Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.10141839_10141979delCA3261045086VHLc.-9_132del
3g.10141886_10141990delCA3261045087VHLc.39_143del (p.Gly14_Leu48del)
3g.10141892_10141951delCA2664399904VHLc.45_104del (p.Glu16_Ala35del)
gnomAD v4
3g.10141915_10141974delCA3261045089VHLc.68_127del (p.Tyr23_Glu42del)
3g.10141915_10141959delCA2516254345VHLc.68_112del (p.Tyr23_Glu37del)
3g.10141915_10142023delCA3261045088VHLc.68_176del (p.Tyr23CysfsTer8)
3g.10141922_10141966delCA2740090896VHLc.75_119del (p.Glu26_Pro40del)
ClinVar dbSNP
3g.10141922_10141981delCA2664399905VHLc.75_134del (p.Glu26_Pro45del)
gnomAD v4
3g.10141922_10142030dupCA3060570556VHLc.75_183dup (p.Val62Ter)
ClinVar
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.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=)
dbSNP
3g.10141935G>TCA351747567VHLc.88G>T (p.Gly30Trp)
ClinVar dbSNP gnomAD v4
3g.10141938delCA2580068386VHLc.91del (p.Glu31ArgfsTer?)
ClinVar dbSNP
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=)
dbSNP
3g.10141936G>TCA351747574VHLc.89G>T (p.Gly30Val)
gnomAD v4
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=)
dbSNP
3g.10141937G>TCA432536245VHLc.90G>T (p.Gly30=)
dbSNP
3g.10141940_10141969dupCA1345065181VHLc.93_122dup (p.Glu41_Glu42insGluSerGlyAlaGluGluSerGlyProGlu)
ClinVar dbSNP
3g.10141938G>ACA351747595VHLc.91G>A (p.Glu31Lys)
ClinVar
3g.10141938G>CCA351747597VHLc.91G>C (p.Glu31Gln)
3g.10141938G=CA1345065183VHLc.91G= (p.Glu31=)
dbSNP
3g.10141938G>TCA351747598VHLc.91G>T (p.Glu31Ter)
ClinVar dbSNP gnomAD v4
3g.10141946_10141960dupCA541213520VHLc.99_113dup (p.Ser38_Gly39insGlyAlaGluGluSer)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.10141946_10141960delCA3046517738VHLc.99_113del (p.Gly34_Ser38del)
ClinVar
3g.10141939A=CA3057222420VHLc.92A= (p.Glu31=)
dbSNP
3g.10141939A>CCA351747599VHLc.92A>C (p.Glu31Ala)
dbSNP
3g.10141939A>GCA351747601VHLc.92A>G (p.Glu31Gly)
ClinVar dbSNP gnomAD v4 COSMIC
3g.10141939A>TCA351747605VHLc.92A>T (p.Glu31Val)
3g.10141940G>ACA432536248VHLc.93G>A (p.Glu31=)
ClinVar dbSNP gnomAD v4
3g.10141940G>CCA351747611VHLc.93G>C (p.Glu31Asp)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.10141940G=CA1345065185VHLc.93G= (p.Glu31=)
dbSNP
3g.10141940G>TCA351747615VHLc.93G>T (p.Glu31Asp)
3g.10141941dupCA2989079290VHLc.94dup (p.Glu32GlyfsTer?)
3g.10141941G>ACA351747616VHLc.94G>A (p.Glu32Lys)
ClinVar dbSNP gnomAD v4
3g.10141941G>CCA351747617VHLc.94G>C (p.Glu32Gln)
ClinVar dbSNP gnomAD v4
3g.10141941G=CA3103965855VHLc.94G= (p.Glu32=)
dbSNP
3g.10141941G>TCA351747620VHLc.94G>T (p.Glu32Ter)
dbSNP gnomAD v4
3g.10141942A=CA1345065187VHLc.95A= (p.Glu32=)
dbSNP
3g.10141942A>CCA351747631VHLc.95A>C (p.Glu32Ala)
3g.10141942A>GCA020549VHLc.95A>G (p.Glu32Gly)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.10141942A>TCA351747625VHLc.95A>T (p.Glu32Val)
ClinVar dbSNP gnomAD v4

Number of alleles fetched