Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.156881581_156881609delinsTGCACGCCCGGCTGCAAGCCCTGGCCCAG | CA1200788906 | NTRK1 | c.2150_2178delinsTGCACGCCCGGCTGCAAGCCCTGGCCCAG (p.Val717=) c.*922_*950delinsTGCACGCCCGGCTGCAAGCCCTGGCCCAG (n.*922_*950delinsTGCACGCCCGGCTGCAAGCCCTGGCCCAG) c.2330_2358delinsTGCACGCCCGGCTGCAAGCCCTGGCCCAG (p.Val777=) c.389_417delinsTGCACGCCCGGCTGCAAGCCCTGGCCCAG c.2321_2349delinsTGCACGCCCGGCTGCAAGCCCTGGCCCAG (p.Val774=) c.2312_2340delinsTGCACGCCCGGCTGCAAGCCCTGGCCCAG (p.Val771=) c.2222_2250delinsTGCACGCCCGGCTGCAAGCCCTGGCCCAG (p.Val741=) n.2783_2811delinsTGCACGCCCGGCTGCAAGCCCTGGCCCAG n.373_401delinsTGCACGCCCGGCTGCAAGCCCTGGCCCAG | |
1 | g.156881586_156881613del | CA891843047 | NTRK1 | c.2155_2182del (p.Ala719LeufsTer?) c.*927_*954del (n.*927_*954del) c.2335_2362del (p.Ala779LeufsTer?) c.394_421del c.2326_2353del (p.Ala776LeufsTer?) c.2317_2344del (p.Ala773LeufsTer?) c.2227_2254del (p.Ala743LeufsTer?) n.2788_2815del n.378_405del | ClinVar dbSNP |
1 | g.156881585C>A | CA342941725 | NTRK1 | c.2154C>A (p.His718Gln) c.*926C>A (n.*926C>A) c.2334C>A (p.His778Gln) c.393C>A c.2325C>A (p.His775Gln) c.2316C>A (p.His772Gln) c.2226C>A (p.His742Gln) n.2787C>A n.377C>A | dbSNP gnomAD v2 |
1 | g.156881585C= | CA1143734134 | NTRK1 | c.2154C= (p.His718=) c.*926C= (n.*926C=) c.2334C= (p.His778=) c.393C= c.2325C= (p.His775=) c.2316C= (p.His772=) c.2226C= (p.His742=) n.2787C= n.377C= | |
1 | g.156881585C>G | CA342941726 | NTRK1 | c.2154C>G (p.His718Gln) c.*926C>G (n.*926C>G) c.2334C>G (p.His778Gln) c.393C>G c.2325C>G (p.His775Gln) c.2316C>G (p.His772Gln) c.2226C>G (p.His742Gln) n.2787C>G n.377C>G | dbSNP |
1 | g.156881585C>T | CA1169634 | NTRK1 | c.2154C>T (p.His718=) c.*926C>T (n.*926C>T) c.2334C>T (p.His778=) c.393C>T c.2325C>T (p.His775=) c.2316C>T (p.His772=) c.2226C>T (p.His742=) n.2787C>T n.377C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.156881586G>A | CA1169635 | NTRK1 | c.2155G>A (p.Ala719Thr) c.*927G>A (n.*927G>A) c.2335G>A (p.Ala779Thr) c.394G>A c.2326G>A (p.Ala776Thr) c.2317G>A (p.Ala773Thr) c.2227G>A (p.Ala743Thr) n.2788G>A n.378G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.156881586G>C | CA342941727 | NTRK1 | c.2155G>C (p.Ala719Pro) c.*927G>C (n.*927G>C) c.2335G>C (p.Ala779Pro) c.394G>C c.2326G>C (p.Ala776Pro) c.2317G>C (p.Ala773Pro) c.2227G>C (p.Ala743Pro) n.2788G>C n.378G>C | dbSNP |
1 | g.156881586G= | CA1144028342 | NTRK1 | c.2155G= (p.Ala719=) c.*927G= (n.*927G=) c.2335G= (p.Ala779=) c.394G= c.2326G= (p.Ala776=) c.2317G= (p.Ala773=) c.2227G= (p.Ala743=) n.2788G= n.378G= | |
1 | g.156881586G>T | CA342941729 | NTRK1 | c.2155G>T (p.Ala719Ser) c.*927G>T (n.*927G>T) c.2335G>T (p.Ala779Ser) c.394G>T c.2326G>T (p.Ala776Ser) c.2317G>T (p.Ala773Ser) c.2227G>T (p.Ala743Ser) n.2788G>T n.378G>T | dbSNP gnomAD v4 |
1 | g.156881590_156881601del | CA2648467752 | NTRK1 | c.2159_2170del (p.Arg720_Ala723del) c.*931_*942del (n.*931_*942del) c.2339_2350del (p.Arg780_Ala783del) c.398_409del c.2330_2341del (p.Arg777_Ala780del) c.2321_2332del (p.Arg774_Ala777del) c.2231_2242del (p.Arg744_Ala747del) n.2792_2803del n.382_393del | gnomAD v4 |
1 | g.156881587C>A | CA342941730 | NTRK1 | c.2156C>A (p.Ala719Asp) c.*928C>A (n.*928C>A) c.2336C>A (p.Ala779Asp) c.395C>A c.2327C>A (p.Ala776Asp) c.2318C>A (p.Ala773Asp) c.2228C>A (p.Ala743Asp) n.2789C>A n.379C>A | |
1 | g.156881587C= | CA1200788924 | NTRK1 | c.2156C= (p.Ala719=) c.*928C= (n.*928C=) c.2336C= (p.Ala779=) c.395C= c.2327C= (p.Ala776=) c.2318C= (p.Ala773=) c.2228C= (p.Ala743=) n.2789C= n.379C= | |
1 | g.156881587C>G | CA342941731 | NTRK1 | c.2156C>G (p.Ala719Gly) c.*928C>G (n.*928C>G) c.2336C>G (p.Ala779Gly) c.395C>G c.2327C>G (p.Ala776Gly) c.2318C>G (p.Ala773Gly) c.2228C>G (p.Ala743Gly) n.2789C>G n.379C>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.156881587C>T | CA342941732 | NTRK1 | c.2156C>T (p.Ala719Val) c.*928C>T (n.*928C>T) c.2336C>T (p.Ala779Val) c.395C>T c.2327C>T (p.Ala776Val) c.2318C>T (p.Ala773Val) c.2228C>T (p.Ala743Val) n.2789C>T n.379C>T | dbSNP |
1 | g.156881588C>A | CA421140670 | NTRK1 | c.2157C>A (p.Ala719=) c.*929C>A (n.*929C>A) c.2337C>A (p.Ala779=) c.396C>A c.2328C>A (p.Ala776=) c.2319C>A (p.Ala773=) c.2229C>A (p.Ala743=) n.2790C>A n.380C>A | gnomAD v4 |
1 | g.156881588C>G | CA421140669 | NTRK1 | c.2157C>G (p.Ala719=) c.*929C>G (n.*929C>G) c.2337C>G (p.Ala779=) c.396C>G c.2328C>G (p.Ala776=) c.2319C>G (p.Ala773=) c.2229C>G (p.Ala743=) n.2790C>G n.380C>G | |
1 | g.156881588C>T | CA421140668 | NTRK1 | c.2157C>T (p.Ala719=) c.*929C>T (n.*929C>T) c.2337C>T (p.Ala779=) c.396C>T c.2328C>T (p.Ala776=) c.2319C>T (p.Ala773=) c.2229C>T (p.Ala743=) n.2790C>T n.380C>T | |
1 | g.156881589C>A | CA421140671 | NTRK1 | c.2158C>A (p.Arg720=) c.*930C>A (n.*930C>A) c.2338C>A (p.Arg780=) c.397C>A c.2329C>A (p.Arg777=) c.2320C>A (p.Arg774=) c.2230C>A (p.Arg744=) n.2791C>A n.381C>A | dbSNP gnomAD v4 |
1 | g.156881589C= | CA1145049910 | NTRK1 | c.2158C= (p.Arg720=) c.*930C= (n.*930C=) c.2338C= (p.Arg780=) c.397C= c.2329C= (p.Arg777=) c.2320C= (p.Arg774=) c.2230C= (p.Arg744=) n.2791C= n.381C= | |
1 | g.156881589C>G | CA342941733 | NTRK1 | c.2158C>G (p.Arg720Gly) c.*930C>G (n.*930C>G) c.2338C>G (p.Arg780Gly) c.397C>G c.2329C>G (p.Arg777Gly) c.2320C>G (p.Arg774Gly) c.2230C>G (p.Arg744Gly) n.2791C>G n.381C>G | dbSNP gnomAD v4 COSMIC |
1 | g.156881589C>T | CA1169636 | NTRK1 | c.2158C>T (p.Arg720Trp) c.*930C>T (n.*930C>T) c.2338C>T (p.Arg780Trp) c.397C>T c.2329C>T (p.Arg777Trp) c.2320C>T (p.Arg774Trp) c.2230C>T (p.Arg744Trp) n.2791C>T n.381C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.156881590G>A | CA1169637 | NTRK1 | c.2159G>A (p.Arg720Gln) c.*931G>A (n.*931G>A) c.2339G>A (p.Arg780Gln) c.398G>A c.2330G>A (p.Arg777Gln) c.2321G>A (p.Arg774Gln) c.2231G>A (p.Arg744Gln) n.2792G>A n.382G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.156881590G>C | CA256268 | NTRK1 | c.2159G>C (p.Arg720Pro) c.*931G>C (n.*931G>C) c.2339G>C (p.Arg780Pro) c.398G>C c.2330G>C (p.Arg777Pro) c.2321G>C (p.Arg774Pro) c.2231G>C (p.Arg744Pro) n.2792G>C n.382G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.156881590G= | CA1140584233 | NTRK1 | c.2159G= (p.Arg720=) c.*931G= (n.*931G=) c.2339G= (p.Arg780=) c.398G= c.2330G= (p.Arg777=) c.2321G= (p.Arg774=) c.2231G= (p.Arg744=) n.2792G= n.382G= | |
1 | g.156881590G>T | CA342941734 | NTRK1 | c.2159G>T (p.Arg720Leu) c.*931G>T (n.*931G>T) c.2339G>T (p.Arg780Leu) c.398G>T c.2330G>T (p.Arg777Leu) c.2321G>T (p.Arg774Leu) c.2231G>T (p.Arg744Leu) n.2792G>T n.382G>T | gnomAD v4 |
1 | g.156881591G>A | CA1169638 | NTRK1 | c.2160G>A (p.Arg720=) c.*932G>A (n.*932G>A) c.2340G>A (p.Arg780=) c.399G>A c.2331G>A (p.Arg777=) c.2322G>A (p.Arg774=) c.2232G>A (p.Arg744=) n.2793G>A n.383G>A | dbSNP ExAC gnomAD v2 |
1 | g.156881591G>C | CA421140673 | NTRK1 | c.2160G>C (p.Arg720=) c.*932G>C (n.*932G>C) c.2340G>C (p.Arg780=) c.399G>C c.2331G>C (p.Arg777=) c.2322G>C (p.Arg774=) c.2232G>C (p.Arg744=) n.2793G>C n.383G>C | dbSNP |
1 | g.156881591G= | CA1148269761 | NTRK1 | c.2160G= (p.Arg720=) c.*932G= (n.*932G=) c.2340G= (p.Arg780=) c.399G= c.2331G= (p.Arg777=) c.2322G= (p.Arg774=) c.2232G= (p.Arg744=) n.2793G= n.383G= | |
1 | g.156881591G>T | CA421140672 | NTRK1 | c.2160G>T (p.Arg720=) c.*932G>T (n.*932G>T) c.2340G>T (p.Arg780=) c.399G>T c.2331G>T (p.Arg777=) c.2322G>T (p.Arg774=) c.2232G>T (p.Arg744=) n.2793G>T n.383G>T | |
1 | g.156881592C>A | CA342941735 | NTRK1 | c.2161C>A (p.Leu721Met) c.*933C>A (n.*933C>A) c.2341C>A (p.Leu781Met) c.400C>A c.2332C>A (p.Leu778Met) c.2323C>A (p.Leu775Met) c.2233C>A (p.Leu745Met) n.2794C>A n.384C>A | |
1 | g.156881592C>G | CA342941736 | NTRK1 | c.2161C>G (p.Leu721Val) c.*933C>G (n.*933C>G) c.2341C>G (p.Leu781Val) c.400C>G c.2332C>G (p.Leu778Val) c.2323C>G (p.Leu775Val) c.2233C>G (p.Leu745Val) n.2794C>G n.384C>G | dbSNP |
1 | g.156881592C>T | CA421140674 | NTRK1 | c.2161C>T (p.Leu721=) c.*933C>T (n.*933C>T) c.2341C>T (p.Leu781=) c.400C>T c.2332C>T (p.Leu778=) c.2323C>T (p.Leu775=) c.2233C>T (p.Leu745=) n.2794C>T n.384C>T | dbSNP gnomAD v4 COSMIC COSMIC |
1 | g.156881593T>A | CA342941737 | NTRK1 | c.2162T>A (p.Leu721Gln) c.*934T>A (n.*934T>A) c.2342T>A (p.Leu781Gln) c.401T>A c.2333T>A (p.Leu778Gln) c.2324T>A (p.Leu775Gln) c.2234T>A (p.Leu745Gln) n.2795T>A n.385T>A | dbSNP |
1 | g.156881593T>C | CA342941738 | NTRK1 | c.2162T>C (p.Leu721Pro) c.*934T>C (n.*934T>C) c.2342T>C (p.Leu781Pro) c.401T>C c.2333T>C (p.Leu778Pro) c.2324T>C (p.Leu775Pro) c.2234T>C (p.Leu745Pro) n.2795T>C n.385T>C | dbSNP |
1 | g.156881593T>G | CA342941739 | NTRK1 | c.2162T>G (p.Leu721Arg) c.*934T>G (n.*934T>G) c.2342T>G (p.Leu781Arg) c.401T>G c.2333T>G (p.Leu778Arg) c.2324T>G (p.Leu775Arg) c.2234T>G (p.Leu745Arg) n.2795T>G n.385T>G | dbSNP |
1 | g.156881594G>A | CA421140675 | NTRK1 | c.2163G>A (p.Leu721=) c.*935G>A (n.*935G>A) c.2343G>A (p.Leu781=) c.402G>A c.2334G>A (p.Leu778=) c.2325G>A (p.Leu775=) c.2235G>A (p.Leu745=) n.2796G>A n.386G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.156881594G>C | CA421140676 | NTRK1 | c.2163G>C (p.Leu721=) c.*935G>C (n.*935G>C) c.2343G>C (p.Leu781=) c.402G>C c.2334G>C (p.Leu778=) c.2325G>C (p.Leu775=) c.2235G>C (p.Leu745=) n.2796G>C n.386G>C | dbSNP |
1 | g.156881594G= | CA1200788942 | NTRK1 | c.2163G= (p.Leu721=) c.*935G= (n.*935G=) c.2343G= (p.Leu781=) c.402G= c.2334G= (p.Leu778=) c.2325G= (p.Leu775=) c.2235G= (p.Leu745=) n.2796G= n.386G= | |
1 | g.156881594G>T | CA421140677 | NTRK1 | c.2163G>T (p.Leu721=) c.*935G>T (n.*935G>T) c.2343G>T (p.Leu781=) c.402G>T c.2334G>T (p.Leu778=) c.2325G>T (p.Leu775=) c.2235G>T (p.Leu745=) n.2796G>T n.386G>T | |
1 | g.156881595C>A | CA342941740 | NTRK1 | c.2164C>A (p.Gln722Lys) c.*936C>A (n.*936C>A) c.2344C>A (p.Gln782Lys) c.403C>A c.2335C>A (p.Gln779Lys) c.2326C>A (p.Gln776Lys) c.2236C>A (p.Gln746Lys) n.2797C>A n.387C>A | dbSNP |
1 | g.156881595C= | CA1200788948 | NTRK1 | c.2164C= (p.Gln722=) c.*936C= (n.*936C=) c.2344C= (p.Gln782=) c.403C= c.2335C= (p.Gln779=) c.2326C= (p.Gln776=) c.2236C= (p.Gln746=) n.2797C= n.387C= | |
1 | g.156881595C>G | CA342941741 | NTRK1 | c.2164C>G (p.Gln722Glu) c.*936C>G (n.*936C>G) c.2344C>G (p.Gln782Glu) c.403C>G c.2335C>G (p.Gln779Glu) c.2326C>G (p.Gln776Glu) c.2236C>G (p.Gln746Glu) n.2797C>G n.387C>G | dbSNP |
1 | g.156881595C>T | CA342941742 | NTRK1 | c.2164C>T (p.Gln722Ter) c.*936C>T (n.*936C>T) c.2344C>T (p.Gln782Ter) c.403C>T c.2335C>T (p.Gln779Ter) c.2326C>T (p.Gln776Ter) c.2236C>T (p.Gln746Ter) n.2797C>T n.387C>T | ClinVar dbSNP gnomAD v4 |
1 | g.156881596A= | CA1200788952 | NTRK1 | c.2165A= (p.Gln722=) c.*937A= (n.*937A=) c.2345A= (p.Gln782=) c.404A= c.2336A= (p.Gln779=) c.2327A= (p.Gln776=) c.2237A= (p.Gln746=) n.2798A= n.388A= | |
1 | g.156881596A>C | CA342941743 | NTRK1 | c.2165A>C (p.Gln722Pro) c.*937A>C (n.*937A>C) c.2345A>C (p.Gln782Pro) c.404A>C c.2336A>C (p.Gln779Pro) c.2327A>C (p.Gln776Pro) c.2237A>C (p.Gln746Pro) n.2798A>C n.388A>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.156881596A>G | CA342941744 | NTRK1 | c.2165A>G (p.Gln722Arg) c.*937A>G (n.*937A>G) c.2345A>G (p.Gln782Arg) c.404A>G c.2336A>G (p.Gln779Arg) c.2327A>G (p.Gln776Arg) c.2237A>G (p.Gln746Arg) n.2798A>G n.388A>G | |
1 | g.156881596A>T | CA342941745 | NTRK1 | c.2165A>T (p.Gln722Leu) c.*937A>T (n.*937A>T) c.2345A>T (p.Gln782Leu) c.404A>T c.2336A>T (p.Gln779Leu) c.2327A>T (p.Gln776Leu) c.2237A>T (p.Gln746Leu) n.2798A>T n.388A>T | |
1 | g.156881597A>C | CA342941747 | NTRK1 | c.2166A>C (p.Gln722His) c.*938A>C (n.*938A>C) c.2346A>C (p.Gln782His) c.405A>C c.2337A>C (p.Gln779His) c.2328A>C (p.Gln776His) c.2238A>C (p.Gln746His) n.2799A>C n.389A>C | dbSNP |
1 | g.156881597A>G | CA421140678 | NTRK1 | c.2166A>G (p.Gln722=) c.*938A>G (n.*938A>G) c.2346A>G (p.Gln782=) c.405A>G c.2337A>G (p.Gln779=) c.2328A>G (p.Gln776=) c.2238A>G (p.Gln746=) n.2799A>G n.389A>G | dbSNP |