Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.32491325_32491331delCA915950907DMDn.2779_2785del
c.2572_2578del (p.Thr858HisfsTer11)
c.2560_2566del (p.Thr854HisfsTer11)
c.94-126128_94-126122del (n.94-126128_94-126122del)
c.94-126617_94-126611del (n.94-126617_94-126611del)
n.336-274264_336-274258del
c.2548_2554del (p.Thr850HisfsTer11)
c.2203_2209del (p.Thr735HisfsTer11)
c.2443_2449del (p.Thr815HisfsTer11)
ClinVar dbSNP
Xg.32491327_32491334delCA2695232031DMDn.2775_2782del
c.2568_2575del (p.Gln856HisfsTer9)
c.2556_2563del (p.Gln852HisfsTer9)
c.94-126132_94-126125del (n.94-126132_94-126125del)
c.94-126621_94-126614del (n.94-126621_94-126614del)
n.336-274268_336-274261del
c.2544_2551del (p.Gln848HisfsTer9)
c.2199_2206del (p.Gln733HisfsTer9)
c.2439_2446del (p.Gln813HisfsTer9)
Xg.32491330delCA2695232032DMDn.2778del
c.2571del (p.Thr858ProfsTer13)
c.2559del (p.Thr854ProfsTer13)
c.94-126129del (n.94-126129del)
c.94-126618del (n.94-126618del)
n.336-274265del
c.2547del (p.Thr850ProfsTer13)
c.2202del (p.Thr735ProfsTer13)
c.2442del (p.Thr815ProfsTer13)
Xg.32491330G>ACA10379494DMDn.2776C>T
c.2569C>T (p.Pro857Ser)
c.2557C>T (p.Pro853Ser)
c.94-126131C>T (n.94-126131C>T)
c.94-126620C>T (n.94-126620C>T)
n.336-274267C>T
c.2545C>T (p.Pro849Ser)
c.2200C>T (p.Pro734Ser)
c.2440C>T (p.Pro814Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.32491330G>CCA412672004DMDn.2776C>G
c.2569C>G (p.Pro857Ala)
c.2557C>G (p.Pro853Ala)
c.94-126131C>G (n.94-126131C>G)
c.94-126620C>G (n.94-126620C>G)
n.336-274267C>G
c.2545C>G (p.Pro849Ala)
c.2200C>G (p.Pro734Ala)
c.2440C>G (p.Pro814Ala)
Xg.32491330G=CA2422829117DMDn.2776C=
c.2569C= (p.Pro857=)
c.2557C= (p.Pro853=)
c.94-126131C= (n.94-126131C=)
c.94-126620C= (n.94-126620C=)
n.336-274267C=
c.2545C= (p.Pro849=)
c.2200C= (p.Pro734=)
c.2440C= (p.Pro814=)
Xg.32491330G>TCA412672006DMDn.2776C>A
c.2569C>A (p.Pro857Thr)
c.2557C>A (p.Pro853Thr)
c.94-126131C>A (n.94-126131C>A)
c.94-126620C>A (n.94-126620C>A)
n.336-274267C>A
c.2545C>A (p.Pro849Thr)
c.2200C>A (p.Pro734Thr)
c.2440C>A (p.Pro814Thr)
Xg.32491331T>ACA412672009DMDn.2775A>T
c.2568A>T (p.Gln856His)
c.2556A>T (p.Gln852His)
c.94-126132A>T (n.94-126132A>T)
c.94-126621A>T (n.94-126621A>T)
n.336-274268A>T
c.2544A>T (p.Gln848His)
c.2199A>T (p.Gln733His)
c.2439A>T (p.Gln813His)
Xg.32491331T>CCA515719996DMDn.2775A>G
c.2568A>G (p.Gln856=)
c.2556A>G (p.Gln852=)
c.94-126132A>G (n.94-126132A>G)
c.94-126621A>G (n.94-126621A>G)
n.336-274268A>G
c.2544A>G (p.Gln848=)
c.2199A>G (p.Gln733=)
c.2439A>G (p.Gln813=)
ClinVar dbSNP gnomAD v4
Xg.32491331T>GCA412672007DMDn.2775A>C
c.2568A>C (p.Gln856His)
c.2556A>C (p.Gln852His)
c.94-126132A>C (n.94-126132A>C)
c.94-126621A>C (n.94-126621A>C)
n.336-274268A>C
c.2544A>C (p.Gln848His)
c.2199A>C (p.Gln733His)
c.2439A>C (p.Gln813His)
Xg.32491332T>ACA412672011DMDn.2774A>T
c.2567A>T (p.Gln856Leu)
c.2555A>T (p.Gln852Leu)
c.94-126133A>T (n.94-126133A>T)
c.94-126622A>T (n.94-126622A>T)
n.336-274269A>T
c.2543A>T (p.Gln848Leu)
c.2198A>T (p.Gln733Leu)
c.2438A>T (p.Gln813Leu)
Xg.32491332T>CCA412672013DMDn.2774A>G
c.2567A>G (p.Gln856Arg)
c.2555A>G (p.Gln852Arg)
c.94-126133A>G (n.94-126133A>G)
c.94-126622A>G (n.94-126622A>G)
n.336-274269A>G
c.2543A>G (p.Gln848Arg)
c.2198A>G (p.Gln733Arg)
c.2438A>G (p.Gln813Arg)
Xg.32491332T>GCA412672015DMDn.2774A>C
c.2567A>C (p.Gln856Pro)
c.2555A>C (p.Gln852Pro)
c.94-126133A>C (n.94-126133A>C)
c.94-126622A>C (n.94-126622A>C)
n.336-274269A>C
c.2543A>C (p.Gln848Pro)
c.2198A>C (p.Gln733Pro)
c.2438A>C (p.Gln813Pro)
dbSNP gnomAD v2 gnomAD v4
Xg.32491332T=CA2422829118DMDn.2774A=
c.2567A= (p.Gln856=)
c.2555A= (p.Gln852=)
c.94-126133A= (n.94-126133A=)
c.94-126622A= (n.94-126622A=)
n.336-274269A=
c.2543A= (p.Gln848=)
c.2198A= (p.Gln733=)
c.2438A= (p.Gln813=)
Xg.32491333G>ACA412672017DMDn.2773C>T
c.2566C>T (p.Gln856Ter)
c.2554C>T (p.Gln852Ter)
c.94-126134C>T (n.94-126134C>T)
c.94-126623C>T (n.94-126623C>T)
n.336-274270C>T
c.2542C>T (p.Gln848Ter)
c.2197C>T (p.Gln733Ter)
c.2437C>T (p.Gln813Ter)
ClinVar
Xg.32491333G>CCA412672018DMDn.2773C>G
c.2566C>G (p.Gln856Glu)
c.2554C>G (p.Gln852Glu)
c.94-126134C>G (n.94-126134C>G)
c.94-126623C>G (n.94-126623C>G)
n.336-274270C>G
c.2542C>G (p.Gln848Glu)
c.2197C>G (p.Gln733Glu)
c.2437C>G (p.Gln813Glu)
Xg.32491333G>TCA412672020DMDn.2773C>A
c.2566C>A (p.Gln856Lys)
c.2554C>A (p.Gln852Lys)
c.94-126134C>A (n.94-126134C>A)
c.94-126623C>A (n.94-126623C>A)
n.336-274270C>A
c.2542C>A (p.Gln848Lys)
c.2197C>A (p.Gln733Lys)
c.2437C>A (p.Gln813Lys)
Xg.32491334G>ACA515719997DMDn.2772C>T
c.2565C>T (p.Ile855=)
c.2553C>T (p.Ile851=)
c.94-126135C>T (n.94-126135C>T)
c.94-126624C>T (n.94-126624C>T)
n.336-274271C>T
c.2541C>T (p.Ile847=)
c.2196C>T (p.Ile732=)
c.2436C>T (p.Ile812=)
ClinVar dbSNP
Xg.32491334G>CCA412672022DMDn.2772C>G
c.2565C>G (p.Ile855Met)
c.2553C>G (p.Ile851Met)
c.94-126135C>G (n.94-126135C>G)
c.94-126624C>G (n.94-126624C>G)
n.336-274271C>G
c.2541C>G (p.Ile847Met)
c.2196C>G (p.Ile732Met)
c.2436C>G (p.Ile812Met)
Xg.32491334G>TCA515719998DMDn.2772C>A
c.2565C>A (p.Ile855=)
c.2553C>A (p.Ile851=)
c.94-126135C>A (n.94-126135C>A)
c.94-126624C>A (n.94-126624C>A)
n.336-274271C>A
c.2541C>A (p.Ile847=)
c.2196C>A (p.Ile732=)
c.2436C>A (p.Ile812=)
ClinVar dbSNP
Xg.32491335A=CA2422829119DMDn.2771T=
c.2564T= (p.Ile855=)
c.2552T= (p.Ile851=)
c.94-126136T= (n.94-126136T=)
c.94-126625T= (n.94-126625T=)
n.336-274272T=
c.2540T= (p.Ile847=)
c.2195T= (p.Ile732=)
c.2435T= (p.Ile812=)
Xg.32491335A>CCA412672024DMDn.2771T>G
c.2564T>G (p.Ile855Ser)
c.2552T>G (p.Ile851Ser)
c.94-126136T>G (n.94-126136T>G)
c.94-126625T>G (n.94-126625T>G)
n.336-274272T>G
c.2540T>G (p.Ile847Ser)
c.2195T>G (p.Ile732Ser)
c.2435T>G (p.Ile812Ser)
Xg.32491335A>GCA412672025DMDn.2771T>C
c.2564T>C (p.Ile855Thr)
c.2552T>C (p.Ile851Thr)
c.94-126136T>C (n.94-126136T>C)
c.94-126625T>C (n.94-126625T>C)
n.336-274272T>C
c.2540T>C (p.Ile847Thr)
c.2195T>C (p.Ile732Thr)
c.2435T>C (p.Ile812Thr)
dbSNP gnomAD v3 gnomAD v4
Xg.32491335A>TCA412672027DMDn.2771T>A
c.2564T>A (p.Ile855Asn)
c.2552T>A (p.Ile851Asn)
c.94-126136T>A (n.94-126136T>A)
c.94-126625T>A (n.94-126625T>A)
n.336-274272T>A
c.2540T>A (p.Ile847Asn)
c.2195T>A (p.Ile732Asn)
c.2435T>A (p.Ile812Asn)
Xg.32491336T>ACA412672029DMDn.2770A>T
c.2563A>T (p.Ile855Phe)
c.2551A>T (p.Ile851Phe)
c.94-126137A>T (n.94-126137A>T)
c.94-126626A>T (n.94-126626A>T)
n.336-274273A>T
c.2539A>T (p.Ile847Phe)
c.2194A>T (p.Ile732Phe)
c.2434A>T (p.Ile812Phe)
Xg.32491336T>CCA412672031DMDn.2770A>G
c.2563A>G (p.Ile855Val)
c.2551A>G (p.Ile851Val)
c.94-126137A>G (n.94-126137A>G)
c.94-126626A>G (n.94-126626A>G)
n.336-274273A>G
c.2539A>G (p.Ile847Val)
c.2194A>G (p.Ile732Val)
c.2434A>G (p.Ile812Val)
Xg.32491336T>GCA412672033DMDn.2770A>C
c.2563A>C (p.Ile855Leu)
c.2551A>C (p.Ile851Leu)
c.94-126137A>C (n.94-126137A>C)
c.94-126626A>C (n.94-126626A>C)
n.336-274273A>C
c.2539A>C (p.Ile847Leu)
c.2194A>C (p.Ile732Leu)
c.2434A>C (p.Ile812Leu)
Xg.32491339dupCA2580100683DMDn.2770dup
c.2563dup (p.Ile855AsnfsTer13)
c.2551dup (p.Ile851AsnfsTer13)
c.94-126137dup (n.94-126137dup)
c.94-126626dup (n.94-126626dup)
n.336-274273dup
c.2539dup (p.Ile847AsnfsTer13)
c.2194dup (p.Ile732AsnfsTer13)
c.2434dup (p.Ile812AsnfsTer13)
ClinVar
Xg.32491337T>ACA412672035DMDn.2769A>T
c.2562A>T (p.Lys854Asn)
c.2550A>T (p.Lys850Asn)
c.94-126138A>T (n.94-126138A>T)
c.94-126627A>T (n.94-126627A>T)
n.336-274274A>T
c.2538A>T (p.Lys846Asn)
c.2193A>T (p.Lys731Asn)
c.2433A>T (p.Lys811Asn)
Xg.32491337T>CCA515719999DMDn.2769A>G
c.2562A>G (p.Lys854=)
c.2550A>G (p.Lys850=)
c.94-126138A>G (n.94-126138A>G)
c.94-126627A>G (n.94-126627A>G)
n.336-274274A>G
c.2538A>G (p.Lys846=)
c.2193A>G (p.Lys731=)
c.2433A>G (p.Lys811=)
Xg.32491337T>GCA412672037DMDn.2769A>C
c.2562A>C (p.Lys854Asn)
c.2550A>C (p.Lys850Asn)
c.94-126138A>C (n.94-126138A>C)
c.94-126627A>C (n.94-126627A>C)
n.336-274274A>C
c.2538A>C (p.Lys846Asn)
c.2193A>C (p.Lys731Asn)
c.2433A>C (p.Lys811Asn)
gnomAD v4
Xg.32491338T>ACA412672039DMDn.2768A>T
c.2561A>T (p.Lys854Ile)
c.2549A>T (p.Lys850Ile)
c.94-126139A>T (n.94-126139A>T)
c.94-126628A>T (n.94-126628A>T)
n.336-274275A>T
c.2537A>T (p.Lys846Ile)
c.2192A>T (p.Lys731Ile)
c.2432A>T (p.Lys811Ile)
Xg.32491338T>CCA412672043DMDn.2768A>G
c.2561A>G (p.Lys854Arg)
c.2549A>G (p.Lys850Arg)
c.94-126139A>G (n.94-126139A>G)
c.94-126628A>G (n.94-126628A>G)
n.336-274275A>G
c.2537A>G (p.Lys846Arg)
c.2192A>G (p.Lys731Arg)
c.2432A>G (p.Lys811Arg)
Xg.32491338T>GCA412672041DMDn.2768A>C
c.2561A>C (p.Lys854Thr)
c.2549A>C (p.Lys850Thr)
c.94-126139A>C (n.94-126139A>C)
c.94-126628A>C (n.94-126628A>C)
n.336-274275A>C
c.2537A>C (p.Lys846Thr)
c.2192A>C (p.Lys731Thr)
c.2432A>C (p.Lys811Thr)
Xg.32491339T>ACA412672046DMDn.2767A>T
c.2560A>T (p.Lys854Ter)
c.2548A>T (p.Lys850Ter)
c.94-126140A>T (n.94-126140A>T)
c.94-126629A>T (n.94-126629A>T)
n.336-274276A>T
c.2536A>T (p.Lys846Ter)
c.2191A>T (p.Lys731Ter)
c.2431A>T (p.Lys811Ter)
dbSNP
Xg.32491339T>CCA412672047DMDn.2767A>G
c.2560A>G (p.Lys854Glu)
c.2548A>G (p.Lys850Glu)
c.94-126140A>G (n.94-126140A>G)
c.94-126629A>G (n.94-126629A>G)
n.336-274276A>G
c.2536A>G (p.Lys846Glu)
c.2191A>G (p.Lys731Glu)
c.2431A>G (p.Lys811Glu)
Xg.32491339T>GCA412672049DMDn.2767A>C
c.2560A>C (p.Lys854Gln)
c.2548A>C (p.Lys850Gln)
c.94-126140A>C (n.94-126140A>C)
c.94-126629A>C (n.94-126629A>C)
n.336-274276A>C
c.2536A>C (p.Lys846Gln)
c.2191A>C (p.Lys731Gln)
c.2431A>C (p.Lys811Gln)
Xg.32491339_32491340delCA2695232033DMDn.2766_2767del
c.2559_2560del (p.Lys854AsnfsTer13)
c.2547_2548del (p.Lys850AsnfsTer13)
c.94-126141_94-126140del (n.94-126141_94-126140del)
c.94-126630_94-126629del (n.94-126630_94-126629del)
n.336-274277_336-274276del
c.2535_2536del (p.Lys846AsnfsTer13)
c.2190_2191del (p.Lys731AsnfsTer13)
c.2430_2431del (p.Lys811AsnfsTer13)
Xg.32491340C>ACA412672052DMDn.2766G>T
c.2559G>T (p.Leu853Phe)
c.2547G>T (p.Leu849Phe)
c.94-126141G>T (n.94-126141G>T)
c.94-126630G>T (n.94-126630G>T)
n.336-274277G>T
c.2535G>T (p.Leu845Phe)
c.2190G>T (p.Leu730Phe)
c.2430G>T (p.Leu810Phe)
Xg.32491340C>GCA412672054DMDn.2766G>C
c.2559G>C (p.Leu853Phe)
c.2547G>C (p.Leu849Phe)
c.94-126141G>C (n.94-126141G>C)
c.94-126630G>C (n.94-126630G>C)
n.336-274277G>C
c.2535G>C (p.Leu845Phe)
c.2190G>C (p.Leu730Phe)
c.2430G>C (p.Leu810Phe)
Xg.32491340C>TCA515720000DMDn.2766G>A
c.2559G>A (p.Leu853=)
c.2547G>A (p.Leu849=)
c.94-126141G>A (n.94-126141G>A)
c.94-126630G>A (n.94-126630G>A)
n.336-274277G>A
c.2535G>A (p.Leu845=)
c.2190G>A (p.Leu730=)
c.2430G>A (p.Leu810=)
COSMIC COSMIC COSMIC
Xg.32491341A>CCA412672061DMDn.2765T>G
c.2558T>G (p.Leu853Trp)
c.2546T>G (p.Leu849Trp)
c.94-126142T>G (n.94-126142T>G)
c.94-126631T>G (n.94-126631T>G)
n.336-274278T>G
c.2534T>G (p.Leu845Trp)
c.2189T>G (p.Leu730Trp)
c.2429T>G (p.Leu810Trp)
ClinVar dbSNP
Xg.32491341A>GCA412672059DMDn.2765T>C
c.2558T>C (p.Leu853Ser)
c.2546T>C (p.Leu849Ser)
c.94-126142T>C (n.94-126142T>C)
c.94-126631T>C (n.94-126631T>C)
n.336-274278T>C
c.2534T>C (p.Leu845Ser)
c.2189T>C (p.Leu730Ser)
c.2429T>C (p.Leu810Ser)
Xg.32491341A>TCA412672057DMDn.2765T>A
c.2558T>A (p.Leu853Ter)
c.2546T>A (p.Leu849Ter)
c.94-126142T>A (n.94-126142T>A)
c.94-126631T>A (n.94-126631T>A)
n.336-274278T>A
c.2534T>A (p.Leu845Ter)
c.2189T>A (p.Leu730Ter)
c.2429T>A (p.Leu810Ter)
dbSNP
Xg.32491342A=CA2422829120DMDn.2764T=
c.2557T= (p.Leu853=)
c.2545T= (p.Leu849=)
c.94-126143T= (n.94-126143T=)
c.94-126632T= (n.94-126632T=)
n.336-274279T=
c.2533T= (p.Leu845=)
c.2188T= (p.Leu730=)
c.2428T= (p.Leu810=)
Xg.32491342A>CCA412672063DMDn.2764T>G
c.2557T>G (p.Leu853Val)
c.2545T>G (p.Leu849Val)
c.94-126143T>G (n.94-126143T>G)
c.94-126632T>G (n.94-126632T>G)
n.336-274279T>G
c.2533T>G (p.Leu845Val)
c.2188T>G (p.Leu730Val)
c.2428T>G (p.Leu810Val)
Xg.32491342A>GCA10379495DMDn.2764T>C
c.2557T>C (p.Leu853=)
c.2545T>C (p.Leu849=)
c.94-126143T>C (n.94-126143T>C)
c.94-126632T>C (n.94-126632T>C)
n.336-274279T>C
c.2533T>C (p.Leu845=)
c.2188T>C (p.Leu730=)
c.2428T>C (p.Leu810=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.32491342A>TCA412672066DMDn.2764T>A
c.2557T>A (p.Leu853Met)
c.2545T>A (p.Leu849Met)
c.94-126143T>A (n.94-126143T>A)
c.94-126632T>A (n.94-126632T>A)
n.336-274279T>A
c.2533T>A (p.Leu845Met)
c.2188T>A (p.Leu730Met)
c.2428T>A (p.Leu810Met)
Xg.32491343C>ACA412672068DMDn.2763G>T
c.2556G>T (p.Trp852Cys)
c.2544G>T (p.Trp848Cys)
c.94-126144G>T (n.94-126144G>T)
c.94-126633G>T (n.94-126633G>T)
n.336-274280G>T
c.2532G>T (p.Trp844Cys)
c.2187G>T (p.Trp729Cys)
c.2427G>T (p.Trp809Cys)
ClinVar dbSNP
Xg.32491343C=CA2422829121DMDn.2763G=
c.2556G= (p.Trp852=)
c.2544G= (p.Trp848=)
c.94-126144G= (n.94-126144G=)
c.94-126633G= (n.94-126633G=)
n.336-274280G=
c.2532G= (p.Trp844=)
c.2187G= (p.Trp729=)
c.2427G= (p.Trp809=)

Number of alleles fetched