| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.28028197_28028211dup | CA645597700 | FLT3 | c.2020_2034dup (p.Leu678_Gly679insIleValAsnLeuLeu) n.2102_2116dup c.1963_1977dup (p.Leu659_Gly660insIleValAsnLeuLeu) c.1495_1509dup (p.Leu503_Gly504insIleValAsnLeuLeu) c.1804_1818dup (p.Leu606_Gly607insIleValAsnLeuLeu) c.1141_1155dup (p.Leu385_Gly386insIleValAsnLeuLeu) c.1123_1137dup (p.Leu379_Gly380insIleValAsnLeuLeu) n.2086_2100dup | COSMIC |
| 13 | g.28028205T>A | CA387652132 | FLT3 | c.2026A>T (p.Asn676Tyr) n.2108A>T c.1969A>T (p.Asn657Tyr) c.1501A>T (p.Asn501Tyr) c.1810A>T (p.Asn604Tyr) c.1147A>T (p.Asn383Tyr) c.1129A>T (p.Asn377Tyr) n.2092A>T | |
| 13 | g.28028205T>C | CA16602569 | FLT3 | c.2026A>G (p.Asn676Asp) n.2108A>G c.1969A>G (p.Asn657Asp) c.1501A>G (p.Asn501Asp) c.1810A>G (p.Asn604Asp) c.1147A>G (p.Asn383Asp) c.1129A>G (p.Asn377Asp) n.2092A>G | ClinVar dbSNP |
| 13 | g.28028205T>G | CA387652133 | FLT3 | c.2026A>C (p.Asn676His) n.2108A>C c.1969A>C (p.Asn657His) c.1501A>C (p.Asn501His) c.1810A>C (p.Asn604His) c.1147A>C (p.Asn383His) c.1129A>C (p.Asn377His) n.2092A>C | |
| 13 | g.28028205T= | CA2080790603 | FLT3 | c.2026A= (p.Asn676=) n.2108A= c.1969A= (p.Asn657=) c.1501A= (p.Asn501=) c.1810A= (p.Asn604=) c.1147A= (p.Asn383=) c.1129A= (p.Asn377=) n.2092A= | |
| 13 | g.28028206C>A | CA483043303 | FLT3 | c.2025G>T (p.Val675=) n.2107G>T c.1968G>T (p.Val656=) c.1500G>T (p.Val500=) c.1809G>T (p.Val603=) c.1146G>T (p.Val382=) c.1128G>T (p.Val376=) n.2091G>T | |
| 13 | g.28028206C= | CA2080790604 | FLT3 | c.2025G= (p.Val675=) n.2107G= c.1968G= (p.Val656=) c.1500G= (p.Val500=) c.1809G= (p.Val603=) c.1146G= (p.Val382=) c.1128G= (p.Val376=) n.2091G= | |
| 13 | g.28028206C>G | CA6928484 | FLT3 | c.2025G>C (p.Val675=) n.2107G>C c.1968G>C (p.Val656=) c.1500G>C (p.Val500=) c.1809G>C (p.Val603=) c.1146G>C (p.Val382=) c.1128G>C (p.Val376=) n.2091G>C | dbSNP ExAC gnomAD v2 |
| 13 | g.28028206C>T | CA483043304 | FLT3 | c.2025G>A (p.Val675=) n.2107G>A c.1968G>A (p.Val656=) c.1500G>A (p.Val500=) c.1809G>A (p.Val603=) c.1146G>A (p.Val382=) c.1128G>A (p.Val376=) n.2091G>A | dbSNP |
| 13 | g.28028207A>C | CA387652134 | FLT3 | c.2024T>G (p.Val675Gly) n.2106T>G c.1967T>G (p.Val656Gly) c.1499T>G (p.Val500Gly) c.1808T>G (p.Val603Gly) c.1145T>G (p.Val382Gly) c.1127T>G (p.Val376Gly) n.2090T>G | |
| 13 | g.28028207A>G | CA387652135 | FLT3 | c.2024T>C (p.Val675Ala) n.2106T>C c.1967T>C (p.Val656Ala) c.1499T>C (p.Val500Ala) c.1808T>C (p.Val603Ala) c.1145T>C (p.Val382Ala) c.1127T>C (p.Val376Ala) n.2090T>C | gnomAD v4 COSMIC |
| 13 | g.28028207A>T | CA387652136 | FLT3 | c.2024T>A (p.Val675Glu) n.2106T>A c.1967T>A (p.Val656Glu) c.1499T>A (p.Val500Glu) c.1808T>A (p.Val603Glu) c.1145T>A (p.Val382Glu) c.1127T>A (p.Val376Glu) n.2090T>A | |
| 13 | g.28028208C>A | CA387652137 | FLT3 | c.2023G>T (p.Val675Leu) n.2105G>T c.1966G>T (p.Val656Leu) c.1498G>T (p.Val500Leu) c.1807G>T (p.Val603Leu) c.1144G>T (p.Val382Leu) c.1126G>T (p.Val376Leu) n.2089G>T | |
| 13 | g.28028208C>G | CA387652138 | FLT3 | c.2023G>C (p.Val675Leu) n.2105G>C c.1966G>C (p.Val656Leu) c.1498G>C (p.Val500Leu) c.1807G>C (p.Val603Leu) c.1144G>C (p.Val382Leu) c.1126G>C (p.Val376Leu) n.2089G>C | |
| 13 | g.28028208C>T | CA387652139 | FLT3 | c.2023G>A (p.Val675Met) n.2105G>A c.1966G>A (p.Val656Met) c.1498G>A (p.Val500Met) c.1807G>A (p.Val603Met) c.1144G>A (p.Val382Met) c.1126G>A (p.Val376Met) n.2089G>A | |
| 13 | g.28028209A>C | CA387652140 | FLT3 | c.2022T>G (p.Ile674Met) n.2104T>G c.1965T>G (p.Ile655Met) c.1497T>G (p.Ile499Met) c.1806T>G (p.Ile602Met) c.1143T>G (p.Ile381Met) c.1125T>G (p.Ile375Met) n.2088T>G | |
| 13 | g.28028209A>G | CA483043310 | FLT3 | c.2022T>C (p.Ile674=) n.2104T>C c.1965T>C (p.Ile655=) c.1497T>C (p.Ile499=) c.1806T>C (p.Ile602=) c.1143T>C (p.Ile381=) c.1125T>C (p.Ile375=) n.2088T>C | gnomAD v4 |
| 13 | g.28028209A>T | CA483043312 | FLT3 | c.2022T>A (p.Ile674=) n.2104T>A c.1965T>A (p.Ile655=) c.1497T>A (p.Ile499=) c.1806T>A (p.Ile602=) c.1143T>A (p.Ile381=) c.1125T>A (p.Ile375=) n.2088T>A | |
| 13 | g.28028210A= | CA2080790605 | FLT3 | c.2021T= (p.Ile674=) n.2103T= c.1964T= (p.Ile655=) c.1496T= (p.Ile499=) c.1805T= (p.Ile602=) c.1142T= (p.Ile381=) c.1124T= (p.Ile375=) n.2087T= | |
| 13 | g.28028210A>C | CA387652141 | FLT3 | c.2021T>G (p.Ile674Ser) n.2103T>G c.1964T>G (p.Ile655Ser) c.1496T>G (p.Ile499Ser) c.1805T>G (p.Ile602Ser) c.1142T>G (p.Ile381Ser) c.1124T>G (p.Ile375Ser) n.2087T>G | |
| 13 | g.28028210A>G | CA6928485 | FLT3 | c.2021T>C (p.Ile674Thr) n.2103T>C c.1964T>C (p.Ile655Thr) c.1496T>C (p.Ile499Thr) c.1805T>C (p.Ile602Thr) c.1142T>C (p.Ile381Thr) c.1124T>C (p.Ile375Thr) n.2087T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.28028210A>T | CA387652142 | FLT3 | c.2021T>A (p.Ile674Asn) n.2103T>A c.1964T>A (p.Ile655Asn) c.1496T>A (p.Ile499Asn) c.1805T>A (p.Ile602Asn) c.1142T>A (p.Ile381Asn) c.1124T>A (p.Ile375Asn) n.2087T>A | |
| 13 | g.28028211T>A | CA387652145 | FLT3 | c.2020A>T (p.Ile674Phe) n.2102A>T c.1963A>T (p.Ile655Phe) c.1495A>T (p.Ile499Phe) c.1804A>T (p.Ile602Phe) c.1141A>T (p.Ile381Phe) c.1123A>T (p.Ile375Phe) n.2086A>T | |
| 13 | g.28028211T>C | CA387652143 | FLT3 | c.2020A>G (p.Ile674Val) n.2102A>G c.1963A>G (p.Ile655Val) c.1495A>G (p.Ile499Val) c.1804A>G (p.Ile602Val) c.1141A>G (p.Ile381Val) c.1123A>G (p.Ile375Val) n.2086A>G | gnomAD v4 |
| 13 | g.28028211T>G | CA387652144 | FLT3 | c.2020A>C (p.Ile674Leu) n.2102A>C c.1963A>C (p.Ile655Leu) c.1495A>C (p.Ile499Leu) c.1804A>C (p.Ile602Leu) c.1141A>C (p.Ile381Leu) c.1123A>C (p.Ile375Leu) n.2086A>C | |
| 13 | g.28028212A>C | CA387652146 | FLT3 | c.2019T>G (p.Asn673Lys) n.2101T>G c.1962T>G (p.Asn654Lys) c.1494T>G (p.Asn498Lys) c.1803T>G (p.Asn601Lys) c.1140T>G (p.Asn380Lys) c.1122T>G (p.Asn374Lys) n.2085T>G | |
| 13 | g.28028212A>G | CA483043319 | FLT3 | c.2019T>C (p.Asn673=) n.2101T>C c.1962T>C (p.Asn654=) c.1494T>C (p.Asn498=) c.1803T>C (p.Asn601=) c.1140T>C (p.Asn380=) c.1122T>C (p.Asn374=) n.2085T>C | |
| 13 | g.28028212A>T | CA387652147 | FLT3 | c.2019T>A (p.Asn673Lys) n.2101T>A c.1962T>A (p.Asn654Lys) c.1494T>A (p.Asn498Lys) c.1803T>A (p.Asn601Lys) c.1140T>A (p.Asn380Lys) c.1122T>A (p.Asn374Lys) n.2085T>A | |
| 13 | g.28028213T>A | CA387652148 | FLT3 | c.2018A>T (p.Asn673Ile) n.2100A>T c.1961A>T (p.Asn654Ile) c.1493A>T (p.Asn498Ile) c.1802A>T (p.Asn601Ile) c.1139A>T (p.Asn380Ile) c.1121A>T (p.Asn374Ile) n.2084A>T | |
| 13 | g.28028213T>C | CA387652149 | FLT3 | c.2018A>G (p.Asn673Ser) n.2100A>G c.1961A>G (p.Asn654Ser) c.1493A>G (p.Asn498Ser) c.1802A>G (p.Asn601Ser) c.1139A>G (p.Asn380Ser) c.1121A>G (p.Asn374Ser) n.2084A>G | |
| 13 | g.28028213T>G | CA387652150 | FLT3 | c.2018A>C (p.Asn673Thr) n.2100A>C c.1961A>C (p.Asn654Thr) c.1493A>C (p.Asn498Thr) c.1802A>C (p.Asn601Thr) c.1139A>C (p.Asn380Thr) c.1121A>C (p.Asn374Thr) n.2084A>C | |
| 13 | g.28028214T>A | CA387652151 | FLT3 | c.2017A>T (p.Asn673Tyr) n.2099A>T c.1960A>T (p.Asn654Tyr) c.1492A>T (p.Asn498Tyr) c.1801A>T (p.Asn601Tyr) c.1138A>T (p.Asn380Tyr) c.1120A>T (p.Asn374Tyr) n.2083A>T | |
| 13 | g.28028214T>C | CA387652152 | FLT3 | c.2017A>G (p.Asn673Asp) n.2099A>G c.1960A>G (p.Asn654Asp) c.1492A>G (p.Asn498Asp) c.1801A>G (p.Asn601Asp) c.1138A>G (p.Asn380Asp) c.1120A>G (p.Asn374Asp) n.2083A>G | |
| 13 | g.28028214T>G | CA387652153 | FLT3 | c.2017A>C (p.Asn673His) n.2099A>C c.1960A>C (p.Asn654His) c.1492A>C (p.Asn498His) c.1801A>C (p.Asn601His) c.1138A>C (p.Asn380His) c.1120A>C (p.Asn374His) n.2083A>C | |
| 13 | g.28028215C>A | CA387652154 | FLT3 | c.2016G>T (p.Glu672Asp) n.2098G>T c.1959G>T (p.Glu653Asp) c.1491G>T (p.Glu497Asp) c.1800G>T (p.Glu600Asp) c.1137G>T (p.Glu379Asp) c.1119G>T (p.Glu373Asp) n.2082G>T | |
| 13 | g.28028215C>G | CA387652155 | FLT3 | c.2016G>C (p.Glu672Asp) n.2098G>C c.1959G>C (p.Glu653Asp) c.1491G>C (p.Glu497Asp) c.1800G>C (p.Glu600Asp) c.1137G>C (p.Glu379Asp) c.1119G>C (p.Glu373Asp) n.2082G>C | |
| 13 | g.28028215C>T | CA483043327 | FLT3 | c.2016G>A (p.Glu672=) n.2098G>A c.1959G>A (p.Glu653=) c.1491G>A (p.Glu497=) c.1800G>A (p.Glu600=) c.1137G>A (p.Glu379=) c.1119G>A (p.Glu373=) n.2082G>A | |
| 13 | g.28028216T>A | CA387652158 | FLT3 | c.2015A>T (p.Glu672Val) n.2097A>T c.1958A>T (p.Glu653Val) c.1490A>T (p.Glu497Val) c.1799A>T (p.Glu600Val) c.1136A>T (p.Glu379Val) c.1118A>T (p.Glu373Val) n.2081A>T | |
| 13 | g.28028216T>C | CA387652157 | FLT3 | c.2015A>G (p.Glu672Gly) n.2097A>G c.1958A>G (p.Glu653Gly) c.1490A>G (p.Glu497Gly) c.1799A>G (p.Glu600Gly) c.1136A>G (p.Glu379Gly) c.1118A>G (p.Glu373Gly) n.2081A>G | |
| 13 | g.28028216T>G | CA387652156 | FLT3 | c.2015A>C (p.Glu672Ala) n.2097A>C c.1958A>C (p.Glu653Ala) c.1490A>C (p.Glu497Ala) c.1799A>C (p.Glu600Ala) c.1136A>C (p.Glu379Ala) c.1118A>C (p.Glu373Ala) n.2081A>C | |
| 13 | g.28028217C>A | CA387652159 | FLT3 | c.2014G>T (p.Glu672Ter) n.2096G>T c.1957G>T (p.Glu653Ter) c.1489G>T (p.Glu497Ter) c.1798G>T (p.Glu600Ter) c.1135G>T (p.Glu379Ter) c.1117G>T (p.Glu373Ter) n.2080G>T | gnomAD v4 |
| 13 | g.28028217C= | CA2080790606 | FLT3 | c.2014G= (p.Glu672=) n.2096G= c.1957G= (p.Glu653=) c.1489G= (p.Glu497=) c.1798G= (p.Glu600=) c.1135G= (p.Glu379=) c.1117G= (p.Glu373=) n.2080G= | |
| 13 | g.28028217C>G | CA387652160 | FLT3 | c.2014G>C (p.Glu672Gln) n.2096G>C c.1957G>C (p.Glu653Gln) c.1489G>C (p.Glu497Gln) c.1798G>C (p.Glu600Gln) c.1135G>C (p.Glu379Gln) c.1117G>C (p.Glu373Gln) n.2080G>C | |
| 13 | g.28028217C>T | CA387652161 | FLT3 | c.2014G>A (p.Glu672Lys) n.2096G>A c.1957G>A (p.Glu653Lys) c.1489G>A (p.Glu497Lys) c.1798G>A (p.Glu600Lys) c.1135G>A (p.Glu379Lys) c.1117G>A (p.Glu373Lys) n.2080G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.28028218G>A | CA6928486 | FLT3 | c.2013C>T (p.His671=) n.2095C>T c.1956C>T (p.His652=) c.1488C>T (p.His496=) c.1797C>T (p.His599=) c.1134C>T (p.His378=) c.1116C>T (p.His372=) n.2079C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.28028218G>C | CA387652162 | FLT3 | c.2013C>G (p.His671Gln) n.2095C>G c.1956C>G (p.His652Gln) c.1488C>G (p.His496Gln) c.1797C>G (p.His599Gln) c.1134C>G (p.His378Gln) c.1116C>G (p.His372Gln) n.2079C>G | dbSNP gnomAD v2 |
| 13 | g.28028218G= | CA2080790607 | FLT3 | c.2013C= (p.His671=) n.2095C= c.1956C= (p.His652=) c.1488C= (p.His496=) c.1797C= (p.His599=) c.1134C= (p.His378=) c.1116C= (p.His372=) n.2079C= | |
| 13 | g.28028218G>T | CA387652163 | FLT3 | c.2013C>A (p.His671Gln) n.2095C>A c.1956C>A (p.His652Gln) c.1488C>A (p.His496Gln) c.1797C>A (p.His599Gln) c.1134C>A (p.His378Gln) c.1116C>A (p.His372Gln) n.2079C>A | |
| 13 | g.28028219T>A | CA387652164 | FLT3 | c.2012A>T (p.His671Leu) n.2094A>T c.1955A>T (p.His652Leu) c.1487A>T (p.His496Leu) c.1796A>T (p.His599Leu) c.1133A>T (p.His378Leu) c.1115A>T (p.His372Leu) n.2078A>T | |
| 13 | g.28028219T>C | CA387652165 | FLT3 | c.2012A>G (p.His671Arg) n.2094A>G c.1955A>G (p.His652Arg) c.1487A>G (p.His496Arg) c.1796A>G (p.His599Arg) c.1133A>G (p.His378Arg) c.1115A>G (p.His372Arg) n.2078A>G |