Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.10141849_10149966delCA2581463473VHLc.2_*320del
c.2_*1del
c.2_*197del
3g.10142071_10149891delCA1139532528VHLc.224_*245del
c.224_704del
c.224_679del
c.224_568del
c.224_445del
c.224_*122del
3g.10143181_10152298delCA2499216371VHLc.340+994_*2333del
c.*17+160_*2529del
ClinVar
3g.10145108_10153342delCA2499216377VHLc.341-1406_*3377del
c.*17+2087_*3573del
c.340+2921_*3377del
ClinVar
3g.10145132_10153366delCA2499216378VHLc.341-1382_*3401del
c.*17+2111_*3597del
c.340+2945_*3401del
ClinVar
3g.10145585_10153156delCA2499216380VHLc.341-929_*3191del
c.*17+2564_*3387del
c.340+3398_*3191del
ClinVar
3g.10146465_10152780delCA2499216382VHLc.341-49_*2815del
c.*18-3322_*3011del
c.341-3322_*2815del
ClinVar
3g.10146480_10149909delCA2581463488VHLc.*18-34_*263del
c.600-3307_722del
c.341-34_697del
c.341-34_586del
c.341-3307_463del
n.477-34_722del
c.*18-3307_*140del
3g.10146514_10149967delCA1139532108VHLc.*18_*321del
c.600-3273_780del
c.341_*2del
c.341-3273_*2del
n.477_780del
c.*18-3273_*198del
3g.10147075_10150956delCA2499216384VHLc.*140+439_*1310del
c.600-2712_1769del
c.463+439_*991del
c.341-2712_*991del
c.*18-2712_*1187del
ClinVar
3g.10147644_10152768delCA2499216385VHLc.463+1008_*2803del
c.*18-2143_*2999del
c.341-2143_*2803del
ClinVar
3g.10148440_10158273delCA2499216386 ClinVar
3g.10148566_10158401delCA2499216387 ClinVar
3g.10148561_10152736delCA2499216388VHLc.464-143_*2771del
c.464-1226_*2771del
c.*18-1226_*2967del
c.341-1226_*2771del
ClinVar
3g.10148615_10158450delCA2499216389 ClinVar
3g.10149787_10149965delCA2580612129VHLc.*141_*319del (n.*141_*319del)
c.600_778del (n.600_778del)
c.575_753del (p.Val192GlufsTer?)
c.464_642del (p.Val155GlufsTer?)
c.341_519del (p.Val114GlufsTer?)
n.600_778del
c.*18_*196del (n.*18_*196del)
3g.10149817_10149828delinsTTGTCCGGAGCCCA1345062315VHLc.*171_*182delinsTTGTCCGGAGCC (n.*171_*182delinsTTGTCCGGAGCC)
c.630_641delinsTTGTCCGGAGCC (n.630_641delinsTTGTCCGGAGCC)
c.605_616delinsTTGTCCGGAGCC (p.Val202=)
c.494_505delinsTTGTCCGGAGCC (p.Val165=)
c.371_382delinsTTGTCCGGAGCC (p.Val124=)
n.630_641delinsTTGTCCGGAGCC
c.*48_*59delinsTTGTCCGGAGCC (n.*48_*59delinsTTGTCCGGAGCC)
3g.10149819_10149829delCA357119VHLc.*173_*183del (n.*173_*183del)
c.632_642del (n.632_642del)
c.607_617del (p.Val203SerfsTer4)
c.496_506del (p.Val166SerfsTer4)
c.373_383del (p.Val125SerfsTer4)
n.632_642del
c.*50_*60del (n.*50_*60del)
ClinVar dbSNP
3g.10149822_10149827delinsTCA16621943VHLc.*176_*181delinsT (n.*176_*181delinsT)
c.635_640delinsT (n.635_640delinsT)
c.610_615delinsT (p.Arg204SerfsTer5)
c.499_504delinsT (p.Arg167SerfsTer5)
c.376_381delinsT (p.Arg126SerfsTer5)
n.635_640delinsT
c.*53_*58delinsT (n.*53_*58delinsT)
3g.10149827_10149842delCA2499216391VHLc.*181_*196del (n.*181_*196del)
c.640_655del (n.640_655del)
c.615_630del (p.Ser205ArgfsTer29)
c.504_519del (p.Ser168ArgfsTer29)
c.381_396del (p.Ser127ArgfsTer29)
n.640_655del
c.*58_*73del (n.*58_*73del)
ClinVar dbSNP
3g.10149830_10149839delCA645525074VHLc.*184_*193del (n.*184_*193del)
c.643_652del (n.643_652del)
c.618_627del (p.Val207ArgfsTer29)
c.507_516del (p.Val170ArgfsTer29)
c.384_393del (p.Val129ArgfsTer29)
n.643_652del
c.*61_*70del (n.*61_*70del)
COSMIC COSMIC
3g.10149826delCA432423300VHLc.*180del (n.*180del)
c.639del (n.639del)
c.614del (p.Ser205ThrfsTer2)
c.503del (p.Ser168ThrfsTer2)
c.380del (p.Ser127ThrfsTer2)
n.639del
c.*57del (n.*57del)
COSMIC
3g.10149826G>ACA351756182VHLc.*180G>A (n.*180G>A)
c.639G>A (n.639G>A)
c.614G>A (p.Ser205Asn)
c.503G>A (p.Ser168Asn)
c.380G>A (p.Ser127Asn)
n.639G>A
c.*57G>A (n.*57G>A)
ClinVar dbSNP
3g.10149826G>CCA351756183VHLc.*180G>C (n.*180G>C)
c.639G>C (n.639G>C)
c.614G>C (p.Ser205Thr)
c.503G>C (p.Ser168Thr)
c.380G>C (p.Ser127Thr)
n.639G>C
c.*57G>C (n.*57G>C)
dbSNP
3g.10149826G=CA1345062362VHLc.*180G= (n.*180G=)
c.639G= (n.639G=)
c.614G= (p.Ser205=)
c.503G= (p.Ser168=)
c.380G= (p.Ser127=)
n.639G=
c.*57G= (n.*57G=)
3g.10149826G>TCA351756184VHLc.*180G>T (n.*180G>T)
c.639G>T (n.639G>T)
c.614G>T (p.Ser205Ile)
c.503G>T (p.Ser168Ile)
c.380G>T (p.Ser127Ile)
n.639G>T
c.*57G>T (n.*57G>T)
dbSNP
3g.10149826_10149827delCA645525076VHLc.*180_*181del (n.*180_*181del)
c.639_640del (n.639_640del)
c.614_615del (p.Ser205ThrfsTer5)
c.503_504del (p.Ser168ThrfsTer5)
c.380_381del (p.Ser127ThrfsTer5)
n.639_640del
c.*57_*58del (n.*57_*58del)
COSMIC
3g.10149826_10149832delCA645525075VHLc.*180_*186del (n.*180_*186del)
c.639_645del (n.639_645del)
c.614_620del (p.Ser205ThrfsTer?)
c.503_509del (p.Ser168ThrfsTer?)
c.380_386del (p.Ser127ThrfsTer?)
n.639_645del
c.*57_*63del (n.*57_*63del)
COSMIC
3g.10149826_10149836delCA2573131812VHLc.*180_*190del (n.*180_*190del)
c.639_649del (n.639_649del)
c.614_624del (p.Ser205ThrfsTer2)
c.503_513del (p.Ser168ThrfsTer2)
c.380_390del (p.Ser127ThrfsTer2)
n.639_649del
c.*57_*67del (n.*57_*67del)
3g.10149827C>ACA351756186VHLc.*181C>A (n.*181C>A)
c.640C>A (n.640C>A)
c.615C>A (p.Ser205Arg)
c.504C>A (p.Ser168Arg)
c.381C>A (p.Ser127Arg)
n.640C>A
c.*58C>A (n.*58C>A)
dbSNP
3g.10149827C=CA1345062368VHLc.*181C= (n.*181C=)
c.640C= (n.640C=)
c.615C= (p.Ser205=)
c.504C= (p.Ser168=)
c.381C= (p.Ser127=)
n.640C=
c.*58C= (n.*58C=)
3g.10149827C>GCA351756185VHLc.*181C>G (n.*181C>G)
c.640C>G (n.640C>G)
c.615C>G (p.Ser205Arg)
c.504C>G (p.Ser168Arg)
c.381C>G (p.Ser127Arg)
n.640C>G
c.*58C>G (n.*58C>G)
dbSNP
3g.10149827C>TCA432423306VHLc.*181C>T (n.*181C>T)
c.640C>T (n.640C>T)
c.615C>T (p.Ser205=)
c.504C>T (p.Ser168=)
c.381C>T (p.Ser127=)
n.640C>T
c.*58C>T (n.*58C>T)
ClinVar dbSNP
3g.10149828dupCA1139655762VHLc.*182dup (n.*182dup)
c.641dup (n.641dup)
c.616dup (p.Leu206ProfsTer5)
c.505dup (p.Leu169ProfsTer5)
c.382dup (p.Leu128ProfsTer5)
n.641dup
c.*59dup (n.*59dup)
ClinVar dbSNP
3g.10149828delCA432423309VHLc.*182del (n.*182del)
c.641del (n.641del)
c.616del (p.Leu206Ter)
c.505del (p.Leu169Ter)
c.382del (p.Leu128Ter)
n.641del
c.*59del (n.*59del)
COSMIC
3g.10149828_10149833delCA645525078VHLc.*182_*187del (n.*182_*187del)
c.641_646del (n.641_646del)
c.616_621del (p.Leu206_Val207del)
c.505_510del (p.Leu169_Val170del)
c.382_387del (p.Leu128_Val129del)
n.641_646del
c.*59_*64del (n.*59_*64del)
COSMIC
3g.10149827_10149834delCA645525077VHLc.*181_*188del (n.*181_*188del)
c.640_647del (n.640_647del)
c.615_622del (p.Ser205ArgfsTer3)
c.504_511del (p.Ser168ArgfsTer3)
c.381_388del (p.Ser127ArgfsTer3)
n.640_647del
c.*58_*65del (n.*58_*65del)
COSMIC
3g.10149828C>ACA351756187VHLc.*182C>A (n.*182C>A)
c.641C>A (n.641C>A)
c.616C>A (p.Leu206Ile)
c.505C>A (p.Leu169Ile)
c.382C>A (p.Leu128Ile)
n.641C>A
c.*59C>A (n.*59C>A)
dbSNP
3g.10149828C=CA1345062374VHLc.*182C= (n.*182C=)
c.641C= (n.641C=)
c.616C= (p.Leu206=)
c.505C= (p.Leu169=)
c.382C= (p.Leu128=)
n.641C=
c.*59C= (n.*59C=)
3g.10149828C>GCA351756188VHLc.*182C>G (n.*182C>G)
c.641C>G (n.641C>G)
c.616C>G (p.Leu206Val)
c.505C>G (p.Leu169Val)
c.382C>G (p.Leu128Val)
n.641C>G
c.*59C>G (n.*59C>G)
ClinVar dbSNP
3g.10149828C>TCA432423313VHLc.*182C>T (n.*182C>T)
c.641C>T (n.641C>T)
c.616C>T (p.Leu206=)
c.505C>T (p.Leu169=)
c.382C>T (p.Leu128=)
n.641C>T
c.*59C>T (n.*59C>T)
COSMIC
3g.10149828_10149829delinsCTCA1345062372VHLc.*182_*183delinsCT (n.*182_*183delinsCT)
c.641_642delinsCT (n.641_642delinsCT)
c.616_617delinsCT (p.Leu206=)
c.505_506delinsCT (p.Leu169=)
c.382_383delinsCT (p.Leu128=)
n.641_642delinsCT
c.*59_*60delinsCT (n.*59_*60delinsCT)
3g.10149829_10149833delCA645525079VHLc.*183_*187del (n.*183_*187del)
c.642_646del (n.642_646del)
c.617_621del (p.Leu206GlnfsTer3)
c.506_510del (p.Leu169GlnfsTer3)
c.383_387del (p.Leu128GlnfsTer3)
n.642_646del
c.*60_*64del (n.*60_*64del)
COSMIC
3g.10149829delCA432423319VHLc.*183del (n.*183del)
c.642del (n.642del)
c.617del (p.Leu206GlnfsTer?)
c.506del (p.Leu169GlnfsTer?)
c.383del (p.Leu128GlnfsTer?)
n.642del
c.*60del (n.*60del)
ClinVar dbSNP gnomAD v2 COSMIC
3g.10149829T>ACA351756189VHLc.*183T>A (n.*183T>A)
c.642T>A (n.642T>A)
c.617T>A (p.Leu206Gln)
c.506T>A (p.Leu169Gln)
c.383T>A (p.Leu128Gln)
n.642T>A
c.*60T>A (n.*60T>A)
dbSNP
3g.10149829T>CCA351756191VHLc.*183T>C (n.*183T>C)
c.642T>C (n.642T>C)
c.617T>C (p.Leu206Pro)
c.506T>C (p.Leu169Pro)
c.383T>C (p.Leu128Pro)
n.642T>C
c.*60T>C (n.*60T>C)
ClinVar dbSNP COSMIC
3g.10149829T>GCA351756190VHLc.*183T>G (n.*183T>G)
c.642T>G (n.642T>G)
c.617T>G (p.Leu206Arg)
c.506T>G (p.Leu169Arg)
c.383T>G (p.Leu128Arg)
n.642T>G
c.*60T>G (n.*60T>G)
3g.10149829T=CA1345062379VHLc.*183T= (n.*183T=)
c.642T= (n.642T=)
c.617T= (p.Leu206=)
c.506T= (p.Leu169=)
c.383T= (p.Leu128=)
n.642T=
c.*60T= (n.*60T=)
3g.10149830delCA432423324VHLc.*184del (n.*184del)
c.643del (n.643del)
c.618del (p.Val207SerfsTer?)
c.507del (p.Val170SerfsTer?)
c.384del (p.Val129SerfsTer?)
n.643del
c.*61del (n.*61del)
COSMIC
3g.10149830A=CA1345062385VHLc.*184A= (n.*184A=)
c.643A= (n.643A=)
c.618A= (p.Leu206=)
c.507A= (p.Leu169=)
c.384A= (p.Leu128=)
n.643A=
c.*61A= (n.*61A=)

Number of alleles fetched