ClinVar Miner

List of variants in gene FOXP1 reported as likely pathogenic

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Total variants: 25
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HGVS dbSNP
GRCh37/hg19 3p13(chr3:71129956-71255015)x1
NM_001244810.1(FOXP1):c.1348+2T>C rs1057518999
NM_001349338.3(FOXP1):c.1096A>G (p.Met366Val)
NM_032682.5(FOXP1):c.1000G>C (p.Asp334His) rs1576028676
NM_032682.5(FOXP1):c.1146+1G>C rs1559650552
NM_032682.5(FOXP1):c.1146+1G>T rs1559650552
NM_032682.5(FOXP1):c.1147-2A>G rs1559621862
NM_032682.5(FOXP1):c.1429-13_1429-3del rs1559617016
NM_032682.5(FOXP1):c.1710_1722+2del rs1559596230
NM_032682.5(FOXP1):c.1722+1G>A rs1553660900
NM_032682.5(FOXP1):c.1889+5G>T rs1553656383
NM_032682.6(FOXP1):c.1064T>C (p.Leu355Pro) rs1064795306
NM_032682.6(FOXP1):c.1177A>T (p.Lys393Ter) rs1553668839
NM_032682.6(FOXP1):c.1240_1241del (p.Leu414fs) rs1064793130
NM_032682.6(FOXP1):c.1267_1268del (p.Val423fs) rs786200948
NM_032682.6(FOXP1):c.1314_1321del (p.Tyr439fs) rs1575806033
NM_032682.6(FOXP1):c.1348G>A (p.Ala450Thr) rs1553668386
NM_032682.6(FOXP1):c.1396C>G (p.Pro466Ala) rs1057518926
NM_032682.6(FOXP1):c.1406C>T (p.Thr469Ile)
NM_032682.6(FOXP1):c.1506C>G (p.Phe502Leu) rs1057524152
NM_032682.6(FOXP1):c.1541G>A (p.Arg514His) rs797045586
NM_032682.6(FOXP1):c.1550T>G (p.Leu517Arg) rs1575757812
NM_032682.6(FOXP1):c.1653_1672dup (p.Asn558fs) rs1559596699
NM_032682.6(FOXP1):c.44C>T (p.Ala15Val) rs532329866
NM_032682.6(FOXP1):c.659dup (p.Gln221fs)

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