Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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 |
1 | g.156868139C>G | CA342933650 | NTRK1 | c.302C>G (p.Ala101Gly) c.464C>G (p.Ala155Gly) c.374C>G (p.Ala125Gly) n.313-5494C>G n.522C>G | dbSNP |
1 | g.156868139C>T | CA342933651 | NTRK1 | c.302C>T (p.Ala101Val) c.464C>T (p.Ala155Val) c.374C>T (p.Ala125Val) n.313-5494C>T n.522C>T | dbSNP gnomAD v4 |
1 | g.156868140C>A | CA421270917 | NTRK1 | c.303C>A (p.Ala101=) c.465C>A (p.Ala155=) c.375C>A (p.Ala125=) n.313-5493C>A n.523C>A | |
1 | g.156868140C>G | CA421270918 | NTRK1 | c.303C>G (p.Ala101=) c.465C>G (p.Ala155=) c.375C>G (p.Ala125=) n.313-5493C>G n.523C>G | |
1 | g.156868140C>T | CA421270919 | NTRK1 | c.303C>T (p.Ala101=) c.465C>T (p.Ala155=) c.375C>T (p.Ala125=) n.313-5493C>T n.523C>T | dbSNP |
1 | g.156868141C>A | CA342933652 | NTRK1 | c.304C>A (p.Leu102Met) c.466C>A (p.Leu156Met) c.376C>A (p.Leu126Met) n.313-5492C>A n.524C>A | dbSNP |
1 | g.156868141C>G | CA342933654 | NTRK1 | c.304C>G (p.Leu102Val) c.466C>G (p.Leu156Val) c.376C>G (p.Leu126Val) n.313-5492C>G n.524C>G | dbSNP |
1 | g.156868141C>T | CA421270923 | NTRK1 | c.304C>T (p.Leu102=) c.466C>T (p.Leu156=) c.376C>T (p.Leu126=) n.313-5492C>T n.524C>T | dbSNP gnomAD v4 |
1 | g.156868142T>A | CA342933660 | NTRK1 | c.305T>A (p.Leu102Gln) c.467T>A (p.Leu156Gln) c.377T>A (p.Leu126Gln) n.313-5491T>A n.525T>A | dbSNP |
1 | g.156868142T>C | CA342933657 | NTRK1 | c.305T>C (p.Leu102Pro) c.467T>C (p.Leu156Pro) c.377T>C (p.Leu126Pro) n.313-5491T>C n.525T>C | |
1 | g.156868142T>G | CA342933658 | NTRK1 | c.305T>G (p.Leu102Arg) c.467T>G (p.Leu156Arg) c.377T>G (p.Leu126Arg) n.313-5491T>G n.525T>G | |
1 | g.156868142T= | CA1200782075 | NTRK1 | c.305T= (p.Leu102=) c.467T= (p.Leu156=) c.377T= (p.Leu126=) n.313-5491T= n.525T= | |
1 | g.156868143G>A | CA421270926 | NTRK1 | c.306G>A (p.Leu102=) c.468G>A (p.Leu156=) c.378G>A (p.Leu126=) n.313-5490G>A n.526G>A | |
1 | g.156868143G>C | CA31108153 | NTRK1 | c.306G>C (p.Leu102=) c.468G>C (p.Leu156=) c.378G>C (p.Leu126=) n.313-5490G>C n.526G>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
1 | g.156868143G= | CA1200782076 | NTRK1 | c.306G= (p.Leu102=) c.468G= (p.Leu156=) c.378G= (p.Leu126=) n.313-5490G= n.526G= | |
1 | g.156868143G>T | CA421270927 | NTRK1 | c.306G>T (p.Leu102=) c.468G>T (p.Leu156=) c.378G>T (p.Leu126=) n.313-5490G>T n.526G>T | |
1 | g.156868144C>A | CA342933662 | NTRK1 | c.307C>A (p.Arg103Ser) c.469C>A (p.Arg157Ser) c.379C>A (p.Arg127Ser) n.313-5489C>A n.527C>A | dbSNP gnomAD v3 gnomAD v4 |
1 | g.156868144C= | CA1141817583 | NTRK1 | c.307C= (p.Arg103=) c.469C= (p.Arg157=) c.379C= (p.Arg127=) n.313-5489C= n.527C= | |
1 | g.156868144C>G | CA342933664 | NTRK1 | c.307C>G (p.Arg103Gly) c.469C>G (p.Arg157Gly) c.379C>G (p.Arg127Gly) n.313-5489C>G n.527C>G | dbSNP gnomAD v4 |
1 | g.156868144C>T | CA1168990 | NTRK1 | c.307C>T (p.Arg103Cys) c.469C>T (p.Arg157Cys) c.379C>T (p.Arg127Cys) n.313-5489C>T n.527C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.156868145G>A | CA1168991 | NTRK1 | c.308G>A (p.Arg103His) c.470G>A (p.Arg157His) c.380G>A (p.Arg127His) n.313-5488G>A n.528G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.156868145G>C | CA342933668 | NTRK1 | c.308G>C (p.Arg103Pro) c.470G>C (p.Arg157Pro) c.380G>C (p.Arg127Pro) n.313-5488G>C n.528G>C | dbSNP |
1 | g.156868145G= | CA1141779603 | NTRK1 | c.308G= (p.Arg103=) c.470G= (p.Arg157=) c.380G= (p.Arg127=) n.313-5488G= n.528G= | |
1 | g.156868145G>T | CA1168992 | NTRK1 | c.308G>T (p.Arg103Leu) c.470G>T (p.Arg157Leu) c.380G>T (p.Arg127Leu) n.313-5488G>T n.528G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.156868146C>A | CA421270931 | NTRK1 | c.309C>A (p.Arg103=) c.471C>A (p.Arg157=) c.381C>A (p.Arg127=) n.313-5487C>A n.529C>A | |
1 | g.156868146C= | CA1200782077 | NTRK1 | c.309C= (p.Arg103=) c.471C= (p.Arg157=) c.381C= (p.Arg127=) n.313-5487C= n.529C= | |
1 | g.156868146C>G | CA421270932 | NTRK1 | c.309C>G (p.Arg103=) c.471C>G (p.Arg157=) c.381C>G (p.Arg127=) n.313-5487C>G n.529C>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.156868146C>T | CA421270933 | NTRK1 | c.309C>T (p.Arg103=) c.471C>T (p.Arg157=) c.381C>T (p.Arg127=) n.313-5487C>T n.529C>T | COSMIC COSMIC |
1 | g.156868147T>A | CA342933671 | NTRK1 | c.310T>A (p.Trp104Arg) c.472T>A (p.Trp158Arg) c.382T>A (p.Trp128Arg) n.313-5486T>A n.530T>A | |
1 | g.156868147T>C | CA342933672 | NTRK1 | c.310T>C (p.Trp104Arg) c.472T>C (p.Trp158Arg) c.382T>C (p.Trp128Arg) n.313-5486T>C n.530T>C | ClinVar gnomAD v4 |
1 | g.156868147T>G | CA342933674 | NTRK1 | c.310T>G (p.Trp104Gly) c.472T>G (p.Trp158Gly) c.382T>G (p.Trp128Gly) n.313-5486T>G n.530T>G | |
1 | g.156868148G>A | CA342933676 | NTRK1 | c.311G>A (p.Trp104Ter) c.473G>A (p.Trp158Ter) c.383G>A (p.Trp128Ter) n.313-5485G>A n.531G>A | dbSNP |
1 | g.156868148G>C | CA342933678 | NTRK1 | c.311G>C (p.Trp104Ser) c.473G>C (p.Trp158Ser) c.383G>C (p.Trp128Ser) n.313-5485G>C n.531G>C | dbSNP |
1 | g.156868148G>T | CA342933679 | NTRK1 | c.311G>T (p.Trp104Leu) c.473G>T (p.Trp158Leu) c.383G>T (p.Trp128Leu) n.313-5485G>T n.531G>T | dbSNP |
1 | g.156868149del | CA2586964208 | NTRK1 | c.312del (p.Trp104CysfsTer?) c.474del (p.Trp158CysfsTer?) c.384del (p.Trp128CysfsTer?) n.313-5484del n.532del | ClinVar |
1 | g.156868149G>A | CA342933682 | NTRK1 | c.312G>A (p.Trp104Ter) c.474G>A (p.Trp158Ter) c.384G>A (p.Trp128Ter) n.313-5484G>A n.532G>A | dbSNP gnomAD v4 |
1 | g.156868149G>C | CA342933686 | NTRK1 | c.312G>C (p.Trp104Cys) c.474G>C (p.Trp158Cys) c.384G>C (p.Trp128Cys) n.313-5484G>C n.532G>C | dbSNP gnomAD v4 |
1 | g.156868149G>T | CA342933684 | NTRK1 | c.312G>T (p.Trp104Cys) c.474G>T (p.Trp158Cys) c.384G>T (p.Trp128Cys) n.313-5484G>T n.532G>T | dbSNP gnomAD v4 |
1 | g.156868150C>A | CA342933688 | NTRK1 | c.313C>A (p.Leu105Ile) c.475C>A (p.Leu159Ile) c.385C>A (p.Leu129Ile) n.313-5483C>A n.533C>A | |
1 | g.156868150C= | CA1200782078 | NTRK1 | c.313C= (p.Leu105=) c.475C= (p.Leu159=) c.385C= (p.Leu129=) n.313-5483C= n.533C= | |
1 | g.156868150C>G | CA342933690 | NTRK1 | c.313C>G (p.Leu105Val) c.475C>G (p.Leu159Val) c.385C>G (p.Leu129Val) n.313-5483C>G n.533C>G | dbSNP |
1 | g.156868150C>T | CA421270937 | NTRK1 | c.313C>T (p.Leu105=) c.475C>T (p.Leu159=) c.385C>T (p.Leu129=) n.313-5483C>T n.533C>T | ClinVar dbSNP |
1 | g.156868151T>A | CA342933692 | NTRK1 | c.314T>A (p.Leu105Gln) c.476T>A (p.Leu159Gln) c.386T>A (p.Leu129Gln) n.313-5482T>A n.534T>A | dbSNP |
1 | g.156868151T>C | CA342933693 | NTRK1 | c.314T>C (p.Leu105Pro) c.476T>C (p.Leu159Pro) c.386T>C (p.Leu129Pro) n.313-5482T>C n.534T>C | dbSNP |
1 | g.156868151T>G | CA342933695 | NTRK1 | c.314T>G (p.Leu105Arg) c.476T>G (p.Leu159Arg) c.386T>G (p.Leu129Arg) n.313-5482T>G n.534T>G | |
1 | g.156868151_156868152dup | CA526673358 | NTRK1 | c.314_315dup (p.Gln106TyrfsTer?) c.476_477dup (p.Gln160TyrfsTer?) c.386_387dup (p.Gln130TyrfsTer?) n.313-5482_313-5481dup n.534_535dup | dbSNP gnomAD v2 |
1 | g.156868152A= | CA1200782079 | NTRK1 | c.315A= (p.Leu105=) c.477A= (p.Leu159=) c.387A= (p.Leu129=) n.313-5481A= n.535A= | |
1 | g.156868152A>C | CA421270945 | NTRK1 | c.315A>C (p.Leu105=) c.477A>C (p.Leu159=) c.387A>C (p.Leu129=) n.313-5481A>C n.535A>C | dbSNP gnomAD v3 gnomAD v4 |
1 | g.156868152A>G | CA421270946 | NTRK1 | c.315A>G (p.Leu105=) c.477A>G (p.Leu159=) c.387A>G (p.Leu129=) n.313-5481A>G n.535A>G | ClinVar dbSNP |
1 | g.156868152A>T | CA421270948 | NTRK1 | c.315A>T (p.Leu105=) c.477A>T (p.Leu159=) c.387A>T (p.Leu129=) n.313-5481A>T n.535A>T | dbSNP |
1 | g.156868153C>A | CA342933698 | NTRK1 | c.316C>A (p.Gln106Lys) c.478C>A (p.Gln160Lys) c.388C>A (p.Gln130Lys) n.313-5480C>A n.536C>A | |
1 | g.156868153C= | CA1200782080 | NTRK1 | c.316C= (p.Gln106=) c.478C= (p.Gln160=) c.388C= (p.Gln130=) n.313-5480C= n.536C= | |
1 | g.156868153C>G | CA342933699 | NTRK1 | c.316C>G (p.Gln106Glu) c.478C>G (p.Gln160Glu) c.388C>G (p.Gln130Glu) n.313-5480C>G n.536C>G | dbSNP |
1 | g.156868153C>T | CA342933702 | NTRK1 | c.316C>T (p.Gln106Ter) c.478C>T (p.Gln160Ter) c.388C>T (p.Gln130Ter) n.313-5480C>T n.536C>T | ClinVar dbSNP |
1 | g.156868154A>C | CA342933703 | NTRK1 | c.317A>C (p.Gln106Pro) c.479A>C (p.Gln160Pro) c.389A>C (p.Gln130Pro) n.313-5479A>C n.537A>C | gnomAD v4 |
1 | g.156868154A>G | CA342933705 | NTRK1 | c.317A>G (p.Gln106Arg) c.479A>G (p.Gln160Arg) c.389A>G (p.Gln130Arg) n.313-5479A>G n.537A>G | dbSNP |
1 | g.156868154A>T | CA342933707 | NTRK1 | c.317A>T (p.Gln106Leu) c.479A>T (p.Gln160Leu) c.389A>T (p.Gln130Leu) n.313-5479A>T n.537A>T | dbSNP |
1 | g.156868155G>A | CA421270949 | NTRK1 | c.318G>A (p.Gln106=) c.480G>A (p.Gln160=) c.390G>A (p.Gln130=) n.313-5478G>A n.538G>A | ClinVar dbSNP gnomAD v4 |
1 | g.156868155G>C | CA342933709 | NTRK1 | c.318G>C (p.Gln106His) c.480G>C (p.Gln160His) c.390G>C (p.Gln130His) n.313-5478G>C n.538G>C | dbSNP |
1 | g.156868155G>T | CA342933710 | NTRK1 | c.318G>T (p.Gln106His) c.480G>T (p.Gln160His) c.390G>T (p.Gln130His) n.313-5478G>T n.538G>T | gnomAD v4 |
1 | g.156868156C>A | CA342933715 | NTRK1 | c.319C>A (p.Arg107Ser) c.481C>A (p.Arg161Ser) c.391C>A (p.Arg131Ser) n.313-5477C>A n.539C>A | dbSNP gnomAD v4 |
1 | g.156868156C= | CA1200782081 | NTRK1 | c.319C= (p.Arg107=) c.481C= (p.Arg161=) c.391C= (p.Arg131=) n.313-5477C= n.539C= | |
1 | g.156868156C>G | CA342933713 | NTRK1 | c.319C>G (p.Arg107Gly) c.481C>G (p.Arg161Gly) c.391C>G (p.Arg131Gly) n.313-5477C>G n.539C>G | dbSNP |
1 | g.156868156C>T | CA1168993 | NTRK1 | c.319C>T (p.Arg107Cys) c.481C>T (p.Arg161Cys) c.391C>T (p.Arg131Cys) n.313-5477C>T n.539C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.156868157G>A | CA1168994 | NTRK1 | c.320G>A (p.Arg107His) c.482G>A (p.Arg161His) c.392G>A (p.Arg131His) n.313-5476G>A n.540G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.156868157G>C | CA342933718 | NTRK1 | c.320G>C (p.Arg107Pro) c.482G>C (p.Arg161Pro) c.392G>C (p.Arg131Pro) n.313-5476G>C n.540G>C | dbSNP COSMIC COSMIC |
1 | g.156868157G= | CA1142354727 | NTRK1 | c.320G= (p.Arg107=) c.482G= (p.Arg161=) c.392G= (p.Arg131=) n.313-5476G= n.540G= | |
1 | g.156868157G>T | CA342933720 | NTRK1 | c.320G>T (p.Arg107Leu) c.482G>T (p.Arg161Leu) c.392G>T (p.Arg131Leu) n.313-5476G>T n.540G>T | |
1 | g.156868158C>A | CA421270955 | NTRK1 | c.321C>A (p.Arg107=) c.483C>A (p.Arg161=) c.393C>A (p.Arg131=) n.313-5475C>A n.541C>A | |
1 | g.156868158C>G | CA421270956 | NTRK1 | c.321C>G (p.Arg107=) c.483C>G (p.Arg161=) c.393C>G (p.Arg131=) n.313-5475C>G n.541C>G | dbSNP |
1 | g.156868158C>T | CA421270957 | NTRK1 | c.321C>T (p.Arg107=) c.483C>T (p.Arg161=) c.393C>T (p.Arg131=) n.313-5475C>T n.541C>T | |
1 | g.156868159T>A | CA342933722 | NTRK1 | c.322T>A (p.Trp108Arg) c.484T>A (p.Trp162Arg) c.394T>A (p.Trp132Arg) n.313-5474T>A n.542T>A | dbSNP gnomAD v2 gnomAD v4 |
1 | g.156868159T>C | CA1168995 | NTRK1 | c.322T>C (p.Trp108Arg) c.484T>C (p.Trp162Arg) c.394T>C (p.Trp132Arg) n.313-5474T>C n.542T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.156868159T>G | CA342933725 | NTRK1 | c.322T>G (p.Trp108Gly) c.484T>G (p.Trp162Gly) c.394T>G (p.Trp132Gly) n.313-5474T>G n.542T>G | |
1 | g.156868159T= | CA1148900117 | NTRK1 | c.322T= (p.Trp108=) c.484T= (p.Trp162=) c.394T= (p.Trp132=) n.313-5474T= n.542T= | |
1 | g.156868160G>A | CA342933726 | NTRK1 | c.323G>A (p.Trp108Ter) c.485G>A (p.Trp162Ter) c.395G>A (p.Trp132Ter) n.313-5473G>A n.543G>A | dbSNP gnomAD v4 |
1 | g.156868160G>C | CA342933728 | NTRK1 | c.323G>C (p.Trp108Ser) c.485G>C (p.Trp162Ser) c.395G>C (p.Trp132Ser) n.313-5473G>C n.543G>C | |
1 | g.156868160G= | CA1200782083 | NTRK1 | c.323G= (p.Trp108=) c.485G= (p.Trp162=) c.395G= (p.Trp132=) n.313-5473G= n.543G= | |
1 | g.156868160G>T | CA342933730 | NTRK1 | c.323G>T (p.Trp108Leu) c.485G>T (p.Trp162Leu) c.395G>T (p.Trp132Leu) n.313-5473G>T n.543G>T | |
1 | g.156868160_156868163delinsGGGA | CA1200782082 | NTRK1 | c.323_326delinsGGGA (p.Trp108=) c.485_488delinsGGGA (p.Trp162=) c.395_398delinsGGGA (p.Trp132=) n.313-5473_313-5470delinsGGGA n.543_546delinsGGGA | |
1 | g.156868161G>A | CA342933732 | NTRK1 | c.324G>A (p.Trp108Ter) c.486G>A (p.Trp162Ter) c.396G>A (p.Trp132Ter) n.313-5472G>A n.544G>A | dbSNP |
1 | g.156868161G>C | CA342933734 | NTRK1 | c.324G>C (p.Trp108Cys) c.486G>C (p.Trp162Cys) c.396G>C (p.Trp132Cys) n.313-5472G>C n.544G>C | dbSNP |
1 | g.156868161G>T | CA342933736 | NTRK1 | c.324G>T (p.Trp108Cys) c.486G>T (p.Trp162Cys) c.396G>T (p.Trp132Cys) n.313-5472G>T n.544G>T | dbSNP |
1 | g.156868169_156868171del | CA1168996 | NTRK1 | c.332_334del (p.Glu111del) c.494_496del (p.Glu165del) c.404_406del (p.Glu135del) n.313-5464_313-5462del n.552_554del | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.156868162G>A | CA342933742 | NTRK1 | c.325G>A (p.Glu109Lys) c.487G>A (p.Glu163Lys) c.397G>A (p.Glu133Lys) n.313-5471G>A n.545G>A | dbSNP gnomAD v4 |
1 | g.156868162G>C | CA342933743 | NTRK1 | c.325G>C (p.Glu109Gln) c.487G>C (p.Glu163Gln) c.397G>C (p.Glu133Gln) n.313-5471G>C n.545G>C | dbSNP |
1 | g.156868162G>T | CA342933740 | NTRK1 | c.325G>T (p.Glu109Ter) c.487G>T (p.Glu163Ter) c.397G>T (p.Glu133Ter) n.313-5471G>T n.545G>T | |
1 | g.156868163A>C | CA342933744 | NTRK1 | c.326A>C (p.Glu109Ala) c.488A>C (p.Glu163Ala) c.398A>C (p.Glu133Ala) n.313-5470A>C n.546A>C | |
1 | g.156868163A>G | CA342933745 | NTRK1 | c.326A>G (p.Glu109Gly) c.488A>G (p.Glu163Gly) c.398A>G (p.Glu133Gly) n.313-5470A>G n.546A>G | dbSNP |
1 | g.156868163A>T | CA342933746 | NTRK1 | c.326A>T (p.Glu109Val) c.488A>T (p.Glu163Val) c.398A>T (p.Glu133Val) n.313-5470A>T n.546A>T | dbSNP |
1 | g.156868164G>A | CA421270970 | NTRK1 | c.327G>A (p.Glu109=) c.489G>A (p.Glu163=) c.399G>A (p.Glu133=) n.313-5469G>A n.547G>A | dbSNP |
1 | g.156868164G>C | CA342933748 | NTRK1 | c.327G>C (p.Glu109Asp) c.489G>C (p.Glu163Asp) c.399G>C (p.Glu133Asp) n.313-5469G>C n.547G>C | |
1 | g.156868164G>T | CA342933750 | NTRK1 | c.327G>T (p.Glu109Asp) c.489G>T (p.Glu163Asp) c.399G>T (p.Glu133Asp) n.313-5469G>T n.547G>T | |
1 | g.156868165G>A | CA342933751 | NTRK1 | c.328G>A (p.Glu110Lys) c.490G>A (p.Glu164Lys) c.400G>A (p.Glu134Lys) n.313-5468G>A n.548G>A | dbSNP |
1 | g.156868165G>C | CA342933752 | NTRK1 | c.328G>C (p.Glu110Gln) c.490G>C (p.Glu164Gln) c.400G>C (p.Glu134Gln) n.313-5468G>C n.548G>C | dbSNP |
1 | g.156868165G>T | CA342933753 | NTRK1 | c.328G>T (p.Glu110Ter) c.490G>T (p.Glu164Ter) c.400G>T (p.Glu134Ter) n.313-5468G>T n.548G>T | |
1 | g.156868166A= | CA1143364267 | NTRK1 | c.329A= (p.Glu110=) c.491A= (p.Glu164=) c.401A= (p.Glu134=) n.313-5467A= n.549A= | |
1 | g.156868166A>C | CA342933755 | NTRK1 | c.329A>C (p.Glu110Ala) c.491A>C (p.Glu164Ala) c.401A>C (p.Glu134Ala) n.313-5467A>C n.549A>C | |
1 | g.156868166A>G | CA31108198 | NTRK1 | c.329A>G (p.Glu110Gly) c.491A>G (p.Glu164Gly) c.401A>G (p.Glu134Gly) n.313-5467A>G n.549A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.156868166A>T | CA342933758 | NTRK1 | c.329A>T (p.Glu110Val) c.491A>T (p.Glu164Val) c.401A>T (p.Glu134Val) n.313-5467A>T n.549A>T | dbSNP |
1 | g.156868167G>A | CA421270974 | NTRK1 | c.330G>A (p.Glu110=) c.492G>A (p.Glu164=) c.402G>A (p.Glu134=) n.313-5466G>A n.550G>A | dbSNP |
1 | g.156868167G>C | CA342933763 | NTRK1 | c.330G>C (p.Glu110Asp) c.492G>C (p.Glu164Asp) c.402G>C (p.Glu134Asp) n.313-5466G>C n.550G>C | gnomAD v4 |
1 | g.156868167G>T | CA342933765 | NTRK1 | c.330G>T (p.Glu110Asp) c.492G>T (p.Glu164Asp) c.402G>T (p.Glu134Asp) n.313-5466G>T n.550G>T | |
1 | g.156868168G>A | CA1168997 | NTRK1 | c.331G>A (p.Glu111Lys) c.493G>A (p.Glu165Lys) c.403G>A (p.Glu135Lys) n.313-5465G>A n.551G>A | dbSNP ExAC gnomAD v2 |
1 | g.156868168G>C | CA342933769 | NTRK1 | c.331G>C (p.Glu111Gln) c.493G>C (p.Glu165Gln) c.403G>C (p.Glu135Gln) n.313-5465G>C n.551G>C | dbSNP |
1 | g.156868168G= | CA1200782084 | NTRK1 | c.331G= (p.Glu111=) c.493G= (p.Glu165=) c.403G= (p.Glu135=) n.313-5465G= n.551G= | |
1 | g.156868168G>T | CA342933767 | NTRK1 | c.331G>T (p.Glu111Ter) c.493G>T (p.Glu165Ter) c.403G>T (p.Glu135Ter) n.313-5465G>T n.551G>T | dbSNP |
1 | g.156868169A>C | CA342933771 | NTRK1 | c.332A>C (p.Glu111Ala) c.494A>C (p.Glu165Ala) c.404A>C (p.Glu135Ala) n.313-5464A>C n.552A>C | |
1 | g.156868169A>G | CA342933773 | NTRK1 | c.332A>G (p.Glu111Gly) c.494A>G (p.Glu165Gly) c.404A>G (p.Glu135Gly) n.313-5464A>G n.552A>G | dbSNP |
1 | g.156868169A>T | CA342933774 | NTRK1 | c.332A>T (p.Glu111Val) c.494A>T (p.Glu165Val) c.404A>T (p.Glu135Val) n.313-5464A>T n.552A>T | gnomAD v4 |
1 | g.156868170G>A | CA421270980 | NTRK1 | c.333G>A (p.Glu111=) c.495G>A (p.Glu165=) c.405G>A (p.Glu135=) n.313-5463G>A n.553G>A | dbSNP |
1 | g.156868170G>C | CA1168998 | NTRK1 | c.333G>C (p.Glu111Asp) c.495G>C (p.Glu165Asp) c.405G>C (p.Glu135Asp) n.313-5463G>C n.553G>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.156868170G= | CA1200782085 | NTRK1 | c.333G= (p.Glu111=) c.495G= (p.Glu165=) c.405G= (p.Glu135=) n.313-5463G= n.553G= | |
1 | g.156868170G>T | CA342933777 | NTRK1 | c.333G>T (p.Glu111Asp) c.495G>T (p.Glu165Asp) c.405G>T (p.Glu135Asp) n.313-5463G>T n.553G>T | |
1 | g.156868172dup | CA2746258418 | NTRK1 | c.335dup (p.Leu113ThrfsTer6) c.497dup (p.Leu167ThrfsTer6) c.407dup (p.Leu137ThrfsTer6) n.313-5461dup n.555dup | |
1 | g.156868171G>A | CA342933779 | NTRK1 | c.334G>A (p.Gly112Arg) c.496G>A (p.Gly166Arg) c.406G>A (p.Gly136Arg) n.313-5462G>A n.554G>A | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
1 | g.156868171G>C | CA342933781 | NTRK1 | c.334G>C (p.Gly112Arg) c.496G>C (p.Gly166Arg) c.406G>C (p.Gly136Arg) n.313-5462G>C n.554G>C | dbSNP |
1 | g.156868171G= | CA1200782086 | NTRK1 | c.334G= (p.Gly112=) c.496G= (p.Gly166=) c.406G= (p.Gly136=) n.313-5462G= n.554G= | |
1 | g.156868171G>T | CA342933783 | NTRK1 | c.334G>T (p.Gly112Ter) c.496G>T (p.Gly166Ter) c.406G>T (p.Gly136Ter) n.313-5462G>T n.554G>T | ClinVar dbSNP |
1 | g.156868172G>A | CA342933785 | NTRK1 | c.335G>A (p.Gly112Glu) c.497G>A (p.Gly166Glu) c.407G>A (p.Gly136Glu) n.313-5461G>A n.555G>A | dbSNP |
1 | g.156868172G>C | CA342933787 | NTRK1 | c.335G>C (p.Gly112Ala) c.497G>C (p.Gly166Ala) c.407G>C (p.Gly136Ala) n.313-5461G>C n.555G>C | dbSNP |
1 | g.156868172G>T | CA342933789 | NTRK1 | c.335G>T (p.Gly112Val) c.497G>T (p.Gly166Val) c.407G>T (p.Gly136Val) n.313-5461G>T n.555G>T | |
1 | g.156868173A>C | CA421270984 | NTRK1 | c.336A>C (p.Gly112=) c.498A>C (p.Gly166=) c.408A>C (p.Gly136=) n.313-5460A>C n.556A>C | |
1 | g.156868173A>G | CA421270985 | NTRK1 | c.336A>G (p.Gly112=) c.498A>G (p.Gly166=) c.408A>G (p.Gly136=) n.313-5460A>G n.556A>G | dbSNP |
1 | g.156868173A>T | CA421270986 | NTRK1 | c.336A>T (p.Gly112=) c.498A>T (p.Gly166=) c.408A>T (p.Gly136=) n.313-5460A>T n.556A>T | dbSNP |
1 | g.156868173_156868174delinsAC | CA1200782087 | NTRK1 | c.336_337delinsAC (p.Gly112=) c.498_499delinsAC (p.Gly166=) c.408_409delinsAC (p.Gly136=) n.313-5460_313-5459delinsAC n.556_557delinsAC | |
1 | g.156868174del | CA916318245 | NTRK1 | c.337del (p.Leu113TrpfsTer30) c.499del (p.Leu167TrpfsTer30) c.409del (p.Leu137TrpfsTer30) n.313-5459del n.557del | dbSNP |
1 | g.156868174C>A | CA342933793 | NTRK1 | c.337C>A (p.Leu113Met) c.499C>A (p.Leu167Met) c.409C>A (p.Leu137Met) n.313-5459C>A n.557C>A | COSMIC COSMIC |
1 | g.156868174C= | CA1200782088 | NTRK1 | c.337C= (p.Leu113=) c.499C= (p.Leu167=) c.409C= (p.Leu137=) n.313-5459C= n.557C= | |
1 | g.156868174C>G | CA342933791 | NTRK1 | c.337C>G (p.Leu113Val) c.499C>G (p.Leu167Val) c.409C>G (p.Leu137Val) n.313-5459C>G n.557C>G | dbSNP |
1 | g.156868174C>T | CA421270988 | NTRK1 | c.337C>T (p.Leu113=) c.499C>T (p.Leu167=) c.409C>T (p.Leu137=) n.313-5459C>T n.557C>T | dbSNP gnomAD v2 gnomAD v4 |
1 | g.156868175T>A | CA342933796 | NTRK1 | c.338T>A (p.Leu113Gln) c.500T>A (p.Leu167Gln) c.410T>A (p.Leu137Gln) n.313-5458T>A n.558T>A | |
1 | g.156868175T>C | CA342933799 | NTRK1 | c.338T>C (p.Leu113Pro) c.500T>C (p.Leu167Pro) c.410T>C (p.Leu137Pro) n.313-5458T>C n.558T>C | gnomAD v4 |
1 | g.156868175T>G | CA1168999 | NTRK1 | c.338T>G (p.Leu113Arg) c.500T>G (p.Leu167Arg) c.410T>G (p.Leu137Arg) n.313-5458T>G n.558T>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.156868175T= | CA1149137837 | NTRK1 | c.338T= (p.Leu113=) c.500T= (p.Leu167=) c.410T= (p.Leu137=) n.313-5458T= n.558T= | |
1 | g.156868176G>A | CA1169000 | NTRK1 | c.339G>A (p.Leu113=) c.501G>A (p.Leu167=) c.411G>A (p.Leu137=) n.313-5457G>A n.559G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.156868176G>C | CA421270996 | NTRK1 | c.339G>C (p.Leu113=) c.501G>C (p.Leu167=) c.411G>C (p.Leu137=) n.313-5457G>C n.559G>C | |
1 | g.156868176G= | CA1200782089 | NTRK1 | c.339G= (p.Leu113=) c.501G= (p.Leu167=) c.411G= (p.Leu137=) n.313-5457G= n.559G= | |
1 | g.156868176G>T | CA421270992 | NTRK1 | c.339G>T (p.Leu113=) c.501G>T (p.Leu167=) c.411G>T (p.Leu137=) n.313-5457G>T n.559G>T | |
1 | g.156868177G>A | CA342933802 | NTRK1 | c.340G>A (p.Gly114Ser) c.502G>A (p.Gly168Ser) c.412G>A (p.Gly138Ser) n.313-5456G>A n.560G>A | |
1 | g.156868177G>C | CA342933803 | NTRK1 | c.340G>C (p.Gly114Arg) c.502G>C (p.Gly168Arg) c.412G>C (p.Gly138Arg) n.313-5456G>C n.560G>C | |
1 | g.156868177G>T | CA342933805 | NTRK1 | c.340G>T (p.Gly114Cys) c.502G>T (p.Gly168Cys) c.412G>T (p.Gly138Cys) n.313-5456G>T n.560G>T | |
1 | g.156868178G>A | CA342933806 | NTRK1 | c.341G>A (p.Gly114Asp) c.503G>A (p.Gly168Asp) c.413G>A (p.Gly138Asp) n.313-5455G>A n.561G>A | dbSNP gnomAD v4 |
1 | g.156868178G>C | CA342933807 | NTRK1 | c.341G>C (p.Gly114Ala) c.503G>C (p.Gly168Ala) c.413G>C (p.Gly138Ala) n.313-5455G>C n.561G>C | |
1 | g.156868178G= | CA1200782090 | NTRK1 | c.341G= (p.Gly114=) c.503G= (p.Gly168=) c.413G= (p.Gly138=) n.313-5455G= n.561G= | |
1 | g.156868178G>T | CA1169001 | NTRK1 | c.341G>T (p.Gly114Val) c.503G>T (p.Gly168Val) c.413G>T (p.Gly138Val) n.313-5455G>T n.561G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.156868179C>A | CA421270999 | NTRK1 | c.342C>A (p.Gly114=) c.504C>A (p.Gly168=) c.414C>A (p.Gly138=) n.313-5454C>A n.562C>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.156868179C= | CA1142001147 | NTRK1 | c.342C= (p.Gly114=) c.504C= (p.Gly168=) c.414C= (p.Gly138=) n.313-5454C= n.562C= | |
1 | g.156868179C>G | CA421271002 | NTRK1 | c.342C>G (p.Gly114=) c.504C>G (p.Gly168=) c.414C>G (p.Gly138=) n.313-5454C>G n.562C>G | dbSNP |
1 | g.156868179C>T | CA1169002 | NTRK1 | c.342C>T (p.Gly114=) c.504C>T (p.Gly168=) c.414C>T (p.Gly138=) n.313-5454C>T n.562C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.156868180G>A | CA1169003 | NTRK1 | c.343G>A (p.Gly115Arg) c.505G>A (p.Gly169Arg) c.415G>A (p.Gly139Arg) n.313-5453G>A n.563G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
1 | g.156868180G>C | CA342933812 | NTRK1 | c.343G>C (p.Gly115Arg) c.505G>C (p.Gly169Arg) c.415G>C (p.Gly139Arg) n.313-5453G>C n.563G>C | |
1 | g.156868180G= | CA1143558389 | NTRK1 | c.343G= (p.Gly115=) c.505G= (p.Gly169=) c.415G= (p.Gly139=) n.313-5453G= n.563G= | |
1 | g.156868180G>T | CA342933813 | NTRK1 | c.343G>T (p.Gly115Ter) c.505G>T (p.Gly169Ter) c.415G>T (p.Gly139Ter) n.313-5453G>T n.563G>T | dbSNP |
1 | g.156868181G>A | CA342933816 | NTRK1 | c.344G>A (p.Gly115Glu) c.506G>A (p.Gly169Glu) c.416G>A (p.Gly139Glu) n.313-5452G>A n.564G>A | dbSNP |
1 | g.156868181G>C | CA342933818 | NTRK1 | c.344G>C (p.Gly115Ala) c.506G>C (p.Gly169Ala) c.416G>C (p.Gly139Ala) n.313-5452G>C n.564G>C | dbSNP |
1 | g.156868181G>T | CA342933820 | NTRK1 | c.344G>T (p.Gly115Val) c.506G>T (p.Gly169Val) c.416G>T (p.Gly139Val) n.313-5452G>T n.564G>T | dbSNP gnomAD v4 |
1 | g.156868182A>C | CA421271009 | NTRK1 | c.345A>C (p.Gly115=) c.507A>C (p.Gly169=) c.417A>C (p.Gly139=) n.313-5451A>C n.565A>C | ClinVar dbSNP |
1 | g.156868182A>G | CA421271010 | NTRK1 | c.345A>G (p.Gly115=) c.507A>G (p.Gly169=) c.417A>G (p.Gly139=) n.313-5451A>G n.565A>G | dbSNP |
1 | g.156868182A>T | CA421271011 | NTRK1 | c.345A>T (p.Gly115=) c.507A>T (p.Gly169=) c.417A>T (p.Gly139=) n.313-5451A>T n.565A>T | dbSNP |
1 | g.156868183G>A | CA342933825 | NTRK1 | c.346G>A (p.Val116Met) c.508G>A (p.Val170Met) c.418G>A (p.Val140Met) n.313-5450G>A n.566G>A | ClinVar dbSNP |
1 | g.156868183G>C | CA342933822 | NTRK1 | c.346G>C (p.Val116Leu) c.508G>C (p.Val170Leu) c.418G>C (p.Val140Leu) n.313-5450G>C n.566G>C | dbSNP gnomAD v4 |
1 | g.156868183G= | CA1200782091 | NTRK1 | c.346G= (p.Val116=) c.508G= (p.Val170=) c.418G= (p.Val140=) n.313-5450G= n.566G= | |
1 | g.156868183G>T | CA342933824 | NTRK1 | c.346G>T (p.Val116Leu) c.508G>T (p.Val170Leu) c.418G>T (p.Val140Leu) n.313-5450G>T n.566G>T | gnomAD v4 |
1 | g.156868184T>A | CA342933829 | NTRK1 | c.347T>A (p.Val116Glu) c.509T>A (p.Val170Glu) c.419T>A (p.Val140Glu) n.313-5449T>A n.567T>A | dbSNP |
1 | g.156868184T>C | CA1169004 | NTRK1 | c.347T>C (p.Val116Ala) c.509T>C (p.Val170Ala) c.419T>C (p.Val140Ala) n.313-5449T>C n.567T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.156868184T>G | CA342933831 | NTRK1 | c.347T>G (p.Val116Gly) c.509T>G (p.Val170Gly) c.419T>G (p.Val140Gly) n.313-5449T>G n.567T>G | dbSNP |
1 | g.156868184T= | CA1143487044 | NTRK1 | c.347T= (p.Val116=) c.509T= (p.Val170=) c.419T= (p.Val140=) n.313-5449T= n.567T= | |
1 | g.156868185G>A | CA421271021 | NTRK1 | c.348G>A (p.Val116=) c.510G>A (p.Val170=) c.420G>A (p.Val140=) n.313-5448G>A n.568G>A | dbSNP |
1 | g.156868185G>C | CA421271022 | NTRK1 | c.348G>C (p.Val116=) c.510G>C (p.Val170=) c.420G>C (p.Val140=) n.313-5448G>C n.568G>C | |
1 | g.156868185G>T | CA421271024 | NTRK1 | c.348G>T (p.Val116=) c.510G>T (p.Val170=) c.420G>T (p.Val140=) n.313-5448G>T n.568G>T | |
1 | g.156868186C>A | CA1169005 | NTRK1 | c.349C>A (p.Pro117Thr) c.511C>A (p.Pro171Thr) c.421C>A (p.Pro141Thr) n.313-5447C>A n.569C>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.156868186C= | CA1143431243 | NTRK1 | c.349C= (p.Pro117=) c.511C= (p.Pro171=) c.421C= (p.Pro141=) n.313-5447C= n.569C= | |
1 | g.156868186C>G | CA342933833 | NTRK1 | c.349C>G (p.Pro117Ala) c.511C>G (p.Pro171Ala) c.421C>G (p.Pro141Ala) n.313-5447C>G n.569C>G | dbSNP |
1 | g.156868186C>T | CA1169006 | NTRK1 | c.349C>T (p.Pro117Ser) c.511C>T (p.Pro171Ser) c.421C>T (p.Pro141Ser) n.313-5447C>T n.569C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.156868187del | CA2648463079 | NTRK1 | c.350del (p.Pro117LeufsTer26) c.512del (p.Pro171LeufsTer26) c.422del (p.Pro141LeufsTer26) n.313-5446del n.570del | gnomAD v4 |
1 | g.156868187C>A | CA342933837 | NTRK1 | c.350C>A (p.Pro117His) c.512C>A (p.Pro171His) c.422C>A (p.Pro141His) n.313-5446C>A n.570C>A | dbSNP |
1 | g.156868187C>G | CA342933839 | NTRK1 | c.350C>G (p.Pro117Arg) c.512C>G (p.Pro171Arg) c.422C>G (p.Pro141Arg) n.313-5446C>G n.570C>G | dbSNP |
1 | g.156868187C>T | CA342933841 | NTRK1 | c.350C>T (p.Pro117Leu) c.512C>T (p.Pro171Leu) c.422C>T (p.Pro141Leu) n.313-5446C>T n.570C>T | |
1 | g.156868188del | CA2573131108 | NTRK1 | c.351del (p.Glu118AsnfsTer25) c.513del (p.Glu172AsnfsTer25) c.423del (p.Glu142AsnfsTer25) n.313-5445del n.571del | ClinVar dbSNP |
1 | g.156868188T>A | CA421271028 | NTRK1 | c.351T>A (p.Pro117=) c.513T>A (p.Pro171=) c.423T>A (p.Pro141=) n.313-5445T>A n.571T>A | dbSNP |
1 | g.156868188T>C | CA421271030 | NTRK1 | c.351T>C (p.Pro117=) c.513T>C (p.Pro171=) c.423T>C (p.Pro141=) n.313-5445T>C n.571T>C | dbSNP |
1 | g.156868188T>G | CA421271029 | NTRK1 | c.351T>G (p.Pro117=) c.513T>G (p.Pro171=) c.423T>G (p.Pro141=) n.313-5445T>G n.571T>G | |
1 | g.156868189G>A | CA31108280 | NTRK1 | c.352G>A (p.Glu118Lys) c.514G>A (p.Glu172Lys) c.424G>A (p.Glu142Lys) n.313-5444G>A n.572G>A | ClinVar dbSNP gnomAD v4 |
1 | g.156868189G>C | CA342933844 | NTRK1 | c.352G>C (p.Glu118Gln) c.514G>C (p.Glu172Gln) c.424G>C (p.Glu142Gln) n.313-5444G>C n.572G>C | dbSNP |
1 | g.156868189G= | CA1143536943 | NTRK1 | c.352G= (p.Glu118=) c.514G= (p.Glu172=) c.424G= (p.Glu142=) n.313-5444G= n.572G= | |
1 | g.156868189G>T | CA342933846 | NTRK1 | c.352G>T (p.Glu118Ter) c.514G>T (p.Glu172Ter) c.424G>T (p.Glu142Ter) n.313-5444G>T n.572G>T | |
1 | g.156868190A>C | CA342933847 | NTRK1 | c.353A>C (p.Glu118Ala) c.515A>C (p.Glu172Ala) c.425A>C (p.Glu142Ala) n.313-5443A>C n.573A>C | |
1 | g.156868190A>G | CA342933850 | NTRK1 | c.353A>G (p.Glu118Gly) c.515A>G (p.Glu172Gly) c.425A>G (p.Glu142Gly) n.313-5443A>G n.573A>G | |
1 | g.156868190A>T | CA342933849 | NTRK1 | c.353A>T (p.Glu118Val) c.515A>T (p.Glu172Val) c.425A>T (p.Glu142Val) n.313-5443A>T n.573A>T | dbSNP |
1 | g.156868191A= | CA1143536945 | NTRK1 | c.354A= (p.Glu118=) c.516A= (p.Glu172=) c.426A= (p.Glu142=) n.313-5442A= n.574A= | |
1 | g.156868191A>C | CA31108285 | NTRK1 | c.354A>C (p.Glu118Asp) c.516A>C (p.Glu172Asp) c.426A>C (p.Glu142Asp) n.313-5442A>C n.574A>C | dbSNP |
1 | g.156868191A>G | CA421271036 | NTRK1 | c.354A>G (p.Glu118=) c.516A>G (p.Glu172=) c.426A>G (p.Glu142=) n.313-5442A>G n.574A>G | dbSNP gnomAD v4 |
1 | g.156868191A>T | CA342933851 | NTRK1 | c.354A>T (p.Glu118Asp) c.516A>T (p.Glu172Asp) c.426A>T (p.Glu142Asp) n.313-5442A>T n.574A>T | dbSNP |
1 | g.156868192C>A | CA342933852 | NTRK1 | c.355C>A (p.Gln119Lys) c.517C>A (p.Gln173Lys) c.427C>A (p.Gln143Lys) n.313-5441C>A n.575C>A | dbSNP |
1 | g.156868192C>G | CA342933854 | NTRK1 | c.355C>G (p.Gln119Glu) c.517C>G (p.Gln173Glu) c.427C>G (p.Gln143Glu) n.313-5441C>G n.575C>G | dbSNP |
1 | g.156868192C>T | CA342933856 | NTRK1 | c.355C>T (p.Gln119Ter) c.517C>T (p.Gln173Ter) c.427C>T (p.Gln143Ter) n.313-5441C>T n.575C>T | |
1 | g.156868193A>C | CA342933859 | NTRK1 | c.356A>C (p.Gln119Pro) c.518A>C (p.Gln173Pro) c.428A>C (p.Gln143Pro) n.313-5440A>C n.576A>C | |
1 | g.156868193A>G | CA342933860 | NTRK1 | c.356A>G (p.Gln119Arg) c.518A>G (p.Gln173Arg) c.428A>G (p.Gln143Arg) n.313-5440A>G n.576A>G | |
1 | g.156868193A>T | CA342933862 | NTRK1 | c.356A>T (p.Gln119Leu) c.518A>T (p.Gln173Leu) c.428A>T (p.Gln143Leu) n.313-5440A>T n.576A>T | |
1 | g.156868194G>A | CA421271039 | NTRK1 | c.357G>A (p.Gln119=) c.519G>A (p.Gln173=) c.429G>A (p.Gln143=) n.313-5439G>A n.577G>A | dbSNP |
1 | g.156868194G>C | CA342933863 | NTRK1 | c.357G>C (p.Gln119His) c.519G>C (p.Gln173His) c.429G>C (p.Gln143His) n.313-5439G>C n.577G>C | dbSNP |
1 | g.156868194G>T | CA342933865 | NTRK1 | c.357G>T (p.Gln119His) c.519G>T (p.Gln173His) c.429G>T (p.Gln143His) n.313-5439G>T n.577G>T | |
1 | g.156868195A= | CA1200782092 | NTRK1 | c.358A= (p.Lys120=) c.520A= (p.Lys174=) c.430A= (p.Lys144=) n.313-5438A= n.578A= | |
1 | g.156868195A>C | CA342933867 | NTRK1 | c.358A>C (p.Lys120Gln) c.520A>C (p.Lys174Gln) c.430A>C (p.Lys144Gln) n.313-5438A>C n.578A>C | gnomAD v4 |
1 | g.156868195A>G | CA342933868 | NTRK1 | c.358A>G (p.Lys120Glu) c.520A>G (p.Lys174Glu) c.430A>G (p.Lys144Glu) n.313-5438A>G n.578A>G | ClinVar dbSNP gnomAD v4 |
1 | g.156868195A>T | CA342933871 | NTRK1 | c.358A>T (p.Lys120Ter) c.520A>T (p.Lys174Ter) c.430A>T (p.Lys144Ter) n.313-5438A>T n.578A>T | |
1 | g.156868196A= | CA1200782093 | NTRK1 | c.359A= (p.Lys120=) c.521A= (p.Lys174=) c.431A= (p.Lys144=) n.313-5437A= n.579A= | |
1 | g.156868196A>C | CA342933873 | NTRK1 | c.359A>C (p.Lys120Thr) c.521A>C (p.Lys174Thr) c.431A>C (p.Lys144Thr) n.313-5437A>C n.579A>C | |
1 | g.156868196A>G | CA342933876 | NTRK1 | c.359A>G (p.Lys120Arg) c.521A>G (p.Lys174Arg) c.431A>G (p.Lys144Arg) n.313-5437A>G n.579A>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
1 | g.156868196A>T | CA342933874 | NTRK1 | c.359A>T (p.Lys120Met) c.521A>T (p.Lys174Met) c.431A>T (p.Lys144Met) n.313-5437A>T n.579A>T | |
1 | g.156868197G>A | CA421271046 | NTRK1 | c.360G>A (p.Lys120=) c.522G>A (p.Lys174=) c.432G>A (p.Lys144=) n.313-5436G>A n.580G>A | dbSNP |
1 | g.156868197G>C | CA342933879 | NTRK1 | c.360G>C (p.Lys120Asn) c.522G>C (p.Lys174Asn) c.432G>C (p.Lys144Asn) n.313-5436G>C n.580G>C | dbSNP |
1 | g.156868197G= | CA1143370860 | NTRK1 | c.360G= (p.Lys120=) c.522G= (p.Lys174=) c.432G= (p.Lys144=) n.313-5436G= n.580G= | |
1 | g.156868197G>T | CA31108291 | NTRK1 | c.360G>T (p.Lys120Asn) c.522G>T (p.Lys174Asn) c.432G>T (p.Lys144Asn) n.313-5436G>T n.580G>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.156868198C>A | CA342933881 | NTRK1 | c.361C>A (p.Leu121Met) c.523C>A (p.Leu175Met) c.433C>A (p.Leu145Met) n.313-5435C>A n.581C>A | dbSNP |
1 | g.156868198C>G | CA342933883 | NTRK1 | c.361C>G (p.Leu121Val) c.523C>G (p.Leu175Val) c.433C>G (p.Leu145Val) n.313-5435C>G n.581C>G | dbSNP |
1 | g.156868198C>T | CA421271047 | NTRK1 | c.361C>T (p.Leu121=) c.523C>T (p.Leu175=) c.433C>T (p.Leu145=) n.313-5435C>T n.581C>T | dbSNP gnomAD v4 |
1 | g.156868199T>A | CA342933886 | NTRK1 | c.362T>A (p.Leu121Gln) c.524T>A (p.Leu175Gln) c.434T>A (p.Leu145Gln) n.313-5434T>A n.582T>A | dbSNP |
1 | g.156868199T>C | CA342933887 | NTRK1 | c.362T>C (p.Leu121Pro) c.524T>C (p.Leu175Pro) c.434T>C (p.Leu145Pro) n.313-5434T>C n.582T>C | |
1 | g.156868199T>G | CA342933889 | NTRK1 | c.362T>G (p.Leu121Arg) c.524T>G (p.Leu175Arg) c.434T>G (p.Leu145Arg) n.313-5434T>G n.582T>G | |
1 | g.156868200del | CA2697464296 | NTRK1 | c.363del (p.Gln122SerfsTer21) c.525del (p.Gln176SerfsTer21) c.435del (p.Gln146SerfsTer21) n.313-5433del n.583del | dbSNP |
1 | g.156868200G>A | CA31108297 | NTRK1 | c.363G>A (p.Leu121=) c.525G>A (p.Leu175=) c.435G>A (p.Leu145=) n.313-5433G>A n.583G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.156868200G>C | CA421271053 | NTRK1 | c.363G>C (p.Leu121=) c.525G>C (p.Leu175=) c.435G>C (p.Leu145=) n.313-5433G>C n.583G>C | dbSNP |
1 | g.156868200G= | CA1200782094 | NTRK1 | c.363G= (p.Leu121=) c.525G= (p.Leu175=) c.435G= (p.Leu145=) n.313-5433G= n.583G= | |
1 | g.156868200G>T | CA421271054 | NTRK1 | c.363G>T (p.Leu121=) c.525G>T (p.Leu175=) c.435G>T (p.Leu145=) n.313-5433G>T n.583G>T | dbSNP |
1 | g.156868201C>A | CA342933891 | NTRK1 | c.364C>A (p.Gln122Lys) c.526C>A (p.Gln176Lys) c.436C>A (p.Gln146Lys) n.313-5432C>A n.584C>A | |
1 | g.156868201C= | CA1200782095 | NTRK1 | c.364C= (p.Gln122=) c.526C= (p.Gln176=) c.436C= (p.Gln146=) n.313-5432C= n.584C= | |
1 | g.156868201C>G | CA342933893 | NTRK1 | c.364C>G (p.Gln122Glu) c.526C>G (p.Gln176Glu) c.436C>G (p.Gln146Glu) n.313-5432C>G n.584C>G | |
1 | g.156868201C>T | CA10584138 | NTRK1 | c.364C>T (p.Gln122Ter) c.526C>T (p.Gln176Ter) c.436C>T (p.Gln146Ter) n.313-5432C>T n.584C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.156868202A= | CA1200782096 | NTRK1 | c.365A= (p.Gln122=) c.527A= (p.Gln176=) c.437A= (p.Gln146=) n.313-5431A= n.585A= | |
1 | g.156868202A>C | CA342933897 | NTRK1 | c.365A>C (p.Gln122Pro) c.527A>C (p.Gln176Pro) c.437A>C (p.Gln146Pro) n.313-5431A>C n.585A>C | |
1 | g.156868202A>G | CA342933899 | NTRK1 | c.365A>G (p.Gln122Arg) c.527A>G (p.Gln176Arg) c.437A>G (p.Gln146Arg) n.313-5431A>G n.585A>G | dbSNP |
1 | g.156868202A>T | CA342933895 | NTRK1 | c.365A>T (p.Gln122Leu) c.527A>T (p.Gln176Leu) c.437A>T (p.Gln146Leu) n.313-5431A>T n.585A>T | dbSNP |
1 | g.156868203G>A | CA31108298 | NTRK1 | c.366G>A (p.Gln122=) c.528G>A (p.Gln176=) c.438G>A (p.Gln146=) n.313-5430G>A n.586G>A | dbSNP |
1 | g.156868203G>C | CA342933901 | NTRK1 | c.366G>C (p.Gln122His) c.528G>C (p.Gln176His) c.438G>C (p.Gln146His) n.313-5430G>C n.586G>C | dbSNP |
1 | g.156868203G= | CA1200782097 | NTRK1 | c.366G= (p.Gln122=) c.528G= (p.Gln176=) c.438G= (p.Gln146=) n.313-5430G= n.586G= | |
1 | g.156868203G>T | CA342933902 | NTRK1 | c.366G>T (p.Gln122His) c.528G>T (p.Gln176His) c.438G>T (p.Gln146His) n.313-5430G>T n.586G>T | COSMIC COSMIC |
1 | g.156868204T>A | CA342933905 | NTRK1 | c.367T>A (p.Cys123Ser) c.529T>A (p.Cys177Ser) c.439T>A (p.Cys147Ser) n.313-5429T>A n.587T>A | dbSNP |
1 | g.156868204T>C | CA342933906 | NTRK1 | c.367T>C (p.Cys123Arg) c.529T>C (p.Cys177Arg) c.439T>C (p.Cys147Arg) n.313-5429T>C n.587T>C | |
1 | g.156868204T>G | CA342933908 | NTRK1 | c.367T>G (p.Cys123Gly) c.529T>G (p.Cys177Gly) c.439T>G (p.Cys147Gly) n.313-5429T>G n.587T>G | |
1 | g.156868205G>A | CA342933910 | NTRK1 | c.368G>A (p.Cys123Tyr) c.530G>A (p.Cys177Tyr) c.440G>A (p.Cys147Tyr) n.313-5428G>A n.588G>A | |
1 | g.156868205G>C | CA342933912 | NTRK1 | c.368G>C (p.Cys123Ser) c.530G>C (p.Cys177Ser) c.440G>C (p.Cys147Ser) n.313-5428G>C n.588G>C | dbSNP |
1 | g.156868205G>T | CA342933914 | NTRK1 | c.368G>T (p.Cys123Phe) c.530G>T (p.Cys177Phe) c.440G>T (p.Cys147Phe) n.313-5428G>T n.588G>T | |
1 | g.156868206T>A | CA342933916 | NTRK1 | c.369T>A (p.Cys123Ter) c.531T>A (p.Cys177Ter) c.441T>A (p.Cys147Ter) n.313-5427T>A n.589T>A | dbSNP |
1 | g.156868206T>C | CA16603449 | NTRK1 | c.369T>C (p.Cys123=) c.531T>C (p.Cys177=) c.441T>C (p.Cys147=) n.313-5427T>C n.589T>C | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.156868206T>G | CA342933918 | NTRK1 | c.369T>G (p.Cys123Trp) c.531T>G (p.Cys177Trp) c.441T>G (p.Cys147Trp) n.313-5427T>G n.589T>G | dbSNP |
1 | g.156868206T= | CA1200782098 | NTRK1 | c.369T= (p.Cys123=) c.531T= (p.Cys177=) c.441T= (p.Cys147=) n.313-5427T= n.589T= | |
1 | g.156868207C>A | CA342933920 | NTRK1 | c.370C>A (p.His124Asn) c.532C>A (p.His178Asn) c.442C>A (p.His148Asn) n.313-5426C>A n.590C>A | |
1 | g.156868207C= | CA1200782099 | NTRK1 | c.370C= (p.His124=) c.532C= (p.His178=) c.442C= (p.His148=) n.313-5426C= n.590C= | |
1 | g.156868207C>G | CA1169007 | NTRK1 | c.370C>G (p.His124Asp) c.532C>G (p.His178Asp) c.442C>G (p.His148Asp) n.313-5426C>G n.590C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.156868207C>T | CA342933923 | NTRK1 | c.370C>T (p.His124Tyr) c.532C>T (p.His178Tyr) c.442C>T (p.His148Tyr) n.313-5426C>T n.590C>T | COSMIC COSMIC |
1 | g.156868208A>C | CA342933925 | NTRK1 | c.371A>C (p.His124Pro) c.533A>C (p.His178Pro) c.443A>C (p.His148Pro) n.313-5425A>C n.591A>C | |
1 | g.156868208A>G | CA342933929 | NTRK1 | c.371A>G (p.His124Arg) c.533A>G (p.His178Arg) c.443A>G (p.His148Arg) n.313-5425A>G n.591A>G | |
1 | g.156868208A>T | CA342933927 | NTRK1 | c.371A>T (p.His124Leu) c.533A>T (p.His178Leu) c.443A>T (p.His148Leu) n.313-5425A>T n.591A>T | dbSNP |
1 | g.156868209T>A | CA342933935 | NTRK1 | c.372T>A (p.His124Gln) c.534T>A (p.His178Gln) c.444T>A (p.His148Gln) n.313-5424T>A n.592T>A | dbSNP |
1 | g.156868209T>C | CA421271072 | NTRK1 | c.372T>C (p.His124=) c.534T>C (p.His178=) c.444T>C (p.His148=) n.313-5424T>C n.592T>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.156868209T>G | CA342933937 | NTRK1 | c.372T>G (p.His124Gln) c.534T>G (p.His178Gln) c.444T>G (p.His148Gln) n.313-5424T>G n.592T>G | dbSNP |
1 | g.156868209T= | CA1200782100 | NTRK1 | c.372T= (p.His124=) c.534T= (p.His178=) c.444T= (p.His148=) n.313-5424T= n.592T= | |
1 | g.156868210G>A | CA342933939 | NTRK1 | c.373G>A (p.Gly125Arg) c.535G>A (p.Gly179Arg) c.445G>A (p.Gly149Arg) n.313-5423G>A n.593G>A | dbSNP gnomAD v4 |
1 | g.156868210G>C | CA342933941 | NTRK1 | c.373G>C (p.Gly125Arg) c.535G>C (p.Gly179Arg) c.445G>C (p.Gly149Arg) n.313-5423G>C n.593G>C | |
1 | g.156868210G= | CA1200782101 | NTRK1 | c.373G= (p.Gly125=) c.535G= (p.Gly179=) c.445G= (p.Gly149=) n.313-5423G= n.593G= | |
1 | g.156868210G>T | CA342933943 | NTRK1 | c.373G>T (p.Gly125Trp) c.535G>T (p.Gly179Trp) c.445G>T (p.Gly149Trp) n.313-5423G>T n.593G>T | dbSNP gnomAD v4 |
1 | g.156868211G>A | CA1169008 | NTRK1 | c.374G>A (p.Gly125Glu) c.536G>A (p.Gly179Glu) c.446G>A (p.Gly149Glu) n.313-5422G>A n.594G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.156868211G>C | CA1169009 | NTRK1 | c.374G>C (p.Gly125Ala) c.536G>C (p.Gly179Ala) c.446G>C (p.Gly149Ala) n.313-5422G>C n.594G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.156868211G= | CA1200782102 | NTRK1 | c.374G= (p.Gly125=) c.536G= (p.Gly179=) c.446G= (p.Gly149=) n.313-5422G= n.594G= | |
1 | g.156868211G>T | CA342933945 | NTRK1 | c.374G>T (p.Gly125Val) c.536G>T (p.Gly179Val) c.446G>T (p.Gly149Val) n.313-5422G>T n.594G>T | |
1 | g.156868212G>A | CA421271085 | NTRK1 | c.375G>A (p.Gly125=) c.537G>A (p.Gly179=) c.447G>A (p.Gly149=) n.313-5421G>A n.595G>A | ClinVar dbSNP gnomAD v4 |
1 | g.156868212G>C | CA421271086 | NTRK1 | c.375G>C (p.Gly125=) c.537G>C (p.Gly179=) c.447G>C (p.Gly149=) n.313-5421G>C n.595G>C | dbSNP |
1 | g.156868212G>T | CA421271087 | NTRK1 | c.375G>T (p.Gly125=) c.537G>T (p.Gly179=) c.447G>T (p.Gly149=) n.313-5421G>T n.595G>T | |
1 | g.156868213C>A | CA342933947 | NTRK1 | c.376C>A (p.Gln126Lys) c.538C>A (p.Gln180Lys) c.448C>A (p.Gln150Lys) n.313-5420C>A n.596C>A | dbSNP |
1 | g.156868213C= | CA1200782103 | NTRK1 | c.376C= (p.Gln126=) c.538C= (p.Gln180=) c.448C= (p.Gln150=) n.313-5420C= n.596C= | |
1 | g.156868213C>G | CA342933948 | NTRK1 | c.376C>G (p.Gln126Glu) c.538C>G (p.Gln180Glu) c.448C>G (p.Gln150Glu) n.313-5420C>G n.596C>G | dbSNP gnomAD v4 |
1 | g.156868213C>T | CA342933950 | NTRK1 | c.376C>T (p.Gln126Ter) c.538C>T (p.Gln180Ter) c.448C>T (p.Gln150Ter) n.313-5420C>T n.596C>T | ClinVar dbSNP gnomAD v4 |
1 | g.156868214A>C | CA342933953 | NTRK1 | c.377A>C (p.Gln126Pro) c.539A>C (p.Gln180Pro) c.449A>C (p.Gln150Pro) n.313-5419A>C n.597A>C | |
1 | g.156868214A>G | CA342933954 | NTRK1 | c.377A>G (p.Gln126Arg) c.539A>G (p.Gln180Arg) c.449A>G (p.Gln150Arg) n.313-5419A>G n.597A>G | |
1 | g.156868214A>T | CA342933951 | NTRK1 | c.377A>T (p.Gln126Leu) c.539A>T (p.Gln180Leu) c.449A>T (p.Gln150Leu) n.313-5419A>T n.597A>T | |
1 | g.156868215A>C | CA342933956 | NTRK1 | c.378A>C (p.Gln126His) c.540A>C (p.Gln180His) c.450A>C (p.Gln150His) n.313-5418A>C n.598A>C | dbSNP |
1 | g.156868215A>G | CA421271095 | NTRK1 | c.378A>G (p.Gln126=) c.540A>G (p.Gln180=) c.450A>G (p.Gln150=) n.313-5418A>G n.598A>G | dbSNP |
1 | g.156868215A>T | CA342933957 | NTRK1 | c.378A>T (p.Gln126His) c.540A>T (p.Gln180His) c.450A>T (p.Gln150His) n.313-5418A>T n.598A>T | dbSNP |
1 | g.156868215_156868216delinsAG | CA1200782104 | NTRK1 | c.378_379delinsAG (p.Gln126=) c.540_541delinsAG (p.Gln180=) c.450_451delinsAG (p.Gln150=) n.313-5418_313-5417delinsAG n.598_599delinsAG | |
1 | g.156868216G>A | CA342933959 | NTRK1 | c.379G>A (p.Gly127Arg) c.541G>A (p.Gly181Arg) c.451G>A (p.Gly151Arg) n.313-5417G>A n.599G>A | |
1 | g.156868216G>C | CA342933960 | NTRK1 | c.379G>C (p.Gly127Arg) c.541G>C (p.Gly181Arg) c.451G>C (p.Gly151Arg) n.313-5417G>C n.599G>C | gnomAD v4 |
1 | g.156868216G>T | CA342933962 | NTRK1 | c.379G>T (p.Gly127Trp) c.541G>T (p.Gly181Trp) c.451G>T (p.Gly151Trp) n.313-5417G>T n.599G>T | gnomAD v4 |
1 | g.156868218del | CA526673359 | NTRK1 | c.381del (p.Leu129TrpfsTer14) c.543del (p.Leu183TrpfsTer14) c.453del (p.Leu153TrpfsTer14) n.313-5415del n.601del | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.156868217G>A | CA342933964 | NTRK1 | c.380G>A (p.Gly127Glu) c.542G>A (p.Gly181Glu) c.452G>A (p.Gly151Glu) n.313-5416G>A n.600G>A | dbSNP |
1 | g.156868217G>C | CA342933966 | NTRK1 | c.380G>C (p.Gly127Ala) c.542G>C (p.Gly181Ala) c.452G>C (p.Gly151Ala) n.313-5416G>C n.600G>C | dbSNP |
1 | g.156868217G>T | CA342933968 | NTRK1 | c.380G>T (p.Gly127Val) c.542G>T (p.Gly181Val) c.452G>T (p.Gly151Val) n.313-5416G>T n.600G>T | |
1 | g.156868218G>A | CA1169010 | NTRK1 | c.381G>A (p.Gly127=) c.543G>A (p.Gly181=) c.453G>A (p.Gly151=) n.313-5415G>A n.601G>A | ClinVar dbSNP ExAC gnomAD v2 |
1 | g.156868218G>C | CA421271108 | NTRK1 | c.381G>C (p.Gly127=) c.543G>C (p.Gly181=) c.453G>C (p.Gly151=) n.313-5415G>C n.601G>C | |
1 | g.156868218G= | CA1200782105 | NTRK1 | c.381G= (p.Gly127=) c.543G= (p.Gly181=) c.453G= (p.Gly151=) n.313-5415G= n.601G= | |
1 | g.156868218G>T | CA421271105 | NTRK1 | c.381G>T (p.Gly127=) c.543G>T (p.Gly181=) c.453G>T (p.Gly151=) n.313-5415G>T n.601G>T | ClinVar dbSNP gnomAD v2 |
1 | g.156868219C>A | CA342933971 | NTRK1 | c.382C>A (p.Pro128Thr) c.544C>A (p.Pro182Thr) c.454C>A (p.Pro152Thr) n.313-5414C>A n.602C>A | dbSNP gnomAD v4 |
1 | g.156868219C= | CA1200782106 | NTRK1 | c.382C= (p.Pro128=) c.544C= (p.Pro182=) c.454C= (p.Pro152=) n.313-5414C= n.602C= | |
1 | g.156868219C>G | CA342933973 | NTRK1 | c.382C>G (p.Pro128Ala) c.544C>G (p.Pro182Ala) c.454C>G (p.Pro152Ala) n.313-5414C>G n.602C>G | ClinVar dbSNP |
1 | g.156868219C>T | CA1169011 | NTRK1 | c.382C>T (p.Pro128Ser) c.544C>T (p.Pro182Ser) c.454C>T (p.Pro152Ser) n.313-5414C>T n.602C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.156868220C>A | CA342933975 | NTRK1 | c.383C>A (p.Pro128His) c.545C>A (p.Pro182His) c.455C>A (p.Pro152His) n.313-5413C>A n.603C>A | dbSNP gnomAD v4 |
1 | g.156868220C= | CA1200782107 | NTRK1 | c.383C= (p.Pro128=) c.545C= (p.Pro182=) c.455C= (p.Pro152=) n.313-5413C= n.603C= | |
1 | g.156868220C>G | CA342933977 | NTRK1 | c.383C>G (p.Pro128Arg) c.545C>G (p.Pro182Arg) c.455C>G (p.Pro152Arg) n.313-5413C>G n.603C>G | dbSNP |
1 | g.156868220C>T | CA342933979 | NTRK1 | c.383C>T (p.Pro128Leu) c.545C>T (p.Pro182Leu) c.455C>T (p.Pro152Leu) n.313-5413C>T n.603C>T | dbSNP gnomAD v2 gnomAD v4 |
1 | g.156868221C>A | CA421271116 | NTRK1 | c.384C>A (p.Pro128=) c.546C>A (p.Pro182=) c.456C>A (p.Pro152=) n.313-5412C>A n.604C>A | |
1 | g.156868221C= | CA1200782108 | NTRK1 | c.384C= (p.Pro128=) c.546C= (p.Pro182=) c.456C= (p.Pro152=) n.313-5412C= n.604C= | |
1 | g.156868221C>G | CA1169012 | NTRK1 | c.384C>G (p.Pro128=) c.546C>G (p.Pro182=) c.456C>G (p.Pro152=) n.313-5412C>G n.604C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.156868221C>T | CA421271117 | NTRK1 | c.384C>T (p.Pro128=) c.546C>T (p.Pro182=) c.456C>T (p.Pro152=) n.313-5412C>T n.604C>T | dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC |
1 | g.156868222C>A | CA342933982 | NTRK1 | c.385C>A (p.Leu129Met) c.547C>A (p.Leu183Met) c.457C>A (p.Leu153Met) n.313-5411C>A n.605C>A | |
1 | g.156868222C= | CA1147019766 | NTRK1 | c.385C= (p.Leu129=) c.547C= (p.Leu183=) c.457C= (p.Leu153=) n.313-5411C= n.605C= | |
1 | g.156868222C>G | CA1169013 | NTRK1 | c.385C>G (p.Leu129Val) c.547C>G (p.Leu183Val) c.457C>G (p.Leu153Val) n.313-5411C>G n.605C>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.156868222C>T | CA421271120 | NTRK1 | c.385C>T (p.Leu129=) c.547C>T (p.Leu183=) c.457C>T (p.Leu153=) n.313-5411C>T n.605C>T | |
1 | g.156868223T>A | CA342933985 | NTRK1 | c.386T>A (p.Leu129Gln) c.548T>A (p.Leu183Gln) c.458T>A (p.Leu153Gln) n.313-5410T>A n.606T>A | |
1 | g.156868223T>C | CA342933986 | NTRK1 | c.386T>C (p.Leu129Pro) c.548T>C (p.Leu183Pro) c.458T>C (p.Leu153Pro) n.313-5410T>C n.606T>C | |
1 | g.156868223T>G | CA342933988 | NTRK1 | c.386T>G (p.Leu129Arg) c.548T>G (p.Leu183Arg) c.458T>G (p.Leu153Arg) n.313-5410T>G n.606T>G | |
1 | g.156868224G>A | CA421271122 | NTRK1 | c.387G>A (p.Leu129=) c.549G>A (p.Leu183=) c.459G>A (p.Leu153=) n.313-5409G>A n.607G>A | dbSNP gnomAD v3 gnomAD v4 |
1 | g.156868224G>C | CA421271124 | NTRK1 | c.387G>C (p.Leu129=) c.549G>C (p.Leu183=) c.459G>C (p.Leu153=) n.313-5409G>C n.607G>C | |
1 | g.156868224G= | CA1200782109 | NTRK1 | c.387G= (p.Leu129=) c.549G= (p.Leu183=) c.459G= (p.Leu153=) n.313-5409G= n.607G= | |
1 | g.156868224G>T | CA31108349 | NTRK1 | c.387G>T (p.Leu129=) c.549G>T (p.Leu183=) c.459G>T (p.Leu153=) n.313-5409G>T n.607G>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.156868224_156868225insCAC | CA2746258419 | NTRK1 | c.387_388insCAC (p.Leu129_Ala130insHis) c.549_550insCAC (p.Leu183_Ala184insHis) c.459_460insCAC (p.Leu153_Ala154insHis) n.313-5409_313-5408insCAC n.607_608insCAC | |
1 | g.156868225G>A | CA342933991 | NTRK1 | c.388G>A (p.Ala130Thr) c.550G>A (p.Ala184Thr) c.460G>A (p.Ala154Thr) n.313-5408G>A n.608G>A | gnomAD v4 |
1 | g.156868225G>C | CA342933993 | NTRK1 | c.388G>C (p.Ala130Pro) c.550G>C (p.Ala184Pro) c.460G>C (p.Ala154Pro) n.313-5408G>C n.608G>C | gnomAD v4 |
1 | g.156868225G>T | CA342933995 | NTRK1 | c.388G>T (p.Ala130Ser) c.550G>T (p.Ala184Ser) c.460G>T (p.Ala154Ser) n.313-5408G>T n.608G>T | |
1 | g.156868230_156868237del | CA2697464552 | NTRK1 | c.393_400del (p.His131GlnfsTer?) c.555_562del (p.His185GlnfsTer?) c.465_472del (p.His155GlnfsTer?) n.313-5403_313-5396del n.613_620del | dbSNP |
1 | g.156868226C>A | CA342933997 | NTRK1 | c.389C>A (p.Ala130Asp) c.551C>A (p.Ala184Asp) c.461C>A (p.Ala154Asp) n.313-5407C>A n.609C>A | gnomAD v4 |
1 | g.156868226C>G | CA342933998 | NTRK1 | c.389C>G (p.Ala130Gly) c.551C>G (p.Ala184Gly) c.461C>G (p.Ala154Gly) n.313-5407C>G n.609C>G | dbSNP |
1 | g.156868226C>T | CA342934000 | NTRK1 | c.389C>T (p.Ala130Val) c.551C>T (p.Ala184Val) c.461C>T (p.Ala154Val) n.313-5407C>T n.609C>T | dbSNP gnomAD v4 |
1 | g.156868228del | CA2648463212 | NTRK1 | c.391del (p.His131ThrfsTer12) c.553del (p.His185ThrfsTer12) c.463del (p.His155ThrfsTer12) n.313-5405del n.611del | gnomAD v4 |
1 | g.156868227C>A | CA421271135 | NTRK1 | c.390C>A (p.Ala130=) c.552C>A (p.Ala184=) c.462C>A (p.Ala154=) n.313-5406C>A n.610C>A | dbSNP |
1 | g.156868227C>G | CA421271136 | NTRK1 | c.390C>G (p.Ala130=) c.552C>G (p.Ala184=) c.462C>G (p.Ala154=) n.313-5406C>G n.610C>G | dbSNP |
1 | g.156868227C>T | CA421271137 | NTRK1 | c.390C>T (p.Ala130=) c.552C>T (p.Ala184=) c.462C>T (p.Ala154=) n.313-5406C>T n.610C>T | dbSNP |
1 | g.156868228C>A | CA342934002 | NTRK1 | c.391C>A (p.His131Asn) c.553C>A (p.His185Asn) c.463C>A (p.His155Asn) n.313-5405C>A n.611C>A | dbSNP gnomAD v4 |
1 | g.156868228C= | CA1200782110 | NTRK1 | c.391C= (p.His131=) c.553C= (p.His185=) c.463C= (p.His155=) n.313-5405C= n.611C= | |
1 | g.156868228C>G | CA342934003 | NTRK1 | c.391C>G (p.His131Asp) c.553C>G (p.His185Asp) c.463C>G (p.His155Asp) n.313-5405C>G n.611C>G | |
1 | g.156868228C>T | CA342934004 | NTRK1 | c.391C>T (p.His131Tyr) c.553C>T (p.His185Tyr) c.463C>T (p.His155Tyr) n.313-5405C>T n.611C>T | ClinVar dbSNP |
1 | g.156868229A>C | CA342934010 | NTRK1 | c.392A>C (p.His131Pro) c.554A>C (p.His185Pro) c.464A>C (p.His155Pro) n.313-5404A>C n.612A>C | |
1 | g.156868229A>G | CA342934008 | NTRK1 | c.392A>G (p.His131Arg) c.554A>G (p.His185Arg) c.464A>G (p.His155Arg) n.313-5404A>G n.612A>G | |
1 | g.156868229A>T | CA342934007 | NTRK1 | c.392A>T (p.His131Leu) c.554A>T (p.His185Leu) c.464A>T (p.His155Leu) n.313-5404A>T n.612A>T | |
1 | g.156868230C>A | CA342934014 | NTRK1 | c.393C>A (p.His131Gln) c.555C>A (p.His185Gln) c.465C>A (p.His155Gln) n.313-5403C>A n.613C>A | dbSNP |
1 | g.156868230C>G | CA342934013 | NTRK1 | c.393C>G (p.His131Gln) c.555C>G (p.His185Gln) c.465C>G (p.His155Gln) n.313-5403C>G n.613C>G | |
1 | g.156868230C>T | CA421271144 | NTRK1 | c.393C>T (p.His131=) c.555C>T (p.His185=) c.465C>T (p.His155=) n.313-5403C>T n.613C>T | dbSNP |
1 | g.156868231A>C | CA342934017 | NTRK1 | c.394A>C (p.Met132Leu) c.556A>C (p.Met186Leu) c.466A>C (p.Met156Leu) n.313-5402A>C n.614A>C | |
1 | g.156868231A>G | CA342934016 | NTRK1 | c.394A>G (p.Met132Val) c.556A>G (p.Met186Val) c.466A>G (p.Met156Val) n.313-5402A>G n.614A>G | |
1 | g.156868231A>T | CA342934019 | NTRK1 | c.394A>T (p.Met132Leu) c.556A>T (p.Met186Leu) c.466A>T (p.Met156Leu) n.313-5402A>T n.614A>T | |
1 | g.156868232T>A | CA342934021 | NTRK1 | c.395T>A (p.Met132Lys) c.557T>A (p.Met186Lys) c.467T>A (p.Met156Lys) n.313-5401T>A n.615T>A | |
1 | g.156868232T>C | CA1169014 | NTRK1 | c.395T>C (p.Met132Thr) c.557T>C (p.Met186Thr) c.467T>C (p.Met156Thr) n.313-5401T>C n.615T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.156868232T>G | CA342934023 | NTRK1 | c.395T>G (p.Met132Arg) c.557T>G (p.Met186Arg) c.467T>G (p.Met156Arg) n.313-5401T>G n.615T>G | |
1 | g.156868232T= | CA1143794233 | NTRK1 | c.395T= (p.Met132=) c.557T= (p.Met186=) c.467T= (p.Met156=) n.313-5401T= n.615T= |