Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.10133799_10141895delCA16043394 ClinVar
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.10141833_10141851delinsCGGCCCGGGTGGTCTGGTCTCCGCA2573052052VHLc.-15_4delinsCGGCCCGGGTGGTCTGGTCTCCG
ClinVar dbSNP
3g.10141837_10141857dupCA2580068376VHLc.-11_10dup (p.Arg3_Arg4insIleAlaGluGlyMetProArg)
ClinVar gnomAD v4
3g.10141836_10141849dupCA10602864VHLc.-12_2dup (p.Met1IlefsTer18)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.10141839_10141852dupCA020491VHLc.-9_5dup (p.Ala5GlufsTer14)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.10141848_10141864delCA645524623VHLc.1_17del (p.Met1GlufsTer20)
COSMIC
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.10141847A=CA1345064722VHLc.-1A= (n.-1A=)
3g.10141847A>CCA896157845VHLc.-1A>C (n.-1A>C)
dbSNP
3g.10141847A>GCA1044994608VHLc.-1A>G (n.-1A>G)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.10141847A>TCA541213516VHLc.-1A>T (n.-1A>T)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.10141847_10141867delCA645524624VHLc.-1_20del
COSMIC
3g.10141847_10141867dupCA896157844VHLc.-1_20dup (p.Glu6_Asn7insLysMetProArgArgAlaGlu)
dbSNP
3g.10141848A=CA1345064728VHLc.1A= (p.Met1=)
3g.10141848A>CCA351747009VHLc.1A>C (p.Met1Leu)
3g.10141848A>GCA351747010VHLc.1A>G (p.Met1Val)
ClinVar dbSNP gnomAD v4
3g.10141848A>TCA16611052VHLc.1A>T (p.Met1Leu)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
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.10141849T>ACA351747011VHLc.2T>A (p.Met1Lys)
ClinVar dbSNP
3g.10141849T>CCA351747012VHLc.2T>C (p.Met1Thr)
dbSNP
3g.10141849T>GCA351747013VHLc.2T>G (p.Met1Arg)
dbSNP
3g.10141850G>ACA020331VHLc.3G>A (p.Met1Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.10141850G>CCA70042122VHLc.3G>C (p.Met1Ile)
ClinVar dbSNP gnomAD v4
3g.10141850G=CA1345064732VHLc.3G= (p.Met1=)
3g.10141850G>TCA040825VHLc.3G>T (p.Met1Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.10141850_10141851delinsGCCA1345064738VHLc.3_4delinsGC (p.Met1=)
3g.10141850_10141851insGTCTCCCA2573136083VHLc.3_4insGTCTCC (p.Met1_Pro2insValSer)
dbSNP
3g.10141851C>ACA351747014VHLc.4C>A (p.Pro2Thr)
ClinVar gnomAD v4
3g.10141851C=CA1345064743VHLc.4C= (p.Pro2=)
3g.10141851C>GCA351747015VHLc.4C>G (p.Pro2Ala)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.10141851C>TCA70042126VHLc.4C>T (p.Pro2Ser)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.10141854delCA915941832VHLc.7del (p.Arg3GlyfsTer11)
ClinVar dbSNP gnomAD v4
3g.10141852C>ACA351747016VHLc.5C>A (p.Pro2His)
ClinVar
3g.10141852C=CA1345064752VHLc.5C= (p.Pro2=)
3g.10141852C>GCA16611054VHLc.5C>G (p.Pro2Arg)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.10141852C>TCA020518VHLc.5C>T (p.Pro2Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.10141853C>ACA432536117VHLc.6C>A (p.Pro2=)
dbSNP gnomAD v4

Number of alleles fetched