ClinVar Miner

List of variants in gene FOXP1 reported as likely benign for History of neurodevelopmental disorder

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Gene type:
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Total variants: 12
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HGVS dbSNP
NM_032682.5(FOXP1):c.1652+4C>T rs572849158
NM_032682.5(FOXP1):c.1890-4C>T rs748164903
NM_032682.6(FOXP1):c.114C>T (p.Asn38=) rs1560102007
NM_032682.6(FOXP1):c.123G>A (p.Thr41=) rs201155996
NM_032682.6(FOXP1):c.135C>T (p.Asp45=) rs749307402
NM_032682.6(FOXP1):c.154G>A (p.Ala52Thr) rs1359632401
NM_032682.6(FOXP1):c.1709A>G (p.Asn570Ser) rs140161845
NM_032682.6(FOXP1):c.1848C>T (p.Asn616=) rs1231630526
NM_032682.6(FOXP1):c.44C>T (p.Ala15Val) rs532329866
NM_032682.6(FOXP1):c.643C>G (p.Pro215Ala) rs146606219
NM_032682.6(FOXP1):c.676A>G (p.Thr226Ala) rs1450633154
NM_032682.6(FOXP1):c.738C>G (p.Gly246=) rs761092367

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