| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.156868122_156868125dup | CA2580061217 | NTRK1 | c.285_288dup (p.His97SerfsTer23) c.447_450dup (p.His151SerfsTer23) c.357_360dup (p.His121SerfsTer23) n.313-5511_313-5508dup n.505_508dup | ClinVar |
| 1 | g.156868125G>A | CA421270908 | NTRK1 | c.288G>A (p.Leu96=) c.450G>A (p.Leu150=) c.360G>A (p.Leu120=) n.313-5508G>A n.508G>A | dbSNP |
| 1 | g.156868125G>C | CA421270909 | NTRK1 | c.288G>C (p.Leu96=) c.450G>C (p.Leu150=) c.360G>C (p.Leu120=) n.313-5508G>C n.508G>C | dbSNP |
| 1 | g.156868125G= | CA1200782072 | NTRK1 | c.288G= (p.Leu96=) c.450G= (p.Leu150=) c.360G= (p.Leu120=) n.313-5508G= n.508G= | |
| 1 | g.156868125G>T | CA1168987 | NTRK1 | c.288G>T (p.Leu96=) c.450G>T (p.Leu150=) c.360G>T (p.Leu120=) n.313-5508G>T n.508G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156868126C>A | CA342933609 | NTRK1 | c.289C>A (p.His97Asn) c.451C>A (p.His151Asn) c.361C>A (p.His121Asn) n.313-5507C>A n.509C>A | |
| 1 | g.156868126C= | CA1200782073 | NTRK1 | c.289C= (p.His97=) c.451C= (p.His151=) c.361C= (p.His121=) n.313-5507C= n.509C= | |
| 1 | g.156868126C>G | CA342933610 | NTRK1 | c.289C>G (p.His97Asp) c.451C>G (p.His151Asp) c.361C>G (p.His121Asp) n.313-5507C>G n.509C>G | dbSNP |
| 1 | g.156868126C>T | CA342933611 | NTRK1 | c.289C>T (p.His97Tyr) c.451C>T (p.His151Tyr) c.361C>T (p.His121Tyr) n.313-5507C>T n.509C>T | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.156868127A= | CA1200782074 | NTRK1 | c.290A= (p.His97=) c.452A= (p.His151=) c.362A= (p.His121=) n.313-5506A= n.510A= | |
| 1 | g.156868127A>C | CA342933612 | NTRK1 | c.290A>C (p.His97Pro) c.452A>C (p.His151Pro) c.362A>C (p.His121Pro) n.313-5506A>C n.510A>C | |
| 1 | g.156868127A>G | CA1168988 | NTRK1 | c.290A>G (p.His97Arg) c.452A>G (p.His151Arg) c.362A>G (p.His121Arg) n.313-5506A>G n.510A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.156868127A>T | CA342933613 | NTRK1 | c.290A>T (p.His97Leu) c.452A>T (p.His151Leu) c.362A>T (p.His121Leu) n.313-5506A>T n.510A>T | dbSNP |
| 1 | g.156868128C>A | CA342933614 | NTRK1 | c.291C>A (p.His97Gln) c.453C>A (p.His151Gln) c.363C>A (p.His121Gln) n.313-5505C>A n.511C>A | |
| 1 | g.156868128C= | CA1143605715 | NTRK1 | c.291C= (p.His97=) c.453C= (p.His151=) c.363C= (p.His121=) n.313-5505C= n.511C= | |
| 1 | g.156868128C>G | CA31108140 | NTRK1 | c.291C>G (p.His97Gln) c.453C>G (p.His151Gln) c.363C>G (p.His121Gln) n.313-5505C>G n.511C>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156868128C>T | CA1168989 | NTRK1 | c.291C>T (p.His97=) c.453C>T (p.His151=) c.363C>T (p.His121=) n.313-5505C>T n.511C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.156868129T>A | CA342933615 | NTRK1 | c.292T>A (p.Cys98Ser) c.454T>A (p.Cys152Ser) c.364T>A (p.Cys122Ser) n.313-5504T>A n.512T>A | |
| 1 | g.156868129T>C | CA342933616 | NTRK1 | c.292T>C (p.Cys98Arg) c.454T>C (p.Cys152Arg) c.364T>C (p.Cys122Arg) n.313-5504T>C n.512T>C | |
| 1 | g.156868129T>G | CA342933617 | NTRK1 | c.292T>G (p.Cys98Gly) c.454T>G (p.Cys152Gly) c.364T>G (p.Cys122Gly) n.313-5504T>G n.512T>G | |
| 1 | g.156868130G>A | CA342933618 | NTRK1 | c.293G>A (p.Cys98Tyr) c.455G>A (p.Cys152Tyr) c.365G>A (p.Cys122Tyr) n.313-5503G>A n.513G>A | dbSNP |
| 1 | g.156868130G>C | CA342933619 | NTRK1 | c.293G>C (p.Cys98Ser) c.455G>C (p.Cys152Ser) c.365G>C (p.Cys122Ser) n.313-5503G>C n.513G>C | dbSNP gnomAD v4 |
| 1 | g.156868130G>T | CA342933620 | NTRK1 | c.293G>T (p.Cys98Phe) c.455G>T (p.Cys152Phe) c.365G>T (p.Cys122Phe) n.313-5503G>T n.513G>T | |
| 1 | g.156868131T>A | CA342933621 | NTRK1 | c.294T>A (p.Cys98Ter) c.456T>A (p.Cys152Ter) c.366T>A (p.Cys122Ter) n.313-5502T>A n.514T>A | dbSNP |
| 1 | g.156868131T>C | CA421270912 | NTRK1 | c.294T>C (p.Cys98=) c.456T>C (p.Cys152=) c.366T>C (p.Cys122=) n.313-5502T>C n.514T>C | ClinVar COSMIC |
| 1 | g.156868131T>G | CA342933622 | NTRK1 | c.294T>G (p.Cys98Trp) c.456T>G (p.Cys152Trp) c.366T>G (p.Cys122Trp) n.313-5502T>G n.514T>G | dbSNP |
| 1 | g.156868132T>A | CA342933623 | NTRK1 | c.295T>A (p.Ser99Thr) c.457T>A (p.Ser153Thr) c.367T>A (p.Ser123Thr) n.313-5501T>A n.515T>A | |
| 1 | g.156868132T>C | CA342933624 | NTRK1 | c.295T>C (p.Ser99Pro) c.457T>C (p.Ser153Pro) c.367T>C (p.Ser123Pro) n.313-5501T>C n.515T>C | dbSNP |
| 1 | g.156868132T>G | CA342933625 | NTRK1 | c.295T>G (p.Ser99Ala) c.457T>G (p.Ser153Ala) c.367T>G (p.Ser123Ala) n.313-5501T>G n.515T>G | |
| 1 | g.156868133C>A | CA342933626 | NTRK1 | c.296C>A (p.Ser99Tyr) c.458C>A (p.Ser153Tyr) c.368C>A (p.Ser123Tyr) n.313-5500C>A n.516C>A | |
| 1 | g.156868133C>G | CA342933627 | NTRK1 | c.296C>G (p.Ser99Cys) c.458C>G (p.Ser153Cys) c.368C>G (p.Ser123Cys) n.313-5500C>G n.516C>G | dbSNP |
| 1 | g.156868133C>T | CA342933628 | NTRK1 | c.296C>T (p.Ser99Phe) c.458C>T (p.Ser153Phe) c.368C>T (p.Ser123Phe) n.313-5500C>T n.516C>T | dbSNP gnomAD v4 |
| 1 | g.156868134T>A | CA421270913 | NTRK1 | c.297T>A (p.Ser99=) c.459T>A (p.Ser153=) c.369T>A (p.Ser123=) n.313-5499T>A n.517T>A | |
| 1 | g.156868134T>C | CA421270915 | NTRK1 | c.297T>C (p.Ser99=) c.459T>C (p.Ser153=) c.369T>C (p.Ser123=) n.313-5499T>C n.517T>C | |
| 1 | g.156868134T>G | CA421270914 | NTRK1 | c.297T>G (p.Ser99=) c.459T>G (p.Ser153=) c.369T>G (p.Ser123=) n.313-5499T>G n.517T>G | |
| 1 | g.156868135T>A | CA342933630 | NTRK1 | c.298T>A (p.Cys100Ser) c.460T>A (p.Cys154Ser) c.370T>A (p.Cys124Ser) n.313-5498T>A n.518T>A | |
| 1 | g.156868135T>C | CA342933631 | NTRK1 | c.298T>C (p.Cys100Arg) c.460T>C (p.Cys154Arg) c.370T>C (p.Cys124Arg) n.313-5498T>C n.518T>C | dbSNP |
| 1 | g.156868135T>G | CA342933629 | NTRK1 | c.298T>G (p.Cys100Gly) c.460T>G (p.Cys154Gly) c.370T>G (p.Cys124Gly) n.313-5498T>G n.518T>G | |
| 1 | g.156868137_156868138del | CA2697462987 | NTRK1 | c.300_301del (p.Ala101ProfsTer17) c.462_463del (p.Ala155ProfsTer17) c.372_373del (p.Ala125ProfsTer17) n.313-5496_313-5495del n.520_521del | dbSNP |
| 1 | g.156868136G>A | CA342933633 | NTRK1 | c.299G>A (p.Cys100Tyr) c.461G>A (p.Cys154Tyr) c.371G>A (p.Cys124Tyr) n.313-5497G>A n.519G>A | |
| 1 | g.156868136G>C | CA342933635 | NTRK1 | c.299G>C (p.Cys100Ser) c.461G>C (p.Cys154Ser) c.371G>C (p.Cys124Ser) n.313-5497G>C n.519G>C | dbSNP |
| 1 | g.156868136G>T | CA342933637 | NTRK1 | c.299G>T (p.Cys100Phe) c.461G>T (p.Cys154Phe) c.371G>T (p.Cys124Phe) n.313-5497G>T n.519G>T | |
| 1 | g.156868136dup | CA2740090266 | NTRK1 | c.299dup (p.Cys100TrpfsTer19) c.461dup (p.Cys154TrpfsTer19) c.371dup (p.Cys124TrpfsTer19) n.313-5497dup n.519dup | ClinVar |
| 1 | g.156868137T>A | CA342933638 | NTRK1 | c.300T>A (p.Cys100Ter) c.462T>A (p.Cys154Ter) c.372T>A (p.Cys124Ter) n.313-5496T>A n.520T>A | |
| 1 | g.156868137T>C | CA421270916 | NTRK1 | c.300T>C (p.Cys100=) c.462T>C (p.Cys154=) c.372T>C (p.Cys124=) n.313-5496T>C n.520T>C | |
| 1 | g.156868137T>G | CA342933640 | NTRK1 | c.300T>G (p.Cys100Trp) c.462T>G (p.Cys154Trp) c.372T>G (p.Cys124Trp) n.313-5496T>G n.520T>G | |
| 1 | g.156868138G>A | CA342933643 | NTRK1 | c.301G>A (p.Ala101Thr) c.463G>A (p.Ala155Thr) c.373G>A (p.Ala125Thr) n.313-5495G>A n.521G>A | gnomAD v4 |
| 1 | g.156868138G>C | CA342933644 | NTRK1 | c.301G>C (p.Ala101Pro) c.463G>C (p.Ala155Pro) c.373G>C (p.Ala125Pro) n.313-5495G>C n.521G>C | dbSNP |
| 1 | g.156868138G>T | CA342933646 | NTRK1 | c.301G>T (p.Ala101Ser) c.463G>T (p.Ala155Ser) c.373G>T (p.Ala125Ser) n.313-5495G>T n.521G>T | dbSNP |
| 1 | g.156868139C>A | CA342933648 | NTRK1 | c.302C>A (p.Ala101Asp) c.464C>A (p.Ala155Asp) c.374C>A (p.Ala125Asp) n.313-5494C>A n.522C>A | dbSNP |