Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.7166172C>A | CA403666215 | INSR | c.1843G>T (p.Val615Phe) n.1818G>T c.244G>T (p.Val82Phe) c.1921G>T (p.Val641Phe) | |
19 | g.7166172C= | CA2320788218 | INSR | c.1843G= (p.Val615=) n.1818G= c.244G= (p.Val82=) c.1921G= (p.Val641=) | |
19 | g.7166172C>G | CA403666214 | INSR | c.1843G>C (p.Val615Leu) n.1818G>C c.244G>C (p.Val82Leu) c.1921G>C (p.Val641Leu) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.7166172C>T | CA403666213 | INSR | c.1843G>A (p.Val615Ile) n.1818G>A c.244G>A (p.Val82Ile) c.1921G>A (p.Val641Ile) | ClinVar dbSNP |
19 | g.7166173A>C | CA403666216 | INSR | c.1842T>G (p.Tyr614Ter) n.1817T>G c.243T>G (p.Tyr81Ter) c.1920T>G (p.Tyr640Ter) | |
19 | g.7166173A>G | CA505199016 | INSR | c.1842T>C (p.Tyr614=) n.1817T>C c.243T>C (p.Tyr81=) c.1920T>C (p.Tyr640=) | |
19 | g.7166173A>T | CA403666217 | INSR | c.1842T>A (p.Tyr614Ter) n.1817T>A c.243T>A (p.Tyr81Ter) c.1920T>A (p.Tyr640Ter) | |
19 | g.7166174T>A | CA403666218 | INSR | c.1841A>T (p.Tyr614Phe) n.1816A>T c.242A>T (p.Tyr81Phe) c.1919A>T (p.Tyr640Phe) | |
19 | g.7166174T>C | CA403666219 | INSR | c.1841A>G (p.Tyr614Cys) n.1816A>G c.242A>G (p.Tyr81Cys) c.1919A>G (p.Tyr640Cys) | |
19 | g.7166174T>G | CA403666220 | INSR | c.1841A>C (p.Tyr614Ser) n.1816A>C c.242A>C (p.Tyr81Ser) c.1919A>C (p.Tyr640Ser) | |
19 | g.7166175A>C | CA403666221 | INSR | c.1840T>G (p.Tyr614Asp) n.1815T>G c.241T>G (p.Tyr81Asp) c.1918T>G (p.Tyr640Asp) | |
19 | g.7166175A>G | CA403666222 | INSR | c.1840T>C (p.Tyr614His) n.1815T>C c.241T>C (p.Tyr81His) c.1918T>C (p.Tyr640His) | |
19 | g.7166175A>T | CA403666223 | INSR | c.1840T>A (p.Tyr614Asn) n.1815T>A c.241T>A (p.Tyr81Asn) c.1918T>A (p.Tyr640Asn) | |
19 | g.7166176A>C | CA403666224 | INSR | c.1839T>G (p.Ile613Met) n.1814T>G c.240T>G (p.Ile80Met) c.1917T>G (p.Ile639Met) | gnomAD v4 |
19 | g.7166176A>G | CA505199024 | INSR | c.1839T>C (p.Ile613=) n.1814T>C c.240T>C (p.Ile80=) c.1917T>C (p.Ile639=) | |
19 | g.7166176A>T | CA505199025 | INSR | c.1839T>A (p.Ile613=) n.1814T>A c.240T>A (p.Ile80=) c.1917T>A (p.Ile639=) | |
19 | g.7166177A>C | CA403666225 | INSR | c.1838T>G (p.Ile613Ser) n.1813T>G c.239T>G (p.Ile80Ser) c.1916T>G (p.Ile639Ser) | |
19 | g.7166177A>G | CA403666226 | INSR | c.1838T>C (p.Ile613Thr) n.1813T>C c.239T>C (p.Ile80Thr) c.1916T>C (p.Ile639Thr) | |
19 | g.7166177A>T | CA403666227 | INSR | c.1838T>A (p.Ile613Asn) n.1813T>A c.239T>A (p.Ile80Asn) c.1916T>A (p.Ile639Asn) | gnomAD v4 |
19 | g.7166178T>A | CA403666230 | INSR | c.1837A>T (p.Ile613Phe) n.1812A>T c.238A>T (p.Ile80Phe) c.1915A>T (p.Ile639Phe) | |
19 | g.7166178T>C | CA403666229 | INSR | c.1837A>G (p.Ile613Val) n.1812A>G c.238A>G (p.Ile80Val) c.1915A>G (p.Ile639Val) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.7166178T>G | CA403666228 | INSR | c.1837A>C (p.Ile613Leu) n.1812A>C c.238A>C (p.Ile80Leu) c.1915A>C (p.Ile639Leu) | |
19 | g.7166178T= | CA2320788219 | INSR | c.1837A= (p.Ile613=) n.1812A= c.238A= (p.Ile80=) c.1915A= (p.Ile639=) | |
19 | g.7166179G>A | CA505199032 | INSR | c.1836C>T (p.Ile612=) n.1811C>T c.237C>T (p.Ile79=) c.1914C>T (p.Ile638=) | |
19 | g.7166179G>C | CA403666231 | INSR | c.1836C>G (p.Ile612Met) n.1811C>G c.237C>G (p.Ile79Met) c.1914C>G (p.Ile638Met) | |
19 | g.7166179G>T | CA505199031 | INSR | c.1836C>A (p.Ile612=) n.1811C>A c.237C>A (p.Ile79=) c.1914C>A (p.Ile638=) | |
19 | g.7166180A>C | CA403666232 | INSR | c.1835T>G (p.Ile612Ser) n.1810T>G c.236T>G (p.Ile79Ser) c.1913T>G (p.Ile638Ser) | |
19 | g.7166180A>G | CA403666233 | INSR | c.1835T>C (p.Ile612Thr) n.1810T>C c.236T>C (p.Ile79Thr) c.1913T>C (p.Ile638Thr) | |
19 | g.7166180A>T | CA403666234 | INSR | c.1835T>A (p.Ile612Asn) n.1810T>A c.236T>A (p.Ile79Asn) c.1913T>A (p.Ile638Asn) | |
19 | g.7166181T>A | CA403666235 | INSR | c.1834A>T (p.Ile612Phe) n.1809A>T c.235A>T (p.Ile79Phe) c.1912A>T (p.Ile638Phe) | |
19 | g.7166181T>C | CA403666236 | INSR | c.1834A>G (p.Ile612Val) n.1809A>G c.235A>G (p.Ile79Val) c.1912A>G (p.Ile638Val) | |
19 | g.7166181T>G | CA403666237 | INSR | c.1834A>C (p.Ile612Leu) n.1809A>C c.235A>C (p.Ile79Leu) c.1912A>C (p.Ile638Leu) | |
19 | g.7166182G>A | CA505199038 | INSR | c.1833C>T (p.Asp611=) n.1808C>T c.234C>T (p.Asp78=) c.1911C>T (p.Asp637=) | |
19 | g.7166182G>C | CA403666238 | INSR | c.1833C>G (p.Asp611Glu) n.1808C>G c.234C>G (p.Asp78Glu) c.1911C>G (p.Asp637Glu) | |
19 | g.7166182G>T | CA403666239 | INSR | c.1833C>A (p.Asp611Glu) n.1808C>A c.234C>A (p.Asp78Glu) c.1911C>A (p.Asp637Glu) | |
19 | g.7166183T>A | CA403666240 | INSR | c.1832A>T (p.Asp611Val) n.1807A>T c.233A>T (p.Asp78Val) c.1910A>T (p.Asp637Val) | |
19 | g.7166183T>C | CA403666241 | INSR | c.1832A>G (p.Asp611Gly) n.1807A>G c.233A>G (p.Asp78Gly) c.1910A>G (p.Asp637Gly) | gnomAD v4 |
19 | g.7166183T>G | CA403666242 | INSR | c.1832A>C (p.Asp611Ala) n.1807A>C c.233A>C (p.Asp78Ala) c.1910A>C (p.Asp637Ala) | |
19 | g.7166184C>A | CA403666245 | INSR | c.1831G>T (p.Asp611Tyr) n.1806G>T c.232G>T (p.Asp78Tyr) c.1909G>T (p.Asp637Tyr) | gnomAD v4 |
19 | g.7166184C= | CA2320788220 | INSR | c.1831G= (p.Asp611=) n.1806G= c.232G= (p.Asp78=) c.1909G= (p.Asp637=) | |
19 | g.7166184C>G | CA403666244 | INSR | c.1831G>C (p.Asp611His) n.1806G>C c.232G>C (p.Asp78His) c.1909G>C (p.Asp637His) | |
19 | g.7166184C>T | CA403666243 | INSR | c.1831G>A (p.Asp611Asn) n.1806G>A c.232G>A (p.Asp78Asn) c.1909G>A (p.Asp637Asn) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7166185A>C | CA403666246 | INSR | c.1830T>G (p.Ser610Arg) n.1805T>G c.231T>G (p.Ser77Arg) c.1908T>G (p.Ser636Arg) | |
19 | g.7166185A>G | CA505199046 | INSR | c.1830T>C (p.Ser610=) n.1805T>C c.231T>C (p.Ser77=) c.1908T>C (p.Ser636=) | gnomAD v4 |
19 | g.7166185A>T | CA403666247 | INSR | c.1830T>A (p.Ser610Arg) n.1805T>A c.231T>A (p.Ser77Arg) c.1908T>A (p.Ser636Arg) | |
19 | g.7166186C>A | CA403666248 | INSR | c.1829G>T (p.Ser610Ile) n.1804G>T c.230G>T (p.Ser77Ile) c.1907G>T (p.Ser636Ile) | |
19 | g.7166186C= | CA2320788221 | INSR | c.1829G= (p.Ser610=) n.1804G= c.230G= (p.Ser77=) c.1907G= (p.Ser636=) | |
19 | g.7166186C>G | CA403666249 | INSR | c.1829G>C (p.Ser610Thr) n.1804G>C c.230G>C (p.Ser77Thr) c.1907G>C (p.Ser636Thr) | |
19 | g.7166186C>T | CA9135748 | INSR | c.1829G>A (p.Ser610Asn) n.1804G>A c.230G>A (p.Ser77Asn) c.1907G>A (p.Ser636Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.7166187T>A | CA403666250 | INSR | c.1828A>T (p.Ser610Cys) n.1803A>T c.229A>T (p.Ser77Cys) c.1906A>T (p.Ser636Cys) | |
19 | g.7166187T>C | CA403666251 | INSR | c.1828A>G (p.Ser610Gly) n.1803A>G c.229A>G (p.Ser77Gly) c.1906A>G (p.Ser636Gly) | |
19 | g.7166187T>G | CA403666252 | INSR | c.1828A>C (p.Ser610Arg) n.1803A>C c.229A>C (p.Ser77Arg) c.1906A>C (p.Ser636Arg) | |
19 | g.7166188C>A | CA403666253 | INSR | c.1827G>T (p.Lys609Asn) n.1802G>T c.228G>T (p.Lys76Asn) c.1905G>T (p.Lys635Asn) | |
19 | g.7166188C= | CA2320788222 | INSR | c.1827G= (p.Lys609=) n.1802G= c.228G= (p.Lys76=) c.1905G= (p.Lys635=) | |
19 | g.7166188C>G | CA403666254 | INSR | c.1827G>C (p.Lys609Asn) n.1802G>C c.228G>C (p.Lys76Asn) c.1905G>C (p.Lys635Asn) | |
19 | g.7166188C>T | CA505199054 | INSR | c.1827G>A (p.Lys609=) n.1802G>A c.228G>A (p.Lys76=) c.1905G>A (p.Lys635=) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.7166189T>A | CA403666255 | INSR | c.1826A>T (p.Lys609Met) n.1801A>T c.227A>T (p.Lys76Met) c.1904A>T (p.Lys635Met) | |
19 | g.7166189T>C | CA403666256 | INSR | c.1826A>G (p.Lys609Arg) n.1801A>G c.227A>G (p.Lys76Arg) c.1904A>G (p.Lys635Arg) | |
19 | g.7166189T>G | CA403666257 | INSR | c.1826A>C (p.Lys609Thr) n.1801A>C c.227A>C (p.Lys76Thr) c.1904A>C (p.Lys635Thr) | |
19 | g.7166190T>A | CA403666260 | INSR | c.1825A>T (p.Lys609Ter) n.1800A>T c.226A>T (p.Lys76Ter) c.1903A>T (p.Lys635Ter) | |
19 | g.7166190T>C | CA403666259 | INSR | c.1825A>G (p.Lys609Glu) n.1800A>G c.226A>G (p.Lys76Glu) c.1903A>G (p.Lys635Glu) | |
19 | g.7166190T>G | CA403666258 | INSR | c.1825A>C (p.Lys609Gln) n.1800A>C c.226A>C (p.Lys76Gln) c.1903A>C (p.Lys635Gln) | |
19 | g.7166191G>A | CA505199058 | INSR | c.1824C>T (p.Ala608=) n.1799C>T c.225C>T (p.Ala75=) c.1902C>T (p.Ala634=) | dbSNP |
19 | g.7166191G>C | CA505199060 | INSR | c.1824C>G (p.Ala608=) n.1799C>G c.225C>G (p.Ala75=) c.1902C>G (p.Ala634=) | |
19 | g.7166191G>T | CA505199061 | INSR | c.1824C>A (p.Ala608=) n.1799C>A c.225C>A (p.Ala75=) c.1902C>A (p.Ala634=) | |
19 | g.7166192G>A | CA9135749 | INSR | c.1823C>T (p.Ala608Val) n.1798C>T c.224C>T (p.Ala75Val) c.1901C>T (p.Ala634Val) | dbSNP ExAC gnomAD v2 |
19 | g.7166192G>C | CA403666261 | INSR | c.1823C>G (p.Ala608Gly) n.1798C>G c.224C>G (p.Ala75Gly) c.1901C>G (p.Ala634Gly) | |
19 | g.7166192G= | CA2320788223 | INSR | c.1823C= (p.Ala608=) n.1798C= c.224C= (p.Ala75=) c.1901C= (p.Ala634=) | |
19 | g.7166192G>T | CA403666262 | INSR | c.1823C>A (p.Ala608Asp) n.1798C>A c.224C>A (p.Ala75Asp) c.1901C>A (p.Ala634Asp) | |
19 | g.7166193C>A | CA403666263 | INSR | c.1822G>T (p.Ala608Ser) n.1797G>T c.223G>T (p.Ala75Ser) c.1900G>T (p.Ala634Ser) | |
19 | g.7166193C= | CA2320788224 | INSR | c.1822G= (p.Ala608=) n.1797G= c.223G= (p.Ala75=) c.1900G= (p.Ala634=) | |
19 | g.7166193C>G | CA403666264 | INSR | c.1822G>C (p.Ala608Pro) n.1797G>C c.223G>C (p.Ala75Pro) c.1900G>C (p.Ala634Pro) | |
19 | g.7166193C>T | CA9135750 | INSR | c.1822G>A (p.Ala608Thr) n.1797G>A c.223G>A (p.Ala75Thr) c.1900G>A (p.Ala634Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.7166196dup | CA2839155200 | INSR | c.1822dup (p.Ala608GlyfsTer4) n.1797dup c.223dup (p.Ala75GlyfsTer4) c.1900dup (p.Ala634GlyfsTer4) | |
19 | g.7166194C>A | CA505199067 | INSR | c.1821G>T (p.Gly607=) n.1796G>T c.222G>T (p.Gly74=) c.1899G>T (p.Gly633=) | |
19 | g.7166194C>G | CA505199065 | INSR | c.1821G>C (p.Gly607=) n.1796G>C c.222G>C (p.Gly74=) c.1899G>C (p.Gly633=) | gnomAD v4 |
19 | g.7166194C>T | CA505199066 | INSR | c.1821G>A (p.Gly607=) n.1796G>A c.222G>A (p.Gly74=) c.1899G>A (p.Gly633=) | |
19 | g.7166195C>A | CA403666265 | INSR | c.1820G>T (p.Gly607Val) n.1795G>T c.221G>T (p.Gly74Val) c.1898G>T (p.Gly633Val) | gnomAD v4 |
19 | g.7166195C>G | CA403666266 | INSR | c.1820G>C (p.Gly607Ala) n.1795G>C c.221G>C (p.Gly74Ala) c.1898G>C (p.Gly633Ala) | |
19 | g.7166195C>T | CA403666267 | INSR | c.1820G>A (p.Gly607Glu) n.1795G>A c.221G>A (p.Gly74Glu) c.1898G>A (p.Gly633Glu) | |
19 | g.7166196C>A | CA403666268 | INSR | c.1819G>T (p.Gly607Trp) n.1794G>T c.220G>T (p.Gly74Trp) c.1897G>T (p.Gly633Trp) | |
19 | g.7166196C>G | CA403666269 | INSR | c.1819G>C (p.Gly607Arg) n.1794G>C c.220G>C (p.Gly74Arg) c.1897G>C (p.Gly633Arg) | |
19 | g.7166196C>T | CA403666270 | INSR | c.1819G>A (p.Gly607Arg) n.1794G>A c.220G>A (p.Gly74Arg) c.1897G>A (p.Gly633Arg) | COSMIC COSMIC |
19 | g.7166197A= | CA2320788225 | INSR | c.1818T= (p.Tyr606=) n.1793T= c.219T= (p.Tyr73=) c.1896T= (p.Tyr632=) | |
19 | g.7166197A>C | CA403666271 | INSR | c.1818T>G (p.Tyr606Ter) n.1793T>G c.219T>G (p.Tyr73Ter) c.1896T>G (p.Tyr632Ter) | |
19 | g.7166197A>G | CA304856187 | INSR | c.1818T>C (p.Tyr606=) n.1793T>C c.219T>C (p.Tyr73=) c.1896T>C (p.Tyr632=) | dbSNP gnomAD v4 |
19 | g.7166197A>T | CA403666272 | INSR | c.1818T>A (p.Tyr606Ter) n.1793T>A c.219T>A (p.Tyr73Ter) c.1896T>A (p.Tyr632Ter) | |
19 | g.7166198T>A | CA403666275 | INSR | c.1817A>T (p.Tyr606Phe) n.1792A>T c.218A>T (p.Tyr73Phe) c.1895A>T (p.Tyr632Phe) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.7166198T>C | CA403666274 | INSR | c.1817A>G (p.Tyr606Cys) n.1792A>G c.218A>G (p.Tyr73Cys) c.1895A>G (p.Tyr632Cys) | gnomAD v4 |
19 | g.7166198T>G | CA403666273 | INSR | c.1817A>C (p.Tyr606Ser) n.1792A>C c.218A>C (p.Tyr73Ser) c.1895A>C (p.Tyr632Ser) | |
19 | g.7166198T= | CA2320788226 | INSR | c.1817A= (p.Tyr606=) n.1792A= c.218A= (p.Tyr73=) c.1895A= (p.Tyr632=) | |
19 | g.7166199A>C | CA403666276 | INSR | c.1816T>G (p.Tyr606Asp) n.1791T>G c.217T>G (p.Tyr73Asp) c.1894T>G (p.Tyr632Asp) | |
19 | g.7166199A>G | CA403666277 | INSR | c.1816T>C (p.Tyr606His) n.1791T>C c.217T>C (p.Tyr73His) c.1894T>C (p.Tyr632His) | |
19 | g.7166199A>T | CA403666278 | INSR | c.1816T>A (p.Tyr606Asn) n.1791T>A c.217T>A (p.Tyr73Asn) c.1894T>A (p.Tyr632Asn) | |
19 | g.7166200G>A | CA505199071 | INSR | c.1815C>T (p.Thr605=) n.1790C>T c.216C>T (p.Thr72=) c.1893C>T (p.Thr631=) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.7166200G>C | CA505199072 | INSR | c.1815C>G (p.Thr605=) n.1790C>G c.216C>G (p.Thr72=) c.1893C>G (p.Thr631=) | |
19 | g.7166200G= | CA2320788227 | INSR | c.1815C= (p.Thr605=) n.1790C= c.216C= (p.Thr72=) c.1893C= (p.Thr631=) | |
19 | g.7166200G>T | CA505199073 | INSR | c.1815C>A (p.Thr605=) n.1790C>A c.216C>A (p.Thr72=) c.1893C>A (p.Thr631=) | |
19 | g.7166201G>A | CA403666279 | INSR | c.1814C>T (p.Thr605Ile) n.1789C>T c.215C>T (p.Thr72Ile) c.1892C>T (p.Thr631Ile) | gnomAD v4 |
19 | g.7166201G>C | CA403666280 | INSR | c.1814C>G (p.Thr605Ser) n.1789C>G c.215C>G (p.Thr72Ser) c.1892C>G (p.Thr631Ser) | |
19 | g.7166201G>T | CA403666281 | INSR | c.1814C>A (p.Thr605Asn) n.1789C>A c.215C>A (p.Thr72Asn) c.1892C>A (p.Thr631Asn) | |
19 | g.7166202T>A | CA403666282 | INSR | c.1813A>T (p.Thr605Ser) n.1788A>T c.214A>T (p.Thr72Ser) c.1891A>T (p.Thr631Ser) | |
19 | g.7166202T>C | CA403666283 | INSR | c.1813A>G (p.Thr605Ala) n.1788A>G c.214A>G (p.Thr72Ala) c.1891A>G (p.Thr631Ala) | gnomAD v4 |
19 | g.7166202T>G | CA403666284 | INSR | c.1813A>C (p.Thr605Pro) n.1788A>C c.214A>C (p.Thr72Pro) c.1891A>C (p.Thr631Pro) | |
19 | g.7166203C>A | CA505199074 | INSR | c.1812G>T (p.Arg604=) n.1787G>T c.213G>T (p.Arg71=) c.1890G>T (p.Arg630=) | |
19 | g.7166203C>G | CA505199075 | INSR | c.1812G>C (p.Arg604=) n.1787G>C c.213G>C (p.Arg71=) c.1890G>C (p.Arg630=) | COSMIC COSMIC |
19 | g.7166203C>T | CA505199076 | INSR | c.1812G>A (p.Arg604=) n.1787G>A c.213G>A (p.Arg71=) c.1890G>A (p.Arg630=) | |
19 | g.7166204C>A | CA403666285 | INSR | c.1811G>T (p.Arg604Leu) n.1786G>T c.212G>T (p.Arg71Leu) c.1889G>T (p.Arg630Leu) | |
19 | g.7166204C= | CA2320788228 | INSR | c.1811G= (p.Arg604=) n.1786G= c.212G= (p.Arg71=) c.1889G= (p.Arg630=) | |
19 | g.7166204C>G | CA403666286 | INSR | c.1811G>C (p.Arg604Pro) n.1786G>C c.212G>C (p.Arg71Pro) c.1889G>C (p.Arg630Pro) | |
19 | g.7166204C>T | CA9135751 | INSR | c.1811G>A (p.Arg604Gln) n.1786G>A c.212G>A (p.Arg71Gln) c.1889G>A (p.Arg630Gln) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7166205G>A | CA9135752 | INSR | c.1810C>T (p.Arg604Trp) n.1785C>T c.211C>T (p.Arg71Trp) c.1888C>T (p.Arg630Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7166205G>C | CA403666287 | INSR | c.1810C>G (p.Arg604Gly) n.1785C>G c.211C>G (p.Arg71Gly) c.1888C>G (p.Arg630Gly) | |
19 | g.7166205G= | CA2320788229 | INSR | c.1810C= (p.Arg604=) n.1785C= c.211C= (p.Arg71=) c.1888C= (p.Arg630=) | |
19 | g.7166205G>T | CA505199078 | INSR | c.1810C>A (p.Arg604=) n.1785C>A c.211C>A (p.Arg71=) c.1888C>A (p.Arg630=) | |
19 | g.7166206G>A | CA505199079 | INSR | c.1809C>T (p.Arg603=) n.1784C>T c.210C>T (p.Arg70=) c.1887C>T (p.Arg629=) | |
19 | g.7166206G>C | CA505199080 | INSR | c.1809C>G (p.Arg603=) n.1784C>G c.210C>G (p.Arg70=) c.1887C>G (p.Arg629=) | |
19 | g.7166206G>T | CA505199081 | INSR | c.1809C>A (p.Arg603=) n.1784C>A c.210C>A (p.Arg70=) c.1887C>A (p.Arg629=) | |
19 | g.7166207C>A | CA403666288 | INSR | c.1808G>T (p.Arg603Leu) n.1783G>T c.209G>T (p.Arg70Leu) c.1886G>T (p.Arg629Leu) | |
19 | g.7166207C= | CA2320788230 | INSR | c.1808G= (p.Arg603=) n.1783G= c.209G= (p.Arg70=) c.1886G= (p.Arg629=) | |
19 | g.7166207C>G | CA403666289 | INSR | c.1808G>C (p.Arg603Pro) n.1783G>C c.209G>C (p.Arg70Pro) c.1886G>C (p.Arg629Pro) | |
19 | g.7166207C>T | CA9135753 | INSR | c.1808G>A (p.Arg603His) n.1783G>A c.209G>A (p.Arg70His) c.1886G>A (p.Arg629His) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
19 | g.7166208G>A | CA9135754 | INSR | c.1807C>T (p.Arg603Cys) n.1782C>T c.208C>T (p.Arg70Cys) c.1885C>T (p.Arg629Cys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.7166208G>C | CA403666290 | INSR | c.1807C>G (p.Arg603Gly) n.1782C>G c.208C>G (p.Arg70Gly) c.1885C>G (p.Arg629Gly) | |
19 | g.7166208G= | CA2320788231 | INSR | c.1807C= (p.Arg603=) n.1782C= c.208C= (p.Arg70=) c.1885C= (p.Arg629=) | |
19 | g.7166208G>T | CA403666291 | INSR | c.1807C>A (p.Arg603Ser) n.1782C>A c.208C>A (p.Arg70Ser) c.1885C>A (p.Arg629Ser) | |
19 | g.7166209T>A | CA403666292 | INSR | c.1806A>T (p.Glu602Asp) n.1781A>T c.207A>T (p.Glu69Asp) c.1884A>T (p.Glu628Asp) | |
19 | g.7166209T>C | CA505199083 | INSR | c.1806A>G (p.Glu602=) n.1781A>G c.207A>G (p.Glu69=) c.1884A>G (p.Glu628=) | |
19 | g.7166209T>G | CA403666293 | INSR | c.1806A>C (p.Glu602Asp) n.1781A>C c.207A>C (p.Glu69Asp) c.1884A>C (p.Glu628Asp) | |
19 | g.7166210T>A | CA403666294 | INSR | c.1805A>T (p.Glu602Val) n.1780A>T c.206A>T (p.Glu69Val) c.1883A>T (p.Glu628Val) | |
19 | g.7166210T>C | CA403666295 | INSR | c.1805A>G (p.Glu602Gly) n.1780A>G c.206A>G (p.Glu69Gly) c.1883A>G (p.Glu628Gly) | |
19 | g.7166210T>G | CA403666296 | INSR | c.1805A>C (p.Glu602Ala) n.1780A>C c.206A>C (p.Glu69Ala) c.1883A>C (p.Glu628Ala) | |
19 | g.7166211C>A | CA403666297 | INSR | c.1804G>T (p.Glu602Ter) n.1779G>T c.205G>T (p.Glu69Ter) c.1882G>T (p.Glu628Ter) | |
19 | g.7166211C>G | CA403666298 | INSR | c.1804G>C (p.Glu602Gln) n.1779G>C c.205G>C (p.Glu69Gln) c.1882G>C (p.Glu628Gln) | |
19 | g.7166211C>T | CA403666299 | INSR | c.1804G>A (p.Glu602Lys) n.1779G>A c.205G>A (p.Glu69Lys) c.1882G>A (p.Glu628Lys) | |
19 | g.7166212A>C | CA403666300 | INSR | c.1803T>G (p.Asp601Glu) n.1778T>G c.204T>G (p.Asp68Glu) c.1881T>G (p.Asp627Glu) | |
19 | g.7166212A>G | CA505199084 | INSR | c.1803T>C (p.Asp601=) n.1778T>C c.204T>C (p.Asp68=) c.1881T>C (p.Asp627=) | gnomAD v4 |
19 | g.7166212A>T | CA403666301 | INSR | c.1803T>A (p.Asp601Glu) n.1778T>A c.204T>A (p.Asp68Glu) c.1881T>A (p.Asp627Glu) | |
19 | g.7166213T>A | CA403666304 | INSR | c.1802A>T (p.Asp601Val) n.1777A>T c.203A>T (p.Asp68Val) c.1880A>T (p.Asp627Val) | |
19 | g.7166213T>C | CA403666302 | INSR | c.1802A>G (p.Asp601Gly) n.1777A>G c.203A>G (p.Asp68Gly) c.1880A>G (p.Asp627Gly) | |
19 | g.7166213T>G | CA403666303 | INSR | c.1802A>C (p.Asp601Ala) n.1777A>C c.203A>C (p.Asp68Ala) c.1880A>C (p.Asp627Ala) | |
19 | g.7166214C>A | CA403666305 | INSR | c.1801G>T (p.Asp601Tyr) n.1776G>T c.202G>T (p.Asp68Tyr) c.1879G>T (p.Asp627Tyr) | |
19 | g.7166214C>G | CA403666306 | INSR | c.1801G>C (p.Asp601His) n.1776G>C c.202G>C (p.Asp68His) c.1879G>C (p.Asp627His) | |
19 | g.7166214C>T | CA403666307 | INSR | c.1801G>A (p.Asp601Asn) n.1776G>A c.202G>A (p.Asp68Asn) c.1879G>A (p.Asp627Asn) | |
19 | g.7166215C>A | CA505199085 | INSR | c.1800G>T (p.Ser600=) n.1775G>T c.201G>T (p.Ser67=) c.1878G>T (p.Ser626=) | |
19 | g.7166215C= | CA2320788232 | INSR | c.1800G= (p.Ser600=) n.1775G= c.201G= (p.Ser67=) c.1878G= (p.Ser626=) | |
19 | g.7166215C>G | CA505199086 | INSR | c.1800G>C (p.Ser600=) n.1775G>C c.201G>C (p.Ser67=) c.1878G>C (p.Ser626=) | |
19 | g.7166215C>T | CA9135755 | INSR | c.1800G>A (p.Ser600=) n.1775G>A c.201G>A (p.Ser67=) c.1878G>A (p.Ser626=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
19 | g.7166216G>A | CA9135756 | INSR | c.1799C>T (p.Ser600Leu) n.1774C>T c.200C>T (p.Ser67Leu) c.1877C>T (p.Ser626Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
19 | g.7166216G>C | CA403666308 | INSR | c.1799C>G (p.Ser600Trp) n.1774C>G c.200C>G (p.Ser67Trp) c.1877C>G (p.Ser626Trp) | |
19 | g.7166216G= | CA2320788233 | INSR | c.1799C= (p.Ser600=) n.1774C= c.200C= (p.Ser67=) c.1877C= (p.Ser626=) | |
19 | g.7166216G>T | CA403666309 | INSR | c.1799C>A (p.Ser600Ter) n.1774C>A c.200C>A (p.Ser67Ter) c.1877C>A (p.Ser626Ter) | |
19 | g.7166216_7166217delinsGA | CA2320788234 | INSR | c.1798_1799delinsTC (p.Ser600=) n.1773_1774delinsTC c.199_200delinsTC (p.Ser67=) c.1876_1877delinsTC (p.Ser626=) | |
19 | g.7166217A>C | CA403666310 | INSR | c.1798T>G (p.Ser600Ala) n.1773T>G c.199T>G (p.Ser67Ala) c.1876T>G (p.Ser626Ala) | |
19 | g.7166217A>G | CA403666311 | INSR | c.1798T>C (p.Ser600Pro) n.1773T>C c.199T>C (p.Ser67Pro) c.1876T>C (p.Ser626Pro) | |
19 | g.7166217A>T | CA403666312 | INSR | c.1798T>A (p.Ser600Thr) n.1773T>A c.199T>A (p.Ser67Thr) c.1876T>A (p.Ser626Thr) | |
19 | g.7166220del | CA2320788235 | INSR | c.1798del (p.Ser600ArgfsTer?) n.1773del c.199del (p.Ser67ArgfsTer?) c.1876del (p.Ser626ArgfsTer?) | dbSNP gnomAD v4 |
19 | g.7166218A>C | CA403666313 | INSR | c.1797T>G (p.Phe599Leu) n.1772T>G c.198T>G (p.Phe66Leu) c.1875T>G (p.Phe625Leu) | |
19 | g.7166218A>G | CA505199087 | INSR | c.1797T>C (p.Phe599=) n.1772T>C c.198T>C (p.Phe66=) c.1875T>C (p.Phe625=) | COSMIC COSMIC |
19 | g.7166218A>T | CA403666314 | INSR | c.1797T>A (p.Phe599Leu) n.1772T>A c.198T>A (p.Phe66Leu) c.1875T>A (p.Phe625Leu) | |
19 | g.7166219A>C | CA403666315 | INSR | c.1796T>G (p.Phe599Cys) n.1771T>G c.197T>G (p.Phe66Cys) c.1874T>G (p.Phe625Cys) | |
19 | g.7166219A>G | CA403666317 | INSR | c.1796T>C (p.Phe599Ser) n.1771T>C c.197T>C (p.Phe66Ser) c.1874T>C (p.Phe625Ser) | |
19 | g.7166219A>T | CA403666316 | INSR | c.1796T>A (p.Phe599Tyr) n.1771T>A c.197T>A (p.Phe66Tyr) c.1874T>A (p.Phe625Tyr) | |
19 | g.7166220A>C | CA403666318 | INSR | c.1795T>G (p.Phe599Val) n.1770T>G c.196T>G (p.Phe66Val) c.1873T>G (p.Phe625Val) | |
19 | g.7166220A>G | CA403666320 | INSR | c.1795T>C (p.Phe599Leu) n.1770T>C c.196T>C (p.Phe66Leu) c.1873T>C (p.Phe625Leu) | |
19 | g.7166220A>T | CA403666319 | INSR | c.1795T>A (p.Phe599Ile) n.1770T>A c.196T>A (p.Phe66Ile) c.1873T>A (p.Phe625Ile) | |
19 | g.7166221G>A | CA505199088 | INSR | c.1794C>T (p.Thr598=) n.1769C>T c.195C>T (p.Thr65=) c.1872C>T (p.Thr624=) | |
19 | g.7166221G>C | CA505199089 | INSR | c.1794C>G (p.Thr598=) n.1769C>G c.195C>G (p.Thr65=) c.1872C>G (p.Thr624=) | |
19 | g.7166221G= | CA2320788236 | INSR | c.1794C= (p.Thr598=) n.1769C= c.195C= (p.Thr65=) c.1872C= (p.Thr624=) | |
19 | g.7166221G>T | CA505199090 | INSR | c.1794C>A (p.Thr598=) n.1769C>A c.195C>A (p.Thr65=) c.1872C>A (p.Thr624=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7166222G>A | CA9135757 | INSR | c.1793C>T (p.Thr598Ile) n.1768C>T c.194C>T (p.Thr65Ile) c.1871C>T (p.Thr624Ile) | dbSNP ExAC gnomAD v2 |
19 | g.7166222G>C | CA403666321 | INSR | c.1793C>G (p.Thr598Ser) n.1768C>G c.194C>G (p.Thr65Ser) c.1871C>G (p.Thr624Ser) | |
19 | g.7166222G= | CA2320788237 | INSR | c.1793C= (p.Thr598=) n.1768C= c.194C= (p.Thr65=) c.1871C= (p.Thr624=) | |
19 | g.7166222G>T | CA403666322 | INSR | c.1793C>A (p.Thr598Asn) n.1768C>A c.194C>A (p.Thr65Asn) c.1871C>A (p.Thr624Asn) | |
19 | g.7166223T>A | CA403666323 | INSR | c.1792A>T (p.Thr598Ser) n.1767A>T c.193A>T (p.Thr65Ser) c.1870A>T (p.Thr624Ser) | |
19 | g.7166223T>C | CA403666324 | INSR | c.1792A>G (p.Thr598Ala) n.1767A>G c.193A>G (p.Thr65Ala) c.1870A>G (p.Thr624Ala) | |
19 | g.7166223T>G | CA403666325 | INSR | c.1792A>C (p.Thr598Pro) n.1767A>C c.193A>C (p.Thr65Pro) c.1870A>C (p.Thr624Pro) | |
19 | g.7166224G>A | CA505199091 | INSR | c.1791C>T (p.Val597=) n.1766C>T c.192C>T (p.Val64=) c.1869C>T (p.Val623=) | gnomAD v4 |
19 | g.7166224G>C | CA505199092 | INSR | c.1791C>G (p.Val597=) n.1766C>G c.192C>G (p.Val64=) c.1869C>G (p.Val623=) | |
19 | g.7166224G>T | CA505199093 | INSR | c.1791C>A (p.Val597=) n.1766C>A c.192C>A (p.Val64=) c.1869C>A (p.Val623=) | |
19 | g.7166225A>C | CA403666326 | INSR | c.1790T>G (p.Val597Gly) n.1765T>G c.191T>G (p.Val64Gly) c.1868T>G (p.Val623Gly) | |
19 | g.7166225A>G | CA403666327 | INSR | c.1790T>C (p.Val597Ala) n.1765T>C c.191T>C (p.Val64Ala) c.1868T>C (p.Val623Ala) | |
19 | g.7166225A>T | CA403666328 | INSR | c.1790T>A (p.Val597Asp) n.1765T>A c.191T>A (p.Val64Asp) c.1868T>A (p.Val623Asp) | |
19 | g.7166226C>A | CA403666329 | INSR | c.1789G>T (p.Val597Phe) n.1764G>T c.190G>T (p.Val64Phe) c.1867G>T (p.Val623Phe) | |
19 | g.7166226C>G | CA403666330 | INSR | c.1789G>C (p.Val597Leu) n.1764G>C c.190G>C (p.Val64Leu) c.1867G>C (p.Val623Leu) | gnomAD v4 |
19 | g.7166226C>T | CA403666331 | INSR | c.1789G>A (p.Val597Ile) n.1764G>A c.190G>A (p.Val64Ile) c.1867G>A (p.Val623Ile) | |
19 | g.7166227C>A | CA505199094 | INSR | c.1788G>T (p.Leu596=) n.1763G>T c.189G>T (p.Leu63=) c.1866G>T (p.Leu622=) | dbSNP |
19 | g.7166227C>G | CA505199095 | INSR | c.1788G>C (p.Leu596=) n.1763G>C c.189G>C (p.Leu63=) c.1866G>C (p.Leu622=) | |
19 | g.7166227C>T | CA505199096 | INSR | c.1788G>A (p.Leu596=) n.1763G>A c.189G>A (p.Leu63=) c.1866G>A (p.Leu622=) | gnomAD v4 |
19 | g.7166228A>C | CA403666334 | INSR | c.1787T>G (p.Leu596Arg) n.1762T>G c.188T>G (p.Leu63Arg) c.1865T>G (p.Leu622Arg) | |
19 | g.7166228A>G | CA403666332 | INSR | c.1787T>C (p.Leu596Pro) n.1762T>C c.188T>C (p.Leu63Pro) c.1865T>C (p.Leu622Pro) | |
19 | g.7166228A>T | CA403666333 | INSR | c.1787T>A (p.Leu596Gln) n.1762T>A c.188T>A (p.Leu63Gln) c.1865T>A (p.Leu622Gln) | |
19 | g.7166229G>A | CA505199097 | INSR | c.1786C>T (p.Leu596=) n.1761C>T c.187C>T (p.Leu63=) c.1864C>T (p.Leu622=) | |
19 | g.7166229G>C | CA403666335 | INSR | c.1786C>G (p.Leu596Val) n.1761C>G c.187C>G (p.Leu63Val) c.1864C>G (p.Leu622Val) | |
19 | g.7166229G>T | CA403666336 | INSR | c.1786C>A (p.Leu596Met) n.1761C>A c.187C>A (p.Leu63Met) c.1864C>A (p.Leu622Met) | |
19 | g.7166230G>A | CA9135758 | INSR | c.1785C>T (p.Thr595=) n.1760C>T c.186C>T (p.Thr62=) c.1863C>T (p.Thr621=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.7166230G>C | CA505199098 | INSR | c.1785C>G (p.Thr595=) n.1760C>G c.186C>G (p.Thr62=) c.1863C>G (p.Thr621=) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.7166230G= | CA2320788238 | INSR | c.1785C= (p.Thr595=) n.1760C= c.186C= (p.Thr62=) c.1863C= (p.Thr621=) | |
19 | g.7166230G>T | CA505199099 | INSR | c.1785C>A (p.Thr595=) n.1760C>A c.186C>A (p.Thr62=) c.1863C>A (p.Thr621=) | |
19 | g.7166231G>A | CA403666337 | INSR | c.1784C>T (p.Thr595Ile) n.1759C>T c.185C>T (p.Thr62Ile) c.1862C>T (p.Thr621Ile) | |
19 | g.7166231G>C | CA403666338 | INSR | c.1784C>G (p.Thr595Ser) n.1759C>G c.185C>G (p.Thr62Ser) c.1862C>G (p.Thr621Ser) | |
19 | g.7166231G>T | CA403666339 | INSR | c.1784C>A (p.Thr595Asn) n.1759C>A c.185C>A (p.Thr62Asn) c.1862C>A (p.Thr621Asn) | |
19 | g.7166232T>A | CA403666340 | INSR | c.1783A>T (p.Thr595Ser) n.1758A>T c.184A>T (p.Thr62Ser) c.1861A>T (p.Thr621Ser) | dbSNP |
19 | g.7166232T>C | CA403666341 | INSR | c.1783A>G (p.Thr595Ala) n.1758A>G c.184A>G (p.Thr62Ala) c.1861A>G (p.Thr621Ala) | |
19 | g.7166232T>G | CA403666342 | INSR | c.1783A>C (p.Thr595Pro) n.1758A>C c.184A>C (p.Thr62Pro) c.1861A>C (p.Thr621Pro) | |
19 | g.7166232T= | CA2320788239 | INSR | c.1783A= (p.Thr595=) n.1758A= c.184A= (p.Thr62=) c.1861A= (p.Thr621=) | |
19 | g.7166233C>A | CA403666343 | INSR | c.1782G>T (p.Lys594Asn) n.1757G>T c.183G>T (p.Lys61Asn) c.1860G>T (p.Lys620Asn) | |
19 | g.7166233C>G | CA403666344 | INSR | c.1782G>C (p.Lys594Asn) n.1757G>C c.183G>C (p.Lys61Asn) c.1860G>C (p.Lys620Asn) | |
19 | g.7166233C>T | CA505199100 | INSR | c.1782G>A (p.Lys594=) n.1757G>A c.183G>A (p.Lys61=) c.1860G>A (p.Lys620=) | |
19 | g.7166234T>A | CA403666347 | INSR | c.1781A>T (p.Lys594Met) n.1756A>T c.182A>T (p.Lys61Met) c.1859A>T (p.Lys620Met) | |
19 | g.7166234T>C | CA403666346 | INSR | c.1781A>G (p.Lys594Arg) n.1756A>G c.182A>G (p.Lys61Arg) c.1859A>G (p.Lys620Arg) | |
19 | g.7166234T>G | CA403666345 | INSR | c.1781A>C (p.Lys594Thr) n.1756A>C c.182A>C (p.Lys61Thr) c.1859A>C (p.Lys620Thr) | |
19 | g.7166235T>A | CA403666348 | INSR | c.1780A>T (p.Lys594Ter) n.1755A>T c.181A>T (p.Lys61Ter) c.1858A>T (p.Lys620Ter) | |
19 | g.7166235T>C | CA403666349 | INSR | c.1780A>G (p.Lys594Glu) n.1755A>G c.181A>G (p.Lys61Glu) c.1858A>G (p.Lys620Glu) | |
19 | g.7166235T>G | CA403666350 | INSR | c.1780A>C (p.Lys594Gln) n.1755A>C c.181A>C (p.Lys61Gln) c.1858A>C (p.Lys620Gln) | |
19 | g.7166236C>A | CA505199103 | INSR | c.1779G>T (p.Val593=) n.1754G>T c.180G>T (p.Val60=) c.1857G>T (p.Val619=) | |
19 | g.7166236C>G | CA505199102 | INSR | c.1779G>C (p.Val593=) n.1754G>C c.180G>C (p.Val60=) c.1857G>C (p.Val619=) | |
19 | g.7166236C>T | CA505199101 | INSR | c.1779G>A (p.Val593=) n.1754G>A c.180G>A (p.Val60=) c.1857G>A (p.Val619=) | |
19 | g.7166237A>C | CA403666351 | INSR | c.1778T>G (p.Val593Gly) n.1753T>G c.179T>G (p.Val60Gly) c.1856T>G (p.Val619Gly) | |
19 | g.7166237A>G | CA403666352 | INSR | c.1778T>C (p.Val593Ala) n.1753T>C c.179T>C (p.Val60Ala) c.1856T>C (p.Val619Ala) | |
19 | g.7166237A>T | CA403666353 | INSR | c.1778T>A (p.Val593Glu) n.1753T>A c.179T>A (p.Val60Glu) c.1856T>A (p.Val619Glu) | |
19 | g.7166238C>A | CA403666356 | INSR | c.1777G>T (p.Val593Leu) n.1752G>T c.178G>T (p.Val60Leu) c.1855G>T (p.Val619Leu) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7166238C= | CA2320788240 | INSR | c.1777G= (p.Val593=) n.1752G= c.178G= (p.Val60=) c.1855G= (p.Val619=) | |
19 | g.7166238C>G | CA403666354 | INSR | c.1777G>C (p.Val593Leu) n.1752G>C c.178G>C (p.Val60Leu) c.1855G>C (p.Val619Leu) | |
19 | g.7166238C>T | CA403666355 | INSR | c.1777G>A (p.Val593Met) n.1752G>A c.178G>A (p.Val60Met) c.1855G>A (p.Val619Met) | |
19 | g.7166239A>C | CA403666357 | INSR | c.1776T>G (p.Phe592Leu) n.1751T>G c.177T>G (p.Phe59Leu) c.1854T>G (p.Phe618Leu) | |
19 | g.7166239A>G | CA505199104 | INSR | c.1776T>C (p.Phe592=) n.1751T>C c.177T>C (p.Phe59=) c.1854T>C (p.Phe618=) | dbSNP |
19 | g.7166239A>T | CA403666358 | INSR | c.1776T>A (p.Phe592Leu) n.1751T>A c.177T>A (p.Phe59Leu) c.1854T>A (p.Phe618Leu) | |
19 | g.7166240A>C | CA403666359 | INSR | c.1775T>G (p.Phe592Cys) n.1750T>G c.176T>G (p.Phe59Cys) c.1853T>G (p.Phe618Cys) | |
19 | g.7166240A>G | CA403666360 | INSR | c.1775T>C (p.Phe592Ser) n.1750T>C c.176T>C (p.Phe59Ser) c.1853T>C (p.Phe618Ser) | |
19 | g.7166240A>T | CA403666361 | INSR | c.1775T>A (p.Phe592Tyr) n.1750T>A c.176T>A (p.Phe59Tyr) c.1853T>A (p.Phe618Tyr) | |
19 | g.7166241A>C | CA403666362 | INSR | c.1774T>G (p.Phe592Val) n.1749T>G c.175T>G (p.Phe59Val) c.1852T>G (p.Phe618Val) | |
19 | g.7166241A>G | CA403666364 | INSR | c.1774T>C (p.Phe592Leu) n.1749T>C c.175T>C (p.Phe59Leu) c.1852T>C (p.Phe618Leu) | |
19 | g.7166241A>T | CA403666363 | INSR | c.1774T>A (p.Phe592Ile) n.1749T>A c.175T>A (p.Phe59Ile) c.1852T>A (p.Phe618Ile) | |
19 | g.7166242G>A | CA304856215 | INSR | c.1773C>T (p.Ile591=) n.1748C>T c.174C>T (p.Ile58=) c.1851C>T (p.Ile617=) | dbSNP |
19 | g.7166242G>C | CA403666365 | INSR | c.1773C>G (p.Ile591Met) n.1748C>G c.174C>G (p.Ile58Met) c.1851C>G (p.Ile617Met) | gnomAD v4 |
19 | g.7166242G= | CA2320788241 | INSR | c.1773C= (p.Ile591=) n.1748C= c.174C= (p.Ile58=) c.1851C= (p.Ile617=) | |
19 | g.7166242G>T | CA505199105 | INSR | c.1773C>A (p.Ile591=) n.1748C>A c.174C>A (p.Ile58=) c.1851C>A (p.Ile617=) | gnomAD v4 |
19 | g.7166243A>C | CA403666366 | INSR | c.1772T>G (p.Ile591Ser) n.1747T>G c.173T>G (p.Ile58Ser) c.1850T>G (p.Ile617Ser) | |
19 | g.7166243A>G | CA403666367 | INSR | c.1772T>C (p.Ile591Thr) n.1747T>C c.173T>C (p.Ile58Thr) c.1850T>C (p.Ile617Thr) | |
19 | g.7166243A>T | CA403666368 | INSR | c.1772T>A (p.Ile591Asn) n.1747T>A c.173T>A (p.Ile58Asn) c.1850T>A (p.Ile617Asn) | |
19 | g.7166244T>A | CA403666369 | INSR | c.1771A>T (p.Ile591Phe) n.1746A>T c.172A>T (p.Ile58Phe) c.1849A>T (p.Ile617Phe) | |
19 | g.7166244T>C | CA403666370 | INSR | c.1771A>G (p.Ile591Val) n.1746A>G c.172A>G (p.Ile58Val) c.1849A>G (p.Ile617Val) | |
19 | g.7166244T>G | CA403666371 | INSR | c.1771A>C (p.Ile591Leu) n.1746A>C c.172A>C (p.Ile58Leu) c.1849A>C (p.Ile617Leu) | |
19 | g.7166245G>A | CA505199106 | INSR | c.1770C>T (p.Ala590=) n.1745C>T c.171C>T (p.Ala57=) c.1848C>T (p.Ala616=) | gnomAD v4 |
19 | g.7166245G>C | CA505199107 | INSR | c.1770C>G (p.Ala590=) n.1745C>G c.171C>G (p.Ala57=) c.1848C>G (p.Ala616=) | |
19 | g.7166245G>T | CA505199108 | INSR | c.1770C>A (p.Ala590=) n.1745C>A c.171C>A (p.Ala57=) c.1848C>A (p.Ala616=) | |
19 | g.7166246G>A | CA403666372 | INSR | c.1769C>T (p.Ala590Val) n.1744C>T c.170C>T (p.Ala57Val) c.1847C>T (p.Ala616Val) | gnomAD v4 |
19 | g.7166246G>C | CA403666373 | INSR | c.1769C>G (p.Ala590Gly) n.1744C>G c.170C>G (p.Ala57Gly) c.1847C>G (p.Ala616Gly) | |
19 | g.7166246G>T | CA403666374 | INSR | c.1769C>A (p.Ala590Asp) n.1744C>A c.170C>A (p.Ala57Asp) c.1847C>A (p.Ala616Asp) | |
19 | g.7166247C>A | CA403666376 | INSR | c.1768G>T (p.Ala590Ser) n.1743G>T c.169G>T (p.Ala57Ser) c.1846G>T (p.Ala616Ser) | |
19 | g.7166247C>G | CA403666377 | INSR | c.1768G>C (p.Ala590Pro) n.1743G>C c.169G>C (p.Ala57Pro) c.1846G>C (p.Ala616Pro) | |
19 | g.7166247C>T | CA403666375 | INSR | c.1768G>A (p.Ala590Thr) n.1743G>A c.169G>A (p.Ala57Thr) c.1846G>A (p.Ala616Thr) | |
19 | g.7166248A= | CA2320788242 | INSR | c.1767T= (p.Tyr589=) n.1742T= c.168T= (p.Tyr56=) c.1845T= (p.Tyr615=) | |
19 | g.7166248A>C | CA403666378 | INSR | c.1767T>G (p.Tyr589Ter) n.1742T>G c.168T>G (p.Tyr56Ter) c.1845T>G (p.Tyr615Ter) | |
19 | g.7166248A>G | CA304856217 | INSR | c.1767T>C (p.Tyr589=) n.1742T>C c.168T>C (p.Tyr56=) c.1845T>C (p.Tyr615=) | dbSNP gnomAD v4 |
19 | g.7166248A>T | CA403666379 | INSR | c.1767T>A (p.Tyr589Ter) n.1742T>A c.168T>A (p.Tyr56Ter) c.1845T>A (p.Tyr615Ter) | |
19 | g.7166249T>A | CA403666380 | INSR | c.1766A>T (p.Tyr589Phe) n.1741A>T c.167A>T (p.Tyr56Phe) c.1844A>T (p.Tyr615Phe) | |
19 | g.7166249T>C | CA403666381 | INSR | c.1766A>G (p.Tyr589Cys) n.1741A>G c.167A>G (p.Tyr56Cys) c.1844A>G (p.Tyr615Cys) | |
19 | g.7166249T>G | CA403666382 | INSR | c.1766A>C (p.Tyr589Ser) n.1741A>C c.167A>C (p.Tyr56Ser) c.1844A>C (p.Tyr615Ser) | |
19 | g.7166250A>C | CA403666383 | INSR | c.1765T>G (p.Tyr589Asp) n.1740T>G c.166T>G (p.Tyr56Asp) c.1843T>G (p.Tyr615Asp) | |
19 | g.7166250A>G | CA403666384 | INSR | c.1765T>C (p.Tyr589His) n.1740T>C c.166T>C (p.Tyr56His) c.1843T>C (p.Tyr615His) | |
19 | g.7166250A>T | CA403666385 | INSR | c.1765T>A (p.Tyr589Asn) n.1740T>A c.166T>A (p.Tyr56Asn) c.1843T>A (p.Tyr615Asn) | |
19 | g.7166251C>A | CA403666386 | INSR | c.1764G>T (p.Gln588His) n.1739G>T c.165G>T (p.Gln55His) c.1842G>T (p.Gln614His) | |
19 | g.7166251C= | CA2320788243 | INSR | c.1764G= (p.Gln588=) n.1739G= c.165G= (p.Gln55=) c.1842G= (p.Gln614=) | |
19 | g.7166251C>G | CA403666387 | INSR | c.1764G>C (p.Gln588His) n.1739G>C c.165G>C (p.Gln55His) c.1842G>C (p.Gln614His) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.7166251C>T | CA505199109 | INSR | c.1764G>A (p.Gln588=) n.1739G>A c.165G>A (p.Gln55=) c.1842G>A (p.Gln614=) | dbSNP gnomAD v4 |
19 | g.7166252T>A | CA403666388 | INSR | c.1763A>T (p.Gln588Leu) n.1738A>T c.164A>T (p.Gln55Leu) c.1841A>T (p.Gln614Leu) | gnomAD v4 |
19 | g.7166252T>C | CA403666389 | INSR | c.1763A>G (p.Gln588Arg) n.1738A>G c.164A>G (p.Gln55Arg) c.1841A>G (p.Gln614Arg) | |
19 | g.7166252T>G | CA403666390 | INSR | c.1763A>C (p.Gln588Pro) n.1738A>C c.164A>C (p.Gln55Pro) c.1841A>C (p.Gln614Pro) | |
19 | g.7166253G>A | CA403666391 | INSR | c.1762C>T (p.Gln588Ter) n.1737C>T c.163C>T (p.Gln55Ter) c.1840C>T (p.Gln614Ter) | gnomAD v4 |
19 | g.7166253G>C | CA403666392 | INSR | c.1762C>G (p.Gln588Glu) n.1737C>G c.163C>G (p.Gln55Glu) c.1840C>G (p.Gln614Glu) | |
19 | g.7166253G>T | CA403666393 | INSR | c.1762C>A (p.Gln588Lys) n.1737C>A c.163C>A (p.Gln55Lys) c.1840C>A (p.Gln614Lys) | |
19 | g.7166253_7166254delinsAA | CA645607108 | INSR | c.1761_1762delinsTT (p.Thr588Ter) n.1736_1737delinsTT c.162_163delinsTT (p.Thr55Ter) c.1839_1840delinsTT (p.Thr614Ter) | COSMIC COSMIC |
19 | g.7166254G>A | CA505199110 | INSR | c.1761C>T (p.Thr587=) n.1736C>T c.162C>T (p.Thr54=) c.1839C>T (p.Thr613=) | dbSNP |
19 | g.7166254G>C | CA505199111 | INSR | c.1761C>G (p.Thr587=) n.1736C>G c.162C>G (p.Thr54=) c.1839C>G (p.Thr613=) | |
19 | g.7166254G= | CA2320788244 | INSR | c.1761C= (p.Thr587=) n.1736C= c.162C= (p.Thr54=) c.1839C= (p.Thr613=) | |
19 | g.7166254G>T | CA304856218 | INSR | c.1761C>A (p.Thr587=) n.1736C>A c.162C>A (p.Thr54=) c.1839C>A (p.Thr613=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7166255G>A | CA403666394 | INSR | c.1760C>T (p.Thr587Ile) n.1735C>T c.161C>T (p.Thr54Ile) c.1838C>T (p.Thr613Ile) | |
19 | g.7166255G>C | CA403666396 | INSR | c.1760C>G (p.Thr587Ser) n.1735C>G c.161C>G (p.Thr54Ser) c.1838C>G (p.Thr613Ser) | |
19 | g.7166255G>T | CA403666395 | INSR | c.1760C>A (p.Thr587Asn) n.1735C>A c.161C>A (p.Thr54Asn) c.1838C>A (p.Thr613Asn) | |
19 | g.7166256T>A | CA403666397 | INSR | c.1759A>T (p.Thr587Ser) n.1734A>T c.160A>T (p.Thr54Ser) c.1837A>T (p.Thr613Ser) | gnomAD v4 |
19 | g.7166256T>C | CA403666398 | INSR | c.1759A>G (p.Thr587Ala) n.1734A>G c.160A>G (p.Thr54Ala) c.1837A>G (p.Thr613Ala) | |
19 | g.7166256T>G | CA403666399 | INSR | c.1759A>C (p.Thr587Pro) n.1734A>C c.160A>C (p.Thr54Pro) c.1837A>C (p.Thr613Pro) | |
19 | g.7166257C>A | CA403666400 | INSR | c.1758G>T (p.Trp586Cys) n.1733G>T c.159G>T (p.Trp53Cys) c.1836G>T (p.Trp612Cys) | |
19 | g.7166257C>G | CA403666401 | INSR | c.1758G>C (p.Trp586Cys) n.1733G>C c.159G>C (p.Trp53Cys) c.1836G>C (p.Trp612Cys) | |
19 | g.7166257C>T | CA403666402 | INSR | c.1758G>A (p.Trp586Ter) n.1733G>A c.159G>A (p.Trp53Ter) c.1836G>A (p.Trp612Ter) | |
19 | g.7166258C>A | CA403666403 | INSR | c.1757G>T (p.Trp586Leu) n.1732G>T c.158G>T (p.Trp53Leu) c.1835G>T (p.Trp612Leu) | |
19 | g.7166258C>G | CA403666404 | INSR | c.1757G>C (p.Trp586Ser) n.1732G>C c.158G>C (p.Trp53Ser) c.1835G>C (p.Trp612Ser) | |
19 | g.7166258C>T | CA403666405 | INSR | c.1757G>A (p.Trp586Ter) n.1732G>A c.158G>A (p.Trp53Ter) c.1835G>A (p.Trp612Ter) | |
19 | g.7166259A= | CA2320788245 | INSR | c.1756T= (p.Trp586=) n.1731T= c.157T= (p.Trp53=) c.1834T= (p.Trp612=) | |
19 | g.7166259A>C | CA403666406 | INSR | c.1756T>G (p.Trp586Gly) n.1731T>G c.157T>G (p.Trp53Gly) c.1834T>G (p.Trp612Gly) | |
19 | g.7166259A>G | CA403666407 | INSR | c.1756T>C (p.Trp586Arg) n.1731T>C c.157T>C (p.Trp53Arg) c.1834T>C (p.Trp612Arg) | |
19 | g.7166259A>T | CA403666408 | INSR | c.1756T>A (p.Trp586Arg) n.1731T>A c.157T>A (p.Trp53Arg) c.1834T>A (p.Trp612Arg) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.7166260G>A | CA505199212 | INSR | c.1755C>T (p.Pro585=) n.1730C>T c.156C>T (p.Pro52=) c.1833C>T (p.Pro611=) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.7166260G>C | CA505199214 | INSR | c.1755C>G (p.Pro585=) n.1730C>G c.156C>G (p.Pro52=) c.1833C>G (p.Pro611=) | |
19 | g.7166260G= | CA2320788246 | INSR | c.1755C= (p.Pro585=) n.1730C= c.156C= (p.Pro52=) c.1833C= (p.Pro611=) | |
19 | g.7166260G>T | CA505199216 | INSR | c.1755C>A (p.Pro585=) n.1730C>A c.156C>A (p.Pro52=) c.1833C>A (p.Pro611=) | |
19 | g.7166261G>A | CA403666409 | INSR | c.1754C>T (p.Pro585Leu) n.1729C>T c.155C>T (p.Pro52Leu) c.1832C>T (p.Pro611Leu) | gnomAD v4 |
19 | g.7166261G>C | CA403666411 | INSR | c.1754C>G (p.Pro585Arg) n.1729C>G c.155C>G (p.Pro52Arg) c.1832C>G (p.Pro611Arg) | |
19 | g.7166261G>T | CA403666410 | INSR | c.1754C>A (p.Pro585His) n.1729C>A c.155C>A (p.Pro52His) c.1832C>A (p.Pro611His) | |
19 | g.7166262G>A | CA403666412 | INSR | c.1753C>T (p.Pro585Ser) n.1728C>T c.154C>T (p.Pro52Ser) c.1831C>T (p.Pro611Ser) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.7166262G>C | CA403666413 | INSR | c.1753C>G (p.Pro585Ala) n.1728C>G c.154C>G (p.Pro52Ala) c.1831C>G (p.Pro611Ala) | |
19 | g.7166262G= | CA2320788247 | INSR | c.1753C= (p.Pro585=) n.1728C= c.154C= (p.Pro52=) c.1831C= (p.Pro611=) | |
19 | g.7166262G>T | CA403666414 | INSR | c.1753C>A (p.Pro585Thr) n.1728C>A c.154C>A (p.Pro52Thr) c.1831C>A (p.Pro611Thr) | |
19 | g.7166263C>A | CA403666415 | INSR | c.1752G>T (p.Lys584Asn) n.1727G>T c.153G>T (p.Lys51Asn) c.1830G>T (p.Lys610Asn) | COSMIC |
19 | g.7166263C>G | CA403666416 | INSR | c.1752G>C (p.Lys584Asn) n.1727G>C c.153G>C (p.Lys51Asn) c.1830G>C (p.Lys610Asn) | |
19 | g.7166263C>T | CA505199224 | INSR | c.1752G>A (p.Lys584=) n.1727G>A c.153G>A (p.Lys51=) c.1830G>A (p.Lys610=) | |
19 | g.7166264T>A | CA403666419 | INSR | c.1751A>T (p.Lys584Met) n.1726A>T c.152A>T (p.Lys51Met) c.1829A>T (p.Lys610Met) | |
19 | g.7166264T>C | CA403666418 | INSR | c.1751A>G (p.Lys584Arg) n.1726A>G c.152A>G (p.Lys51Arg) c.1829A>G (p.Lys610Arg) | |
19 | g.7166264T>G | CA403666417 | INSR | c.1751A>C (p.Lys584Thr) n.1726A>C c.152A>C (p.Lys51Thr) c.1829A>C (p.Lys610Thr) | |
19 | g.7166265T>A | CA403666420 | INSR | c.1750A>T (p.Lys584Ter) n.1725A>T c.151A>T (p.Lys51Ter) c.1828A>T (p.Lys610Ter) | |
19 | g.7166265T>C | CA403666421 | INSR | c.1750A>G (p.Lys584Glu) n.1725A>G c.151A>G (p.Lys51Glu) c.1828A>G (p.Lys610Glu) | COSMIC COSMIC |
19 | g.7166265T>G | CA403666422 | INSR | c.1750A>C (p.Lys584Gln) n.1725A>C c.151A>C (p.Lys51Gln) c.1828A>C (p.Lys610Gln) | |
19 | g.7166266G>A | CA505199236 | INSR | c.1749C>T (p.Leu583=) n.1724C>T c.150C>T (p.Leu50=) c.1827C>T (p.Leu609=) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.7166266G>C | CA505199237 | INSR | c.1749C>G (p.Leu583=) n.1724C>G c.150C>G (p.Leu50=) c.1827C>G (p.Leu609=) | dbSNP gnomAD v4 COSMIC COSMIC |
19 | g.7166266G= | CA2320788248 | INSR | c.1749C= (p.Leu583=) n.1724C= c.150C= (p.Leu50=) c.1827C= (p.Leu609=) | |
19 | g.7166266G>T | CA505199239 | INSR | c.1749C>A (p.Leu583=) n.1724C>A c.150C>A (p.Leu50=) c.1827C>A (p.Leu609=) | |
19 | g.7166267A>C | CA403666423 | INSR | c.1748T>G (p.Leu583Arg) n.1723T>G c.149T>G (p.Leu50Arg) c.1826T>G (p.Leu609Arg) | |
19 | g.7166267A>G | CA403666424 | INSR | c.1748T>C (p.Leu583Pro) n.1723T>C c.149T>C (p.Leu50Pro) c.1826T>C (p.Leu609Pro) | |
19 | g.7166267A>T | CA403666425 | INSR | c.1748T>A (p.Leu583His) n.1723T>A c.149T>A (p.Leu50His) c.1826T>A (p.Leu609His) | |
19 | g.7166268G>A | CA403666426 | INSR | c.1747C>T (p.Leu583Phe) n.1722C>T c.148C>T (p.Leu50Phe) c.1825C>T (p.Leu609Phe) | |
19 | g.7166268G>C | CA403666428 | INSR | c.1747C>G (p.Leu583Val) n.1722C>G c.148C>G (p.Leu50Val) c.1825C>G (p.Leu609Val) | |
19 | g.7166268G>T | CA403666427 | INSR | c.1747C>A (p.Leu583Ile) n.1722C>A c.148C>A (p.Leu50Ile) c.1825C>A (p.Leu609Ile) | |
19 | g.7166269A>C | CA505199248 | INSR | c.1746T>G (p.Gly582=) n.1721T>G c.147T>G (p.Gly49=) c.1824T>G (p.Gly608=) | |
19 | g.7166269A>G | CA505199250 | INSR | c.1746T>C (p.Gly582=) n.1721T>C c.147T>C (p.Gly49=) c.1824T>C (p.Gly608=) | |
19 | g.7166269A>T | CA505199252 | INSR | c.1746T>A (p.Gly582=) n.1721T>A c.147T>A (p.Gly49=) c.1824T>A (p.Gly608=) | |
19 | g.7166270C>A | CA403666429 | INSR | c.1745G>T (p.Gly582Val) n.1720G>T c.146G>T (p.Gly49Val) c.1823G>T (p.Gly608Val) | |
19 | g.7166270C>G | CA403666430 | INSR | c.1745G>C (p.Gly582Ala) n.1720G>C c.146G>C (p.Gly49Ala) c.1823G>C (p.Gly608Ala) | |
19 | g.7166270C>T | CA403666431 | INSR | c.1745G>A (p.Gly582Asp) n.1720G>A c.146G>A (p.Gly49Asp) c.1823G>A (p.Gly608Asp) | gnomAD v4 COSMIC COSMIC |
19 | g.7166271C>A | CA403666432 | INSR | c.1744G>T (p.Gly582Cys) n.1719G>T c.145G>T (p.Gly49Cys) c.1822G>T (p.Gly608Cys) | |
19 | g.7166271C>G | CA403666433 | INSR | c.1744G>C (p.Gly582Arg) n.1719G>C c.145G>C (p.Gly49Arg) c.1822G>C (p.Gly608Arg) | |
19 | g.7166271C>T | CA403666434 | INSR | c.1744G>A (p.Gly582Ser) n.1719G>A c.145G>A (p.Gly49Ser) c.1822G>A (p.Gly608Ser) | |
19 | g.7166272C>A | CA505199265 | INSR | c.1743G>T (p.Arg581=) n.1718G>T c.144G>T (p.Arg48=) c.1821G>T (p.Arg607=) | |
19 | g.7166272C= | CA2320788249 | INSR | c.1743G= (p.Arg581=) n.1718G= c.144G= (p.Arg48=) c.1821G= (p.Arg607=) | |
19 | g.7166272C>G | CA505199262 | INSR | c.1743G>C (p.Arg581=) n.1718G>C c.144G>C (p.Arg48=) c.1821G>C (p.Arg607=) | |
19 | g.7166272C>T | CA505199264 | INSR | c.1743G>A (p.Arg581=) n.1718G>A c.144G>A (p.Arg48=) c.1821G>A (p.Arg607=) | dbSNP gnomAD v2 gnomAD v4 |