Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154969329_154969448delCA2695237407F8c.893_1009+3del
c.*769_*885+3del
c.788_904+3del
Xg.154969368C>ACA414917702F8c.972G>T (p.Gln324His)
c.*848G>T (n.*848G>T)
c.867G>T (p.Gln289His)
Xg.154969368C>GCA414917703F8c.972G>C (p.Gln324His)
c.*848G>C (n.*848G>C)
c.867G>C (p.Gln289His)
Xg.154969368C>TCA519367140F8c.972G>A (p.Gln324=)
c.*848G>A (n.*848G>A)
c.867G>A (p.Gln289=)
Xg.154969369T>ACA414917705F8c.971A>T (p.Gln324Leu)
c.*847A>T (n.*847A>T)
c.866A>T (p.Gln289Leu)
Xg.154969369T>CCA414917707F8c.971A>G (p.Gln324Arg)
c.*847A>G (n.*847A>G)
c.866A>G (p.Gln289Arg)
Xg.154969369T>GCA414917709F8c.971A>C (p.Gln324Pro)
c.*847A>C (n.*847A>C)
c.866A>C (p.Gln289Pro)
Xg.154969370G>ACA414917712F8c.970C>T (p.Gln324Ter)
c.*846C>T (n.*846C>T)
c.865C>T (p.Gln289Ter)
Xg.154969370G>CCA414917713F8c.970C>G (p.Gln324Glu)
c.*846C>G (n.*846C>G)
c.865C>G (p.Gln289Glu)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.154969370G=CA2466848981F8c.970C= (p.Gln324=)
c.*846C= (n.*846C=)
c.865C= (p.Gln289=)
Xg.154969370G>TCA501127F8c.970C>A (p.Gln324Lys)
c.*846C>A (n.*846C>A)
c.865C>A (p.Gln289Lys)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.154969371T>ACA519367150F8c.969A>T (p.Gly323=)
c.*845A>T (n.*845A>T)
c.864A>T (p.Gly288=)
Xg.154969371T>CCA519367152F8c.969A>G (p.Gly323=)
c.*845A>G (n.*845A>G)
c.864A>G (p.Gly288=)
Xg.154969371T>GCA519367153F8c.969A>C (p.Gly323=)
c.*845A>C (n.*845A>C)
c.864A>C (p.Gly288=)
Xg.154969372C>ACA414917720F8c.968G>T (p.Gly323Val)
c.*844G>T (n.*844G>T)
c.863G>T (p.Gly288Val)
Xg.154969372C>GCA414917719F8c.968G>C (p.Gly323Ala)
c.*844G>C (n.*844G>C)
c.863G>C (p.Gly288Ala)
Xg.154969372C>TCA414917717F8c.968G>A (p.Gly323Glu)
c.*844G>A (n.*844G>A)
c.863G>A (p.Gly288Glu)
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)

Number of alleles fetched