ClinVar Miner

List of variants in gene FOXP1 reported as pathogenic for not provided

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Gene type:
ClinVar version:
Total variants: 48
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HGVS dbSNP gnomAD frequency
GRCh37/hg19 3p13(chr3:70857459-71259544)x1
GRCh37/hg19 3p13(chr3:71081905-71227572)x1
NC_000003.11:g.(?_71247333)_(71480567_?)del
NM_001349338.3(FOXP1):c.1031_1032insT (p.Gln344fs) rs2107612882
NM_001349338.3(FOXP1):c.1071del (p.Asp358fs) rs1553678501
NM_001349338.3(FOXP1):c.1087C>T (p.Gln363Ter) rs745448468
NM_001349338.3(FOXP1):c.1146+1G>A rs1559650552
NM_001349338.3(FOXP1):c.1172_1175del (p.Leu391fs) rs2037949810
NM_001349338.3(FOXP1):c.1177A>T (p.Lys393Ter) rs1553668839
NM_001349338.3(FOXP1):c.1216_1219dup (p.Pro407fs)
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.1264del (p.Ser422fs) rs2107316329
NM_001349338.3(FOXP1):c.1265_1266del (p.Ser422fs) rs1064796914
NM_001349338.3(FOXP1):c.1317C>A (p.Tyr439Ter) rs794727155
NM_001349338.3(FOXP1):c.1317_1320dup (p.Asp441fs)
NM_001349338.3(FOXP1):c.1319C>G (p.Ser440Ter) rs2037906065
NM_001349338.3(FOXP1):c.1321_1324del (p.Asp441fs)
NM_001349338.3(FOXP1):c.1329C>A (p.Tyr443Ter) rs1064793944
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.1396C>A (p.Pro466Thr) rs1057518926
NM_001349338.3(FOXP1):c.1409A>G (p.Tyr470Cys) rs769448730
NM_001349338.3(FOXP1):c.1426C>T (p.Gln476Ter) rs2107310122
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.1556T>C (p.Leu519Pro)
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.1624C>T (p.Gln542Ter) rs794727215
NM_001349338.3(FOXP1):c.1652+5G>A rs794727216
NM_001349338.3(FOXP1):c.1670_1685dup (p.Ser562fs) rs398124429
NM_001349338.3(FOXP1):c.1717_1722+5del rs1553660890
NM_001349338.3(FOXP1):c.1722G>A (p.Gln574=) rs2107155481
NM_001349338.3(FOXP1):c.1889+1G>T rs1553656387
NM_001349338.3(FOXP1):c.214C>T (p.Gln72Ter) rs2107748579
NM_001349338.3(FOXP1):c.447dup (p.Gln150fs) rs2050059649
NM_001349338.3(FOXP1):c.508G>T (p.Glu170Ter)
NM_001349338.3(FOXP1):c.511C>T (p.Gln171Ter)
NM_001349338.3(FOXP1):c.529C>T (p.Gln177Ter) rs1559807265
NM_001349338.3(FOXP1):c.574C>T (p.Gln192Ter) rs1057524732
NM_001349338.3(FOXP1):c.622C>T (p.Gln208Ter) rs1553709881
NM_001349338.3(FOXP1):c.838C>T (p.Gln280Ter)
NM_001349338.3(FOXP1):c.870-2A>G
NM_001349338.3(FOXP1):c.909T>G (p.Tyr303Ter)
NM_001349338.3(FOXP1):c.972delA (p.Lys325fs)

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