Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.184631845C>A | CA359106040 | CASP3 | c.403G>T (p.Asp135Tyr) n.471G>T n.3368G>T c.*152G>T (n.*152G>T) c.430G>T (p.Asp144Tyr) c.325G>T (p.Asp109Tyr) | |
4 | g.184631845C= | CA1519179785 | CASP3 | c.403G= (p.Asp135=) n.471G= n.3368G= c.*152G= (n.*152G=) c.430G= (p.Asp144=) c.325G= (p.Asp109=) | |
4 | g.184631845C>G | CA359106041 | CASP3 | c.403G>C (p.Asp135His) n.471G>C n.3368G>C c.*152G>C (n.*152G>C) c.430G>C (p.Asp144His) c.325G>C (p.Asp109His) | dbSNP |
4 | g.184631845C>T | CA359106039 | CASP3 | c.403G>A (p.Asp135Asn) n.471G>A n.3368G>A c.*152G>A (n.*152G>A) c.430G>A (p.Asp144Asn) c.325G>A (p.Asp109Asn) | dbSNP |
4 | g.184631846A>C | CA442737645 | CASP3 | c.402T>G (p.Val134=) n.470T>G n.3367T>G c.*151T>G (n.*151T>G) c.429T>G (p.Val143=) c.324T>G (p.Val108=) | COSMIC |
4 | g.184631846A>G | CA442737643 | CASP3 | c.402T>C (p.Val134=) n.470T>C n.3367T>C c.*151T>C (n.*151T>C) c.429T>C (p.Val143=) c.324T>C (p.Val108=) | |
4 | g.184631846A>T | CA442737644 | CASP3 | c.402T>A (p.Val134=) n.470T>A n.3367T>A c.*151T>A (n.*151T>A) c.429T>A (p.Val143=) c.324T>A (p.Val108=) | |
4 | g.184631847A>C | CA359106042 | CASP3 | c.401T>G (p.Val134Gly) n.469T>G n.3366T>G c.*150T>G (n.*150T>G) c.428T>G (p.Val143Gly) c.323T>G (p.Val108Gly) | |
4 | g.184631847A>G | CA359106043 | CASP3 | c.401T>C (p.Val134Ala) n.469T>C n.3366T>C c.*150T>C (n.*150T>C) c.428T>C (p.Val143Ala) c.323T>C (p.Val108Ala) | |
4 | g.184631847A>T | CA359106044 | CASP3 | c.401T>A (p.Val134Asp) n.469T>A n.3366T>A c.*150T>A (n.*150T>A) c.428T>A (p.Val143Asp) c.323T>A (p.Val108Asp) | |
4 | g.184631848C>A | CA359106045 | CASP3 | c.400G>T (p.Val134Phe) n.468G>T n.3365G>T c.*149G>T (n.*149G>T) c.427G>T (p.Val143Phe) c.322G>T (p.Val108Phe) | COSMIC |
4 | g.184631848C= | CA1519179789 | CASP3 | c.400G= (p.Val134=) n.468G= n.3365G= c.*149G= (n.*149G=) c.427G= (p.Val143=) c.322G= (p.Val108=) | |
4 | g.184631848C>G | CA359106046 | CASP3 | c.400G>C (p.Val134Leu) n.468G>C n.3365G>C c.*149G>C (n.*149G>C) c.427G>C (p.Val143Leu) c.322G>C (p.Val108Leu) | |
4 | g.184631848C>T | CA359106047 | CASP3 | c.400G>A (p.Val134Ile) n.468G>A n.3365G>A c.*149G>A (n.*149G>A) c.427G>A (p.Val143Ile) c.322G>A (p.Val108Ile) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.184631849A= | CA1519179794 | CASP3 | c.399T= (p.Pro133=) n.467T= n.3364T= c.*148T= (n.*148T=) c.426T= (p.Pro142=) c.321T= (p.Pro107=) | |
4 | g.184631849A>C | CA442737652 | CASP3 | c.399T>G (p.Pro133=) n.467T>G n.3364T>G c.*148T>G (n.*148T>G) c.426T>G (p.Pro142=) c.321T>G (p.Pro107=) | |
4 | g.184631849A>G | CA442737653 | CASP3 | c.399T>C (p.Pro133=) n.467T>C n.3364T>C c.*148T>C (n.*148T>C) c.426T>C (p.Pro142=) c.321T>C (p.Pro107=) | |
4 | g.184631849A>T | CA3154030 | CASP3 | c.399T>A (p.Pro133=) n.467T>A n.3364T>A c.*148T>A (n.*148T>A) c.426T>A (p.Pro142=) c.321T>A (p.Pro107=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.184631850G>A | CA359106048 | CASP3 | c.398C>T (p.Pro133Leu) n.466C>T n.3363C>T c.*147C>T (n.*147C>T) c.425C>T (p.Pro142Leu) c.320C>T (p.Pro107Leu) | |
4 | g.184631850G>C | CA359106049 | CASP3 | c.398C>G (p.Pro133Arg) n.466C>G n.3363C>G c.*147C>G (n.*147C>G) c.425C>G (p.Pro142Arg) c.320C>G (p.Pro107Arg) | |
4 | g.184631850G>T | CA359106050 | CASP3 | c.398C>A (p.Pro133His) n.466C>A n.3363C>A c.*147C>A (n.*147C>A) c.425C>A (p.Pro142His) c.320C>A (p.Pro107His) | |
4 | g.184631851G>A | CA112459078 | CASP3 | c.397C>T (p.Pro133Ser) n.465C>T n.3362C>T c.*146C>T (n.*146C>T) c.424C>T (p.Pro142Ser) c.319C>T (p.Pro107Ser) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.184631851G>C | CA359106051 | CASP3 | c.397C>G (p.Pro133Ala) n.465C>G n.3362C>G c.*146C>G (n.*146C>G) c.424C>G (p.Pro142Ala) c.319C>G (p.Pro107Ala) | |
4 | g.184631851G= | CA1519179799 | CASP3 | c.397C= (p.Pro133=) n.465C= n.3362C= c.*146C= (n.*146C=) c.424C= (p.Pro142=) c.319C= (p.Pro107=) | |
4 | g.184631851G>T | CA359106052 | CASP3 | c.397C>A (p.Pro133Thr) n.465C>A n.3362C>A c.*146C>A (n.*146C>A) c.424C>A (p.Pro142Thr) c.319C>A (p.Pro107Thr) | |
4 | g.184631852T>A | CA442737659 | CASP3 | c.396A>T (p.Gly132=) n.464A>T n.3361A>T c.*145A>T (n.*145A>T) c.423A>T (p.Gly141=) c.318A>T (p.Gly106=) | gnomAD v4 |
4 | g.184631852T>C | CA442737660 | CASP3 | c.396A>G (p.Gly132=) n.464A>G n.3361A>G c.*145A>G (n.*145A>G) c.423A>G (p.Gly141=) c.318A>G (p.Gly106=) | gnomAD v4 |
4 | g.184631852T>G | CA442737662 | CASP3 | c.396A>C (p.Gly132=) n.464A>C n.3361A>C c.*145A>C (n.*145A>C) c.423A>C (p.Gly141=) c.318A>C (p.Gly106=) | |
4 | g.184631853C>A | CA359106055 | CASP3 | c.395G>T (p.Gly132Val) n.463G>T n.3360G>T c.*144G>T (n.*144G>T) c.422G>T (p.Gly141Val) c.317G>T (p.Gly106Val) | |
4 | g.184631853C>G | CA359106053 | CASP3 | c.395G>C (p.Gly132Ala) n.463G>C n.3360G>C c.*144G>C (n.*144G>C) c.422G>C (p.Gly141Ala) c.317G>C (p.Gly106Ala) | |
4 | g.184631853C>T | CA359106054 | CASP3 | c.395G>A (p.Gly132Glu) n.463G>A n.3360G>A c.*144G>A (n.*144G>A) c.422G>A (p.Gly141Glu) c.317G>A (p.Gly106Glu) | |
4 | g.184631854C>A | CA359106056 | CASP3 | c.394G>T (p.Gly132Ter) n.462G>T n.3359G>T c.*143G>T (n.*143G>T) c.421G>T (p.Gly141Ter) c.316G>T (p.Gly106Ter) | |
4 | g.184631854C>G | CA359106057 | CASP3 | c.394G>C (p.Gly132Arg) n.462G>C n.3359G>C c.*143G>C (n.*143G>C) c.421G>C (p.Gly141Arg) c.316G>C (p.Gly106Arg) | |
4 | g.184631854C>T | CA359106058 | CASP3 | c.394G>A (p.Gly132Arg) n.462G>A n.3359G>A c.*143G>A (n.*143G>A) c.421G>A (p.Gly141Arg) c.316G>A (p.Gly106Arg) | |
4 | g.184631855A= | CA1519179809 | CASP3 | c.393T= (p.Asn131=) n.461T= n.3358T= c.*142T= (n.*142T=) c.420T= (p.Asn140=) c.315T= (p.Asn105=) | |
4 | g.184631855A>C | CA359106059 | CASP3 | c.393T>G (p.Asn131Lys) n.461T>G n.3358T>G c.*142T>G (n.*142T>G) c.420T>G (p.Asn140Lys) c.315T>G (p.Asn105Lys) | |
4 | g.184631855A>G | CA3154031 | CASP3 | c.393T>C (p.Asn131=) n.461T>C n.3358T>C c.*142T>C (n.*142T>C) c.420T>C (p.Asn140=) c.315T>C (p.Asn105=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.184631855A>T | CA359106060 | CASP3 | c.393T>A (p.Asn131Lys) n.461T>A n.3358T>A c.*142T>A (n.*142T>A) c.420T>A (p.Asn140Lys) c.315T>A (p.Asn105Lys) | |
4 | g.184631856T>A | CA359106061 | CASP3 | c.392A>T (p.Asn131Ile) n.460A>T n.3357A>T c.*141A>T (n.*141A>T) c.419A>T (p.Asn140Ile) c.314A>T (p.Asn105Ile) | |
4 | g.184631856T>C | CA359106062 | CASP3 | c.392A>G (p.Asn131Ser) n.460A>G n.3357A>G c.*141A>G (n.*141A>G) c.419A>G (p.Asn140Ser) c.314A>G (p.Asn105Ser) | |
4 | g.184631856T>G | CA359106063 | CASP3 | c.392A>C (p.Asn131Thr) n.460A>C n.3357A>C c.*141A>C (n.*141A>C) c.419A>C (p.Asn140Thr) c.314A>C (p.Asn105Thr) | |
4 | g.184631857T>A | CA359106064 | CASP3 | c.391A>T (p.Asn131Tyr) n.459A>T n.3356A>T c.*140A>T (n.*140A>T) c.418A>T (p.Asn140Tyr) c.313A>T (p.Asn105Tyr) | |
4 | g.184631857T>C | CA359106065 | CASP3 | c.391A>G (p.Asn131Asp) n.459A>G n.3356A>G c.*140A>G (n.*140A>G) c.418A>G (p.Asn140Asp) c.313A>G (p.Asn105Asp) | |
4 | g.184631857T>G | CA359106066 | CASP3 | c.391A>C (p.Asn131His) n.459A>C n.3356A>C c.*140A>C (n.*140A>C) c.418A>C (p.Asn140His) c.313A>C (p.Asn105His) | |
4 | g.184631858T>A | CA442737673 | CASP3 | c.390A>T (p.Thr130=) n.458A>T n.3355A>T c.*139A>T (n.*139A>T) c.417A>T (p.Thr139=) c.312A>T (p.Thr104=) | |
4 | g.184631858T>C | CA442737674 | CASP3 | c.390A>G (p.Thr130=) n.458A>G n.3355A>G c.*139A>G (n.*139A>G) c.417A>G (p.Thr139=) c.312A>G (p.Thr104=) | |
4 | g.184631858T>G | CA442737676 | CASP3 | c.390A>C (p.Thr130=) n.458A>C n.3355A>C c.*139A>C (n.*139A>C) c.417A>C (p.Thr139=) c.312A>C (p.Thr104=) | |
4 | g.184631859G>A | CA359106067 | CASP3 | c.389C>T (p.Thr130Ile) n.457C>T n.3354C>T c.*138C>T (n.*138C>T) c.416C>T (p.Thr139Ile) c.311C>T (p.Thr104Ile) | |
4 | g.184631859G>C | CA359106069 | CASP3 | c.389C>G (p.Thr130Arg) n.457C>G n.3354C>G c.*138C>G (n.*138C>G) c.416C>G (p.Thr139Arg) c.311C>G (p.Thr104Arg) | |
4 | g.184631859G>T | CA359106068 | CASP3 | c.389C>A (p.Thr130Lys) n.457C>A n.3354C>A c.*138C>A (n.*138C>A) c.416C>A (p.Thr139Lys) c.311C>A (p.Thr104Lys) |