Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.130317591C>TCA12798544ASAP1c.186+40426G>A (p.=)
c.165+40426G>A (p.=)
c.*168+40426G>A (p.=)
n.96+23251G>A
c.-120-27453G>A (p.=)
c.10-80597G>A (p.=)
n.2820C>T
n.2635C>T
n.2663C>T
c.51+40091G>A (p.=)
dbSNP gnomAD
8g.130317603T>GCA186052979ASAP1c.186+40414A>C (p.=)
c.165+40414A>C (p.=)
c.*168+40414A>C (p.=)
n.96+23239A>C
c.-120-27465A>C (p.=)
c.10-80609A>C (p.=)
n.2832T>G
n.2647T>G
n.2675T>G
c.51+40079A>C (p.=)
dbSNP
8g.130317604C>ACA186052980ASAP1c.186+40413G>T (p.=)
c.165+40413G>T (p.=)
c.*168+40413G>T (p.=)
n.96+23238G>T
c.-120-27466G>T (p.=)
c.10-80610G>T (p.=)
n.2833C>A
n.2648C>A
n.2676C>A
c.51+40078G>T (p.=)
dbSNP gnomAD
8g.130317611T>CCA186052981ASAP1c.186+40406A>G (p.=)
c.165+40406A>G (p.=)
c.*168+40406A>G (p.=)
n.96+23231A>G
c.-120-27473A>G (p.=)
c.10-80617A>G (p.=)
n.2840T>C
n.2655T>C
n.2683T>C
c.51+40071A>G (p.=)
dbSNP
8g.130317613T>CCA186052982ASAP1c.186+40404A>G (p.=)
c.165+40404A>G (p.=)
c.*168+40404A>G (p.=)
n.96+23229A>G
c.-120-27475A>G (p.=)
c.10-80619A>G (p.=)
n.2842T>C
n.2657T>C
n.2685T>C
c.51+40069A>G (p.=)
dbSNP
8g.130317626A>GCA847450418ASAP1c.186+40391T>C (p.=)
c.165+40391T>C (p.=)
c.*168+40391T>C (p.=)
n.96+23216T>C
c.-120-27488T>C (p.=)
c.10-80632T>C (p.=)
n.2855A>G
n.2670A>G
n.2698A>G
c.51+40056T>C (p.=)
8g.130317629A>CCA1119189204ASAP1c.186+40388T>G (p.=)
c.165+40388T>G (p.=)
c.*168+40388T>G (p.=)
n.96+23213T>G
c.-120-27491T>G (p.=)
c.10-80635T>G (p.=)
n.2858A>C
n.2673A>C
n.2701A>C
c.51+40053T>G (p.=)
8g.130317640A>CCA1119189207ASAP1c.186+40377T>G (p.=)
c.165+40377T>G (p.=)
c.*168+40377T>G (p.=)
n.96+23202T>G
c.-120-27502T>G (p.=)
c.10-80646T>G (p.=)
n.2869A>C
n.2684A>C
n.2712A>C
c.51+40042T>G (p.=)
8g.130317645T>ACA1119189208ASAP1c.186+40372A>T (p.=)
c.165+40372A>T (p.=)
c.*168+40372A>T (p.=)
n.96+23197A>T
c.-120-27507A>T (p.=)
c.10-80651A>T (p.=)
n.2874T>A
n.2689T>A
n.2717T>A
c.51+40037A>T (p.=)
8g.130317646T>ACA847450421ASAP1c.186+40371A>T (p.=)
c.165+40371A>T (p.=)
c.*168+40371A>T (p.=)
n.96+23196A>T
c.-120-27508A>T (p.=)
c.10-80652A>T (p.=)
n.2875T>A
n.2690T>A
n.2718T>A
c.51+40036A>T (p.=)
8g.130317646T>CCA186052983ASAP1c.186+40371A>G (p.=)
c.165+40371A>G (p.=)
c.*168+40371A>G (p.=)
n.96+23196A>G
c.-120-27508A>G (p.=)
c.10-80652A>G (p.=)
n.2875T>C
n.2690T>C
n.2718T>C
c.51+40036A>G (p.=)
dbSNP
8g.130317647A>GCA186052984ASAP1c.186+40370T>C (p.=)
c.165+40370T>C (p.=)
c.*168+40370T>C (p.=)
n.96+23195T>C
c.-120-27509T>C (p.=)
c.10-80653T>C (p.=)
n.2876A>G
n.2691A>G
n.2719A>G
c.51+40035T>C (p.=)
dbSNP
8g.130317649T>CCA186052985ASAP1c.186+40368A>G (p.=)
c.165+40368A>G (p.=)
c.*168+40368A>G (p.=)
n.96+23193A>G
c.-120-27511A>G (p.=)
c.10-80655A>G (p.=)
n.2878T>C
n.2693T>C
n.2721T>C
c.51+40033A>G (p.=)
dbSNP gnomAD
8g.130317650G>TCA847450425ASAP1c.186+40367C>A (p.=)
c.165+40367C>A (p.=)
c.*168+40367C>A (p.=)
n.96+23192C>A
c.-120-27512C>A (p.=)
c.10-80656C>A (p.=)
n.2879G>T
n.2694G>T
n.2722G>T
c.51+40032C>A (p.=)
8g.130317651C>TCA847450428ASAP1c.186+40366G>A (p.=)
c.165+40366G>A (p.=)
c.*168+40366G>A (p.=)
n.96+23191G>A
c.-120-27513G>A (p.=)
c.10-80657G>A (p.=)
n.2880C>T
n.2695C>T
n.2723C>T
c.51+40031G>A (p.=)
8g.130317655T>ACA1119189210ASAP1c.186+40362A>T (p.=)
c.165+40362A>T (p.=)
c.*168+40362A>T (p.=)
n.96+23187A>T
c.-120-27517A>T (p.=)
c.10-80661A>T (p.=)
n.2884T>A
n.2699T>A
n.2727T>A
c.51+40027A>T (p.=)
8g.130317673C>ACA1119189212ASAP1c.186+40344G>T (p.=)
c.165+40344G>T (p.=)
c.*168+40344G>T (p.=)
n.96+23169G>T
c.-120-27535G>T (p.=)
c.10-80679G>T (p.=)
n.2902C>A
n.2717C>A
n.2745C>A
c.51+40009G>T (p.=)
8g.130317679T>CCA847450431ASAP1c.186+40338A>G (p.=)
c.165+40338A>G (p.=)
c.*168+40338A>G (p.=)
n.96+23163A>G
c.-120-27541A>G (p.=)
c.10-80685A>G (p.=)
n.2908T>C
n.2723T>C
n.2751T>C
c.51+40003A>G (p.=)
8g.130317682T>GCA847450432ASAP1c.186+40335A>C (p.=)
c.165+40335A>C (p.=)
c.*168+40335A>C (p.=)
n.96+23160A>C
c.-120-27544A>C (p.=)
c.10-80688A>C (p.=)
n.2911T>G
n.2726T>G
n.2754T>G
c.51+40000A>C (p.=)
8g.130317683G>ACA1119189214ASAP1c.186+40334C>T (p.=)
c.165+40334C>T (p.=)
c.*168+40334C>T (p.=)
n.96+23159C>T
c.-120-27545C>T (p.=)
c.10-80689C>T (p.=)
n.2912G>A
n.2727G>A
n.2755G>A
c.51+39999C>T (p.=)
8g.130317683G>CCA847450434ASAP1c.186+40334C>G (p.=)
c.165+40334C>G (p.=)
c.*168+40334C>G (p.=)
n.96+23159C>G
c.-120-27545C>G (p.=)
c.10-80689C>G (p.=)
n.2912G>C
n.2727G>C
n.2755G>C
c.51+39999C>G (p.=)
8g.130317686C>TCA186052986ASAP1c.186+40331G>A (p.=)
c.165+40331G>A (p.=)
c.*168+40331G>A (p.=)
n.96+23156G>A
c.-120-27548G>A (p.=)
c.10-80692G>A (p.=)
n.2915C>T
n.2730C>T
n.2758C>T
c.51+39996G>A (p.=)
dbSNP gnomAD
8g.130317688T>GCA186052987ASAP1c.186+40329A>C (p.=)
c.165+40329A>C (p.=)
c.*168+40329A>C (p.=)
n.96+23154A>C
c.-120-27550A>C (p.=)
c.10-80694A>C (p.=)
n.2917T>G
n.2732T>G
n.2760T>G
c.51+39994A>C (p.=)
dbSNP gnomAD

Number of alleles fetched