Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.115286603C>A | CA341837060 | NGF,NGF-AS1 | c.193G>T (p.Gly65Trp) c.-279G>T (n.-279G>T) c.358G>T (p.Gly120Trp) n.207+3363C>A | |
1 | g.115286603C= | CA1190533518 | NGF,NGF-AS1 | c.193G= (p.Gly65=) c.-279G= (n.-279G=) c.358G= (p.Gly120=) n.207+3363C= | |
1 | g.115286603C>G | CA341837061 | NGF,NGF-AS1 | c.193G>C (p.Gly65Arg) c.-279G>C (n.-279G>C) c.358G>C (p.Gly120Arg) n.207+3363C>G | COSMIC |
1 | g.115286603C>T | CA1023032 | NGF,NGF-AS1 | c.193G>A (p.Gly65Arg) c.-279G>A (n.-279G>A) c.358G>A (p.Gly120Arg) n.207+3363C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.115286604C>A | CA420185385 | NGF,NGF-AS1 | c.192G>T (p.Ala64=) c.-280G>T (n.-280G>T) c.357G>T (p.Ala119=) n.207+3364C>A | |
1 | g.115286604C= | CA1190533519 | NGF,NGF-AS1 | c.192G= (p.Ala64=) c.-280G= (n.-280G=) c.357G= (p.Ala119=) n.207+3364C= | |
1 | g.115286604C>G | CA420185387 | NGF,NGF-AS1 | c.192G>C (p.Ala64=) c.-280G>C (n.-280G>C) c.357G>C (p.Ala119=) n.207+3364C>G | |
1 | g.115286604C>T | CA1023033 | NGF,NGF-AS1 | c.192G>A (p.Ala64=) c.-280G>A (n.-280G>A) c.357G>A (p.Ala119=) n.207+3364C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.115286605G>A | CA1023034 | NGF,NGF-AS1 | c.191C>T (p.Ala64Val) c.-281C>T (n.-281C>T) c.356C>T (p.Ala119Val) n.207+3365G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.115286605G>C | CA341837062 | NGF,NGF-AS1 | c.191C>G (p.Ala64Gly) c.-281C>G (n.-281C>G) c.356C>G (p.Ala119Gly) n.207+3365G>C | gnomAD v4 |
1 | g.115286605G= | CA1143459560 | NGF,NGF-AS1 | c.191C= (p.Ala64=) c.-281C= (n.-281C=) c.356C= (p.Ala119=) n.207+3365G= | |
1 | g.115286605G>T | CA1023035 | NGF,NGF-AS1 | c.191C>A (p.Ala64Glu) c.-281C>A (n.-281C>A) c.356C>A (p.Ala119Glu) n.207+3365G>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.115286606C>A | CA341837065 | NGF,NGF-AS1 | c.190G>T (p.Ala64Ser) c.-282G>T (n.-282G>T) c.355G>T (p.Ala119Ser) n.207+3366C>A | |
1 | g.115286606C>G | CA341837063 | NGF,NGF-AS1 | c.190G>C (p.Ala64Pro) c.-282G>C (n.-282G>C) c.355G>C (p.Ala119Pro) n.207+3366C>G | |
1 | g.115286606C>T | CA341837064 | NGF,NGF-AS1 | c.190G>A (p.Ala64Thr) c.-282G>A (n.-282G>A) c.355G>A (p.Ala119Thr) n.207+3366C>T | |
1 | g.115286607C>A | CA420185393 | NGF,NGF-AS1 | c.189G>T (p.Val63=) c.-283G>T (n.-283G>T) c.354G>T (p.Val118=) n.207+3367C>A | COSMIC |
1 | g.115286607C= | CA1190533520 | NGF,NGF-AS1 | c.189G= (p.Val63=) c.-283G= (n.-283G=) c.354G= (p.Val118=) n.207+3367C= | |
1 | g.115286607C>G | CA420185392 | NGF,NGF-AS1 | c.189G>C (p.Val63=) c.-283G>C (n.-283G>C) c.354G>C (p.Val118=) n.207+3367C>G | |
1 | g.115286607C>T | CA1023036 | NGF,NGF-AS1 | c.189G>A (p.Val63=) c.-283G>A (n.-283G>A) c.354G>A (p.Val118=) n.207+3367C>T | dbSNP ExAC gnomAD v2 COSMIC |
1 | g.115286608A= | CA1190533521 | NGF,NGF-AS1 | c.188T= (p.Val63=) c.-284T= (n.-284T=) c.353T= (p.Val118=) n.207+3368A= | |
1 | g.115286608A>C | CA341837066 | NGF,NGF-AS1 | c.188T>G (p.Val63Gly) c.-284T>G (n.-284T>G) c.353T>G (p.Val118Gly) n.207+3368A>C | |
1 | g.115286608A>G | CA1023037 | NGF,NGF-AS1 | c.188T>C (p.Val63Ala) c.-284T>C (n.-284T>C) c.353T>C (p.Val118Ala) n.207+3368A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.115286608A>T | CA341837067 | NGF,NGF-AS1 | c.188T>A (p.Val63Glu) c.-284T>A (n.-284T>A) c.353T>A (p.Val118Glu) n.207+3368A>T | |
1 | g.115286609C>A | CA341837068 | NGF,NGF-AS1 | c.187G>T (p.Val63Leu) c.-285G>T (n.-285G>T) c.352G>T (p.Val118Leu) n.207+3369C>A | |
1 | g.115286609C= | CA1190533522 | NGF,NGF-AS1 | c.187G= (p.Val63=) c.-285G= (n.-285G=) c.352G= (p.Val118=) n.207+3369C= | |
1 | g.115286609C>G | CA1023039 | NGF,NGF-AS1 | c.187G>C (p.Val63Leu) c.-285G>C (n.-285G>C) c.352G>C (p.Val118Leu) n.207+3369C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.115286609C>T | CA1023038 | NGF,NGF-AS1 | c.187G>A (p.Val63Met) c.-285G>A (n.-285G>A) c.352G>A (p.Val118Met) n.207+3369C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.115286609_115286610insCCTG | CA2551056711 | NGF,NGF-AS1 | c.186_187insCAGG (p.Val63GlnfsTer17) c.-286_-285insCAGG (n.-286_-285insCAGG) c.351_352insCAGG (p.Val118GlnfsTer17) n.207+3369_207+3370insCCTG | |
1 | g.115286610G>A | CA1023040 | NGF,NGF-AS1 | c.186C>T (p.Arg62=) c.-286C>T (n.-286C>T) c.351C>T (p.Arg117=) n.207+3370G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
1 | g.115286610G>C | CA420185401 | NGF,NGF-AS1 | c.186C>G (p.Arg62=) c.-286C>G (n.-286C>G) c.351C>G (p.Arg117=) n.207+3370G>C | |
1 | g.115286610G= | CA1190533523 | NGF,NGF-AS1 | c.186C= (p.Arg62=) c.-286C= (n.-286C=) c.351C= (p.Arg117=) n.207+3370G= | |
1 | g.115286610G>T | CA420185400 | NGF,NGF-AS1 | c.186C>A (p.Arg62=) c.-286C>A (n.-286C>A) c.351C>A (p.Arg117=) n.207+3370G>T | |
1 | g.115286611C>A | CA341837069 | NGF,NGF-AS1 | c.185G>T (p.Arg62Leu) c.-287G>T (n.-287G>T) c.350G>T (p.Arg117Leu) n.207+3371C>A | |
1 | g.115286611C= | CA1143651790 | NGF,NGF-AS1 | c.185G= (p.Arg62=) c.-287G= (n.-287G=) c.350G= (p.Arg117=) n.207+3371C= | |
1 | g.115286611C>G | CA341837070 | NGF,NGF-AS1 | c.185G>C (p.Arg62Pro) c.-287G>C (n.-287G>C) c.350G>C (p.Arg117Pro) n.207+3371C>G | gnomAD v4 |
1 | g.115286611C>T | CA1023041 | NGF,NGF-AS1 | c.185G>A (p.Arg62His) c.-287G>A (n.-287G>A) c.350G>A (p.Arg117His) n.207+3371C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.115286612G>A | CA1023042 | NGF,NGF-AS1 | c.184C>T (p.Arg62Cys) c.-288C>T (n.-288C>T) c.349C>T (p.Arg117Cys) n.207+3372G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.115286612G>C | CA341837071 | NGF,NGF-AS1 | c.184C>G (p.Arg62Gly) c.-288C>G (n.-288C>G) c.349C>G (p.Arg117Gly) n.207+3372G>C | gnomAD v4 |
1 | g.115286612G= | CA1190533524 | NGF,NGF-AS1 | c.184C= (p.Arg62=) c.-288C= (n.-288C=) c.349C= (p.Arg117=) n.207+3372G= | |
1 | g.115286612G>T | CA341837072 | NGF,NGF-AS1 | c.184C>A (p.Arg62Ser) c.-288C>A (n.-288C>A) c.349C>A (p.Arg117Ser) n.207+3372G>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.115286613T>A | CA420185404 | NGF,NGF-AS1 | c.183A>T (p.Ala61=) c.-289A>T (n.-289A>T) c.348A>T (p.Ala116=) n.207+3373T>A | |
1 | g.115286613T>C | CA420185406 | NGF,NGF-AS1 | c.183A>G (p.Ala61=) c.-289A>G (n.-289A>G) c.348A>G (p.Ala116=) n.207+3373T>C | |
1 | g.115286613T>G | CA420185405 | NGF,NGF-AS1 | c.183A>C (p.Ala61=) c.-289A>C (n.-289A>C) c.348A>C (p.Ala116=) n.207+3373T>G | |
1 | g.115286613_115286616del | CA2513612349 | NGF,NGF-AS1 | c.180_183del (p.Arg62TrpfsTer?) c.-292_-289del (n.-292_-289del) c.345_348del (p.Arg117TrpfsTer?) n.207+3373_207+3376del | |
1 | g.115286614G>A | CA341837073 | NGF,NGF-AS1 | c.182C>T (p.Ala61Val) c.-290C>T (n.-290C>T) c.347C>T (p.Ala116Val) n.207+3374G>A | dbSNP |
1 | g.115286614G>C | CA341837074 | NGF,NGF-AS1 | c.182C>G (p.Ala61Gly) c.-290C>G (n.-290C>G) c.347C>G (p.Ala116Gly) n.207+3374G>C | |
1 | g.115286614G= | CA1190533525 | NGF,NGF-AS1 | c.182C= (p.Ala61=) c.-290C= (n.-290C=) c.347C= (p.Ala116=) n.207+3374G= | |
1 | g.115286614G>T | CA341837075 | NGF,NGF-AS1 | c.182C>A (p.Ala61Glu) c.-290C>A (n.-290C>A) c.347C>A (p.Ala116Glu) n.207+3374G>T | gnomAD v4 |
1 | g.115286615C>A | CA341837076 | NGF,NGF-AS1 | c.181G>T (p.Ala61Ser) c.-291G>T (n.-291G>T) c.346G>T (p.Ala116Ser) n.207+3375C>A | |
1 | g.115286615C>G | CA341837077 | NGF,NGF-AS1 | c.181G>C (p.Ala61Pro) c.-291G>C (n.-291G>C) c.346G>C (p.Ala116Pro) n.207+3375C>G |