Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.70757986A=CA1918399620ADAMTS14c.2962A= (p.Ile988=)
c.2971A= (p.Ile991=)
c.2461A= (p.Ile821=)
c.2035A= (p.Ile679=)
c.*41A= (n.*41A=)
c.1531A= (p.Ile511=)
10g.70757986A>CCA377108821ADAMTS14c.2962A>C (p.Ile988Leu)
c.2971A>C (p.Ile991Leu)
c.2461A>C (p.Ile821Leu)
c.2035A>C (p.Ile679Leu)
c.*41A>C (n.*41A>C)
c.1531A>C (p.Ile511Leu)
10g.70757986A>GCA5540291ADAMTS14c.2962A>G (p.Ile988Val)
c.2971A>G (p.Ile991Val)
c.2461A>G (p.Ile821Val)
c.2035A>G (p.Ile679Val)
c.*41A>G (n.*41A>G)
c.1531A>G (p.Ile511Val)
dbSNP ExAC
10g.70757986A>TCA377108822ADAMTS14c.2962A>T (p.Ile988Phe)
c.2971A>T (p.Ile991Phe)
c.2461A>T (p.Ile821Phe)
c.2035A>T (p.Ile679Phe)
c.*41A>T (n.*41A>T)
c.1531A>T (p.Ile511Phe)
10g.70757987T>ACA377108823ADAMTS14c.2963T>A (p.Ile988Asn)
c.2972T>A (p.Ile991Asn)
c.2462T>A (p.Ile821Asn)
c.2036T>A (p.Ile679Asn)
c.*42T>A (n.*42T>A)
c.1532T>A (p.Ile511Asn)
10g.70757987T>CCA377108824ADAMTS14c.2963T>C (p.Ile988Thr)
c.2972T>C (p.Ile991Thr)
c.2462T>C (p.Ile821Thr)
c.2036T>C (p.Ile679Thr)
c.*42T>C (n.*42T>C)
c.1532T>C (p.Ile511Thr)
10g.70757987T>GCA377108825ADAMTS14c.2963T>G (p.Ile988Ser)
c.2972T>G (p.Ile991Ser)
c.2462T>G (p.Ile821Ser)
c.2036T>G (p.Ile679Ser)
c.*42T>G (n.*42T>G)
c.1532T>G (p.Ile511Ser)
10g.70757988C>ACA470056185ADAMTS14c.2964C>A (p.Ile988=)
c.2973C>A (p.Ile991=)
c.2463C>A (p.Ile821=)
c.2037C>A (p.Ile679=)
c.*43C>A (n.*43C>A)
c.1533C>A (p.Ile511=)
gnomAD v4
10g.70757988C=CA1918399621ADAMTS14c.2964C= (p.Ile988=)
c.2973C= (p.Ile991=)
c.2463C= (p.Ile821=)
c.2037C= (p.Ile679=)
c.*43C= (n.*43C=)
c.1533C= (p.Ile511=)
10g.70757988C>GCA377108826ADAMTS14c.2964C>G (p.Ile988Met)
c.2973C>G (p.Ile991Met)
c.2463C>G (p.Ile821Met)
c.2037C>G (p.Ile679Met)
c.*43C>G (n.*43C>G)
c.1533C>G (p.Ile511Met)
10g.70757988C>TCA470056186ADAMTS14c.2964C>T (p.Ile988=)
c.2973C>T (p.Ile991=)
c.2463C>T (p.Ile821=)
c.2037C>T (p.Ile679=)
c.*43C>T (n.*43C>T)
c.1533C>T (p.Ile511=)
dbSNP gnomAD v2 gnomAD v4
10g.70757989C>ACA377108827ADAMTS14c.2965C>A (p.Gln989Lys)
c.2974C>A (p.Gln992Lys)
c.2464C>A (p.Gln822Lys)
c.2038C>A (p.Gln680Lys)
c.*44C>A (n.*44C>A)
c.1534C>A (p.Gln512Lys)
10g.70757989C=CA1918399622ADAMTS14c.2965C= (p.Gln989=)
c.2974C= (p.Gln992=)
c.2464C= (p.Gln822=)
c.2038C= (p.Gln680=)
c.*44C= (n.*44C=)
c.1534C= (p.Gln512=)
10g.70757989C>GCA377108828ADAMTS14c.2965C>G (p.Gln989Glu)
c.2974C>G (p.Gln992Glu)
c.2464C>G (p.Gln822Glu)
c.2038C>G (p.Gln680Glu)
c.*44C>G (n.*44C>G)
c.1534C>G (p.Gln512Glu)
10g.70757989C>TCA377108829ADAMTS14c.2965C>T (p.Gln989Ter)
c.2974C>T (p.Gln992Ter)
c.2464C>T (p.Gln822Ter)
c.2038C>T (p.Gln680Ter)
c.*44C>T (n.*44C>T)
c.1534C>T (p.Gln512Ter)
10g.70757990delCA2609525950ADAMTS14c.2966del (p.Gln989ArgfsTer?)
c.2975del (p.Gln992ArgfsTer?)
c.2465del (p.Gln822ArgfsTer?)
c.2039del (p.Gln680ArgfsTer?)
c.*45del (n.*45del)
c.1535del (p.Gln512ArgfsTer?)
gnomAD v4
10g.70757990A=CA1918399623ADAMTS14c.2966A= (p.Gln989=)
c.2975A= (p.Gln992=)
c.2465A= (p.Gln822=)
c.2039A= (p.Gln680=)
c.*45A= (n.*45A=)
c.1535A= (p.Gln512=)
10g.70757990A>CCA377108830ADAMTS14c.2966A>C (p.Gln989Pro)
c.2975A>C (p.Gln992Pro)
c.2465A>C (p.Gln822Pro)
c.2039A>C (p.Gln680Pro)
c.*45A>C (n.*45A>C)
c.1535A>C (p.Gln512Pro)
10g.70757990A>GCA377108831ADAMTS14c.2966A>G (p.Gln989Arg)
c.2975A>G (p.Gln992Arg)
c.2465A>G (p.Gln822Arg)
c.2039A>G (p.Gln680Arg)
c.*45A>G (n.*45A>G)
c.1535A>G (p.Gln512Arg)
dbSNP gnomAD v4
10g.70757990A>TCA377108832ADAMTS14c.2966A>T (p.Gln989Leu)
c.2975A>T (p.Gln992Leu)
c.2465A>T (p.Gln822Leu)
c.2039A>T (p.Gln680Leu)
c.*45A>T (n.*45A>T)
c.1535A>T (p.Gln512Leu)
10g.70757990dupCA668031003ADAMTS14c.2966dup (p.Gln990AlafsTer20)
c.2975dup (p.Gln993AlafsTer20)
c.2465dup (p.Gln823AlafsTer20)
c.2039dup (p.Gln681AlafsTer20)
c.*45dup (n.*45dup)
c.1535dup (p.Gln513AlafsTer20)
dbSNP gnomAD v3 gnomAD v4
10g.70757991G>ACA5540292ADAMTS14c.2967G>A (p.Gln989=)
c.2976G>A (p.Gln992=)
c.2466G>A (p.Gln822=)
c.2040G>A (p.Gln680=)
c.*46G>A (n.*46G>A)
c.1536G>A (p.Gln512=)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.70757991G>CCA377108834ADAMTS14c.2967G>C (p.Gln989His)
c.2976G>C (p.Gln992His)
c.2466G>C (p.Gln822His)
c.2040G>C (p.Gln680His)
c.*46G>C (n.*46G>C)
c.1536G>C (p.Gln512His)
10g.70757991G=CA1918399624ADAMTS14c.2967G= (p.Gln989=)
c.2976G= (p.Gln992=)
c.2466G= (p.Gln822=)
c.2040G= (p.Gln680=)
c.*46G= (n.*46G=)
c.1536G= (p.Gln512=)
10g.70757991G>TCA377108833ADAMTS14c.2967G>T (p.Gln989His)
c.2976G>T (p.Gln992His)
c.2466G>T (p.Gln822His)
c.2040G>T (p.Gln680His)
c.*46G>T (n.*46G>T)
c.1536G>T (p.Gln512His)
gnomAD v4
10g.70757992C>ACA377108837ADAMTS14c.2968C>A (p.Gln990Lys)
c.2977C>A (p.Gln993Lys)
c.2467C>A (p.Gln823Lys)
c.2041C>A (p.Gln681Lys)
c.*47C>A (n.*47C>A)
c.1537C>A (p.Gln513Lys)
10g.70757992C>GCA377108835ADAMTS14c.2968C>G (p.Gln990Glu)
c.2977C>G (p.Gln993Glu)
c.2467C>G (p.Gln823Glu)
c.2041C>G (p.Gln681Glu)
c.*47C>G (n.*47C>G)
c.1537C>G (p.Gln513Glu)
10g.70757992C>TCA377108836ADAMTS14c.2968C>T (p.Gln990Ter)
c.2977C>T (p.Gln993Ter)
c.2467C>T (p.Gln823Ter)
c.2041C>T (p.Gln681Ter)
c.*47C>T (n.*47C>T)
c.1537C>T (p.Gln513Ter)
gnomAD v4
10g.70757993A>CCA377108838ADAMTS14c.2969A>C (p.Gln990Pro)
c.2978A>C (p.Gln993Pro)
c.2468A>C (p.Gln823Pro)
c.2042A>C (p.Gln681Pro)
c.*48A>C (n.*48A>C)
c.1538A>C (p.Gln513Pro)
10g.70757993A>GCA377108839ADAMTS14c.2969A>G (p.Gln990Arg)
c.2978A>G (p.Gln993Arg)
c.2468A>G (p.Gln823Arg)
c.2042A>G (p.Gln681Arg)
c.*48A>G (n.*48A>G)
c.1538A>G (p.Gln513Arg)
10g.70757993A>TCA377108840ADAMTS14c.2969A>T (p.Gln990Leu)
c.2978A>T (p.Gln993Leu)
c.2468A>T (p.Gln823Leu)
c.2042A>T (p.Gln681Leu)
c.*48A>T (n.*48A>T)
c.1538A>T (p.Gln513Leu)
gnomAD v4
10g.70757994G>ACA470056190ADAMTS14c.2970G>A (p.Gln990=)
c.2979G>A (p.Gln993=)
c.2469G>A (p.Gln823=)
c.2043G>A (p.Gln681=)
c.*49G>A (n.*49G>A)
c.1539G>A (p.Gln513=)
10g.70757994G>CCA377108841ADAMTS14c.2970G>C (p.Gln990His)
c.2979G>C (p.Gln993His)
c.2469G>C (p.Gln823His)
c.2043G>C (p.Gln681His)
c.*49G>C (n.*49G>C)
c.1539G>C (p.Gln513His)
10g.70757994G>TCA377108842ADAMTS14c.2970G>T (p.Gln990His)
c.2979G>T (p.Gln993His)
c.2469G>T (p.Gln823His)
c.2043G>T (p.Gln681His)
c.*49G>T (n.*49G>T)
c.1539G>T (p.Gln513His)
gnomAD v4
10g.70757995C>ACA470056191ADAMTS14c.2971C>A (p.Arg991=)
c.2980C>A (p.Arg994=)
c.2470C>A (p.Arg824=)
c.2044C>A (p.Arg682=)
c.*50C>A (n.*50C>A)
c.1540C>A (p.Arg514=)
10g.70757995C=CA1918399625ADAMTS14c.2971C= (p.Arg991=)
c.2980C= (p.Arg994=)
c.2470C= (p.Arg824=)
c.2044C= (p.Arg682=)
c.*50C= (n.*50C=)
c.1540C= (p.Arg514=)
10g.70757995C>GCA377108843ADAMTS14c.2971C>G (p.Arg991Gly)
c.2980C>G (p.Arg994Gly)
c.2470C>G (p.Arg824Gly)
c.2044C>G (p.Arg682Gly)
c.*50C>G (n.*50C>G)
c.1540C>G (p.Arg514Gly)
10g.70757995C>TCA5540293ADAMTS14c.2971C>T (p.Arg991Trp)
c.2980C>T (p.Arg994Trp)
c.2470C>T (p.Arg824Trp)
c.2044C>T (p.Arg682Trp)
c.*50C>T (n.*50C>T)
c.1540C>T (p.Arg514Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.70757995_70757996delinsCGCA1918399626ADAMTS14c.2971_2972delinsCG (p.Arg991=)
c.2980_2981delinsCG (p.Arg994=)
c.2470_2471delinsCG (p.Arg824=)
c.2044_2045delinsCG (p.Arg682=)
c.*50_*51delinsCG (n.*50_*51delinsCG)
c.1540_1541delinsCG (p.Arg514=)
10g.70757996G>ACA5540294ADAMTS14c.2972G>A (p.Arg991Gln)
c.2981G>A (p.Arg994Gln)
c.2471G>A (p.Arg824Gln)
c.2045G>A (p.Arg682Gln)
c.*51G>A (n.*51G>A)
c.1541G>A (p.Arg514Gln)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.70757996G>CCA377108844ADAMTS14c.2972G>C (p.Arg991Pro)
c.2981G>C (p.Arg994Pro)
c.2471G>C (p.Arg824Pro)
c.2045G>C (p.Arg682Pro)
c.*51G>C (n.*51G>C)
c.1541G>C (p.Arg514Pro)
10g.70757996G=CA1918399627ADAMTS14c.2972G= (p.Arg991=)
c.2981G= (p.Arg994=)
c.2471G= (p.Arg824=)
c.2045G= (p.Arg682=)
c.*51G= (n.*51G=)
c.1541G= (p.Arg514=)
10g.70757996G>TCA5540295ADAMTS14c.2972G>T (p.Arg991Leu)
c.2981G>T (p.Arg994Leu)
c.2471G>T (p.Arg824Leu)
c.2045G>T (p.Arg682Leu)
c.*51G>T (n.*51G>T)
c.1541G>T (p.Arg514Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.70757997delCA668031022ADAMTS14c.2973del (p.Gln992ArgfsTer?)
c.2982del (p.Gln995ArgfsTer?)
c.2472del (p.Gln825ArgfsTer?)
c.2046del (p.Gln683ArgfsTer?)
c.*52del (n.*52del)
c.1542del (p.Gln515ArgfsTer?)
dbSNP gnomAD v3 gnomAD v4
10g.70757997G>ACA470056192ADAMTS14c.2973G>A (p.Arg991=)
c.2982G>A (p.Arg994=)
c.2472G>A (p.Arg824=)
c.2046G>A (p.Arg682=)
c.*52G>A (n.*52G>A)
c.1542G>A (p.Arg514=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.70757997G>CCA470056194ADAMTS14c.2973G>C (p.Arg991=)
c.2982G>C (p.Arg994=)
c.2472G>C (p.Arg824=)
c.2046G>C (p.Arg682=)
c.*52G>C (n.*52G>C)
c.1542G>C (p.Arg514=)
10g.70757997G=CA1918399628ADAMTS14c.2973G= (p.Arg991=)
c.2982G= (p.Arg994=)
c.2472G= (p.Arg824=)
c.2046G= (p.Arg682=)
c.*52G= (n.*52G=)
c.1542G= (p.Arg514=)
10g.70757997G>TCA5540296ADAMTS14c.2973G>T (p.Arg991=)
c.2982G>T (p.Arg994=)
c.2472G>T (p.Arg824=)
c.2046G>T (p.Arg682=)
c.*52G>T (n.*52G>T)
c.1542G>T (p.Arg514=)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.70757998C>ACA377108847ADAMTS14c.2974C>A (p.Gln992Lys)
c.2983C>A (p.Gln995Lys)
c.2473C>A (p.Gln825Lys)
c.2047C>A (p.Gln683Lys)
c.*53C>A (n.*53C>A)
c.1543C>A (p.Gln515Lys)
10g.70757998C=CA1918399629ADAMTS14c.2974C= (p.Gln992=)
c.2983C= (p.Gln995=)
c.2473C= (p.Gln825=)
c.2047C= (p.Gln683=)
c.*53C= (n.*53C=)
c.1543C= (p.Gln515=)

Number of alleles fetched