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_10141966delCA2740090896VHLc.75_119del (p.Glu26_Pro40del)
ClinVar
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.10141950_10141964dupCA658655747VHLc.103_117dup (p.Gly39_Pro40insAlaGluGluSerGly)
ClinVar dbSNP
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.10141961_10141966delCA2664399906VHLc.114_119del (p.Gly39_Pro40del)
gnomAD v4
3g.10141960_10142004delCA2664399907VHLc.113_157del (p.Ser38Ter)
gnomAD v4
3g.10141962G>ACA351747863VHLc.115G>A (p.Gly39Ser)
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
3g.10141962G>CCA039367VHLc.115G>C (p.Gly39Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.10141962G=CA1345065267VHLc.115G= (p.Gly39=)
3g.10141962G>TCA351747874VHLc.115G>T (p.Gly39Cys)
gnomAD v4
3g.10141963G>ACA351747884VHLc.116G>A (p.Gly39Asp)
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
3g.10141963G>CCA351747880VHLc.116G>C (p.Gly39Ala)
ClinVar
3g.10141963G=CA1345065269VHLc.116G= (p.Gly39=)
3g.10141963G>TCA70042314VHLc.116G>T (p.Gly39Val)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.10141964C>ACA432536335VHLc.117C>A (p.Gly39=)
3g.10141964C=CA1345065274VHLc.117C= (p.Gly39=)
3g.10141964C>GCA432536336VHLc.117C>G (p.Gly39=)
ClinVar dbSNP
3g.10141964C>TCA16604418VHLc.117C>T (p.Gly39=)
ClinVar dbSNP gnomAD v4
3g.10141965C>ACA039380VHLc.118C>A (p.Pro40Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.10141965C=CA1345065280VHLc.118C= (p.Pro40=)
3g.10141965C>GCA351747889VHLc.118C>G (p.Pro40Ala)
ClinVar dbSNP gnomAD v4
3g.10141965C>TCA351747893VHLc.118C>T (p.Pro40Ser)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.10141966C>ACA351747894VHLc.119C>A (p.Pro40Gln)
ClinVar gnomAD v4
3g.10141966C=CA1345065283VHLc.119C= (p.Pro40=)
3g.10141966C>GCA351747895VHLc.119C>G (p.Pro40Arg)
ClinVar dbSNP gnomAD v4

Number of alleles fetched