| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.115286592G>A | CA420185368 | NGF,NGF-AS1 | c.204C>T (p.Arg68=) c.-268C>T (n.-268C>T) c.369C>T (p.Arg123=) n.207+3352G>A | |
| 1 | g.115286592G>C | CA420185370 | NGF,NGF-AS1 | c.204C>G (p.Arg68=) c.-268C>G (n.-268C>G) c.369C>G (p.Arg123=) n.207+3352G>C | |
| 1 | g.115286592G>T | CA420185369 | NGF,NGF-AS1 | c.204C>A (p.Arg68=) c.-268C>A (n.-268C>A) c.369C>A (p.Arg123=) n.207+3352G>T | |
| 1 | g.115286593C>A | CA341837041 | NGF,NGF-AS1 | c.203G>T (p.Arg68Leu) c.-269G>T (n.-269G>T) c.368G>T (p.Arg123Leu) n.207+3353C>A | |
| 1 | g.115286593C= | CA1144180365 | NGF,NGF-AS1 | c.203G= (p.Arg68=) c.-269G= (n.-269G=) c.368G= (p.Arg123=) n.207+3353C= | |
| 1 | g.115286593C>G | CA341837042 | NGF,NGF-AS1 | c.203G>C (p.Arg68Pro) c.-269G>C (n.-269G>C) c.368G>C (p.Arg123Pro) n.207+3353C>G | |
| 1 | g.115286593C>T | CA1023027 | NGF,NGF-AS1 | c.203G>A (p.Arg68His) c.-269G>A (n.-269G>A) c.368G>A (p.Arg123His) n.207+3353C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.115286594G>A | CA1023028 | NGF,NGF-AS1 | c.202C>T (p.Arg68Cys) c.-270C>T (n.-270C>T) c.367C>T (p.Arg123Cys) n.207+3354G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 1 | g.115286594G>C | CA1023029 | NGF,NGF-AS1 | c.202C>G (p.Arg68Gly) c.-270C>G (n.-270C>G) c.367C>G (p.Arg123Gly) n.207+3354G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.115286594G= | CA1147649128 | NGF,NGF-AS1 | c.202C= (p.Arg68=) c.-270C= (n.-270C=) c.367C= (p.Arg123=) n.207+3354G= | |
| 1 | g.115286594G>T | CA341837043 | NGF,NGF-AS1 | c.202C>A (p.Arg68Ser) c.-270C>A (n.-270C>A) c.367C>A (p.Arg123Ser) n.207+3354G>T | |
| 1 | g.115286595G>A | CA420185374 | NGF,NGF-AS1 | c.201C>T (p.Thr67=) c.-271C>T (n.-271C>T) c.366C>T (p.Thr122=) n.207+3355G>A | |
| 1 | g.115286595G>C | CA1023030 | NGF,NGF-AS1 | c.201C>G (p.Thr67=) c.-271C>G (n.-271C>G) c.366C>G (p.Thr122=) n.207+3355G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.115286595G= | CA1190533514 | NGF,NGF-AS1 | c.201C= (p.Thr67=) c.-271C= (n.-271C=) c.366C= (p.Thr122=) n.207+3355G= | |
| 1 | g.115286595G>T | CA420185375 | NGF,NGF-AS1 | c.201C>A (p.Thr67=) c.-271C>A (n.-271C>A) c.366C>A (p.Thr122=) n.207+3355G>T | ClinVar dbSNP gnomAD v4 |
| 1 | g.115286596G>A | CA341837044 | NGF,NGF-AS1 | c.200C>T (p.Thr67Ile) c.-272C>T (n.-272C>T) c.365C>T (p.Thr122Ile) n.207+3356G>A | |
| 1 | g.115286596G>C | CA341837045 | NGF,NGF-AS1 | c.200C>G (p.Thr67Ser) c.-272C>G (n.-272C>G) c.365C>G (p.Thr122Ser) n.207+3356G>C | |
| 1 | g.115286596G>T | CA341837046 | NGF,NGF-AS1 | c.200C>A (p.Thr67Asn) c.-272C>A (n.-272C>A) c.365C>A (p.Thr122Asn) n.207+3356G>T | |
| 1 | g.115286597T>A | CA341837047 | NGF,NGF-AS1 | c.199A>T (p.Thr67Ser) c.-273A>T (n.-273A>T) c.364A>T (p.Thr122Ser) n.207+3357T>A | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.115286597T>C | CA341837048 | NGF,NGF-AS1 | c.199A>G (p.Thr67Ala) c.-273A>G (n.-273A>G) c.364A>G (p.Thr122Ala) n.207+3357T>C | |
| 1 | g.115286597T>G | CA341837049 | NGF,NGF-AS1 | c.199A>C (p.Thr67Pro) c.-273A>C (n.-273A>C) c.364A>C (p.Thr122Pro) n.207+3357T>G | |
| 1 | g.115286597T= | CA1190533515 | NGF,NGF-AS1 | c.199A= (p.Thr67=) c.-273A= (n.-273A=) c.364A= (p.Thr122=) n.207+3357T= | |
| 1 | g.115286598C>A | CA341837050 | NGF,NGF-AS1 | c.198G>T (p.Gln66His) c.-274G>T (n.-274G>T) c.363G>T (p.Gln121His) n.207+3358C>A | |
| 1 | g.115286598C>G | CA341837051 | NGF,NGF-AS1 | c.198G>C (p.Gln66His) c.-274G>C (n.-274G>C) c.363G>C (p.Gln121His) n.207+3358C>G | gnomAD v4 |
| 1 | g.115286598C>T | CA420185377 | NGF,NGF-AS1 | c.198G>A (p.Gln66=) c.-274G>A (n.-274G>A) c.363G>A (p.Gln121=) n.207+3358C>T | |
| 1 | g.115286599T>A | CA341837052 | NGF,NGF-AS1 | c.197A>T (p.Gln66Leu) c.-275A>T (n.-275A>T) c.362A>T (p.Gln121Leu) n.207+3359T>A | |
| 1 | g.115286599T>C | CA341837054 | NGF,NGF-AS1 | c.197A>G (p.Gln66Arg) c.-275A>G (n.-275A>G) c.362A>G (p.Gln121Arg) n.207+3359T>C | gnomAD v4 |
| 1 | g.115286599T>G | CA341837053 | NGF,NGF-AS1 | c.197A>C (p.Gln66Pro) c.-275A>C (n.-275A>C) c.362A>C (p.Gln121Pro) n.207+3359T>G | |
| 1 | g.115286600G>A | CA341837055 | NGF,NGF-AS1 | c.196C>T (p.Gln66Ter) c.-276C>T (n.-276C>T) c.361C>T (p.Gln121Ter) n.207+3360G>A | |
| 1 | g.115286600G>C | CA341837056 | NGF,NGF-AS1 | c.196C>G (p.Gln66Glu) c.-276C>G (n.-276C>G) c.361C>G (p.Gln121Glu) n.207+3360G>C | |
| 1 | g.115286600G= | CA1190533516 | NGF,NGF-AS1 | c.196C= (p.Gln66=) c.-276C= (n.-276C=) c.361C= (p.Gln121=) n.207+3360G= | |
| 1 | g.115286600G>T | CA1023031 | NGF,NGF-AS1 | c.196C>A (p.Gln66Lys) c.-276C>A (n.-276C>A) c.361C>A (p.Gln121Lys) n.207+3360G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.115286601C>A | CA420185381 | NGF,NGF-AS1 | c.195G>T (p.Gly65=) c.-277G>T (n.-277G>T) c.360G>T (p.Gly120=) n.207+3361C>A | |
| 1 | g.115286601C= | CA1190533517 | NGF,NGF-AS1 | c.195G= (p.Gly65=) c.-277G= (n.-277G=) c.360G= (p.Gly120=) n.207+3361C= | |
| 1 | g.115286601C>G | CA420185383 | NGF,NGF-AS1 | c.195G>C (p.Gly65=) c.-277G>C (n.-277G>C) c.360G>C (p.Gly120=) n.207+3361C>G | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.115286601C>T | CA420185384 | NGF,NGF-AS1 | c.195G>A (p.Gly65=) c.-277G>A (n.-277G>A) c.360G>A (p.Gly120=) n.207+3361C>T | gnomAD v4 |
| 1 | g.115286602C>A | CA341837057 | NGF,NGF-AS1 | c.194G>T (p.Gly65Val) c.-278G>T (n.-278G>T) c.359G>T (p.Gly120Val) n.207+3362C>A | |
| 1 | g.115286602C>G | CA341837058 | NGF,NGF-AS1 | c.194G>C (p.Gly65Ala) c.-278G>C (n.-278G>C) c.359G>C (p.Gly120Ala) n.207+3362C>G | |
| 1 | g.115286602C>T | CA341837059 | NGF,NGF-AS1 | c.194G>A (p.Gly65Glu) c.-278G>A (n.-278G>A) c.359G>A (p.Gly120Glu) n.207+3362C>T | |
| 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= |