Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.120738864G>ACA482146783ACADSc.978G>A (p.Leu326=)
c.966G>A (p.Leu322=)
12g.120738864G>CCA482146784ACADSc.978G>C (p.Leu326=)
c.966G>C (p.Leu322=)
12g.120738864G>TCA482146785ACADSc.978G>T (p.Leu326=)
c.966G>T (p.Leu322=)
12g.120738865C>ACA386601506ACADSc.979C>A (p.Leu327Met)
c.967C>A (p.Leu323Met)
12g.120738865C>GCA386601507ACADSc.979C>G (p.Leu327Val)
c.967C>G (p.Leu323Val)
12g.120738865C>TCA482146788ACADSc.979C>T (p.Leu327=)
c.967C>T (p.Leu323=)
gnomAD v4
12g.120738866_120738869delCA912973555ACADSc.980_983del (p.Leu327ProfsTer7)
c.968_971del (p.Leu323ProfsTer7)
12g.120738866T>ACA386601510ACADSc.980T>A (p.Leu327Gln)
c.968T>A (p.Leu323Gln)
12g.120738866T>CCA386601509ACADSc.980T>C (p.Leu327Pro)
c.968T>C (p.Leu323Pro)
12g.120738866T>GCA386601508ACADSc.980T>G (p.Leu327Arg)
c.968T>G (p.Leu323Arg)
12g.120738866_120738869delinsTGACCA2067555552ACADSc.980_983delinsTGAC (p.Leu327=)
c.968_971delinsTGAC (p.Leu323=)
12g.120738867G>ACA482146791ACADSc.981G>A (p.Leu327=)
c.969G>A (p.Leu323=)
12g.120738867G>CCA482146790ACADSc.981G>C (p.Leu327=)
c.969G>C (p.Leu323=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.120738867G=CA2067555553ACADSc.981G= (p.Leu327=)
c.969G= (p.Leu323=)
12g.120738867G>TCA482146789ACADSc.981G>T (p.Leu327=)
c.969G>T (p.Leu323=)
gnomAD v4
12g.120738867_120738869delCA608059988ACADSc.981_983del (p.Thr328del)
c.969_971del (p.Thr324del)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.120738868A=CA2067555554ACADSc.982A= (p.Thr328=)
c.970A= (p.Thr324=)
12g.120738868A>CCA386601511ACADSc.982A>C (p.Thr328Pro)
c.970A>C (p.Thr324Pro)
gnomAD v4
12g.120738868A>GCA386601512ACADSc.982A>G (p.Thr328Ala)
c.970A>G (p.Thr324Ala)
dbSNP gnomAD v2 gnomAD v4
12g.120738868A>TCA386601513ACADSc.982A>T (p.Thr328Ser)
c.970A>T (p.Thr324Ser)
COSMIC
12g.120738869C>ACA386601514ACADSc.983C>A (p.Thr328Asn)
c.971C>A (p.Thr324Asn)
12g.120738869C>GCA386601515ACADSc.983C>G (p.Thr328Ser)
c.971C>G (p.Thr324Ser)
12g.120738869C>TCA386601516ACADSc.983C>T (p.Thr328Ile)
c.971C>T (p.Thr324Ile)
12g.120738870C>ACA482146795ACADSc.984C>A (p.Thr328=)
c.972C>A (p.Thr324=)
12g.120738870C>GCA482146796ACADSc.984C>G (p.Thr328=)
c.972C>G (p.Thr324=)
12g.120738870C>TCA482146797ACADSc.984C>T (p.Thr328=)
c.972C>T (p.Thr324=)
ClinVar
12g.120738871T>ACA386601517ACADSc.985T>A (p.Trp329Arg)
c.973T>A (p.Trp325Arg)
12g.120738871T>CCA386601518ACADSc.985T>C (p.Trp329Arg)
c.973T>C (p.Trp325Arg)
12g.120738871T>GCA386601519ACADSc.985T>G (p.Trp329Gly)
c.973T>G (p.Trp325Gly)
12g.120738872G>ACA386601520ACADSc.986G>A (p.Trp329Ter)
c.974G>A (p.Trp325Ter)
12g.120738872G>CCA386601521ACADSc.986G>C (p.Trp329Ser)
c.974G>C (p.Trp325Ser)
12g.120738872G>TCA386601522ACADSc.986G>T (p.Trp329Leu)
c.974G>T (p.Trp325Leu)
12g.120738873G>ACA386601525ACADSc.987G>A (p.Trp329Ter)
c.975G>A (p.Trp325Ter)
12g.120738873G>CCA386601524ACADSc.987G>C (p.Trp329Cys)
c.975G>C (p.Trp325Cys)
12g.120738873G>TCA386601523ACADSc.987G>T (p.Trp329Cys)
c.975G>T (p.Trp325Cys)
12g.120738874C>ACA6831152ACADSc.988C>A (p.Arg330Ser)
c.976C>A (p.Arg326Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.120738874C=CA2067555555ACADSc.988C= (p.Arg330=)
c.976C= (p.Arg326=)
12g.120738874C>GCA386601526ACADSc.988C>G (p.Arg330Gly)
c.976C>G (p.Arg326Gly)
12g.120738874C>TCA312222ACADSc.988C>T (p.Arg330Cys)
c.976C>T (p.Arg326Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.120738874_120738876delinsCGCCA2067555556ACADSc.988_990delinsCGC (p.Arg330=)
c.976_978delinsCGC (p.Arg326=)
12g.120738874_120738876delinsTGTCA312246ACADSc.988_990delinsTGT (p.Arg330Cys)
c.976_978delinsTGT (p.Arg326Cys)
ClinVar dbSNP
12g.120738875G>ACA6831153ACADSc.989G>A (p.Arg330His)
c.977G>A (p.Arg326His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.120738875G>CCA6831154ACADSc.989G>C (p.Arg330Pro)
c.977G>C (p.Arg326Pro)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.120738875G=CA2067555557ACADSc.989G= (p.Arg330=)
c.977G= (p.Arg326=)
12g.120738875G>TCA386601527ACADSc.989G>T (p.Arg330Leu)
c.977G>T (p.Arg326Leu)
12g.120738875_120738876delinsATCA645372922ACADSc.989_990delinsAT (p.Arg330His)
c.977_978delinsAT (p.Arg326His)
ClinVar dbSNP
12g.120738875_120738876delinsGCCA2067555558ACADSc.989_990delinsGC (p.Arg330=)
c.977_978delinsGC (p.Arg326=)
12g.120738875_120738876delinsTTCA2739277338ACADSc.989_990delinsTT (p.Arg330Leu)
c.977_978delinsTT (p.Arg326Leu)
ClinVar
12g.120738876C>ACA244494714ACADSc.990C>A (p.Arg330=)
c.978C>A (p.Arg326=)
dbSNP
12g.120738876C=CA2067555559ACADSc.990C= (p.Arg330=)
c.978C= (p.Arg326=)

Number of alleles fetched