| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.28018497_28018500delinsCATG | CA2080781422 | FLT3 | c.2508_2511delinsCATG (p.Ile836=) c.*420_*423delinsCATG (n.*420_*423delinsCATG) n.2722_2725delinsCATG c.2451_2454delinsCATG (p.Ile817=) c.1983_1986delinsCATG (p.Ile661=) c.2292_2295delinsCATG (p.Ile764=) c.1629_1632delinsCATG (p.Ile543=) c.1611_1614delinsCATG (p.Ile537=) n.2706_2709delinsCATG | |
| 13 | g.28018500_28018502del | CA16602772 | FLT3 | c.2508_2510del (p.Ile836del) c.*420_*422del (n.*420_*422del) n.2722_2724del c.2451_2453del (p.Ile817del) c.1983_1985del (p.Ile661del) c.2292_2294del (p.Ile764del) c.1629_1631del (p.Ile543del) c.1611_1613del (p.Ile537del) n.2706_2708del | ClinVar dbSNP COSMIC COSMIC COSMIC |
| 13 | g.28018500G>A | CA483042233 | FLT3 | c.2508C>T (p.Ile836=) c.*420C>T (n.*420C>T) n.2722C>T c.2451C>T (p.Ile817=) c.1983C>T (p.Ile661=) c.2292C>T (p.Ile764=) c.1629C>T (p.Ile543=) c.1611C>T (p.Ile537=) n.2706C>T | dbSNP |
| 13 | g.28018500G>C | CA16602446 | FLT3 | c.2508C>G (p.Ile836Met) c.*420C>G (n.*420C>G) n.2722C>G c.2451C>G (p.Ile817Met) c.1983C>G (p.Ile661Met) c.2292C>G (p.Ile764Met) c.1629C>G (p.Ile543Met) c.1611C>G (p.Ile537Met) n.2706C>G | ClinVar dbSNP COSMIC |
| 13 | g.28018500G= | CA2080781440 | FLT3 | c.2508C= (p.Ile836=) c.*420C= (n.*420C=) n.2722C= c.2451C= (p.Ile817=) c.1983C= (p.Ile661=) c.2292C= (p.Ile764=) c.1629C= (p.Ile543=) c.1611C= (p.Ile537=) n.2706C= | |
| 13 | g.28018500G>T | CA483042234 | FLT3 | c.2508C>A (p.Ile836=) c.*420C>A (n.*420C>A) n.2722C>A c.2451C>A (p.Ile817=) c.1983C>A (p.Ile661=) c.2292C>A (p.Ile764=) c.1629C>A (p.Ile543=) c.1611C>A (p.Ile537=) n.2706C>A | dbSNP COSMIC |
| 13 | g.28018500_28018501insGGGGGGCGGGAG | CA645597691 | FLT3 | c.2508_2509insTCCCGCCCCCCC (p.Ile836_Met837insSerArgProPro) c.*420_*421insTCCCGCCCCCCC (n.*420_*421insTCCCGCCCCCCC) n.2722_2723insTCCCGCCCCCCC c.2451_2452insTCCCGCCCCCCC (p.Ile817_Met818insSerArgProPro) c.1983_1984insTCCCGCCCCCCC (p.Ile661_Met662insSerArgProPro) c.2292_2293insTCCCGCCCCCCC (p.Ile764_Met765insSerArgProPro) c.1629_1630insTCCCGCCCCCCC (p.Ile543_Met544insSerArgProPro) c.1611_1612insTCCCGCCCCCCC (p.Ile537_Met538insSerArgProPro) n.2706_2707insTCCCGCCCCCCC | COSMIC |
| 13 | g.28018500_28018502delinsAAA | CA645597693 | FLT3 | c.2506_2508delinsTTT (p.Ile836Phe) c.*418_*420delinsTTT (n.*418_*420delinsTTT) n.2720_2722delinsTTT c.2449_2451delinsTTT (p.Ile817Phe) c.1981_1983delinsTTT (p.Ile661Phe) c.2290_2292delinsTTT (p.Ile764Phe) c.1627_1629delinsTTT (p.Ile543Phe) c.1609_1611delinsTTT (p.Ile537Phe) n.2704_2706delinsTTT | COSMIC |
| 13 | g.28018500_28018505del | CA645597692 | FLT3 | c.2503_2508del (p.Asp835_Ile836del) c.*415_*420del (n.*415_*420del) n.2717_2722del c.2446_2451del (p.Asp816_Ile817del) c.1978_1983del (p.Asp660_Ile661del) c.2287_2292del (p.Asp763_Ile764del) c.1624_1629del (p.Asp542_Ile543del) c.1606_1611del (p.Asp536_Ile537del) n.2701_2706del | dbSNP COSMIC |
| 13 | g.28018501A= | CA2080781449 | FLT3 | c.2507T= (p.Ile836=) c.*419T= (n.*419T=) n.2721T= c.2450T= (p.Ile817=) c.1982T= (p.Ile661=) c.2291T= (p.Ile764=) c.1628T= (p.Ile543=) c.1610T= (p.Ile537=) n.2705T= | |
| 13 | g.28018501A>C | CA16603127 | FLT3 | c.2507T>G (p.Ile836Ser) c.*419T>G (n.*419T>G) n.2721T>G c.2450T>G (p.Ile817Ser) c.1982T>G (p.Ile661Ser) c.2291T>G (p.Ile764Ser) c.1628T>G (p.Ile543Ser) c.1610T>G (p.Ile537Ser) n.2705T>G | ClinVar dbSNP COSMIC |
| 13 | g.28018501A>G | CA387650198 | FLT3 | c.2507T>C (p.Ile836Thr) c.*419T>C (n.*419T>C) n.2721T>C c.2450T>C (p.Ile817Thr) c.1982T>C (p.Ile661Thr) c.2291T>C (p.Ile764Thr) c.1628T>C (p.Ile543Thr) c.1610T>C (p.Ile537Thr) n.2705T>C | dbSNP COSMIC |
| 13 | g.28018501A>T | CA387650199 | FLT3 | c.2507T>A (p.Ile836Asn) c.*419T>A (n.*419T>A) n.2721T>A c.2450T>A (p.Ile817Asn) c.1982T>A (p.Ile661Asn) c.2291T>A (p.Ile764Asn) c.1628T>A (p.Ile543Asn) c.1610T>A (p.Ile537Asn) n.2705T>A | dbSNP |
| 13 | g.28018501_28018502delinsTCCAA | CA645597694 | FLT3 | c.2506_2507delinsTTGGA (p.Ile836delinsLeuAsp) c.*418_*419delinsTTGGA (n.*418_*419delinsTTGGA) n.2720_2721delinsTTGGA c.2449_2450delinsTTGGA (p.Ile817delinsLeuAsp) c.1981_1982delinsTTGGA (p.Ile661delinsLeuAsp) c.2290_2291delinsTTGGA (p.Ile764delinsLeuAsp) c.1627_1628delinsTTGGA (p.Ile543delinsLeuAsp) c.1609_1610delinsTTGGA (p.Ile537delinsLeuAsp) n.2704_2705delinsTTGGA | COSMIC |
| 13 | g.28018502T>A | CA16603131 | FLT3 | c.2506A>T (p.Ile836Phe) c.*418A>T (n.*418A>T) n.2720A>T c.2449A>T (p.Ile817Phe) c.1981A>T (p.Ile661Phe) c.2290A>T (p.Ile764Phe) c.1627A>T (p.Ile543Phe) c.1609A>T (p.Ile537Phe) n.2704A>T | ClinVar dbSNP |
| 13 | g.28018502T>C | CA16603129 | FLT3 | c.2506A>G (p.Ile836Val) c.*418A>G (n.*418A>G) n.2720A>G c.2449A>G (p.Ile817Val) c.1981A>G (p.Ile661Val) c.2290A>G (p.Ile764Val) c.1627A>G (p.Ile543Val) c.1609A>G (p.Ile537Val) n.2704A>G | ClinVar dbSNP |
| 13 | g.28018502T>G | CA16602447 | FLT3 | c.2506A>C (p.Ile836Leu) c.*418A>C (n.*418A>C) n.2720A>C c.2449A>C (p.Ile817Leu) c.1981A>C (p.Ile661Leu) c.2290A>C (p.Ile764Leu) c.1627A>C (p.Ile543Leu) c.1609A>C (p.Ile537Leu) n.2704A>C | ClinVar dbSNP COSMIC |
| 13 | g.28018502T= | CA2080781464 | FLT3 | c.2506A= (p.Ile836=) c.*418A= (n.*418A=) n.2720A= c.2449A= (p.Ile817=) c.1981A= (p.Ile661=) c.2290A= (p.Ile764=) c.1627A= (p.Ile543=) c.1609A= (p.Ile537=) n.2704A= | |
| 13 | g.28018502_28018504del | CA645597695 | FLT3 | c.2504_2506del (p.Asp835_Ile836delinsVal) c.*416_*418del (n.*416_*418del) n.2718_2720del c.2447_2449del (p.Asp816_Ile817delinsVal) c.1979_1981del (p.Asp660_Ile661delinsVal) c.2288_2290del (p.Asp763_Ile764delinsVal) c.1625_1627del (p.Asp542_Ile543delinsVal) c.1607_1609del (p.Asp536_Ile537delinsVal) n.2702_2704del | dbSNP COSMIC |
| 13 | g.28018502_28018505delinsTATC | CA2080781467 | FLT3 | c.2503_2506delinsGATA (p.Asp835=) c.*415_*418delinsGATA (n.*415_*418delinsGATA) n.2717_2720delinsGATA c.2446_2449delinsGATA (p.Asp816=) c.1978_1981delinsGATA (p.Asp660=) c.2287_2290delinsGATA (p.Asp763=) c.1624_1627delinsGATA (p.Asp542=) c.1606_1609delinsGATA (p.Asp536=) n.2701_2704delinsGATA | |
| 13 | g.28018503A= | CA2080781483 | FLT3 | c.2505T= (p.Asp835=) c.*417T= (n.*417T=) n.2719T= c.2448T= (p.Asp816=) c.1980T= (p.Asp660=) c.2289T= (p.Asp763=) c.1626T= (p.Asp542=) c.1608T= (p.Asp536=) n.2703T= | |
| 13 | g.28018503A>C | CA16602448 | FLT3 | c.2505T>G (p.Asp835Glu) c.*417T>G (n.*417T>G) n.2719T>G c.2448T>G (p.Asp816Glu) c.1980T>G (p.Asp660Glu) c.2289T>G (p.Asp763Glu) c.1626T>G (p.Asp542Glu) c.1608T>G (p.Asp536Glu) n.2703T>G | ClinVar dbSNP |
| 13 | g.28018503A>G | CA483042235 | FLT3 | c.2505T>C (p.Asp835=) c.*417T>C (n.*417T>C) n.2719T>C c.2448T>C (p.Asp816=) c.1980T>C (p.Asp660=) c.2289T>C (p.Asp763=) c.1626T>C (p.Asp542=) c.1608T>C (p.Asp536=) n.2703T>C | |
| 13 | g.28018503A>T | CA16602449 | FLT3 | c.2505T>A (p.Asp835Glu) c.*417T>A (n.*417T>A) n.2719T>A c.2448T>A (p.Asp816Glu) c.1980T>A (p.Asp660Glu) c.2289T>A (p.Asp763Glu) c.1626T>A (p.Asp542Glu) c.1608T>A (p.Asp536Glu) n.2703T>A | ClinVar dbSNP |
| 13 | g.28018503_28018505del | CA280214 | FLT3 | c.2503_2505del (p.Asp835del) c.*415_*417del (n.*415_*417del) n.2717_2719del c.2446_2448del (p.Asp816del) c.1978_1980del (p.Asp660del) c.2287_2289del (p.Asp763del) c.1624_1626del (p.Asp542del) c.1606_1608del (p.Asp536del) n.2701_2703del | ClinVar dbSNP COSMIC COSMIC |
| 13 | g.28018503_28018505delinsGAT | CA923726226 | FLT3 | c.2503_2505delinsATC (p.Asp835Ile) c.*415_*417delinsATC (n.*415_*417delinsATC) n.2717_2719delinsATC c.2446_2448delinsATC (p.Asp816Ile) c.1978_1980delinsATC (p.Asp660Ile) c.2287_2289delinsATC (p.Asp763Ile) c.1624_1626delinsATC (p.Asp542Ile) c.1606_1608delinsATC (p.Asp536Ile) n.2701_2703delinsATC | |
| 13 | g.28018503_28018505delinsTAT | CA923726227 | FLT3 | c.2503_2505delinsATA (p.Asp835Ile) c.*415_*417delinsATA (n.*415_*417delinsATA) n.2717_2719delinsATA c.2446_2448delinsATA (p.Asp816Ile) c.1978_1980delinsATA (p.Asp660Ile) c.2287_2289delinsATA (p.Asp763Ile) c.1624_1626delinsATA (p.Asp542Ile) c.1606_1608delinsATA (p.Asp536Ile) n.2701_2703delinsATA | |
| 13 | g.28018504_28018509del | CA645597696 | FLT3 | c.2500_2505del (p.Arg834_Asp835del) c.*412_*417del (n.*412_*417del) n.2714_2719del c.2443_2448del (p.Arg815_Asp816del) c.1975_1980del (p.Arg659_Asp660del) c.2284_2289del (p.Arg762_Asp763del) c.1621_1626del (p.Arg541_Asp542del) c.1603_1608del (p.Arg535_Asp536del) n.2698_2703del | COSMIC |
| 13 | g.28018504T>A | CA126344 | FLT3 | c.2504A>T (p.Asp835Val) c.*416A>T (n.*416A>T) n.2718A>T c.2447A>T (p.Asp816Val) c.1979A>T (p.Asp660Val) c.2288A>T (p.Asp763Val) c.1625A>T (p.Asp542Val) c.1607A>T (p.Asp536Val) n.2702A>T | ClinVar dbSNP COSMIC |
| 13 | g.28018504T>C | CA387650200 | FLT3 | c.2504A>G (p.Asp835Gly) c.*416A>G (n.*416A>G) n.2718A>G c.2447A>G (p.Asp816Gly) c.1979A>G (p.Asp660Gly) c.2288A>G (p.Asp763Gly) c.1625A>G (p.Asp542Gly) c.1607A>G (p.Asp536Gly) n.2702A>G | dbSNP |
| 13 | g.28018504T>G | CA16602450 | FLT3 | c.2504A>C (p.Asp835Ala) c.*416A>C (n.*416A>C) n.2718A>C c.2447A>C (p.Asp816Ala) c.1979A>C (p.Asp660Ala) c.2288A>C (p.Asp763Ala) c.1625A>C (p.Asp542Ala) c.1607A>C (p.Asp536Ala) n.2702A>C | ClinVar dbSNP COSMIC |
| 13 | g.28018504T= | CA2080781493 | FLT3 | c.2504A= (p.Asp835=) c.*416A= (n.*416A=) n.2718A= c.2447A= (p.Asp816=) c.1979A= (p.Asp660=) c.2288A= (p.Asp763=) c.1625A= (p.Asp542=) c.1607A= (p.Asp536=) n.2702A= | |
| 13 | g.28018504_28018505delinsAA | CA16602563 | FLT3 | c.2503_2504delinsTT (p.Asp835Phe) c.*415_*416delinsTT (n.*415_*416delinsTT) n.2717_2718delinsTT c.2446_2447delinsTT (p.Asp816Phe) c.1978_1979delinsTT (p.Asp660Phe) c.2287_2288delinsTT (p.Asp763Phe) c.1624_1625delinsTT (p.Asp542Phe) c.1606_1607delinsTT (p.Asp536Phe) n.2701_2702delinsTT | ClinVar dbSNP COSMIC |
| 13 | g.28018504_28018505delinsAT | CA923726224 | FLT3 | c.2503_2504delinsAT (p.Asp835Ile) c.*415_*416delinsAT (n.*415_*416delinsAT) n.2717_2718delinsAT c.2446_2447delinsAT (p.Asp816Ile) c.1978_1979delinsAT (p.Asp660Ile) c.2287_2288delinsAT (p.Asp763Ile) c.1624_1625delinsAT (p.Asp542Ile) c.1606_1607delinsAT (p.Asp536Ile) n.2701_2702delinsAT | |
| 13 | g.28018504_28018505delinsTC | CA2080781497 | FLT3 | c.2503_2504delinsGA (p.Asp835=) c.*415_*416delinsGA (n.*415_*416delinsGA) n.2717_2718delinsGA c.2446_2447delinsGA (p.Asp816=) c.1978_1979delinsGA (p.Asp660=) c.2287_2288delinsGA (p.Asp763=) c.1624_1625delinsGA (p.Asp542=) c.1606_1607delinsGA (p.Asp536=) n.2701_2702delinsGA | |
| 13 | g.28018505C>A | CA126347 | FLT3 | c.2503G>T (p.Asp835Tyr) c.*415G>T (n.*415G>T) n.2717G>T c.2446G>T (p.Asp816Tyr) c.1978G>T (p.Asp660Tyr) c.2287G>T (p.Asp763Tyr) c.1624G>T (p.Asp542Tyr) c.1606G>T (p.Asp536Tyr) n.2701G>T | ClinVar dbSNP COSMIC |
| 13 | g.28018505C= | CA2080781510 | FLT3 | c.2503G= (p.Asp835=) c.*415G= (n.*415G=) n.2717G= c.2446G= (p.Asp816=) c.1978G= (p.Asp660=) c.2287G= (p.Asp763=) c.1624G= (p.Asp542=) c.1606G= (p.Asp536=) n.2701G= | |
| 13 | g.28018505C>G | CA280208 | FLT3 | c.2503G>C (p.Asp835His) c.*415G>C (n.*415G>C) n.2717G>C c.2446G>C (p.Asp816His) c.1978G>C (p.Asp660His) c.2287G>C (p.Asp763His) c.1624G>C (p.Asp542His) c.1606G>C (p.Asp536His) n.2701G>C | ClinVar dbSNP COSMIC |
| 13 | g.28018505C>T | CA280211 | FLT3 | c.2503G>A (p.Asp835Asn) c.*415G>A (n.*415G>A) n.2717G>A c.2446G>A (p.Asp816Asn) c.1978G>A (p.Asp660Asn) c.2287G>A (p.Asp763Asn) c.1624G>A (p.Asp542Asn) c.1606G>A (p.Asp536Asn) n.2701G>A | ClinVar dbSNP COSMIC |
| 13 | g.28018506T>A | CA483042238 | FLT3 | c.2502A>T (p.Arg834=) c.*414A>T (n.*414A>T) n.2716A>T c.2445A>T (p.Arg815=) c.1977A>T (p.Arg659=) c.2286A>T (p.Arg762=) c.1623A>T (p.Arg541=) c.1605A>T (p.Arg535=) n.2700A>T | dbSNP |
| 13 | g.28018506T>C | CA483042236 | FLT3 | c.2502A>G (p.Arg834=) c.*414A>G (n.*414A>G) n.2716A>G c.2445A>G (p.Arg815=) c.1977A>G (p.Arg659=) c.2286A>G (p.Arg762=) c.1623A>G (p.Arg541=) c.1605A>G (p.Arg535=) n.2700A>G | |
| 13 | g.28018506T>G | CA483042237 | FLT3 | c.2502A>C (p.Arg834=) c.*414A>C (n.*414A>C) n.2716A>C c.2445A>C (p.Arg815=) c.1977A>C (p.Arg659=) c.2286A>C (p.Arg762=) c.1623A>C (p.Arg541=) c.1605A>C (p.Arg535=) n.2700A>C | dbSNP |
| 13 | g.28018506T= | CA2080781513 | FLT3 | c.2502A= (p.Arg834=) c.*414A= (n.*414A=) n.2716A= c.2445A= (p.Arg815=) c.1977A= (p.Arg659=) c.2286A= (p.Arg762=) c.1623A= (p.Arg541=) c.1605A= (p.Arg535=) n.2700A= | |
| 13 | g.28018507C>A | CA387650201 | FLT3 | c.2501G>T (p.Arg834Leu) c.*413G>T (n.*413G>T) n.2715G>T c.2444G>T (p.Arg815Leu) c.1976G>T (p.Arg659Leu) c.2285G>T (p.Arg762Leu) c.1622G>T (p.Arg541Leu) c.1604G>T (p.Arg535Leu) n.2699G>T | gnomAD v4 |
| 13 | g.28018507C= | CA2080781516 | FLT3 | c.2501G= (p.Arg834=) c.*413G= (n.*413G=) n.2715G= c.2444G= (p.Arg815=) c.1976G= (p.Arg659=) c.2285G= (p.Arg762=) c.1622G= (p.Arg541=) c.1604G= (p.Arg535=) n.2699G= | |
| 13 | g.28018507C>G | CA387650203 | FLT3 | c.2501G>C (p.Arg834Pro) c.*413G>C (n.*413G>C) n.2715G>C c.2444G>C (p.Arg815Pro) c.1976G>C (p.Arg659Pro) c.2285G>C (p.Arg762Pro) c.1622G>C (p.Arg541Pro) c.1604G>C (p.Arg535Pro) n.2699G>C | dbSNP gnomAD v4 |
| 13 | g.28018507C>T | CA387650202 | FLT3 | c.2501G>A (p.Arg834Gln) c.*413G>A (n.*413G>A) n.2715G>A c.2444G>A (p.Arg815Gln) c.1976G>A (p.Arg659Gln) c.2285G>A (p.Arg762Gln) c.1622G>A (p.Arg541Gln) c.1604G>A (p.Arg535Gln) n.2699G>A | dbSNP gnomAD v4 COSMIC |
| 13 | g.28018508G>A | CA6928305 | FLT3 | c.2500C>T (p.Arg834Ter) c.*412C>T (n.*412C>T) n.2714C>T c.2443C>T (p.Arg815Ter) c.1975C>T (p.Arg659Ter) c.2284C>T (p.Arg762Ter) c.1621C>T (p.Arg541Ter) c.1603C>T (p.Arg535Ter) n.2698C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 13 | g.28018508G>C | CA387650204 | FLT3 | c.2500C>G (p.Arg834Gly) c.*412C>G (n.*412C>G) n.2714C>G c.2443C>G (p.Arg815Gly) c.1975C>G (p.Arg659Gly) c.2284C>G (p.Arg762Gly) c.1621C>G (p.Arg541Gly) c.1603C>G (p.Arg535Gly) n.2698C>G | dbSNP |
| 13 | g.28018508G= | CA2080781519 | FLT3 | c.2500C= (p.Arg834=) c.*412C= (n.*412C=) n.2714C= c.2443C= (p.Arg815=) c.1975C= (p.Arg659=) c.2284C= (p.Arg762=) c.1621C= (p.Arg541=) c.1603C= (p.Arg535=) n.2698C= |