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.10141922_10141981delCA2664399905VHLc.75_134del (p.Glu26_Pro45del)
gnomAD v4
3g.10141930_10141975delinsACGGCGGGGAGGAGTCGGGCGCCGAGGAGTCCGGCCCGGAAGAGTCCA1345065141VHLc.83_128delinsACGGCGGGGAGGAGTCGGGCGCCGAGGAGTCCGGCCCGGAAGAGTC (p.Asp28=)
3g.10141935_10141979delCA541213519VHLc.88_132del (p.Gly30_Gly44del)
dbSNP gnomAD v2 gnomAD v4
3g.10141936_10142144delCA2573050894VHLc.89_297del (p.Gly30AspfsTer?)
3g.10141940_10141969dupCA1345065181VHLc.93_122dup (p.Glu41_Glu42insGluSerGlyAlaGluGluSerGlyProGlu)
ClinVar dbSNP
3g.10141945_10141990delinsCGGGCGCCGAGGAGTCCGGCCCGGAAGAGTCCGGCCCGGAGGAACTCA1345065203VHLc.98_143delinsCGGGCGCCGAGGAGTCCGGCCCGGAAGAGTCCGGCCCGGAGGAACT (p.Ser33=)
3g.10141959_10142003dupCA915941834VHLc.112_156dup (p.Glu52_Glu53insSerGlyProGluGluSerGlyProGluGluLeuGlyAlaGluGlu)
ClinVar dbSNP gnomAD v4
3g.10141959_10142003delCA1139655723VHLc.112_156del (p.Ser38_Glu52del)
ClinVar dbSNP gnomAD v4
3g.10141955_10141969dupCA896158356VHLc.108_122dup (p.Glu41_Glu42insGluSerGlyProGlu)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.10141955_10141970delinsGGAGTCCGGCCCGGAACA1345065249VHLc.108_123delinsGGAGTCCGGCCCGGAA (p.Glu36=)
3g.10141970_10141984dupCA541213522VHLc.123_137dup (p.Glu46_Glu47insGluSerGlyProGlu)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.10141970_10141984delCA039321VHLc.123_137del (p.Glu42_Glu46del)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.10141960_10142004delCA2664399907VHLc.113_157del (p.Ser38Ter)
gnomAD v4
3g.10141968G>ACA351747902VHLc.121G>A (p.Glu41Lys)
ClinVar dbSNP gnomAD v4
3g.10141968G>CCA351747904VHLc.121G>C (p.Glu41Gln)
dbSNP
3g.10141968G=CA1345065290VHLc.121G= (p.Glu41=)
3g.10141968G>TCA351747922VHLc.121G>T (p.Glu41Ter)
dbSNP gnomAD v4
3g.10141969A=CA1345065292VHLc.122A= (p.Glu41=)
3g.10141969A>CCA351747928VHLc.122A>C (p.Glu41Ala)
ClinVar dbSNP
3g.10141969A>GCA351747932VHLc.122A>G (p.Glu41Gly)
ClinVar dbSNP COSMIC
3g.10141969A>TCA351747936VHLc.122A>T (p.Glu41Val)
ClinVar dbSNP COSMIC
3g.10141970A>CCA351747951VHLc.123A>C (p.Glu41Asp)
ClinVar
3g.10141970A>GCA432536340VHLc.123A>G (p.Glu41=)
ClinVar dbSNP gnomAD v4
3g.10141970A>TCA351747945VHLc.123A>T (p.Glu41Asp)
3g.10141970_10141973delCA2573136081VHLc.123_126del (p.Glu41AspfsTer25)
ClinVar dbSNP
3g.10141971G>ACA351747955VHLc.124G>A (p.Glu42Lys)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.10141971G>CCA351747976VHLc.124G>C (p.Glu42Gln)
ClinVar dbSNP gnomAD v4
3g.10141971G=CA1345065294VHLc.124G= (p.Glu42=)
3g.10141971G>TCA351747958VHLc.124G>T (p.Glu42Ter)
gnomAD v4
3g.10141972A=CA1345065298VHLc.125A= (p.Glu42=)
3g.10141972A>CCA16617782VHLc.125A>C (p.Glu42Ala)
ClinVar dbSNP gnomAD v4
3g.10141972A>GCA351747982VHLc.125A>G (p.Glu42Gly)
ClinVar dbSNP gnomAD v4
3g.10141972A>TCA351747985VHLc.125A>T (p.Glu42Val)
COSMIC
3g.10141973delCA16602177VHLc.126del (p.Glu42AspfsTer25)
3g.10141973G>ACA432536341VHLc.126G>A (p.Glu42=)

Number of alleles fetched