Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.156880011_156880038delCA2739275328NTRK1c.1879_1906del (p.Thr627ProfsTer?)
c.*651_*678del (n.*651_*678del)
c.2059_2086del (p.Thr687ProfsTer?)
c.27_54del
c.2050_2077del (p.Thr684ProfsTer?)
c.2041_2068del (p.Thr681ProfsTer?)
c.1951_1978del (p.Thr651ProfsTer?)
n.2512_2539del
n.11_38del
ClinVar
1g.156880019G>ACA16603452NTRK1c.1887G>A (p.Leu629=)
c.*659G>A (n.*659G>A)
c.2067G>A (p.Leu689=)
c.35G>A
c.2058G>A (p.Leu686=)
c.2049G>A (p.Leu683=)
c.1959G>A (p.Leu653=)
n.2520G>A
n.19G>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.156880019G>CCA421140441NTRK1c.1887G>C (p.Leu629=)
c.*659G>C (n.*659G>C)
c.2067G>C (p.Leu689=)
c.35G>C
c.2058G>C (p.Leu686=)
c.2049G>C (p.Leu683=)
c.1959G>C (p.Leu653=)
n.2520G>C
n.19G>C
dbSNP
1g.156880019G=CA1200784374NTRK1c.1887G= (p.Leu629=)
c.*659G= (n.*659G=)
c.2067G= (p.Leu689=)
c.35G=
c.2058G= (p.Leu686=)
c.2049G= (p.Leu683=)
c.1959G= (p.Leu653=)
n.2520G=
n.19G=
1g.156880019G>TCA421140442NTRK1c.1887G>T (p.Leu629=)
c.*659G>T (n.*659G>T)
c.2067G>T (p.Leu689=)
c.35G>T
c.2058G>T (p.Leu686=)
c.2049G>T (p.Leu683=)
c.1959G>T (p.Leu653=)
n.2520G>T
n.19G>T
gnomAD v4
1g.156880020C>ACA342940255NTRK1c.1888C>A (p.Pro630Thr)
c.*660C>A (n.*660C>A)
c.2068C>A (p.Pro690Thr)
c.36C>A
c.2059C>A (p.Pro687Thr)
c.2050C>A (p.Pro684Thr)
c.1960C>A (p.Pro654Thr)
n.2521C>A
n.20C>A
dbSNP
1g.156880020C=CA1200784379NTRK1c.1888C= (p.Pro630=)
c.*660C= (n.*660C=)
c.2068C= (p.Pro690=)
c.36C=
c.2059C= (p.Pro687=)
c.2050C= (p.Pro684=)
c.1960C= (p.Pro654=)
n.2521C=
n.20C=
1g.156880020C>GCA342940257NTRK1c.1888C>G (p.Pro630Ala)
c.*660C>G (n.*660C>G)
c.2068C>G (p.Pro690Ala)
c.36C>G
c.2059C>G (p.Pro687Ala)
c.2050C>G (p.Pro684Ala)
c.1960C>G (p.Pro654Ala)
n.2521C>G
n.20C>G
dbSNP
1g.156880020C>TCA342940256NTRK1c.1888C>T (p.Pro630Ser)
c.*660C>T (n.*660C>T)
c.2068C>T (p.Pro690Ser)
c.36C>T
c.2059C>T (p.Pro687Ser)
c.2050C>T (p.Pro684Ser)
c.1960C>T (p.Pro654Ser)
n.2521C>T
n.20C>T
ClinVar dbSNP gnomAD v4
1g.156880021C>ACA342940258NTRK1c.1889C>A (p.Pro630His)
c.*661C>A (n.*661C>A)
c.2069C>A (p.Pro690His)
c.37C>A
c.2060C>A (p.Pro687His)
c.2051C>A (p.Pro684His)
c.1961C>A (p.Pro654His)
n.2522C>A
n.21C>A
dbSNP
1g.156880021C>GCA342940259NTRK1c.1889C>G (p.Pro630Arg)
c.*661C>G (n.*661C>G)
c.2069C>G (p.Pro690Arg)
c.37C>G
c.2060C>G (p.Pro687Arg)
c.2051C>G (p.Pro684Arg)
c.1961C>G (p.Pro654Arg)
n.2522C>G
n.21C>G
dbSNP
1g.156880021C>TCA342940260NTRK1c.1889C>T (p.Pro630Leu)
c.*661C>T (n.*661C>T)
c.2069C>T (p.Pro690Leu)
c.37C>T
c.2060C>T (p.Pro687Leu)
c.2051C>T (p.Pro684Leu)
c.1961C>T (p.Pro654Leu)
n.2522C>T
n.21C>T
dbSNP
1g.156880021_156880022delinsTTCA645518204NTRK1c.1889_1890delinsTT (p.Pro630Leu)
c.*661_*662delinsTT (n.*661_*662delinsTT)
c.2069_2070delinsTT (p.Pro690Leu)
c.37_38delinsTT
c.2060_2061delinsTT (p.Pro687Leu)
c.2051_2052delinsTT (p.Pro684Leu)
c.1961_1962delinsTT (p.Pro654Leu)
n.2522_2523delinsTT
n.21_22delinsTT
COSMIC COSMIC
1g.156880022C>ACA421140444NTRK1c.1890C>A (p.Pro630=)
c.*662C>A (n.*662C>A)
c.2070C>A (p.Pro690=)
c.38C>A
c.2061C>A (p.Pro687=)
c.2052C>A (p.Pro684=)
c.1962C>A (p.Pro654=)
n.2523C>A
n.22C>A
dbSNP
1g.156880022C=CA1140628665NTRK1c.1890C= (p.Pro630=)
c.*662C= (n.*662C=)
c.2070C= (p.Pro690=)
c.38C=
c.2061C= (p.Pro687=)
c.2052C= (p.Pro684=)
c.1962C= (p.Pro654=)
n.2523C=
n.22C=
1g.156880022C>GCA1169560NTRK1c.1890C>G (p.Pro630=)
c.*662C>G (n.*662C>G)
c.2070C>G (p.Pro690=)
c.38C>G
c.2061C>G (p.Pro687=)
c.2052C>G (p.Pro684=)
c.1962C>G (p.Pro654=)
n.2523C>G
n.22C>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.156880022C>TCA31124424NTRK1c.1890C>T (p.Pro630=)
c.*662C>T (n.*662C>T)
c.2070C>T (p.Pro690=)
c.38C>T
c.2061C>T (p.Pro687=)
c.2052C>T (p.Pro684=)
c.1962C>T (p.Pro654=)
n.2523C>T
n.22C>T
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.156880023A=CA1200784385NTRK1c.1891A= (p.Ile631=)
c.*663A= (n.*663A=)
c.2071A= (p.Ile691=)
c.39A=
c.2062A= (p.Ile688=)
c.2053A= (p.Ile685=)
c.1963A= (p.Ile655=)
n.2524A=
n.23A=
1g.156880023A>CCA342940261NTRK1c.1891A>C (p.Ile631Leu)
c.*663A>C (n.*663A>C)
c.2071A>C (p.Ile691Leu)
c.39A>C
c.2062A>C (p.Ile688Leu)
c.2053A>C (p.Ile685Leu)
c.1963A>C (p.Ile655Leu)
n.2524A>C
n.23A>C
dbSNP
1g.156880023A>GCA342940262NTRK1c.1891A>G (p.Ile631Val)
c.*663A>G (n.*663A>G)
c.2071A>G (p.Ile691Val)
c.39A>G
c.2062A>G (p.Ile688Val)
c.2053A>G (p.Ile685Val)
c.1963A>G (p.Ile655Val)
n.2524A>G
n.23A>G
dbSNP
1g.156880023A>TCA342940263NTRK1c.1891A>T (p.Ile631Phe)
c.*663A>T (n.*663A>T)
c.2071A>T (p.Ile691Phe)
c.39A>T
c.2062A>T (p.Ile688Phe)
c.2053A>T (p.Ile685Phe)
c.1963A>T (p.Ile655Phe)
n.2524A>T
n.23A>T
dbSNP
1g.156880024T>ACA342940266NTRK1c.1892T>A (p.Ile631Asn)
c.*664T>A (n.*664T>A)
c.2072T>A (p.Ile691Asn)
c.40T>A
c.2063T>A (p.Ile688Asn)
c.2054T>A (p.Ile685Asn)
c.1964T>A (p.Ile655Asn)
n.2525T>A
n.24T>A
1g.156880024T>CCA342940268NTRK1c.1892T>C (p.Ile631Thr)
c.*664T>C (n.*664T>C)
c.2072T>C (p.Ile691Thr)
c.40T>C
c.2063T>C (p.Ile688Thr)
c.2054T>C (p.Ile685Thr)
c.1964T>C (p.Ile655Thr)
n.2525T>C
n.24T>C
gnomAD v4
1g.156880024T>GCA342940269NTRK1c.1892T>G (p.Ile631Ser)
c.*664T>G (n.*664T>G)
c.2072T>G (p.Ile691Ser)
c.40T>G
c.2063T>G (p.Ile688Ser)
c.2054T>G (p.Ile685Ser)
c.1964T>G (p.Ile655Ser)
n.2525T>G
n.24T>G
1g.156880025T>ACA421140445NTRK1c.1893T>A (p.Ile631=)
c.*665T>A (n.*665T>A)
c.2073T>A (p.Ile691=)
c.41T>A
c.2064T>A (p.Ile688=)
c.2055T>A (p.Ile685=)
c.1965T>A (p.Ile655=)
n.2526T>A
n.25T>A
1g.156880025T>CCA421140446NTRK1c.1893T>C (p.Ile631=)
c.*665T>C (n.*665T>C)
c.2073T>C (p.Ile691=)
c.41T>C
c.2064T>C (p.Ile688=)
c.2055T>C (p.Ile685=)
c.1965T>C (p.Ile655=)
n.2526T>C
n.25T>C
1g.156880025T>GCA342940271NTRK1c.1893T>G (p.Ile631Met)
c.*665T>G (n.*665T>G)
c.2073T>G (p.Ile691Met)
c.41T>G
c.2064T>G (p.Ile688Met)
c.2055T>G (p.Ile685Met)
c.1965T>G (p.Ile655Met)
n.2526T>G
n.25T>G
1g.156880026C>ACA342940273NTRK1c.1894C>A (p.Arg632Ser)
c.*666C>A (n.*666C>A)
c.2074C>A (p.Arg692Ser)
c.42C>A
c.2065C>A (p.Arg689Ser)
c.2056C>A (p.Arg686Ser)
c.1966C>A (p.Arg656Ser)
n.2527C>A
n.26C>A
gnomAD v4
1g.156880026C=CA1200784386NTRK1c.1894C= (p.Arg632=)
c.*666C= (n.*666C=)
c.2074C= (p.Arg692=)
c.42C=
c.2065C= (p.Arg689=)
c.2056C= (p.Arg686=)
c.1966C= (p.Arg656=)
n.2527C=
n.26C=
1g.156880026C>GCA342940272NTRK1c.1894C>G (p.Arg632Gly)
c.*666C>G (n.*666C>G)
c.2074C>G (p.Arg692Gly)
c.42C>G
c.2065C>G (p.Arg689Gly)
c.2056C>G (p.Arg686Gly)
c.1966C>G (p.Arg656Gly)
n.2527C>G
n.26C>G
dbSNP gnomAD v4
1g.156880026C>TCA1169561NTRK1c.1894C>T (p.Arg632Cys)
c.*666C>T (n.*666C>T)
c.2074C>T (p.Arg692Cys)
c.42C>T
c.2065C>T (p.Arg689Cys)
c.2056C>T (p.Arg686Cys)
c.1966C>T (p.Arg656Cys)
n.2527C>T
n.26C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
1g.156880027G>ACA1169562NTRK1c.1895G>A (p.Arg632His)
c.*667G>A (n.*667G>A)
c.2075G>A (p.Arg692His)
c.43G>A
c.2066G>A (p.Arg689His)
c.2057G>A (p.Arg686His)
c.1967G>A (p.Arg656His)
n.2528G>A
n.27G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC
1g.156880027G>CCA342940274NTRK1c.1895G>C (p.Arg632Pro)
c.*667G>C (n.*667G>C)
c.2075G>C (p.Arg692Pro)
c.43G>C
c.2066G>C (p.Arg689Pro)
c.2057G>C (p.Arg686Pro)
c.1967G>C (p.Arg656Pro)
n.2528G>C
n.27G>C
dbSNP gnomAD v4
1g.156880027G=CA1200784390NTRK1c.1895G= (p.Arg632=)
c.*667G= (n.*667G=)
c.2075G= (p.Arg692=)
c.43G=
c.2066G= (p.Arg689=)
c.2057G= (p.Arg686=)
c.1967G= (p.Arg656=)
n.2528G=
n.27G=
1g.156880027G>TCA342940276NTRK1c.1895G>T (p.Arg632Leu)
c.*667G>T (n.*667G>T)
c.2075G>T (p.Arg692Leu)
c.43G>T
c.2066G>T (p.Arg689Leu)
c.2057G>T (p.Arg686Leu)
c.1967G>T (p.Arg656Leu)
n.2528G>T
n.27G>T
dbSNP gnomAD v4
1g.156880028C>ACA421140447NTRK1c.1896C>A (p.Arg632=)
c.*668C>A (n.*668C>A)
c.2076C>A (p.Arg692=)
c.44C>A
c.2067C>A (p.Arg689=)
c.2058C>A (p.Arg686=)
c.1968C>A (p.Arg656=)
n.2529C>A
n.28C>A
1g.156880028C>GCA421140448NTRK1c.1896C>G (p.Arg632=)
c.*668C>G (n.*668C>G)
c.2076C>G (p.Arg692=)
c.44C>G
c.2067C>G (p.Arg689=)
c.2058C>G (p.Arg686=)
c.1968C>G (p.Arg656=)
n.2529C>G
n.28C>G
dbSNP
1g.156880028C>TCA421140449NTRK1c.1896C>T (p.Arg632=)
c.*668C>T (n.*668C>T)
c.2076C>T (p.Arg692=)
c.44C>T
c.2067C>T (p.Arg689=)
c.2058C>T (p.Arg686=)
c.1968C>T (p.Arg656=)
n.2529C>T
n.28C>T
ClinVar dbSNP
1g.156880029T>ACA342940277NTRK1c.1897T>A (p.Trp633Arg)
c.*669T>A (n.*669T>A)
c.2077T>A (p.Trp693Arg)
c.45T>A
c.2068T>A (p.Trp690Arg)
c.2059T>A (p.Trp687Arg)
c.1969T>A (p.Trp657Arg)
n.2530T>A
n.29T>A
1g.156880029T>CCA342940279NTRK1c.1897T>C (p.Trp633Arg)
c.*669T>C (n.*669T>C)
c.2077T>C (p.Trp693Arg)
c.45T>C
c.2068T>C (p.Trp690Arg)
c.2059T>C (p.Trp687Arg)
c.1969T>C (p.Trp657Arg)
n.2530T>C
n.29T>C
1g.156880029T>GCA342940280NTRK1c.1897T>G (p.Trp633Gly)
c.*669T>G (n.*669T>G)
c.2077T>G (p.Trp693Gly)
c.45T>G
c.2068T>G (p.Trp690Gly)
c.2059T>G (p.Trp687Gly)
c.1969T>G (p.Trp657Gly)
n.2530T>G
n.29T>G
1g.156880030G>ACA342940282NTRK1c.1898G>A (p.Trp633Ter)
c.*670G>A (n.*670G>A)
c.2078G>A (p.Trp693Ter)
c.46G>A
c.2069G>A (p.Trp690Ter)
c.2060G>A (p.Trp687Ter)
c.1970G>A (p.Trp657Ter)
n.2531G>A
n.30G>A
ClinVar dbSNP
1g.156880030G>CCA342940283NTRK1c.1898G>C (p.Trp633Ser)
c.*670G>C (n.*670G>C)
c.2078G>C (p.Trp693Ser)
c.46G>C
c.2069G>C (p.Trp690Ser)
c.2060G>C (p.Trp687Ser)
c.1970G>C (p.Trp657Ser)
n.2531G>C
n.30G>C
dbSNP
1g.156880030G=CA1200784392NTRK1c.1898G= (p.Trp633=)
c.*670G= (n.*670G=)
c.2078G= (p.Trp693=)
c.46G=
c.2069G= (p.Trp690=)
c.2060G= (p.Trp687=)
c.1970G= (p.Trp657=)
n.2531G=
n.30G=
1g.156880030G>TCA342940285NTRK1c.1898G>T (p.Trp633Leu)
c.*670G>T (n.*670G>T)
c.2078G>T (p.Trp693Leu)
c.46G>T
c.2069G>T (p.Trp690Leu)
c.2060G>T (p.Trp687Leu)
c.1970G>T (p.Trp657Leu)
n.2531G>T
n.30G>T
1g.156880031G>ACA342940286NTRK1c.1899G>A (p.Trp633Ter)
c.*671G>A (n.*671G>A)
c.2079G>A (p.Trp693Ter)
c.47G>A
c.2070G>A (p.Trp690Ter)
c.2061G>A (p.Trp687Ter)
c.1971G>A (p.Trp657Ter)
n.2532G>A
n.31G>A
dbSNP COSMIC COSMIC
1g.156880031G>CCA342940287NTRK1c.1899G>C (p.Trp633Cys)
c.*671G>C (n.*671G>C)
c.2079G>C (p.Trp693Cys)
c.47G>C
c.2070G>C (p.Trp690Cys)
c.2061G>C (p.Trp687Cys)
c.1971G>C (p.Trp657Cys)
n.2532G>C
n.31G>C
dbSNP
1g.156880031G>TCA342940288NTRK1c.1899G>T (p.Trp633Cys)
c.*671G>T (n.*671G>T)
c.2079G>T (p.Trp693Cys)
c.47G>T
c.2070G>T (p.Trp690Cys)
c.2061G>T (p.Trp687Cys)
c.1971G>T (p.Trp657Cys)
n.2532G>T
n.31G>T
1g.156880032A>CCA342940291NTRK1c.1900A>C (p.Met634Leu)
c.*672A>C (n.*672A>C)
c.2080A>C (p.Met694Leu)
c.48A>C
c.2071A>C (p.Met691Leu)
c.2062A>C (p.Met688Leu)
c.1972A>C (p.Met658Leu)
n.2533A>C
n.32A>C
dbSNP
1g.156880032A>GCA342940290NTRK1c.1900A>G (p.Met634Val)
c.*672A>G (n.*672A>G)
c.2080A>G (p.Met694Val)
c.48A>G
c.2071A>G (p.Met691Val)
c.2062A>G (p.Met688Val)
c.1972A>G (p.Met658Val)
n.2533A>G
n.32A>G

Number of alleles fetched