Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154969329_154969448delCA2695237407F8c.893_1009+3del
c.*769_*885+3del
c.788_904+3del
Xg.154969373C>ACA414917726F8c.967G>T (p.Gly323Ter)
c.*843G>T (n.*843G>T)
c.862G>T (p.Gly288Ter)
Xg.154969373C>GCA414917723F8c.967G>C (p.Gly323Arg)
c.*843G>C (n.*843G>C)
c.862G>C (p.Gly288Arg)
Xg.154969373C>TCA414917724F8c.967G>A (p.Gly323Arg)
c.*843G>A (n.*843G>A)
c.862G>A (p.Gly288Arg)
ClinVar dbSNP
Xg.154969374A=CA2466848982F8c.966T= (p.Leu322=)
c.*842T= (n.*842T=)
c.861T= (p.Leu287=)
Xg.154969374A>CCA519367166F8c.966T>G (p.Leu322=)
c.*842T>G (n.*842T>G)
c.861T>G (p.Leu287=)
Xg.154969374A>GCA519367170F8c.966T>C (p.Leu322=)
c.*842T>C (n.*842T>C)
c.861T>C (p.Leu287=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.154969374A>TCA519367168F8c.966T>A (p.Leu322=)
c.*842T>A (n.*842T>A)
c.861T>A (p.Leu287=)
Xg.154969375A>CCA414917728F8c.965T>G (p.Leu322Arg)
c.*841T>G (n.*841T>G)
c.860T>G (p.Leu287Arg)
Xg.154969375A>GCA414917733F8c.965T>C (p.Leu322Pro)
c.*841T>C (n.*841T>C)
c.860T>C (p.Leu287Pro)
Xg.154969375A>TCA414917735F8c.965T>A (p.Leu322His)
c.*841T>A (n.*841T>A)
c.860T>A (p.Leu287His)
Xg.154969376G>ACA414917737F8c.964C>T (p.Leu322Phe)
c.*840C>T (n.*840C>T)
c.859C>T (p.Leu287Phe)
Xg.154969376G>CCA414917739F8c.964C>G (p.Leu322Val)
c.*840C>G (n.*840C>G)
c.859C>G (p.Leu287Val)
Xg.154969376G>TCA414917741F8c.964C>A (p.Leu322Ile)
c.*840C>A (n.*840C>A)
c.859C>A (p.Leu287Ile)
Xg.154969377G>ACA519367178F8c.963C>T (p.Asp321=)
c.*839C>T (n.*839C>T)
c.858C>T (p.Asp286=)
gnomAD v4
Xg.154969377G>CCA414917743F8c.963C>G (p.Asp321Glu)
c.*839C>G (n.*839C>G)
c.858C>G (p.Asp286Glu)
Xg.154969377G>TCA414917745F8c.963C>A (p.Asp321Glu)
c.*839C>A (n.*839C>A)
c.858C>A (p.Asp286Glu)
Xg.154969378T>ACA414917747F8c.962A>T (p.Asp321Val)
c.*838A>T (n.*838A>T)
c.857A>T (p.Asp286Val)
Xg.154969378T>CCA414917749F8c.962A>G (p.Asp321Gly)
c.*838A>G (n.*838A>G)
c.857A>G (p.Asp286Gly)
gnomAD v4
Xg.154969378T>GCA414917750F8c.962A>C (p.Asp321Ala)
c.*838A>C (n.*838A>C)
c.857A>C (p.Asp286Ala)
Xg.154969379C>ACA414917756F8c.961G>T (p.Asp321Tyr)
c.*837G>T (n.*837G>T)
c.856G>T (p.Asp286Tyr)
Xg.154969379C>GCA414917752F8c.961G>C (p.Asp321His)
c.*837G>C (n.*837G>C)
c.856G>C (p.Asp286His)
Xg.154969379C>TCA414917754F8c.961G>A (p.Asp321Asn)
c.*837G>A (n.*837G>A)
c.856G>A (p.Asp286Asn)
Xg.154969380C>ACA414917757F8c.960G>T (p.Met320Ile)
c.*836G>T (n.*836G>T)
c.855G>T (p.Met285Ile)
Xg.154969380C>GCA414917759F8c.960G>C (p.Met320Ile)
c.*836G>C (n.*836G>C)
c.855G>C (p.Met285Ile)
Xg.154969380C>TCA414917760F8c.960G>A (p.Met320Ile)
c.*836G>A (n.*836G>A)
c.855G>A (p.Met285Ile)
Xg.154969382_154969384delCA2695237427F8c.958_960del (p.Met320del)
c.*834_*836del (n.*834_*836del)
c.853_855del (p.Met285del)
Xg.154969381A>CCA414917761F8c.959T>G (p.Met320Arg)
c.*835T>G (n.*835T>G)
c.854T>G (p.Met285Arg)
Xg.154969381A>GCA414917762F8c.959T>C (p.Met320Thr)
c.*835T>C (n.*835T>C)
c.854T>C (p.Met285Thr)
Xg.154969381A>TCA414917764F8c.959T>A (p.Met320Lys)
c.*835T>A (n.*835T>A)
c.854T>A (p.Met285Lys)
Xg.154969382T>ACA414917766F8c.958A>T (p.Met320Leu)
c.*834A>T (n.*834A>T)
c.853A>T (p.Met285Leu)
Xg.154969382T>CCA414917767F8c.958A>G (p.Met320Val)
c.*834A>G (n.*834A>G)
c.853A>G (p.Met285Val)
Xg.154969382T>GCA414917769F8c.958A>C (p.Met320Leu)
c.*834A>C (n.*834A>C)
c.853A>C (p.Met285Leu)
Xg.154969383_154969391delCA2695237430F8c.950_958del (p.Thr317_Leu319del)
c.*826_*834del (n.*826_*834del)
c.845_853del (p.Thr282_Leu284del)
Xg.154969383C>ACA414917771F8c.957G>T (p.Leu319Phe)
c.*833G>T (n.*833G>T)
c.852G>T (p.Leu284Phe)
Xg.154969383C>GCA414917773F8c.957G>C (p.Leu319Phe)
c.*833G>C (n.*833G>C)
c.852G>C (p.Leu284Phe)
Xg.154969383C>TCA519367203F8c.957G>A (p.Leu319=)
c.*833G>A (n.*833G>A)
c.852G>A (p.Leu284=)
Xg.154969384A>CCA414917774F8c.956T>G (p.Leu319Trp)
c.*832T>G (n.*832T>G)
c.851T>G (p.Leu284Trp)
Xg.154969384A>GCA414917778F8c.956T>C (p.Leu319Ser)
c.*832T>C (n.*832T>C)
c.851T>C (p.Leu284Ser)
Xg.154969384A>TCA414917776F8c.956T>A (p.Leu319Ter)
c.*832T>A (n.*832T>A)
c.851T>A (p.Leu284Ter)
Xg.154969385delCA2695237431F8c.956del (p.Leu319Ter)
c.*832del (n.*832del)
c.851del (p.Leu284Ter)
Xg.154969385A=CA2466848983F8c.955T= (p.Leu319=)
c.*831T= (n.*831T=)
c.850T= (p.Leu284=)
Xg.154969385A>CCA414917780F8c.955T>G (p.Leu319Val)
c.*831T>G (n.*831T>G)
c.850T>G (p.Leu284Val)
Xg.154969385A>GCA519367207F8c.955T>C (p.Leu319=)
c.*831T>C (n.*831T>C)
c.850T>C (p.Leu284=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.154969385A>TCA414917781F8c.955T>A (p.Leu319Met)
c.*831T>A (n.*831T>A)
c.850T>A (p.Leu284Met)
Xg.154969387_154969388delCA2695237432F8c.954_955del (p.Leu319AspfsTer18)
c.*830_*831del (n.*830_*831del)
c.849_850del (p.Leu284AspfsTer18)
Xg.154969386G>ACA519367209F8c.954C>T (p.Leu318=)
c.*830C>T (n.*830C>T)
c.849C>T (p.Leu283=)
Xg.154969386G>CCA519367210F8c.954C>G (p.Leu318=)
c.*830C>G (n.*830C>G)
c.849C>G (p.Leu283=)
Xg.154969386G>TCA519367211F8c.954C>A (p.Leu318=)
c.*830C>A (n.*830C>A)
c.849C>A (p.Leu283=)
Xg.154969387delCA2695237433F8c.953del (p.Leu318ProfsTer2)
c.*829del (n.*829del)
c.848del (p.Leu283ProfsTer2)

Number of alleles fetched