ClinVar Miner

List of variants in gene FOXP1 reported by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 151
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HGVS dbSNP gnomAD frequency
NM_001349338.3(FOXP1):c.1889+20C>A rs7638391 0.94569
NM_001349338.3(FOXP1):c.-11-33T>A rs9855825 0.68941
NM_001349338.3(FOXP1):c.1722+137A>G rs9874207 0.63398
NM_001349338.3(FOXP1):c.181-213C>T rs3843363 0.58729
NM_001349338.3(FOXP1):c.1146+151T>C rs6802472 0.43060
NM_001349338.3(FOXP1):c.974+269A>T rs11128203 0.38769
NM_001349338.3(FOXP1):c.180+537A>T rs2293138 0.35336
NM_001349338.3(FOXP1):c.283-212A>G rs1288979 0.26965
NM_001349338.3(FOXP1):c.180+435G>A rs2293137 0.18945
NM_001349338.3(FOXP1):c.180+49T>C rs2037474 0.18939
NM_001349338.3(FOXP1):c.-91G>A rs17008544 0.15079
NM_001349338.3(FOXP1):c.420+243A>G rs1871148 0.12393
NM_001349338.3(FOXP1):c.180+96T>C rs939845 0.09446
NM_001349338.3(FOXP1):c.1652+806A>C rs3755733 0.07934
NM_001349338.3(FOXP1):c.-11-64C>T rs78495442 0.05088
NM_001349338.3(FOXP1):c.-11-52C>T rs78369780 0.04524
NM_001349338.3(FOXP1):c.1428+90G>C rs11924812 0.03826
NM_001349338.3(FOXP1):c.1889+149A>G rs17008086 0.03565
NM_001349338.3(FOXP1):c.1890-15G>T rs7639736 0.03466
NM_001349338.3(FOXP1):c.975-231G>A rs17008125 0.03253
NM_001349338.3(FOXP1):c.181-50C>T rs17008224 0.03159
NM_001349338.3(FOXP1):c.974+133G>A rs17008134 0.03063
NM_001349338.3(FOXP1):c.664+264C>T rs1288976 0.03005
NM_001349338.3(FOXP1):c.181-321C>G rs9985362 0.02935
NM_001349338.3(FOXP1):c.181-18054A>G rs58847217 0.02361
NM_001349338.3(FOXP1):c.1889+205A>G rs11928045 0.02166
NM_001349338.3(FOXP1):c.510+108T>C rs4555486 0.01117
NM_001349338.3(FOXP1):c.511-248G>C rs11914321 0.01024
NM_001349338.3(FOXP1):c.181-262T>C rs79522164 0.00948
NM_001349338.3(FOXP1):c.181-29G>A rs113050068 0.00886
NM_001349338.3(FOXP1):c.1722+179C>T rs111425991 0.00812
NM_001349338.3(FOXP1):c.282+211T>C rs115531620 0.00743
NM_001349338.3(FOXP1):c.180+289C>T rs141808088 0.00725
NM_001349338.3(FOXP1):c.869+134G>A rs145314293 0.00530
NM_001349338.3(FOXP1):c.1652+839C>G rs184390493 0.00455
NM_001349338.3(FOXP1):c.1890-137G>A rs139747537 0.00429
NM_001349338.3(FOXP1):c.1062+265G>A rs374214924 0.00399
NM_001349338.3(FOXP1):c.1722+63A>G rs189960519 0.00376
NM_001349338.3(FOXP1):c.-11-71A>T rs144226924 0.00316
NM_001349338.3(FOXP1):c.1652+403A>G rs76145927 0.00298
NM_001349338.3(FOXP1):c.1428+173A>G rs140116317 0.00274
NM_001349338.3(FOXP1):c.181-18423_181-18422insC rs1553753128 0.00262
NM_001349338.3(FOXP1):c.181-13T>G rs139264797 0.00220
NM_001349338.3(FOXP1):c.1702C>T (p.Pro568Ser) rs147674680 0.00185
NM_001349338.3(FOXP1):c.1709A>G (p.Asn570Ser) rs140161845 0.00140
NM_001349338.3(FOXP1):c.643C>G (p.Pro215Ala) rs146606219 0.00118
NM_001349338.3(FOXP1):c.1413A>G (p.Ala471=) rs144080925 0.00088
NM_001349338.3(FOXP1):c.1825G>A (p.Ala609Thr) rs147537388 0.00067
NM_001349338.3(FOXP1):c.1890-5T>C rs187666567 0.00059
NM_001349338.3(FOXP1):c.1333G>A (p.Val445Met) rs147756430 0.00044
NM_001349338.3(FOXP1):c.1762G>A (p.Ala588Thr) rs202173892 0.00034
NM_001349338.3(FOXP1):c.123G>A (p.Thr41=) rs201155996 0.00030
NM_001349338.3(FOXP1):c.855T>G (p.Thr285=) rs141007926 0.00029
NM_001349338.3(FOXP1):c.1217C>G (p.Thr406Ser) rs200355554 0.00016
NM_001349338.3(FOXP1):c.936C>T (p.Gly312=) rs61753356 0.00016
NM_001349338.3(FOXP1):c.44C>T (p.Ala15Val) rs532329866 0.00015
NM_001349338.3(FOXP1):c.13T>C (p.Ser5Pro) rs762898505 0.00012
NM_001349338.3(FOXP1):c.1233C>T (p.Thr411=) rs147995584 0.00004
NM_001349338.3(FOXP1):c.1359G>A (p.Ala453=) rs766683691 0.00004
NM_001349338.3(FOXP1):c.888C>T (p.His296=) rs144274165 0.00004
NM_001349338.3(FOXP1):c.1764T>C (p.Ala588=) rs765482675 0.00003
NM_001349338.3(FOXP1):c.2020G>A (p.Glu674Lys) rs368167189 0.00003
NM_001349338.3(FOXP1):c.288C>T (p.Pro96=) rs528713688 0.00003
NM_001349338.3(FOXP1):c.1768A>G (p.Met590Val) rs201446635 0.00002
NM_001349338.3(FOXP1):c.316G>A (p.Val106Ile) rs755709669 0.00002
NM_001349338.3(FOXP1):c.-447+5G>A rs1337469829 0.00001
NM_001349338.3(FOXP1):c.1297G>A (p.Gly433Arg) rs1468570529 0.00001
NM_001349338.3(FOXP1):c.1355T>C (p.Ile452Thr) rs1234343955 0.00001
NM_001349338.3(FOXP1):c.155C>T (p.Ala52Val) rs757649540 0.00001
NM_001349338.3(FOXP1):c.1641A>G (p.Gln547=) rs886058864 0.00001
NM_001349338.3(FOXP1):c.1964C>T (p.Ala655Val) rs762475508 0.00001
NM_001349338.3(FOXP1):c.321C>T (p.Ile107=) rs747108471 0.00001
NM_001349338.3(FOXP1):c.444A>G (p.Lys148=) rs763673991 0.00001
NM_001349338.3(FOXP1):c.*56dup rs112773801
NM_001349338.3(FOXP1):c.-11-29T>A rs56850311
NM_001349338.3(FOXP1):c.1062+128ATTTT[11] rs59993750
NM_001349338.3(FOXP1):c.1062+128ATTTT[12] rs59993750
NM_001349338.3(FOXP1):c.1062+128ATTTT[13] rs59993750
NM_001349338.3(FOXP1):c.1062+128ATTTT[14] rs59993750
NM_001349338.3(FOXP1):c.1062+128ATTTT[15] rs59993750
NM_001349338.3(FOXP1):c.1062+128ATTTT[9] rs59993750
NM_001349338.3(FOXP1):c.1064T>C (p.Leu355Pro) rs1064795306
NM_001349338.3(FOXP1):c.1067C>T (p.Ala356Val) rs2107494409
NM_001349338.3(FOXP1):c.1071del (p.Asp358fs) rs1553678501
NM_001349338.3(FOXP1):c.1095G>T (p.Met365Ile)
NM_001349338.3(FOXP1):c.1127C>T (p.Pro376Leu)
NM_001349338.3(FOXP1):c.1146+10_1146+12del rs199543140
NM_001349338.3(FOXP1):c.1146+1G>A rs1559650552
NM_001349338.3(FOXP1):c.1146+5G>C rs1553678368
NM_001349338.3(FOXP1):c.1162A>T (p.Ser388Cys)
NM_001349338.3(FOXP1):c.1177A>T (p.Lys393Ter) rs1553668839
NM_001349338.3(FOXP1):c.1237C>G (p.Pro413Ala) rs2107317317
NM_001349338.3(FOXP1):c.1239_1265dup (p.Leu414_Ser422dup) rs2107316260
NM_001349338.3(FOXP1):c.1240_1241del (p.Leu414fs) rs1064793130
NM_001349338.3(FOXP1):c.1240dup (p.Leu414fs) rs797044652
NM_001349338.3(FOXP1):c.1264T>C (p.Ser422Pro)
NM_001349338.3(FOXP1):c.1265_1266del (p.Ser422fs) rs1064796914
NM_001349338.3(FOXP1):c.1313G>A (p.Arg438Gln) rs2037908174
NM_001349338.3(FOXP1):c.1314_1321del (p.Tyr439fs) rs1575806033
NM_001349338.3(FOXP1):c.1329C>G (p.Tyr443Ter) rs1064793944
NM_001349338.3(FOXP1):c.1348G>A (p.Ala450Thr) rs1553668386
NM_001349338.3(FOXP1):c.1365C>G (p.Asn455Lys)
NM_001349338.3(FOXP1):c.136A>G (p.Ile46Val)
NM_001349338.3(FOXP1):c.1409A>G (p.Tyr470Cys) rs769448730
NM_001349338.3(FOXP1):c.1540C>T (p.Arg514Cys) rs869025203
NM_001349338.3(FOXP1):c.1541G>A (p.Arg514His) rs797045586
NM_001349338.3(FOXP1):c.1544_1569dup (p.Val524fs) rs886041821
NM_001349338.3(FOXP1):c.1561A>G (p.Lys521Glu) rs1553663113
NM_001349338.3(FOXP1):c.1573C>T (p.Arg525Ter) rs112795301
NM_001349338.3(FOXP1):c.1574G>A (p.Arg525Gln) rs1553663084
NM_001349338.3(FOXP1):c.157C>T (p.His53Tyr)
NM_001349338.3(FOXP1):c.1631G>A (p.Arg544Gln) rs2036497448
NM_001349338.3(FOXP1):c.1635G>A (p.Arg545=)
NM_001349338.3(FOXP1):c.1652+5G>A rs794727216
NM_001349338.3(FOXP1):c.1653-3C>G rs1332032295
NM_001349338.3(FOXP1):c.165GCA[3] (p.Gln60del)
NM_001349338.3(FOXP1):c.1717_1722+5del rs1553660890
NM_001349338.3(FOXP1):c.1722G>C (p.Gln574His) rs2107155481
NM_001349338.3(FOXP1):c.181G>A (p.Ala61Thr)
NM_001349338.3(FOXP1):c.1822G>C (p.Gly608Arg)
NM_001349338.3(FOXP1):c.1849G>A (p.Glu617Lys) rs1323763108
NM_001349338.3(FOXP1):c.184C>T (p.Leu62Phe) rs538443416
NM_001349338.3(FOXP1):c.1872A>T (p.Arg624Ser)
NM_001349338.3(FOXP1):c.1889+1G>T rs1553656387
NM_001349338.3(FOXP1):c.1889+5G>T rs1553656383
NM_001349338.3(FOXP1):c.1891C>T (p.His631Tyr) rs2106858982
NM_001349338.3(FOXP1):c.18G>T (p.Gly6=)
NM_001349338.3(FOXP1):c.1949C>A (p.Ser650Tyr) rs2106857321
NM_001349338.3(FOXP1):c.1956_1958del (p.Thr654del)
NM_001349338.3(FOXP1):c.1961C>T (p.Thr654Ile)
NM_001349338.3(FOXP1):c.1963G>A (p.Ala655Thr)
NM_001349338.3(FOXP1):c.291G>A (p.Val97=)
NM_001349338.3(FOXP1):c.320T>C (p.Ile107Thr)
NM_001349338.3(FOXP1):c.356_367del (p.Gln119_Ser122del)
NM_001349338.3(FOXP1):c.511-3C>A rs778983019
NM_001349338.3(FOXP1):c.520G>A (p.Val174Met) rs2106977104
NM_001349338.3(FOXP1):c.529C>T (p.Gln177Ter) rs1559807265
NM_001349338.3(FOXP1):c.564G>A (p.Met188Ile)
NM_001349338.3(FOXP1):c.574C>T (p.Gln192Ter) rs1057524732
NM_001349338.3(FOXP1):c.602G>A (p.Arg201His) rs1450448594
NM_001349338.3(FOXP1):c.607G>A (p.Gly203Ser) rs2106974116
NM_001349338.3(FOXP1):c.625C>T (p.Pro209Ser)
NM_001349338.3(FOXP1):c.665-7_665-4del rs1453915867
NM_001349338.3(FOXP1):c.728A>G (p.Glu243Gly)
NM_001349338.3(FOXP1):c.773G>A (p.Cys258Tyr)
NM_001349338.3(FOXP1):c.821A>G (p.His274Arg)
NM_001349338.3(FOXP1):c.869+3A>G
NM_001349338.3(FOXP1):c.870-2A>G
NM_001349338.3(FOXP1):c.870-74dup rs151011253
NM_001349338.3(FOXP1):c.963A>T (p.Gln321His) rs900526015
NM_032682.6(FOXP1):c.1379A>G (p.Lys460Arg) rs2107310819

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