Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.55432033T>C | CA551380705 | CLOCK,TMEM165 | c.*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 |
4 | g.55432033T= | CA1459095754 | CLOCK,TMEM165 | c.*3382A= (n.*3382A=) c.352+7390T= c.408+7390T= c.898+7390T= (n.898+7390T=) | |
4 | g.55432033_55432037delinsTAACA | CA1459095755 | CLOCK,TMEM165 | c.*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) | |
4 | g.55432037_55432040del | CA796386550 | CLOCK,TMEM165 | c.*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 |
4 | g.55432040C>A | CA2670685416 | CLOCK,TMEM165 | c.*3375G>T (n.*3375G>T) c.352+7397C>A c.408+7397C>A c.898+7397C>A (n.898+7397C>A) | gnomAD v4 |
4 | g.55432041T>C | CA2670685417 | CLOCK,TMEM165 | c.*3374A>G (n.*3374A>G) c.352+7398T>C c.408+7398T>C c.898+7398T>C (n.898+7398T>C) | gnomAD v4 |
4 | g.55432042A= | CA1459095756 | CLOCK,TMEM165 | c.*3373T= (n.*3373T=) c.352+7399A= c.408+7399A= c.898+7399A= (n.898+7399A=) | |
4 | g.55432042A>T | CA796386554 | CLOCK,TMEM165 | c.*3373T>A (n.*3373T>A) c.352+7399A>T c.408+7399A>T c.898+7399A>T (n.898+7399A>T) | dbSNP |
4 | g.55432043T>G | CA2670685418 | CLOCK,TMEM165 | c.*3372A>C (n.*3372A>C) c.352+7400T>G c.408+7400T>G c.898+7400T>G (n.898+7400T>G) | gnomAD v4 |
4 | g.55432044T>C | CA2670685419 | CLOCK,TMEM165 | c.*3371A>G (n.*3371A>G) c.352+7401T>C c.408+7401T>C c.898+7401T>C (n.898+7401T>C) | gnomAD v4 |
4 | g.55432046C= | CA1459095757 | CLOCK,TMEM165 | c.*3369G= (n.*3369G=) c.352+7403C= c.408+7403C= c.898+7403C= (n.898+7403C=) | |
4 | g.55432046C>G | CA96894358 | CLOCK,TMEM165 | c.*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 |
4 | g.55432048A= | CA1459095758 | CLOCK,TMEM165 | c.*3367T= (n.*3367T=) c.352+7405A= c.408+7405A= c.898+7405A= (n.898+7405A=) | |
4 | g.55432048A>T | CA1459095759 | CLOCK,TMEM165 | c.*3367T>A (n.*3367T>A) c.352+7405A>T c.408+7405A>T c.898+7405A>T (n.898+7405A>T) | dbSNP |
4 | g.55432049A>C | CA2705955199 | CLOCK,TMEM165 | c.*3366T>G (n.*3366T>G) c.352+7406A>C c.408+7406A>C c.898+7406A>C (n.898+7406A>C) | dbSNP |
4 | g.55432050T>C | CA1062735923 | CLOCK,TMEM165 | c.*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 |
4 | g.55432050T= | CA1459095760 | CLOCK,TMEM165 | c.*3365A= (n.*3365A=) c.352+7407T= c.408+7407T= c.898+7407T= (n.898+7407T=) | |
4 | g.55432051C>A | CA2568236435 | CLOCK,TMEM165 | c.*3364G>T (n.*3364G>T) c.352+7408C>A c.408+7408C>A c.898+7408C>A (n.898+7408C>A) | gnomAD v4 |
4 | g.55432051C>T | CA2670685420 | CLOCK,TMEM165 | c.*3364G>A (n.*3364G>A) c.352+7408C>T c.408+7408C>T c.898+7408C>T (n.898+7408C>T) | gnomAD v4 |
4 | g.55432052A>T | CA2536098735 | CLOCK,TMEM165 | c.*3363T>A (n.*3363T>A) c.352+7409A>T c.408+7409A>T c.898+7409A>T (n.898+7409A>T) | |
4 | g.55432056G>A | CA1062735925 | CLOCK,TMEM165 | c.*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 |
4 | g.55432056G>C | CA1459095762 | CLOCK,TMEM165 | c.*3359C>G (n.*3359C>G) c.352+7413G>C c.408+7413G>C c.898+7413G>C (n.898+7413G>C) | dbSNP |
4 | g.55432056G= | CA1459095761 | CLOCK,TMEM165 | c.*3359C= (n.*3359C=) c.352+7413G= c.408+7413G= c.898+7413G= (n.898+7413G=) | |
4 | g.55432056G>T | CA2670685421 | CLOCK,TMEM165 | c.*3359C>A (n.*3359C>A) c.352+7413G>T c.408+7413G>T c.898+7413G>T (n.898+7413G>T) | gnomAD v4 |
4 | g.55432057C>A | CA96894363 | CLOCK,TMEM165 | c.*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 |
4 | g.55432057C= | CA1459095763 | CLOCK,TMEM165 | c.*3358G= (n.*3358G=) c.352+7414C= c.408+7414C= c.898+7414C= (n.898+7414C=) | |
4 | g.55432060C>A | CA2670685422 | CLOCK,TMEM165 | c.*3355G>T (n.*3355G>T) c.352+7417C>A c.408+7417C>A c.898+7417C>A (n.898+7417C>A) | gnomAD v4 |
4 | g.55432060_55432063delinsCTTG | CA1459095764 | CLOCK,TMEM165 | c.*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) | |
4 | g.55432061T>C | CA796386592 | CLOCK,TMEM165 | c.*3354A>G (n.*3354A>G) c.352+7418T>C c.408+7418T>C c.898+7418T>C (n.898+7418T>C) | dbSNP gnomAD v4 |
4 | g.55432061T= | CA1459095765 | CLOCK,TMEM165 | c.*3354A= (n.*3354A=) c.352+7418T= c.408+7418T= c.898+7418T= (n.898+7418T=) | |
4 | g.55432063_55432065del | CA796386588 | CLOCK,TMEM165 | c.*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 |
4 | g.55432062T>C | CA551380707 | CLOCK,TMEM165 | c.*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 |
4 | g.55432062T= | CA1459095766 | CLOCK,TMEM165 | c.*3353A= (n.*3353A=) c.352+7419T= c.408+7419T= c.898+7419T= (n.898+7419T=) | |
4 | g.55432069A>G | CA2670685423 | CLOCK,TMEM165 | c.*3346T>C (n.*3346T>C) c.352+7426A>G c.408+7426A>G c.898+7426A>G (n.898+7426A>G) | gnomAD v4 |
4 | g.55432070C>A | CA796386602 | CLOCK,TMEM165 | c.*3345G>T (n.*3345G>T) c.352+7427C>A c.408+7427C>A c.898+7427C>A (n.898+7427C>A) | dbSNP |
4 | g.55432070C= | CA1459095767 | CLOCK,TMEM165 | c.*3345G= (n.*3345G=) c.352+7427C= c.408+7427C= c.898+7427C= (n.898+7427C=) | |
4 | g.55432073T>C | CA96894365 | CLOCK,TMEM165 | c.*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 |
4 | g.55432073T= | CA1459095768 | CLOCK,TMEM165 | c.*3342A= (n.*3342A=) c.352+7430T= c.408+7430T= c.898+7430T= (n.898+7430T=) | |
4 | g.55432077A= | CA1459095769 | CLOCK,TMEM165 | c.*3338T= (n.*3338T=) c.352+7434A= c.408+7434A= c.898+7434A= (n.898+7434A=) | |
4 | g.55432077A>G | CA1459095770 | CLOCK,TMEM165 | c.*3338T>C (n.*3338T>C) c.352+7434A>G c.408+7434A>G c.898+7434A>G (n.898+7434A>G) | dbSNP |
4 | g.55432079T>C | CA2670685424 | CLOCK,TMEM165 | c.*3336A>G (n.*3336A>G) c.352+7436T>C c.408+7436T>C c.898+7436T>C (n.898+7436T>C) | gnomAD v4 |
4 | g.55432080C>A | CA2670685425 | CLOCK,TMEM165 | c.*3335G>T (n.*3335G>T) c.352+7437C>A c.408+7437C>A c.898+7437C>A (n.898+7437C>A) | gnomAD v4 |
4 | g.55432085G>T | CA2670685426 | CLOCK,TMEM165 | c.*3330C>A (n.*3330C>A) c.352+7442G>T c.408+7442G>T c.898+7442G>T (n.898+7442G>T) | gnomAD v4 |
4 | g.55432086C>A | CA2670685427 | CLOCK,TMEM165 | c.*3329G>T (n.*3329G>T) c.352+7443C>A c.408+7443C>A c.898+7443C>A (n.898+7443C>A) | gnomAD v4 |
4 | g.55432087C>A | CA2670685428 | CLOCK,TMEM165 | c.*3328G>T (n.*3328G>T) c.352+7444C>A c.408+7444C>A c.898+7444C>A (n.898+7444C>A) | gnomAD v4 |
4 | g.55432087C= | CA1459095771 | CLOCK,TMEM165 | c.*3328G= (n.*3328G=) c.352+7444C= c.408+7444C= c.898+7444C= (n.898+7444C=) | |
4 | g.55432087C>T | CA551380711 | CLOCK,TMEM165 | c.*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 |
4 | g.55432088A>G | CA2670685429 | CLOCK,TMEM165 | c.*3327T>C (n.*3327T>C) c.352+7445A>G c.408+7445A>G c.898+7445A>G (n.898+7445A>G) | gnomAD v4 |
4 | g.55432088A>T | CA2670685430 | CLOCK,TMEM165 | c.*3327T>A (n.*3327T>A) c.352+7445A>T c.408+7445A>T c.898+7445A>T (n.898+7445A>T) | gnomAD v4 |
4 | g.55432089G>T | CA2670685431 | CLOCK,TMEM165 | c.*3326C>A (n.*3326C>A) c.352+7446G>T c.408+7446G>T c.898+7446G>T (n.898+7446G>T) | gnomAD v4 |