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.10141892_10141951delCA2664399904VHLc.45_104del (p.Glu16_Ala35del)
gnomAD v4
3g.10141915_10141959delCA2516254345VHLc.68_112del (p.Tyr23_Glu37del)
3g.10141922_10141966delCA2740090896VHLc.75_119del (p.Glu26_Pro40del)
ClinVar
3g.10141922_10141981delCA2664399905VHLc.75_134del (p.Glu26_Pro45del)
gnomAD v4
3g.10141923G>ACA351747440VHLc.76G>A (p.Glu26Lys)
ClinVar dbSNP COSMIC
3g.10141923G>CCA351747441VHLc.76G>C (p.Glu26Gln)
ClinVar
3g.10141923G=CA1345065120VHLc.76G= (p.Glu26=)
3g.10141923G>TCA351747444VHLc.76G>T (p.Glu26Ter)
3g.10141924A>CCA351747449VHLc.77A>C (p.Glu26Ala)
gnomAD v4
3g.10141924A>GCA351747453VHLc.77A>G (p.Glu26Gly)
ClinVar dbSNP COSMIC
3g.10141924A>TCA351747457VHLc.77A>T (p.Glu26Val)
dbSNP
3g.10141925A>CCA351747463VHLc.78A>C (p.Glu26Asp)
3g.10141925A>GCA432536224VHLc.78A>G (p.Glu26=)
dbSNP
3g.10141925A>TCA351747460VHLc.78A>T (p.Glu26Asp)
3g.10141926G>ACA351747466VHLc.79G>A (p.Glu27Lys)
dbSNP
3g.10141926G>CCA351747469VHLc.79G>C (p.Glu27Gln)
dbSNP
3g.10141926G>TCA351747471VHLc.79G>T (p.Glu27Ter)
3g.10141927A>CCA351747474VHLc.80A>C (p.Glu27Ala)
3g.10141927A>GCA351747476VHLc.80A>G (p.Glu27Gly)
ClinVar dbSNP gnomAD v4
3g.10141927A>TCA351747480VHLc.80A>T (p.Glu27Val)
3g.10141928A=CA1345065124VHLc.81A= (p.Glu27=)
3g.10141928A>CCA351747482VHLc.81A>C (p.Glu27Asp)
ClinVar
3g.10141928A>GCA432536226VHLc.81A>G (p.Glu27=)
COSMIC
3g.10141928A>TCA351747483VHLc.81A>T (p.Glu27Asp)
dbSNP
3g.10141929G>ACA351747487VHLc.82G>A (p.Asp28Asn)
ClinVar dbSNP gnomAD v4
3g.10141929G>CCA351747494VHLc.82G>C (p.Asp28His)
ClinVar dbSNP
3g.10141929G=CA1345065135VHLc.82G= (p.Asp28=)
3g.10141929G>TCA351747497VHLc.82G>T (p.Asp28Tyr)
dbSNP gnomAD v4
3g.10141930_10141947dupCA16042062VHLc.83_100dup (p.Ser33_Gly34insAspGlyGlyGluGluSer)
ClinVar dbSNP
3g.10141930A>CCA351747504VHLc.83A>C (p.Asp28Ala)
dbSNP
3g.10141930A>GCA351747510VHLc.83A>G (p.Asp28Gly)
ClinVar dbSNP COSMIC
3g.10141930A>TCA351747502VHLc.83A>T (p.Asp28Val)
ClinVar dbSNP COSMIC
3g.10141930_10141975delinsACGGCGGGGAGGAGTCGGGCGCCGAGGAGTCCGGCCCGGAAGAGTCCA1345065141VHLc.83_128delinsACGGCGGGGAGGAGTCGGGCGCCGAGGAGTCCGGCCCGGAAGAGTC (p.Asp28=)
3g.10141931C>ACA351747516VHLc.84C>A (p.Asp28Glu)
dbSNP gnomAD v4
3g.10141931C=CA1345065145VHLc.84C= (p.Asp28=)

Number of alleles fetched