T (p.Val696=) | gnomAD v4 |
X | g.154362776C>G | CA519709195 | FLNA | c.2289G>C (p.Val763=) c.2208G>C (p.Val736=) c.2346G>C (n.2346G>C) c.279+2660G>C c.2568G>C (n.2568G>C) c.2245G>C (n.2245G>C) c.2088G>C (p.Val696=) | |
X | g.154362776C>T | CA519709196 | FLNA | c.2289G>A (p.Val763=) c.2208G>A (p.Val736=) c.2346G>A (n.2346G>A) c.279+2660G>A c.2568G>A (n.2568G>A) c.2245G>A (n.2245G>A) c.2088G>A (p.Val696=) | |
X | g.154362777A>C | CA415237579 | FLNA | c.2288T>G (p.Val763Gly) c.2207T>G (p.Val736Gly) c.2345T>G (n.2345T>G) c.279+2659T>G c.2567T>G (n.2567T>G) c.2244T>G (n.2244T>G) c.2087T>G (p.Val696Gly) | |
X | g.154362777A>G | CA415237580 | FLNA | c.2288T>C (p.Val763Ala) c.2207T>C (p.Val736Ala) c.2345T>C (n.2345T>C) c.279+2659T>C c.2567T>C (n.2567T>C) c.2244T>C (n.2244T>C) c.2087T>C (p.Val696Ala) | |
X | g.154362777A>T | CA415237581 | FLNA | c.2288T>A (p.Val763Glu) c.2207T>A (p.Val736Glu) c.2345T>A (n.2345T>A) c.279+2659T>A c.2567T>A (n.2567T>A) c.2244T>A (n.2244T>A) c.2087T>A (p.Val696Glu) | |
X | g.154362778C>A | CA415237582 | FLNA | c.2287G>T (p.Val763Leu) c.2206G>T (p.Val736Leu) c.2344G>T (n.2344G>T) c.279+2658G>T c.2566G>T (n.2566G>T) c.2243G>T (n.2243G>T) c.2086G>T (p.Val696Leu) | gnomAD v4 |
X | g.154362778C>G | CA415237583 | FLNA | c.2287G>C (p.Val763Leu) c.2206G>C (p.Val736Leu) c.2344G>C (n.2344G>C) c.279+2658G>C c.2566G>C (n.2566G>C) c.2243G>C (n.2243G>C) c.2086G>C (p.Val696Leu) | |
X | g.154362778C>T | CA415237584 | FLNA | c.2287G>A (p.Val763Met) c.2206G>A (p.Val736Met) c.2344G>A (n.2344G>A) c.279+2658G>A c.2566G>A (n.2566G>A) c.2243G>A (n.2243G>A) c.2086G>A (p.Val696Met) | |
X | g.154362779A>C | CA415237585 | FLNA | c.2286T>G (p.Asn762Lys) c.2205T>G (p.Asn735Lys) c.2343T>G (n.2343T>G) c.279+2657T>G c.2565T>G (n.2565T>G) c.2242T>G (n.2242T>G) c.2085T>G (p.Asn695Lys) | |
X | g.154362779A>G | CA519709199 | FLNA | c.2286T>C (p.Asn762=) c.2205T>C (p.Asn735=) c.2343T>C (n.2343T>C) c.279+2657T>C c.2565T>C (n.2565T>C) c.2242T>C (n.2242T>C) c.2085T>C (p.Asn695=) | |
X | g.154362779A>T | CA415237586 | FLNA | c.2286T>A (p.Asn762Lys) c.2205T>A (p.Asn735Lys) c.2343T>A (n.2343T>A) c.279+2657T>A c.2565T>A (n.2565T>A) c.2242T>A (n.2242T>A) c.2085T>A (p.Asn695Lys) |