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.10141930_10141947dupCA16042062VHLc.83_100dup (p.Ser33_Gly34insAspGlyGlyGluGluSer)
ClinVar dbSNP
3g.10141930_10141975delinsACGGCGGGGAGGAGTCGGGCGCCGAGGAGTCCGGCCCGGAAGAGTCCA1345065141VHLc.83_128delinsACGGCGGGGAGGAGTCGGGCGCCGAGGAGTCCGGCCCGGAAGAGTC (p.Asp28=)
3g.10141935_10141979delCA541213519VHLc.88_132del (p.Gly30_Gly44del)
dbSNP gnomAD v2 gnomAD v4
3g.10141932G>ACA351747529VHLc.85G>A (p.Gly29Ser)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.10141932G>CCA351747532VHLc.85G>C (p.Gly29Arg)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.10141932G=CA1345065149VHLc.85G= (p.Gly29=)
3g.10141932G>TCA351747534VHLc.85G>T (p.Gly29Cys)
ClinVar dbSNP gnomAD v4
3g.10141933G>ACA351747540VHLc.86G>A (p.Gly29Asp)
dbSNP COSMIC
3g.10141933G>CCA351747542VHLc.86G>C (p.Gly29Ala)
ClinVar dbSNP
3g.10141933G=CA1345065156VHLc.86G= (p.Gly29=)
3g.10141933G>TCA351747555VHLc.86G>T (p.Gly29Val)
dbSNP gnomAD v4
3g.10141933_10141934delinsGCCA1345065160VHLc.86_87delinsGC (p.Gly29=)
3g.10141933_10141934delinsTTCA10584228VHLc.86_87delinsTT (p.Gly29Val)
ClinVar dbSNP
3g.10141934C>ACA432536238VHLc.87C>A (p.Gly29=)
ClinVar dbSNP gnomAD v4
3g.10141934C=CA1345065165VHLc.87C= (p.Gly29=)
3g.10141934C>GCA432536240VHLc.87C>G (p.Gly29=)
3g.10141934C>TCA70042244VHLc.87C>T (p.Gly29=)
ClinVar dbSNP gnomAD v4
3g.10141935G>ACA70042258VHLc.88G>A (p.Gly30Arg)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.10141935G>CCA351747563VHLc.88G>C (p.Gly30Arg)
ClinVar dbSNP
3g.10141935G=CA1345065170VHLc.88G= (p.Gly30=)
3g.10141935G>TCA351747567VHLc.88G>T (p.Gly30Trp)
ClinVar dbSNP gnomAD v4
3g.10141938delCA2580068386VHLc.91del (p.Glu31ArgfsTer?)
ClinVar
3g.10141937_10141938delCA645524627VHLc.90_91del (p.Glu31GlyfsTer?)
COSMIC COSMIC
3g.10141936G>ACA16617781VHLc.89G>A (p.Gly30Glu)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.10141936G>CCA351747570VHLc.89G>C (p.Gly30Ala)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.10141936G=CA1345065177VHLc.89G= (p.Gly30=)
3g.10141936G>TCA351747574VHLc.89G>T (p.Gly30Val)
gnomAD v4
3g.10141936_10142144delCA2573050894VHLc.89_297del (p.Gly30AspfsTer?)
3g.10141937G>ACA432536244VHLc.90G>A (p.Gly30=)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.10141937G>CCA70042260VHLc.90G>C (p.Gly30=)
dbSNP
3g.10141937G=CA1345065182VHLc.90G= (p.Gly30=)

Number of alleles fetched