ClinVar Miner

List of variants in gene FOXP1 reported as likely pathogenic

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Total variants: 17
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HGVS dbSNP
GRCh37/hg19 3p13(chr3:71129956-71255015)x1
NM_001244810.1(FOXP1):c.1348+2T>C rs1057518999
NM_001244810.1(FOXP1):c.1396C>G (p.Pro466Ala) rs1057518926
NM_032682.5(FOXP1):c.1064T>C (p.Leu355Pro) rs1064795306
NM_032682.5(FOXP1):c.1146+1G>C
NM_032682.5(FOXP1):c.1147-2A>G
NM_032682.5(FOXP1):c.1177A>T (p.Lys393Ter) rs1553668839
NM_032682.5(FOXP1):c.1267_1268delGT (p.Val423Hisfs) rs786200948
NM_032682.5(FOXP1):c.1348G>A (p.Ala450Thr) rs1553668386
NM_032682.5(FOXP1):c.1429-13_1429-3del
NM_032682.5(FOXP1):c.1506C>G (p.Phe502Leu) rs1057524152
NM_032682.5(FOXP1):c.1541G>A (p.Arg514His) rs797045586
NM_032682.5(FOXP1):c.1653_1672dup (p.Asn558Ilefs)
NM_032682.5(FOXP1):c.1710_1722+2del
NM_032682.5(FOXP1):c.1722+1G>A rs1553660900
NM_032682.5(FOXP1):c.1889+5G>T rs1553656383
NM_032682.5(FOXP1):c.44C>T (p.Ala15Val) rs532329866

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