Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.104914914C=CA1869959230ABCA1c.-92-11143G= (p.=)
c.-115+13021G= (p.=)
c.-156+13021G= (p.=)
n.999-3748C=
n.20+2574C=
n.222-11143G=
9g.104914914C>TCA1869959231ABCA1c.-92-11143G>A (p.=)
c.-115+13021G>A (p.=)
c.-156+13021G>A (p.=)
n.999-3748C>T
n.20+2574C>T
n.222-11143G>A
9g.104914917C=CA1869959232ABCA1c.-92-11146G= (p.=)
c.-115+13018G= (p.=)
c.-156+13018G= (p.=)
n.999-3745C=
n.20+2577C=
n.222-11146G=
9g.104914918dupCA858080410ABCA1c.-92-11147dup (p.=)
c.-115+13017dup (p.=)
c.-156+13017dup (p.=)
n.999-3744dup
n.20+2578dup
n.222-11147dup
dbSNP
9g.104914920G>ACA1127652775ABCA1c.-92-11149C>T (p.=)
c.-115+13015C>T (p.=)
c.-156+13015C>T (p.=)
n.999-3742G>A
n.20+2580G>A
n.222-11149C>T
9g.104914920G=CA1869959233ABCA1c.-92-11149C= (p.=)
c.-115+13015C= (p.=)
c.-156+13015C= (p.=)
n.999-3742G=
n.20+2580G=
n.222-11149C=
9g.104914922G=CA1869959234ABCA1c.-92-11151C= (p.=)
c.-115+13013C= (p.=)
c.-156+13013C= (p.=)
n.999-3740G=
n.20+2582G=
n.222-11151C=
9g.104914922G>TCA1869959235ABCA1c.-92-11151C>A (p.=)
c.-115+13013C>A (p.=)
c.-156+13013C>A (p.=)
n.999-3740G>T
n.20+2582G>T
n.222-11151C>A
9g.104914924G>ACA858080413ABCA1c.-92-11153C>T (p.=)
c.-115+13011C>T (p.=)
c.-156+13011C>T (p.=)
n.999-3738G>A
n.20+2584G>A
n.222-11153C>T
9g.104914924G=CA1869959236ABCA1c.-92-11153C= (p.=)
c.-115+13011C= (p.=)
c.-156+13011C= (p.=)
n.999-3738G=
n.20+2584G=
n.222-11153C=
9g.104914925C>ACA589855452ABCA1c.-92-11154G>T (p.=)
c.-115+13010G>T (p.=)
c.-156+13010G>T (p.=)
n.999-3737C>A
n.20+2585C>A
n.222-11154G>T
gnomAD
9g.104914925C=CA1869959237ABCA1c.-92-11154G= (p.=)
c.-115+13010G= (p.=)
c.-156+13010G= (p.=)
n.999-3737C=
n.20+2585C=
n.222-11154G=
9g.104914926T>CCA1869959239ABCA1c.-92-11155A>G (p.=)
c.-115+13009A>G (p.=)
c.-156+13009A>G (p.=)
n.999-3736T>C
n.20+2586T>C
n.222-11155A>G
9g.104914926T=CA1869959238ABCA1c.-92-11155A= (p.=)
c.-115+13009A= (p.=)
c.-156+13009A= (p.=)
n.999-3736T=
n.20+2586T=
n.222-11155A=
9g.104914928G=CA1869959240ABCA1c.-92-11157C= (p.=)
c.-115+13007C= (p.=)
c.-156+13007C= (p.=)
n.999-3734G=
n.20+2588G=
n.222-11157C=
9g.104914929_104914930insCACA1127652776ABCA1c.-92-11158_-92-11157insGT (p.=)
c.-115+13006_-115+13007insGT (p.=)
c.-156+13006_-156+13007insGT (p.=)
n.999-3733_999-3732insCA
n.20+2589_20+2590insCA
n.222-11158_222-11157insGT
dbSNP
9g.104914930G>CCA13035774ABCA1c.-92-11159C>G (p.=)
c.-115+13005C>G (p.=)
c.-156+13005C>G (p.=)
n.999-3732G>C
n.20+2590G>C
n.222-11159C>G
dbSNP gnomAD
9g.104914930G=CA1869959241ABCA1c.-92-11159C= (p.=)
c.-115+13005C= (p.=)
c.-156+13005C= (p.=)
n.999-3732G=
n.20+2590G=
n.222-11159C=
9g.104914932G>ACA197399681ABCA1c.-92-11161C>T (p.=)
c.-115+13003C>T (p.=)
c.-156+13003C>T (p.=)
n.999-3730G>A
n.20+2592G>A
n.222-11161C>T
dbSNP
9g.104914932G>CCA1869959243ABCA1c.-92-11161C>G (p.=)
c.-115+13003C>G (p.=)
c.-156+13003C>G (p.=)
n.999-3730G>C
n.20+2592G>C
n.222-11161C>G
9g.104914932G=CA1869959242ABCA1c.-92-11161C= (p.=)
c.-115+13003C= (p.=)
c.-156+13003C= (p.=)
n.999-3730G=
n.20+2592G=
n.222-11161C=
9g.104914934A=CA1869959244ABCA1c.-92-11163T= (p.=)
c.-115+13001T= (p.=)
c.-156+13001T= (p.=)
n.999-3728A=
n.20+2594A=
n.222-11163T=
9g.104914934A>GCA858080417ABCA1c.-92-11163T>C (p.=)
c.-115+13001T>C (p.=)
c.-156+13001T>C (p.=)
n.999-3728A>G
n.20+2594A>G
n.222-11163T>C
9g.104914934A>TCA1869959245ABCA1c.-92-11163T>A (p.=)
c.-115+13001T>A (p.=)
c.-156+13001T>A (p.=)
n.999-3728A>T
n.20+2594A>T
n.222-11163T>A
9g.104914936C=CA1869959246ABCA1c.-92-11165G= (p.=)
c.-115+12999G= (p.=)
c.-156+12999G= (p.=)
n.999-3726C=
n.20+2596C=
n.222-11165G=
9g.104914936C>GCA915802837ABCA1c.-92-11165G>C (p.=)
c.-115+12999G>C (p.=)
c.-156+12999G>C (p.=)
n.999-3726C>G
n.20+2596C>G
n.222-11165G>C
gnomAD
9g.104914940G>ACA1127652781ABCA1c.-92-11169C>T (p.=)
c.-115+12995C>T (p.=)
c.-156+12995C>T (p.=)
n.999-3722G>A
n.20+2600G>A
n.222-11169C>T
9g.104914940G=CA1869959247ABCA1c.-92-11169C= (p.=)
c.-115+12995C= (p.=)
c.-156+12995C= (p.=)
n.999-3722G=
n.20+2600G=
n.222-11169C=
9g.104914941A=CA1869959248ABCA1c.-92-11170T= (p.=)
c.-115+12994T= (p.=)
c.-156+12994T= (p.=)
n.999-3721A=
n.20+2601A=
n.222-11170T=
9g.104914941A>TCA858080419ABCA1c.-92-11170T>A (p.=)
c.-115+12994T>A (p.=)
c.-156+12994T>A (p.=)
n.999-3721A>T
n.20+2601A>T
n.222-11170T>A
9g.104914942T>CCA197399683ABCA1c.-92-11171A>G (p.=)
c.-115+12993A>G (p.=)
c.-156+12993A>G (p.=)
n.999-3720T>C
n.20+2602T>C
n.222-11171A>G
dbSNP gnomAD
9g.104914942T=CA1869959249ABCA1c.-92-11171A= (p.=)
c.-115+12993A= (p.=)
c.-156+12993A= (p.=)
n.999-3720T=
n.20+2602T=
n.222-11171A=
9g.104914944G>ACA858080421ABCA1c.-92-11173C>T (p.=)
c.-115+12991C>T (p.=)
c.-156+12991C>T (p.=)
n.999-3718G>A
n.20+2604G>A
n.222-11173C>T
9g.104914944G=CA1869959250ABCA1c.-92-11173C= (p.=)
c.-115+12991C= (p.=)
c.-156+12991C= (p.=)
n.999-3718G=
n.20+2604G=
n.222-11173C=
9g.104914947G>ACA589855461ABCA1c.-92-11176C>T (p.=)
c.-115+12988C>T (p.=)
c.-156+12988C>T (p.=)
n.999-3715G>A
n.20+2607G>A
n.222-11176C>T
gnomAD
9g.104914947G>CCA589855462ABCA1c.-92-11176C>G (p.=)
c.-115+12988C>G (p.=)
c.-156+12988C>G (p.=)
n.999-3715G>C
n.20+2607G>C
n.222-11176C>G
gnomAD
9g.104914947G=CA1869959251ABCA1c.-92-11176C= (p.=)
c.-115+12988C= (p.=)
c.-156+12988C= (p.=)
n.999-3715G=
n.20+2607G=
n.222-11176C=
9g.104914950C=CA1869959252ABCA1c.-92-11179G= (p.=)
c.-115+12985G= (p.=)
c.-156+12985G= (p.=)
n.999-3712C=
n.20+2610C=
n.222-11179G=
9g.104914950C>TCA858080423ABCA1c.-92-11179G>A (p.=)
c.-115+12985G>A (p.=)
c.-156+12985G>A (p.=)
n.999-3712C>T
n.20+2610C>T
n.222-11179G>A
9g.104914956C>ACA589855467ABCA1c.-92-11185G>T (p.=)
c.-115+12979G>T (p.=)
c.-156+12979G>T (p.=)
n.999-3706C>A
n.20+2616C>A
n.222-11185G>T
gnomAD
9g.104914956C=CA1869959253ABCA1c.-92-11185G= (p.=)
c.-115+12979G= (p.=)
c.-156+12979G= (p.=)
n.999-3706C=
n.20+2616C=
n.222-11185G=
9g.104914960T>CCA589855470ABCA1c.-92-11189A>G (p.=)
c.-115+12975A>G (p.=)
c.-156+12975A>G (p.=)
n.999-3702T>C
n.20+2620T>C
n.222-11189A>G
gnomAD
9g.104914960T=CA1869959254ABCA1c.-92-11189A= (p.=)
c.-115+12975A= (p.=)
c.-156+12975A= (p.=)
n.999-3702T=
n.20+2620T=
n.222-11189A=
9g.104914969T>CCA1869959256ABCA1c.-92-11198A>G (p.=)
c.-115+12966A>G (p.=)
c.-156+12966A>G (p.=)
n.999-3693T>C
n.20+2629T>C
n.222-11198A>G
9g.104914969T=CA1869959255ABCA1c.-92-11198A= (p.=)
c.-115+12966A= (p.=)
c.-156+12966A= (p.=)
n.999-3693T=
n.20+2629T=
n.222-11198A=
9g.104914973A=CA1869959257ABCA1c.-92-11202T= (p.=)
c.-115+12962T= (p.=)
c.-156+12962T= (p.=)
n.999-3689A=
n.20+2633A=
n.222-11202T=
9g.104914973A>GCA858080428ABCA1c.-92-11202T>C (p.=)
c.-115+12962T>C (p.=)
c.-156+12962T>C (p.=)
n.999-3689A>G
n.20+2633A>G
n.222-11202T>C
9g.104914974T>CCA589855473ABCA1c.-92-11203A>G (p.=)
c.-115+12961A>G (p.=)
c.-156+12961A>G (p.=)
n.999-3688T>C
n.20+2634T>C
n.222-11203A>G
gnomAD
9g.104914974T=CA1869959258ABCA1c.-92-11203A= (p.=)
c.-115+12961A= (p.=)
c.-156+12961A= (p.=)
n.999-3688T=
n.20+2634T=
n.222-11203A=
9g.104914979C=CA1869959259ABCA1c.-92-11208G= (p.=)
c.-115+12956G= (p.=)
c.-156+12956G= (p.=)
n.999-3683C=
n.20+2639C=
n.222-11208G=

Number of alleles fetched