Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.10141774_10142062delCA3266346840VHLc.-74_215del
3g.10141773_10142082dupCA3266346844VHLc.-75_235dup (p.Arg79ProfsTer51)
3g.10141776_10142091dupCA3266346841VHLc.-72_244dup (p.Arg82HisfsTer50)
3g.10141915_10142023delCA3261045088VHLc.68_176del (p.Tyr23CysfsTer8)
3g.10141922_10142030dupCA3060570556VHLc.75_183dup (p.Val62Ter)
ClinVar
3g.10141960_10142004delCA2664399907VHLc.113_157del (p.Ser38Ter)
gnomAD v4
3g.10141970_10142082dupCA3266346853VHLc.123_235dup (p.Arg79GlnfsTer26)
3g.10141970_10142088dupCA3266346854VHLc.123_241dup (p.Pro81GlnfsTer26)
3g.10141982_10142005delinsGGAGGAACTGGGCGCCGAGGAGGACA1345065328VHLc.135_158delinsGGAGGAACTGGGCGCCGAGGAGGA (p.Pro45=)
3g.10141985_10142007delCA896158519VHLc.138_160del (p.Glu46AspfsTer?)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.10142004_10142006delCA2580614138VHLc.157_159del (p.Glu53del)
ClinVar dbSNP
3g.10142001_10142013delCA645524631VHLc.154_166del (p.Glu52ProfsTer11)
COSMIC
3g.10142002_10142043delCA645524632VHLc.155_196del (p.Glu52_Ser65del)
COSMIC
3g.10142001_10142055delCA3266346858VHLc.154_208del (p.Glu52SerfsTer?)
3g.10142002_10142051delCA3266346860VHLc.155_204del (p.Glu52AlafsTer?)
3g.10142001_10142061delCA3266346859VHLc.154_214del (p.Glu52ProfsTer?)
3g.10142003_10142004delinsAACA3104826042VHLc.156_157delinsAA (p.Glu53Lys)
dbSNP
3g.10142004_10142010delCA645524633VHLc.157_163del (p.Glu53ArgfsTer12)
COSMIC
3g.10142004G>ACA351748391VHLc.157G>A (p.Glu53Lys)
ClinVar dbSNP
3g.10142004G>CCA351748398VHLc.157G>C (p.Glu53Gln)
ClinVar
3g.10142004G=CA3057222432VHLc.157G= (p.Glu53=)
dbSNP
3g.10142004G>TCA351748408VHLc.157G>T (p.Glu53Ter)
dbSNP
3g.10142005A=CA3057222433VHLc.158A= (p.Glu53=)
dbSNP
3g.10142005A>CCA351748426VHLc.158A>C (p.Glu53Ala)
3g.10142005A>GCA351748429VHLc.158A>G (p.Glu53Gly)
ClinVar dbSNP gnomAD v4
3g.10142005A>TCA351748434VHLc.158A>T (p.Glu53Val)
dbSNP
3g.10142006G>ACA432536362VHLc.159G>A (p.Glu53=)
ClinVar dbSNP gnomAD v4 COSMIC
3g.10142006G>CCA351748444VHLc.159G>C (p.Glu53Asp)
ClinVar dbSNP gnomAD v4
3g.10142006G=CA1345065410VHLc.159G= (p.Glu53=)
dbSNP
3g.10142006G>TCA351748440VHLc.159G>T (p.Glu53Asp)
ClinVar gnomAD v4
3g.10142007_10142016delCA645524634VHLc.160_169del (p.Met54GlyfsTer10)
COSMIC
3g.10142007_10142021delCA645524635VHLc.160_174del (p.Met54_Arg58del)
COSMIC
3g.10142007delCA2586965629VHLc.160del (p.Met54TrpfsTer13)
3g.10142007A=CA1345065415VHLc.160A= (p.Met54=)
dbSNP
3g.10142007A>CCA351748450VHLc.160A>C (p.Met54Leu)
3g.10142007A>GCA351748453VHLc.160A>G (p.Met54Val)
ClinVar dbSNP gnomAD v4
3g.10142007A>TCA351748458VHLc.160A>T (p.Met54Leu)
ClinVar dbSNP gnomAD v4
3g.10142007_10142008delCA913189210VHLc.160_161del (p.Met54GlyfsTer?)
3g.10142007_10142019delCA645524637VHLc.160_172del (p.Met54GlyfsTer9)
COSMIC
3g.10142007_10142022delCA645524636VHLc.160_175del (p.Met54ArgfsTer8)
COSMIC
3g.10142008delCA645524638VHLc.161del (p.Met54ArgfsTer13)
COSMIC
3g.10142008T>ACA351748466VHLc.161T>A (p.Met54Lys)
3g.10142008T>CCA351748468VHLc.161T>C (p.Met54Thr)
ClinVar dbSNP
3g.10142008T>GCA351748469VHLc.161T>G (p.Met54Arg)
ClinVar dbSNP
3g.10142008T=CA1345065421VHLc.161T= (p.Met54=)
dbSNP
3g.10142008dupCA2497028723VHLc.161dup (p.Met54IlefsTer?)
3g.10142008_10142009delinsTGCA1345065424VHLc.161_162delinsTG (p.Met54=)
3g.10142009G>ACA351748478VHLc.162G>A (p.Met54Ile)
ClinVar dbSNP
3g.10142009G>CCA351748485VHLc.162G>C (p.Met54Ile)
3g.10142009G=CA3057222434VHLc.162G= (p.Met54=)
dbSNP

Number of alleles fetched