ClinVar Miner

List of variants in gene FOXP1 studied for intellectual disability

Included ClinVar conditions (613):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 148
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HGVS dbSNP gnomAD frequency
NM_001349338.3(FOXP1):c.1889+20C>A rs7638391 0.94569
NM_001349338.3(FOXP1):c.44C>T (p.Ala15Val) rs532329866 0.00015
NM_001349338.3(FOXP1):c.179A>G (p.Gln60Arg) rs374060287 0.00005
NM_001349338.3(FOXP1):c.119A>T (p.Glu40Val) rs765070623 0.00004
NM_001349338.3(FOXP1):c.2020G>A (p.Glu674Lys) rs368167189 0.00003
NM_001349338.3(FOXP1):c.301A>G (p.Met101Val) rs564508875 0.00003
NM_001349338.3(FOXP1):c.181-17916C>T rs1257120372 0.00002
NM_001349338.3(FOXP1):c.8A>G (p.Gln3Arg) rs898658081 0.00002
NM_001349338.3(FOXP1):c.1147-350G>A rs1027620151 0.00001
NM_001349338.3(FOXP1):c.1652+4C>T rs572849158 0.00001
NM_001349338.3(FOXP1):c.1747C>T (p.Pro583Ser) rs1423437984 0.00001
NM_001349338.3(FOXP1):c.1982T>C (p.Phe661Ser) rs759325225 0.00001
GRCh37/hg19 3p13(chr3:71021211-71181046)x1
NM_001244810.1:c.(?_181-50)_(282+50_?)del
NM_001349338.3(FOXP1):c.-11-36045A>C
NM_001349338.3(FOXP1):c.-297-21308G>T rs904697606
NM_001349338.3(FOXP1):c.-298+4925_-298+4928dup rs2107843453
NM_001349338.3(FOXP1):c.1000G>C (p.Asp334His) rs1576028676
NM_001349338.3(FOXP1):c.1028T>G (p.Val343Gly) rs2107612907
NM_001349338.3(FOXP1):c.1078_1079del (p.Glu360fs)
NM_001349338.3(FOXP1):c.1103dup (p.His368fs) rs2040036225
NM_001349338.3(FOXP1):c.1131del (p.Ala378fs)
NM_001349338.3(FOXP1):c.1146+1G>A rs1559650552
NM_001349338.3(FOXP1):c.1146+1G>C rs1559650552
NM_001349338.3(FOXP1):c.1146+5G>C rs1553678368
NM_001349338.3(FOXP1):c.1147-1_1161dup
NM_001349338.3(FOXP1):c.1147-25_1161dup
NM_001349338.3(FOXP1):c.1147-2A>G rs1559621862
NM_001349338.3(FOXP1):c.116G>C (p.Gly39Ala)
NM_001349338.3(FOXP1):c.1172_1175del (p.Leu391fs) rs2037949810
NM_001349338.3(FOXP1):c.1183G>A (p.Ala395Thr) rs376351360
NM_001349338.3(FOXP1):c.1201C>T (p.Gln401Ter) rs1234028937
NM_001349338.3(FOXP1):c.1223C>T (p.Thr408Met)
NM_001349338.3(FOXP1):c.1240_1241del (p.Leu414fs) rs1064793130
NM_001349338.3(FOXP1):c.1240dup (p.Leu414fs) rs797044652
NM_001349338.3(FOXP1):c.1241del (p.Leu414fs)
NM_001349338.3(FOXP1):c.1248dup (p.Val417fs) rs2037930387
NM_001349338.3(FOXP1):c.1267_1268del (p.Val423fs) rs786200948
NM_001349338.3(FOXP1):c.1270A>G (p.Ile424Val)
NM_001349338.3(FOXP1):c.1286T>G (p.Met429Arg)
NM_001349338.3(FOXP1):c.1287_1291dup (p.Thr431fs) rs1575806352
NM_001349338.3(FOXP1):c.1291_1292del (p.Thr431fs) rs1559620376
NM_001349338.3(FOXP1):c.1313G>A (p.Arg438Gln) rs2037908174
NM_001349338.3(FOXP1):c.1317C>G (p.Tyr439Ter) rs794727155
NM_001349338.3(FOXP1):c.1321_1324dup (p.Lys442fs)
NM_001349338.3(FOXP1):c.1329C>A (p.Tyr443Ter) rs1064793944
NM_001349338.3(FOXP1):c.1333_1335delinsAA (p.Val445fs)
NM_001349338.3(FOXP1):c.1348+1G>C rs1559619762
NM_001349338.3(FOXP1):c.1349-1G>A
NM_001349338.3(FOXP1):c.1349-5_1350del rs1135401796
NM_001349338.3(FOXP1):c.1350A>T (p.Ala450=) rs2037865324
NM_001349338.3(FOXP1):c.1393A>G (p.Arg465Gly) rs869025202
NM_001349338.3(FOXP1):c.1394G>C (p.Arg465Thr) rs1553668196
NM_001349338.3(FOXP1):c.1396C>G (p.Pro466Ala) rs1057518926
NM_001349338.3(FOXP1):c.1397C>T (p.Pro466Leu)
NM_001349338.3(FOXP1):c.139G>C (p.Gly47Arg)
NM_001349338.3(FOXP1):c.1406C>T (p.Thr469Ile) rs2037853932
NM_001349338.3(FOXP1):c.1409A>T (p.Tyr470Phe) rs769448730
NM_001349338.3(FOXP1):c.1420_1423del (p.Ile474fs) rs2037850716
NM_001349338.3(FOXP1):c.1420_1427del (p.Ile474fs) rs2037850257
NM_001349338.3(FOXP1):c.1426C>T (p.Gln476Ter) rs2107310122
NM_001349338.3(FOXP1):c.1426_1428+1del rs1575803923
NM_001349338.3(FOXP1):c.1427A>C (p.Gln476Pro) rs2107310071
NM_001349338.3(FOXP1):c.1534dup (p.Ala512fs) rs2107201851
NM_001349338.3(FOXP1):c.1538T>C (p.Val513Ala) rs1553663140
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.1541G>C (p.Arg514Pro) rs797045586
NM_001349338.3(FOXP1):c.1544A>G (p.His515Arg) rs2036511353
NM_001349338.3(FOXP1):c.1547del (p.Asn516fs)
NM_001349338.3(FOXP1):c.1550T>G (p.Leu517Arg) rs1575757812
NM_001349338.3(FOXP1):c.1552dup (p.Ser518fs)
NM_001349338.3(FOXP1):c.1553G>A (p.Ser518Asn) rs2107200789
NM_001349338.3(FOXP1):c.1556T>C (p.Leu519Pro)
NM_001349338.3(FOXP1):c.1567T>C (p.Phe523Leu)
NM_001349338.3(FOXP1):c.1568T>C (p.Phe523Ser) rs1559602593
NM_001349338.3(FOXP1):c.1569_1570insA (p.Val524fs)
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.1590del (p.Ala532fs)
NM_001349338.3(FOXP1):c.1595C>T (p.Ala532Val)
NM_001349338.3(FOXP1):c.159C>A (p.His53Gln) rs777378675
NM_001349338.3(FOXP1):c.1600T>C (p.Trp534Arg) rs587777855
NM_001349338.3(FOXP1):c.1601G>A (p.Trp534Ter)
NM_001349338.3(FOXP1):c.1630C>T (p.Arg544Ter)
NM_001349338.3(FOXP1):c.1652+418G>A rs2107186686
NM_001349338.3(FOXP1):c.1652+546dup
NM_001349338.3(FOXP1):c.1652+5G>A rs794727216
NM_001349338.3(FOXP1):c.1652+5G>C rs794727216
NM_001349338.3(FOXP1):c.1653-19_1653-2dup
NM_001349338.3(FOXP1):c.1653-1G>A rs1575741313
NM_001349338.3(FOXP1):c.1653-2A>T rs1559596756
NM_001349338.3(FOXP1):c.1653_1669del (p.Asn552fs) rs2107156767
NM_001349338.3(FOXP1):c.165GCA[3] (p.Gln60del)
NM_001349338.3(FOXP1):c.1664T>C (p.Leu555Pro) rs2036062834
NM_001349338.3(FOXP1):c.1690G>A (p.Ala564Thr)
NM_001349338.3(FOXP1):c.1718_1722+8del rs2036047362
NM_001349338.3(FOXP1):c.1722+5G>C
NM_001349338.3(FOXP1):c.1729_1730delinsTGAA (p.Met577Ter)
NM_001349338.3(FOXP1):c.1798A>G (p.Ser600Gly) rs970358469
NM_001349338.3(FOXP1):c.180+200C>A
NM_001349338.3(FOXP1):c.1833G>T (p.Glu611Asp)
NM_001349338.3(FOXP1):c.1879A>G (p.Met627Val)
NM_001349338.3(FOXP1):c.1888G>A (p.Val630Met) rs772816590
NM_001349338.3(FOXP1):c.1888G>T (p.Val630Leu) rs772816590
NM_001349338.3(FOXP1):c.1891C>T (p.His631Tyr) rs2106858982
NM_001349338.3(FOXP1):c.1946T>C (p.Leu649Pro)
NM_001349338.3(FOXP1):c.2018del (p.Asn673fs) rs2106854788
NM_001349338.3(FOXP1):c.282+16777A>G
NM_001349338.3(FOXP1):c.319A>G (p.Ile107Val) rs1440752852
NM_001349338.3(FOXP1):c.319A>T (p.Ile107Phe)
NM_001349338.3(FOXP1):c.34A>T (p.Asn12Tyr) rs2108382372
NM_001349338.3(FOXP1):c.381G>C (p.Gln127His)
NM_001349338.3(FOXP1):c.38G>T (p.Gly13Val) rs2108382290
NM_001349338.3(FOXP1):c.407T>A (p.Leu136His) rs1576458423
NM_001349338.3(FOXP1):c.427del (p.Leu143fs)
NM_001349338.3(FOXP1):c.482_483dup (p.Gln162fs)
NM_001349338.3(FOXP1):c.484C>T (p.Gln162Ter) rs2107113697
NM_001349338.3(FOXP1):c.488del (p.His163fs) rs2107113481
NM_001349338.3(FOXP1):c.490G>A (p.Ala164Thr) rs1252621833
NM_001349338.3(FOXP1):c.494del (p.Gly165fs) rs2107113374
NM_001349338.3(FOXP1):c.501delinsTGTTGTTTT (p.Gln167fs)
NM_001349338.3(FOXP1):c.511-3C>G rs778983019
NM_001349338.3(FOXP1):c.573dup (p.Gln192fs)
NM_001349338.3(FOXP1):c.580C>T (p.Gln194Ter)
NM_001349338.3(FOXP1):c.59C>T (p.Ser20Leu)
NM_001349338.3(FOXP1):c.604C>T (p.Gln202Ter)
NM_001349338.3(FOXP1):c.606del (p.Gly203fs) rs1553709907
NM_001349338.3(FOXP1):c.619A>G (p.Ile207Val)
NM_001349338.3(FOXP1):c.622C>T (p.Gln208Ter) rs1553709881
NM_001349338.3(FOXP1):c.659dup (p.Gln221fs) rs2049106504
NM_001349338.3(FOXP1):c.696_705del (p.Leu231_Trp232insTer)
NM_001349338.3(FOXP1):c.738del (p.Asn247fs) rs2106872055
NM_001349338.3(FOXP1):c.775G>C (p.Val259Leu)
NM_001349338.3(FOXP1):c.802T>A (p.Ser268Thr)
NM_001349338.3(FOXP1):c.825del (p.Ser276fs) rs2106870085
NM_001349338.3(FOXP1):c.844_845del (p.Val283fs) rs1576373932
NM_001349338.3(FOXP1):c.869+1G>A rs763837297
NM_001349338.3(FOXP1):c.869G>C (p.Ser290Thr) rs2106869182
NM_001349338.3(FOXP1):c.870-1G>C rs1576175491
NM_001349338.3(FOXP1):c.910G>T (p.Gly304Ter)
NM_001349338.3(FOXP1):c.913_914del (p.His305fs)
NM_001349338.3(FOXP1):c.930G>A (p.Trp310Ter)
NM_001349338.3(FOXP1):c.945del (p.Val316fs) rs2044341412
NM_001349338.3(FOXP1):c.94C>A (p.Leu32Ile)
NM_001349338.3(FOXP1):c.952G>A (p.Glu318Lys)
NM_001349338.3(FOXP1):c.975-2A>C rs1553685707
NM_001349338.3(FOXP1):c.975-2A>G rs1553685707

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