Chr Mutation (hg38) CAid Gene Transcript Linkouts
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.10147075_10150956delCA2499216384VHLc.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.464-1226_*2771del
c.*18-1226_*2967del
c.341-1226_*2771del
ClinVar
3g.10148615_10158450delCA2499216389 ClinVar
3g.10150259G>ACA10614392VHLc.*294G>A (p.=)
c.*490G>A (p.=)
ClinVar dbSNP gnomAD
3g.10150259G=CA1345063453VHLc.*294G= (p.=)
c.*490G= (p.=)
3g.10150260T=CA1345063456VHLc.*295T= (p.=)
c.*491T= (p.=)
3g.10150261A=CA1345063463VHLc.*296A= (p.=)
c.*492A= (p.=)
3g.10150261A>GCA70052851VHLc.*296A>G (p.=)
c.*492A>G (p.=)
dbSNP
3g.10150261dupCA916832779VHLc.*296dup (p.=)
c.*492dup (p.=)
dbSNP
3g.10150265G>ACA1345063467VHLc.*300G>A (p.=)
c.*496G>A (p.=)
3g.10150265G=CA1345063465VHLc.*300G= (p.=)
c.*496G= (p.=)
3g.10150268A=CA1345063469VHLc.*303A= (p.=)
c.*499A= (p.=)
3g.10150268A>TCA10614821VHLc.*303A>T (p.=)
c.*499A>T (p.=)
ClinVar dbSNP gnomAD
3g.10150273G=CA1345063472VHLc.*308G= (p.=)
c.*504G= (p.=)
3g.10150273G>TCA896166511VHLc.*308G>T (p.=)
c.*504G>T (p.=)
3g.10150274T>CCA1345063476VHLc.*309T>C (p.=)
c.*505T>C (p.=)
3g.10150274T=CA1345063474VHLc.*309T= (p.=)
c.*505T= (p.=)
3g.10150284A=CA1345063479VHLc.*319A= (p.=)
c.*515A= (p.=)
3g.10150284A>GCA1345063481VHLc.*319A>G (p.=)
c.*515A>G (p.=)
3g.10150287A=CA1345063485VHLc.*322A= (p.=)
c.*518A= (p.=)
3g.10150287A>GCA70052875VHLc.*322A>G (p.=)
c.*518A>G (p.=)
dbSNP gnomAD
3g.10150289A=CA1345063489VHLc.*324A= (p.=)
c.*520A= (p.=)
3g.10150289A>GCA70052876VHLc.*324A>G (p.=)
c.*520A>G (p.=)
dbSNP
3g.10150291C=CA1345063493VHLc.*326C= (p.=)
c.*522C= (p.=)
3g.10150291C>TCA896166515VHLc.*326C>T (p.=)
c.*522C>T (p.=)
3g.10150292G>ACA540877282VHLc.*327G>A (p.=)
c.*523G>A (p.=)
ClinVar gnomAD
3g.10150292G=CA1345063496VHLc.*327G= (p.=)
c.*523G= (p.=)
3g.10150297A>CCA2513016345VHLc.*332A>C (p.=)
c.*528A>C (p.=)
3g.10150301dupCA2545815688VHLc.*336dup (p.=)
c.*532dup (p.=)
3g.10150302A=CA1345063500VHLc.*337A= (p.=)
c.*533A= (p.=)
3g.10150302A>CCA1345063498VHLc.*337A>C (p.=)
c.*533A>C (p.=)
3g.10150304G>ACA896166519VHLc.*339G>A (p.=)
c.*535G>A (p.=)
3g.10150304G=CA1345063501VHLc.*339G= (p.=)
c.*535G= (p.=)
3g.10150308G=CA1345063502VHLc.*343G= (p.=)
c.*539G= (p.=)
3g.10150308G>TCA1345063503VHLc.*343G>T (p.=)
c.*539G>T (p.=)
3g.10150314G=CA1345063505VHLc.*349G= (p.=)
c.*545G= (p.=)
3g.10150314G>TCA10614396VHLc.*349G>T (p.=)
c.*545G>T (p.=)
ClinVar dbSNP
3g.10150315C=CA1345063510VHLc.*350C= (p.=)
c.*546C= (p.=)
3g.10150315C>TCA1345063512VHLc.*350C>T (p.=)
c.*546C>T (p.=)
3g.10150316A=CA1345063516VHLc.*351A= (p.=)
c.*547A= (p.=)
3g.10150316A>GCA70052880VHLc.*351A>G (p.=)
c.*547A>G (p.=)
dbSNP
3g.10150320G>ACA540877283VHLc.*355G>A (p.=)
c.*551G>A (p.=)
gnomAD

Number of alleles fetched