ClinVar Miner

List of variants in gene FOXP1 reported as pathogenic

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Gene type:
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Total variants: 41
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HGVS dbSNP
GRCh37/hg19 3p13(chr3:71008556-71049017)x1
NC_000003.10:g.(71109689_?)_(?_71508061)del
NM_032682.5(FOXP1):c.1071del (p.Asp358fs) rs1553678501
NM_032682.5(FOXP1):c.1146+5G>C rs1553678368
NM_032682.5(FOXP1):c.1240_1241del (p.Leu414fs) rs1064793130
NM_032682.5(FOXP1):c.1240dup (p.Leu414fs) rs797044652
NM_032682.5(FOXP1):c.1263_1264CT[1] (p.Ser422fs) rs1064796914
NM_032682.5(FOXP1):c.1289_1290AC[1] (p.Thr431fs) rs1559620376
NM_032682.5(FOXP1):c.1317C>A (p.Tyr439Ter) rs794727155
NM_032682.5(FOXP1):c.1317C>G (p.Tyr439Ter) rs794727155
NM_032682.5(FOXP1):c.1329C>A (p.Tyr443Ter) rs1064793944
NM_032682.5(FOXP1):c.1329C>G (p.Tyr443Ter) rs1064793944
NM_032682.5(FOXP1):c.1348+1G>C rs1559619762
NM_032682.5(FOXP1):c.1349-5_1350del rs1135401796
NM_032682.5(FOXP1):c.1393A>G (p.Arg465Gly) rs869025202
NM_032682.5(FOXP1):c.1394G>C (p.Arg465Thr) rs1553668196
NM_032682.5(FOXP1):c.1409A>G (p.Tyr470Cys) rs769448730
NM_032682.5(FOXP1):c.1476T>A (p.Tyr492Ter) rs1559616778
NM_032682.5(FOXP1):c.1489C>T (p.Arg497Ter) rs775136381
NM_032682.5(FOXP1):c.1507C>T (p.Arg503Ter) rs797045584
NM_032682.5(FOXP1):c.1507del (p.Arg503fs) rs1553667322
NM_032682.5(FOXP1):c.1540C>T (p.Arg514Cys) rs869025203
NM_032682.5(FOXP1):c.1541G>A (p.Arg514His) rs797045586
NM_032682.5(FOXP1):c.1544_1569dup (p.Val524fs) rs886041821
NM_032682.5(FOXP1):c.1573C>T (p.Arg525Ter) rs112795301
NM_032682.5(FOXP1):c.1574G>A (p.Arg525Gln) rs1553663084
NM_032682.5(FOXP1):c.1600T>C (p.Trp534Arg) rs587777855
NM_032682.5(FOXP1):c.1624C>T (p.Gln542Ter) rs794727215
NM_032682.5(FOXP1):c.1630C>T (p.Arg544Ter) rs1559602356
NM_032682.5(FOXP1):c.1652+5G>A rs794727216
NM_032682.5(FOXP1):c.1653-2A>T rs1559596756
NM_032682.5(FOXP1):c.1670_1685dup (p.Ser562fs) rs398124429
NM_032682.5(FOXP1):c.1717_1722+5del rs1553660890
NM_032682.5(FOXP1):c.1889+1G>T rs1553656387
NM_032682.5(FOXP1):c.529C>T (p.Gln177Ter) rs1559807265
NM_032682.5(FOXP1):c.574C>T (p.Gln192Ter) rs1057524732
NM_032682.5(FOXP1):c.598C>T (p.Gln200Ter) rs1553709919
NM_032682.5(FOXP1):c.606del (p.Gly203fs) rs1553709907
NM_032682.5(FOXP1):c.622C>T (p.Gln208Ter) rs1553709881
NM_032682.5(FOXP1):c.869+1G>A rs763837297
NM_032682.5(FOXP1):c.975-2A>C rs1553685707

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