Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.10135142_10142466delCA2499216338 ClinVar
3g.10135142_10143568delCA2499216339 ClinVar
3g.10137026_10145481delCA2499216340 ClinVar
3g.10137102_10143357delCA2499216341 ClinVar
3g.10139220_10148953delCA2499216342 ClinVar
3g.10139708_10142406delCA2499216343 ClinVar
3g.10139761_10142459delCA2499216344 ClinVar
3g.10140648_10148414delCA2499216345 ClinVar
3g.10140738_10142535delCA2499216346 ClinVar
3g.10141523_10142610delCA2499216347VHLc.-325_340+423del
ClinVar
3g.10141635_10149787delCA2581463472VHLc.-213_464del
c.-213_341del
c.-213_*18del
3g.10141847_10149786delCA1139532106VHLc.-1_*141-1del
c.-1_575-1del
c.-1_464-1del
c.-1_341-1del
c.-1_*18-1del
3g.10141849_10149966delCA2581463473VHLc.2_*320del
c.2_*1del
c.2_*197del
3g.10141848_10142187delCA2581463474VHLc.1_340del (p.Met1SerfsTer3)
c.1_340del (p.Met1ValfsTer?)
c.1_340del (p.Met1CysfsTer4)
3g.10141848_10146636delCA2581463475VHLc.1_*140del
c.1_600-3151del
c.1_463del
c.1_341-3151del
c.1_*18-3151del
3g.10141936_10142144delCA2573050894VHLc.89_297del (p.Gly30AspfsTer?)
3g.10142071_10149891delCA1139532528VHLc.224_*245del
c.224_704del
c.224_679del
c.224_568del
c.224_445del
c.224_*122del
3g.10142074_10142168delCA645524728VHLc.227_321del (p.Phe76SerfsTer?)
c.227_321del (p.Phe76SerfsTer24)
c.227_321del (p.Phe76SerfsTer25)
COSMIC
3g.10142124_10142141delCA891843321VHLc.277_294del (p.Gly93_Tyr98del)
ClinVar dbSNP
3g.10142129_10142144delCA645524800VHLc.282_297del (p.Pro95ArgfsTer17)
c.282_297del (p.Pro95ArgfsTer?)
c.282_297del (p.Pro95ArgfsTer18)
COSMIC
3g.10142134_10142154delCA2573106190VHLc.287_307del (p.Gln96_Pro102del)
3g.10142130_10142144delCA645524807VHLc.283_297del (p.Pro95_Pro99del)
COSMIC
3g.10142135_10142141delinsGCCCTACCA1345066214VHLc.288_294delinsGCCCTAC (p.Gln96=)
3g.10142136_10142140delinsCCCTACA1345066219VHLc.289_293delinsCCCTA (p.Pro97=)
3g.10142139_10142143delCA645524818VHLc.292_296del (p.Tyr98AsnfsTer?)
COSMIC
3g.10142138_10142143delCA915941835VHLc.291_296del (p.Tyr98_Pro99del)
ClinVar dbSNP
3g.10142137_10142146delCA645524817VHLc.290_299del (p.Pro97ArgfsTer17)
c.290_299del (p.Pro97ArgfsTer?)
c.290_299del (p.Pro97ArgfsTer18)
COSMIC
3g.10142139_10142142delCA913189504VHLc.292_295del (p.Tyr98GlnfsTer18)
c.292_295del (p.Tyr98GlnfsTer?)
c.292_295del (p.Tyr98GlnfsTer19)
ClinVar dbSNP
3g.10142137_10142149delinsCCTACCCAACGCTCA1345066230VHLc.290_302delinsCCTACCCAACGCT (p.Pro97=)
3g.10142138_10142149delCA915941836VHLc.291_302del (p.Tyr98_Leu101del)
ClinVar dbSNP
3g.10142138_10142157delCA645524819VHLc.291_310del (p.Tyr98HisfsTer?)
c.291_310del (p.Tyr98HisfsTer27)
c.291_310del (p.Tyr98HisfsTer28)
COSMIC
3g.10142140delCA432420516VHLc.293del (p.Tyr98SerfsTer19)
c.293del (p.Tyr98SerfsTer?)
c.293del (p.Tyr98SerfsTer20)
COSMIC
3g.10142140A=CA1345066267VHLc.293A= (p.Tyr98=)
3g.10142140A>CCA279916VHLc.293A>C (p.Tyr98Ser)
ClinVar dbSNP COSMIC
3g.10142140A>GCA357072VHLc.293A>G (p.Tyr98Cys)
ClinVar dbSNP COSMIC
3g.10142140A>TCA351750888VHLc.293A>T (p.Tyr98Phe)
COSMIC
3g.10142140dupCA357009VHLc.293dup (p.Tyr98Ter)
ClinVar dbSNP
3g.10142141C>ACA351750889VHLc.294C>A (p.Tyr98Ter)
gnomAD v4 COSMIC
3g.10142141C=CA1345066277VHLc.294C= (p.Tyr98=)
3g.10142141C>GCA16621910VHLc.294C>G (p.Tyr98Ter)
ClinVar dbSNP COSMIC
3g.10142141C>TCA432420517VHLc.294C>T (p.Tyr98=)
ClinVar dbSNP gnomAD v4
3g.10142143dupCA357055VHLc.296dup (p.Thr100AsnfsTer?)
ClinVar dbSNP
3g.10142143delCA432420518VHLc.296del (p.Pro99GlnfsTer18)
c.296del (p.Pro99GlnfsTer?)
c.296del (p.Pro99GlnfsTer19)
COSMIC COSMIC
3g.10142143_10142155delCA658655621VHLc.296_308del (p.Pro99LeufsTer14)
c.296_308del (p.Pro99LeufsTer?)
c.296_308del (p.Pro99LeufsTer15)
3g.10142141_10142142insACA432420519VHLc.294_295insA (p.Pro99ThrfsTer?)
3g.10142142C>ACA351750899VHLc.295C>A (p.Pro99Thr)
ClinVar dbSNP
3g.10142142C=CA1345066284VHLc.295C= (p.Pro99=)
3g.10142142C>GCA040169VHLc.295C>G (p.Pro99Ala)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.10142142C>TCA351750914VHLc.295C>T (p.Pro99Ser)
3g.10142143C>ACA351750933VHLc.296C>A (p.Pro99Gln)
gnomAD v4

Number of alleles fetched