ClinVar Miner

List of variants in gene FOXP1 studied for not provided

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Gene type:
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Total variants: 50
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HGVS dbSNP
GRCh37/hg19 3p13(chr3:71161687-71591240)x3
GRCh37/hg19 3p13(chr3:71319916-71564385)x3
GRCh37/hg19 3p13(chr3:71363860-71500334)x1
GRCh37/hg19 3p13(chr3:71383767-71397385)x1
GRCh37/hg19 3p13(chr3:71505403-71509083)x3
GRCh37/hg19 3p13(chr3:71631606-71652888)x1
NM_032682.5(FOXP1):c.1064T>C (p.Leu355Pro) rs1064795306
NM_032682.5(FOXP1):c.1071del (p.Asp358fs) rs1553678501
NM_032682.5(FOXP1):c.1146+19C>G rs140060227
NM_032682.5(FOXP1):c.1146+1G>T
NM_032682.5(FOXP1):c.1146+5G>C rs1553678368
NM_032682.5(FOXP1):c.1177A>T (p.Lys393Ter) rs1553668839
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.1317C>A (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.1344G>A (p.Ser448=) rs143503790
NM_032682.5(FOXP1):c.1348G>A (p.Ala450Thr) rs1553668386
NM_032682.5(FOXP1):c.1383C>T (p.Asn461=) rs372403441
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.1506C>G (p.Phe502Leu) rs1057524152
NM_032682.5(FOXP1):c.1507C>T (p.Arg503Ter) rs797045584
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.1561A>G (p.Lys521Glu) rs1553663113
NM_032682.5(FOXP1):c.1573C>T (p.Arg525Ter) rs112795301
NM_032682.5(FOXP1):c.1624C>T (p.Gln542Ter) rs794727215
NM_032682.5(FOXP1):c.1652+403A>G rs76145927
NM_032682.5(FOXP1):c.1652+5G>A rs794727216
NM_032682.5(FOXP1):c.1653_1672dup (p.Asn558fs) rs1559596699
NM_032682.5(FOXP1):c.1670_1685dup (p.Ser562fs) rs398124429
NM_032682.5(FOXP1):c.1675A>T (p.Met559Leu) rs764023352
NM_032682.5(FOXP1):c.1702C>T (p.Pro568Ser) rs147674680
NM_032682.5(FOXP1):c.1710_1722+2del rs1559596230
NM_032682.5(FOXP1):c.1717_1722+5del rs1553660890
NM_032682.5(FOXP1):c.1722+1G>A rs1553660900
NM_032682.5(FOXP1):c.181-13T>G rs139264797
NM_032682.5(FOXP1):c.1889+1G>T rs1553656387
NM_032682.5(FOXP1):c.1889+5G>T rs1553656383
NM_032682.5(FOXP1):c.1902C>T (p.His634=) rs749771909
NM_032682.5(FOXP1):c.2020G>A (p.Glu674Lys) rs368167189
NM_032682.5(FOXP1):c.526A>T (p.Thr176Ser) rs1004143711
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.622C>T (p.Gln208Ter) rs1553709881
NM_032682.5(FOXP1):c.64G>A (p.Gly22Ser) rs794727811

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