Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154969471A=CA2466849030F8c.869T= (p.Leu290=)
c.*745T= (n.*745T=)
c.764T= (p.Leu255=)
Xg.154969471A>CCA414918137F8c.869T>G (p.Leu290Arg)
c.*745T>G (n.*745T>G)
c.764T>G (p.Leu255Arg)
Xg.154969471A>GCA414918139F8c.869T>C (p.Leu290Pro)
c.*745T>C (n.*745T>C)
c.764T>C (p.Leu255Pro)
 dbSNP
Xg.154969471A>TCA414918138F8c.869T>A (p.Leu290His)
c.*745T>A (n.*745T>A)
c.764T>A (p.Leu255His)
Xg.154969472G>ACA414918141F8c.868C>T (p.Leu290Phe)
c.*744C>T (n.*744C>T)
c.763C>T (p.Leu255Phe)
Xg.154969472G>CCA414918143F8c.868C>G (p.Leu290Val)
c.*744C>G (n.*744C>G)
c.763C>G (p.Leu255Val)
Xg.154969472G>TCA414918144F8c.868C>A (p.Leu290Ile)
c.*744C>A (n.*744C>A)
c.763C>A (p.Leu255Ile)
 COSMIC COSMIC
Xg.154969473G>ACA337337638F8c.867C>T (p.Phe289=)
c.*743C>T (n.*743C>T)
c.762C>T (p.Phe254=)
 dbSNP gnomAD v4
Xg.154969473G>CCA414918145F8c.867C>G (p.Phe289Leu)
c.*743C>G (n.*743C>G)
c.762C>G (p.Phe254Leu)
Xg.154969473G=CA2466849031F8c.867C= (p.Phe289=)
c.*743C= (n.*743C=)
c.762C= (p.Phe254=)
Xg.154969473G>TCA414918147F8c.867C>A (p.Phe289Leu)
c.*743C>A (n.*743C>A)
c.762C>A (p.Phe254Leu)
Xg.154969474A>CCA414918150F8c.866T>G (p.Phe289Cys)
c.*742T>G (n.*742T>G)
c.761T>G (p.Phe254Cys)
Xg.154969474A>GCA414918151F8c.866T>C (p.Phe289Ser)
c.*742T>C (n.*742T>C)
c.761T>C (p.Phe254Ser)
Xg.154969474A>TCA414918152F8c.866T>A (p.Phe289Tyr)
c.*742T>A (n.*742T>A)
c.761T>A (p.Phe254Tyr)
Xg.154969475A>CCA414918157F8c.865T>G (p.Phe289Val)
c.*741T>G (n.*741T>G)
c.760T>G (p.Phe254Val)
Xg.154969475A>GCA414918155F8c.865T>C (p.Phe289Leu)
c.*741T>C (n.*741T>C)
c.760T>C (p.Phe254Leu)
Xg.154969475A>TCA414918153F8c.865T>A (p.Phe289Ile)
c.*741T>A (n.*741T>A)
c.760T>A (p.Phe254Ile)
Xg.154969476T>ACA519367536F8c.864A>T (p.Ile288=)
c.*740A>T (n.*740A>T)
c.759A>T (p.Ile253=)
Xg.154969476T>CCA414918159F8c.864A>G (p.Ile288Met)
c.*740A>G (n.*740A>G)
c.759A>G (p.Ile253Met)
Xg.154969476T>GCA519367538F8c.864A>C (p.Ile288=)
c.*740A>C (n.*740A>C)
c.759A>C (p.Ile253=)
Xg.154969477A>CCA414918165F8c.863T>G (p.Ile288Arg)
c.*739T>G (n.*739T>G)
c.758T>G (p.Ile253Arg)
Xg.154969477A>GCA414918161F8c.863T>C (p.Ile288Thr)
c.*739T>C (n.*739T>C)
c.758T>C (p.Ile253Thr)
Xg.154969477A>TCA414918163F8c.863T>A (p.Ile288Lys)
c.*739T>A (n.*739T>A)
c.758T>A (p.Ile253Lys)
Xg.154969478T>ACA414918167F8c.862A>T (p.Ile288Leu)
c.*738A>T (n.*738A>T)
c.757A>T (p.Ile253Leu)
Xg.154969478T>CCA414918170F8c.862A>G (p.Ile288Val)
c.*738A>G (n.*738A>G)
c.757A>G (p.Ile253Val)
 dbSNP gnomAD v2 gnomAD v4
Xg.154969478T>GCA414918172F8c.862A>C (p.Ile288Leu)
c.*738A>C (n.*738A>C)
c.757A>C (p.Ile253Leu)
Xg.154969478T=CA2466849032F8c.862A= (p.Ile288=)
c.*738A= (n.*738A=)
c.757A= (p.Ile253=)
Xg.154969479delCA2695237470F8c.862del (p.Ile288TyrfsTer10)
c.*738del (n.*738del)
c.757del (p.Ile253TyrfsTer10)
Xg.154969479T>ACA519367547F8c.861A>T (p.Ser287=)
c.*737A>T (n.*737A>T)
c.756A>T (p.Ser252=)
Xg.154969479T>CCA519367549F8c.861A>G (p.Ser287=)
c.*737A>G (n.*737A>G)
c.756A>G (p.Ser252=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.154969479T>GCA519367551F8c.861A>C (p.Ser287=)
c.*737A>C (n.*737A>C)
c.756A>C (p.Ser252=)
Xg.154969479T=CA2466849033F8c.861A= (p.Ser287=)
c.*737A= (n.*737A=)
c.756A= (p.Ser252=)
Xg.154969480G>ACA414918174F8c.860C>T (p.Ser287Leu)
c.*736C>T (n.*736C>T)
c.755C>T (p.Ser252Leu)
Xg.154969480G>CCA414918176F8c.860C>G (p.Ser287Ter)
c.*736C>G (n.*736C>G)
c.755C>G (p.Ser252Ter)
 dbSNP
Xg.154969480G=CA2466849034F8c.860C= (p.Ser287=)
c.*736C= (n.*736C=)
c.755C= (p.Ser252=)
Xg.154969480G>TCA414918178F8c.860C>A (p.Ser287Ter)
c.*736C>A (n.*736C>A)
c.755C>A (p.Ser252Ter)
 dbSNP
Xg.154969481A>CCA414918180F8c.859T>G (p.Ser287Ala)
c.*735T>G (n.*735T>G)
c.754T>G (p.Ser252Ala)
Xg.154969481A>GCA414918182F8c.859T>C (p.Ser287Pro)
c.*735T>C (n.*735T>C)
c.754T>C (p.Ser252Pro)
Xg.154969481A>TCA414918184F8c.859T>A (p.Ser287Thr)
c.*735T>A (n.*735T>A)
c.754T>A (p.Ser252Thr)
Xg.154969482G>ACA519367560F8c.858C>T (p.His286=)
c.*734C>T (n.*734C>T)
c.753C>T (p.His251=)
 gnomAD v4
Xg.154969482G>CCA414918187F8c.858C>G (p.His286Gln)
c.*734C>G (n.*734C>G)
c.753C>G (p.His251Gln)
 dbSNP
Xg.154969482G=CA2466849035F8c.858C= (p.His286=)
c.*734C= (n.*734C=)
c.753C= (p.His251=)
Xg.154969482G>TCA414918185F8c.858C>A (p.His286Gln)
c.*734C>A (n.*734C>A)
c.753C>A (p.His251Gln)
Xg.154969483T>ACA414918189F8c.857A>T (p.His286Leu)
c.*733A>T (n.*733A>T)
c.752A>T (p.His251Leu)
Xg.154969483T>CCA414918191F8c.857A>G (p.His286Arg)
c.*733A>G (n.*733A>G)
c.752A>G (p.His251Arg)
 dbSNP
Xg.154969483T>GCA414918192F8c.857A>C (p.His286Pro)
c.*733A>C (n.*733A>C)
c.752A>C (p.His251Pro)
Xg.154969483T=CA2466849036F8c.857A= (p.His286=)
c.*733A= (n.*733A=)
c.752A= (p.His251=)
Xg.154969483dupCA2695237471F8c.857dup (p.His286GlnfsTer?)
c.*733dup (n.*733dup)
c.752dup (p.His251GlnfsTer?)
Xg.154969484G>ACA414918193F8c.856C>T (p.His286Tyr)
c.*732C>T (n.*732C>T)
c.751C>T (p.His251Tyr)
 dbSNP
Xg.154969484G>CCA414918194F8c.856C>G (p.His286Asp)
c.*732C>G (n.*732C>G)
c.751C>G (p.His251Asp)

Number of alleles fetched