ClinVar Miner

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

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Gene type:
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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_001349338.3(FOXP1):c.1016C>A (p.Ala339Asp)
NM_001349338.3(FOXP1):c.1021T>C (p.Cys341Arg) rs2107612940
NM_001349338.3(FOXP1):c.1064T>C (p.Leu355Pro) rs1064795306
NM_001349338.3(FOXP1):c.1096A>G (p.Met366Val) rs2040037008
NM_001349338.3(FOXP1):c.1146+1G>T rs1559650552
NM_001349338.3(FOXP1):c.1146+5G>C rs1553678368
NM_001349338.3(FOXP1):c.1240_1241del (p.Leu414fs) rs1064793130
NM_001349338.3(FOXP1):c.1314_1321del (p.Tyr439fs) rs1575806033
NM_001349338.3(FOXP1):c.1406C>T (p.Thr469Ile) rs2037853932
NM_001349338.3(FOXP1):c.1428+1G>C
NM_001349338.3(FOXP1):c.1540C>T (p.Arg514Cys) rs869025203
NM_001349338.3(FOXP1):c.1574G>A (p.Arg525Gln) rs1553663084
NM_001349338.3(FOXP1):c.1643_1652+3del
NM_001349338.3(FOXP1):c.1652+5G>A rs794727216
NM_001349338.3(FOXP1):c.1653-31_1653-26del rs2107157863
NM_001349338.3(FOXP1):c.1653_1672dup (p.Asn558fs) rs1559596699
NM_001349338.3(FOXP1):c.1710_1722+2del rs1559596230
NM_001349338.3(FOXP1):c.1722+1G>A rs1553660900
NM_001349338.3(FOXP1):c.1722G>C (p.Gln574His) rs2107155481
NM_001349338.3(FOXP1):c.1889+5G>T rs1553656383
NM_001349338.3(FOXP1):c.312_313del (p.Gln105fs)
NM_001349338.3(FOXP1):c.511-3C>A rs778983019

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