Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.55432033T>CCA551380705CLOCK,TMEM165c.*3382A>G (n.*3382A>G)
c.352+7390T>C
c.408+7390T>C
c.898+7390T>C (n.898+7390T>C)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.55432033T=CA1459095754CLOCK,TMEM165c.*3382A= (n.*3382A=)
c.352+7390T=
c.408+7390T=
c.898+7390T= (n.898+7390T=)
4g.55432033_55432037delinsTAACACA1459095755CLOCK,TMEM165c.*3378_*3382delinsTGTTA (n.*3378_*3382delinsTGTTA)
c.352+7390_352+7394delinsTAACA
c.408+7390_408+7394delinsTAACA
c.898+7390_898+7394delinsTAACA (n.898+7390_898+7394delinsTAACA)
4g.55432037_55432040delCA796386550CLOCK,TMEM165c.*3378_*3381del (n.*3378_*3381del)
c.352+7394_352+7397del
c.408+7394_408+7397del
c.898+7394_898+7397del (n.898+7394_898+7397del)
dbSNP gnomAD v3 gnomAD v4
4g.55432040C>ACA2670685416CLOCK,TMEM165c.*3375G>T (n.*3375G>T)
c.352+7397C>A
c.408+7397C>A
c.898+7397C>A (n.898+7397C>A)
gnomAD v4
4g.55432041T>CCA2670685417CLOCK,TMEM165c.*3374A>G (n.*3374A>G)
c.352+7398T>C
c.408+7398T>C
c.898+7398T>C (n.898+7398T>C)
gnomAD v4
4g.55432042A=CA1459095756CLOCK,TMEM165c.*3373T= (n.*3373T=)
c.352+7399A=
c.408+7399A=
c.898+7399A= (n.898+7399A=)
4g.55432042A>TCA796386554CLOCK,TMEM165c.*3373T>A (n.*3373T>A)
c.352+7399A>T
c.408+7399A>T
c.898+7399A>T (n.898+7399A>T)
dbSNP
4g.55432043T>GCA2670685418CLOCK,TMEM165c.*3372A>C (n.*3372A>C)
c.352+7400T>G
c.408+7400T>G
c.898+7400T>G (n.898+7400T>G)
gnomAD v4
4g.55432044T>CCA2670685419CLOCK,TMEM165c.*3371A>G (n.*3371A>G)
c.352+7401T>C
c.408+7401T>C
c.898+7401T>C (n.898+7401T>C)
gnomAD v4
4g.55432046C=CA1459095757CLOCK,TMEM165c.*3369G= (n.*3369G=)
c.352+7403C=
c.408+7403C=
c.898+7403C= (n.898+7403C=)
4g.55432046C>GCA96894358CLOCK,TMEM165c.*3369G>C (n.*3369G>C)
c.352+7403C>G
c.408+7403C>G
c.898+7403C>G (n.898+7403C>G)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.55432048A=CA1459095758CLOCK,TMEM165c.*3367T= (n.*3367T=)
c.352+7405A=
c.408+7405A=
c.898+7405A= (n.898+7405A=)
4g.55432048A>TCA1459095759CLOCK,TMEM165c.*3367T>A (n.*3367T>A)
c.352+7405A>T
c.408+7405A>T
c.898+7405A>T (n.898+7405A>T)
dbSNP
4g.55432049A>CCA2705955199CLOCK,TMEM165c.*3366T>G (n.*3366T>G)
c.352+7406A>C
c.408+7406A>C
c.898+7406A>C (n.898+7406A>C)
dbSNP
4g.55432050T>CCA1062735923CLOCK,TMEM165c.*3365A>G (n.*3365A>G)
c.352+7407T>C
c.408+7407T>C
c.898+7407T>C (n.898+7407T>C)
dbSNP gnomAD v3 gnomAD v4
4g.55432050T=CA1459095760CLOCK,TMEM165c.*3365A= (n.*3365A=)
c.352+7407T=
c.408+7407T=
c.898+7407T= (n.898+7407T=)
4g.55432051C>ACA2568236435CLOCK,TMEM165c.*3364G>T (n.*3364G>T)
c.352+7408C>A
c.408+7408C>A
c.898+7408C>A (n.898+7408C>A)
gnomAD v4
4g.55432051C>TCA2670685420CLOCK,TMEM165c.*3364G>A (n.*3364G>A)
c.352+7408C>T
c.408+7408C>T
c.898+7408C>T (n.898+7408C>T)
gnomAD v4
4g.55432052A>TCA2536098735CLOCK,TMEM165c.*3363T>A (n.*3363T>A)
c.352+7409A>T
c.408+7409A>T
c.898+7409A>T (n.898+7409A>T)
4g.55432056G>ACA1062735925CLOCK,TMEM165c.*3359C>T (n.*3359C>T)
c.352+7413G>A
c.408+7413G>A
c.898+7413G>A (n.898+7413G>A)
dbSNP gnomAD v3 gnomAD v4
4g.55432056G>CCA1459095762CLOCK,TMEM165c.*3359C>G (n.*3359C>G)
c.352+7413G>C
c.408+7413G>C
c.898+7413G>C (n.898+7413G>C)
dbSNP
4g.55432056G=CA1459095761CLOCK,TMEM165c.*3359C= (n.*3359C=)
c.352+7413G=
c.408+7413G=
c.898+7413G= (n.898+7413G=)
4g.55432056G>TCA2670685421CLOCK,TMEM165c.*3359C>A (n.*3359C>A)
c.352+7413G>T
c.408+7413G>T
c.898+7413G>T (n.898+7413G>T)
gnomAD v4
4g.55432057C>ACA96894363CLOCK,TMEM165c.*3358G>T (n.*3358G>T)
c.352+7414C>A
c.408+7414C>A
c.898+7414C>A (n.898+7414C>A)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.55432057C=CA1459095763CLOCK,TMEM165c.*3358G= (n.*3358G=)
c.352+7414C=
c.408+7414C=
c.898+7414C= (n.898+7414C=)
4g.55432060C>ACA2670685422CLOCK,TMEM165c.*3355G>T (n.*3355G>T)
c.352+7417C>A
c.408+7417C>A
c.898+7417C>A (n.898+7417C>A)
gnomAD v4
4g.55432060_55432063delinsCTTGCA1459095764CLOCK,TMEM165c.*3352_*3355delinsCAAG (n.*3352_*3355delinsCAAG)
c.352+7417_352+7420delinsCTTG
c.408+7417_408+7420delinsCTTG
c.898+7417_898+7420delinsCTTG (n.898+7417_898+7420delinsCTTG)
4g.55432061T>CCA796386592CLOCK,TMEM165c.*3354A>G (n.*3354A>G)
c.352+7418T>C
c.408+7418T>C
c.898+7418T>C (n.898+7418T>C)
dbSNP gnomAD v4
4g.55432061T=CA1459095765CLOCK,TMEM165c.*3354A= (n.*3354A=)
c.352+7418T=
c.408+7418T=
c.898+7418T= (n.898+7418T=)
4g.55432063_55432065delCA796386588CLOCK,TMEM165c.*3352_*3354del (n.*3352_*3354del)
c.352+7420_352+7422del
c.408+7420_408+7422del
c.898+7420_898+7422del (n.898+7420_898+7422del)
dbSNP gnomAD v3 gnomAD v4
4g.55432062T>CCA551380707CLOCK,TMEM165c.*3353A>G (n.*3353A>G)
c.352+7419T>C
c.408+7419T>C
c.898+7419T>C (n.898+7419T>C)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.55432062T=CA1459095766CLOCK,TMEM165c.*3353A= (n.*3353A=)
c.352+7419T=
c.408+7419T=
c.898+7419T= (n.898+7419T=)
4g.55432069A>GCA2670685423CLOCK,TMEM165c.*3346T>C (n.*3346T>C)
c.352+7426A>G
c.408+7426A>G
c.898+7426A>G (n.898+7426A>G)
gnomAD v4
4g.55432070C>ACA796386602CLOCK,TMEM165c.*3345G>T (n.*3345G>T)
c.352+7427C>A
c.408+7427C>A
c.898+7427C>A (n.898+7427C>A)
dbSNP
4g.55432070C=CA1459095767CLOCK,TMEM165c.*3345G= (n.*3345G=)
c.352+7427C=
c.408+7427C=
c.898+7427C= (n.898+7427C=)
4g.55432073T>CCA96894365CLOCK,TMEM165c.*3342A>G (n.*3342A>G)
c.352+7430T>C
c.408+7430T>C
c.898+7430T>C (n.898+7430T>C)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.55432073T=CA1459095768CLOCK,TMEM165c.*3342A= (n.*3342A=)
c.352+7430T=
c.408+7430T=
c.898+7430T= (n.898+7430T=)
4g.55432077A=CA1459095769CLOCK,TMEM165c.*3338T= (n.*3338T=)
c.352+7434A=
c.408+7434A=
c.898+7434A= (n.898+7434A=)
4g.55432077A>GCA1459095770CLOCK,TMEM165c.*3338T>C (n.*3338T>C)
c.352+7434A>G
c.408+7434A>G
c.898+7434A>G (n.898+7434A>G)
dbSNP
4g.55432079T>CCA2670685424CLOCK,TMEM165c.*3336A>G (n.*3336A>G)
c.352+7436T>C
c.408+7436T>C
c.898+7436T>C (n.898+7436T>C)
gnomAD v4
4g.55432080C>ACA2670685425CLOCK,TMEM165c.*3335G>T (n.*3335G>T)
c.352+7437C>A
c.408+7437C>A
c.898+7437C>A (n.898+7437C>A)
gnomAD v4
4g.55432085G>TCA2670685426CLOCK,TMEM165c.*3330C>A (n.*3330C>A)
c.352+7442G>T
c.408+7442G>T
c.898+7442G>T (n.898+7442G>T)
gnomAD v4
4g.55432086C>ACA2670685427CLOCK,TMEM165c.*3329G>T (n.*3329G>T)
c.352+7443C>A
c.408+7443C>A
c.898+7443C>A (n.898+7443C>A)
gnomAD v4
4g.55432087C>ACA2670685428CLOCK,TMEM165c.*3328G>T (n.*3328G>T)
c.352+7444C>A
c.408+7444C>A
c.898+7444C>A (n.898+7444C>A)
gnomAD v4
4g.55432087C=CA1459095771CLOCK,TMEM165c.*3328G= (n.*3328G=)
c.352+7444C=
c.408+7444C=
c.898+7444C= (n.898+7444C=)
4g.55432087C>TCA551380711CLOCK,TMEM165c.*3328G>A (n.*3328G>A)
c.352+7444C>T
c.408+7444C>T
c.898+7444C>T (n.898+7444C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.55432088A>GCA2670685429CLOCK,TMEM165c.*3327T>C (n.*3327T>C)
c.352+7445A>G
c.408+7445A>G
c.898+7445A>G (n.898+7445A>G)
gnomAD v4
4g.55432088A>TCA2670685430CLOCK,TMEM165c.*3327T>A (n.*3327T>A)
c.352+7445A>T
c.408+7445A>T
c.898+7445A>T (n.898+7445A>T)
gnomAD v4
4g.55432089G>TCA2670685431CLOCK,TMEM165c.*3326C>A (n.*3326C>A)
c.352+7446G>T
c.408+7446G>T
c.898+7446G>T (n.898+7446G>T)
gnomAD v4

Number of alleles fetched