Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.156881581_156881609delinsTGCACGCCCGGCTGCAAGCCCTGGCCCAGCA1200788906NTRK1c.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
1g.156881586_156881613delCA891843047NTRK1c.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
1g.156881585C>ACA342941725NTRK1c.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
1g.156881585C=CA1143734134NTRK1c.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=
1g.156881585C>GCA342941726NTRK1c.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
1g.156881585C>TCA1169634NTRK1c.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
1g.156881586G>ACA1169635NTRK1c.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
1g.156881586G>CCA342941727NTRK1c.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
1g.156881586G=CA1144028342NTRK1c.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=
1g.156881586G>TCA342941729NTRK1c.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
1g.156881590_156881601delCA2648467752NTRK1c.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
1g.156881587C>ACA342941730NTRK1c.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
1g.156881587C=CA1200788924NTRK1c.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=
1g.156881587C>GCA342941731NTRK1c.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
1g.156881587C>TCA342941732NTRK1c.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
1g.156881588C>ACA421140670NTRK1c.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
1g.156881588C>GCA421140669NTRK1c.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
1g.156881588C>TCA421140668NTRK1c.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
1g.156881589C>ACA421140671NTRK1c.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
1g.156881589C=CA1145049910NTRK1c.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=
1g.156881589C>GCA342941733NTRK1c.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
1g.156881589C>TCA1169636NTRK1c.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
1g.156881590G>ACA1169637NTRK1c.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
1g.156881590G>CCA256268NTRK1c.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
1g.156881590G=CA1140584233NTRK1c.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=
1g.156881590G>TCA342941734NTRK1c.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
1g.156881591G>ACA1169638NTRK1c.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
1g.156881591G>CCA421140673NTRK1c.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
1g.156881591G=CA1148269761NTRK1c.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=
1g.156881591G>TCA421140672NTRK1c.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
1g.156881592C>ACA342941735NTRK1c.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
1g.156881592C>GCA342941736NTRK1c.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
1g.156881592C>TCA421140674NTRK1c.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
1g.156881593T>ACA342941737NTRK1c.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
1g.156881593T>CCA342941738NTRK1c.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
1g.156881593T>GCA342941739NTRK1c.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
1g.156881594G>ACA421140675NTRK1c.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
1g.156881594G>CCA421140676NTRK1c.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
1g.156881594G=CA1200788942NTRK1c.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=
1g.156881594G>TCA421140677NTRK1c.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
1g.156881595C>ACA342941740NTRK1c.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
1g.156881595C=CA1200788948NTRK1c.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=
1g.156881595C>GCA342941741NTRK1c.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
1g.156881595C>TCA342941742NTRK1c.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
1g.156881596A=CA1200788952NTRK1c.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=
1g.156881596A>CCA342941743NTRK1c.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
1g.156881596A>GCA342941744NTRK1c.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
1g.156881596A>TCA342941745NTRK1c.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
1g.156881597A>CCA342941747NTRK1c.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
1g.156881597A>GCA421140678NTRK1c.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

Number of alleles fetched