ClinVar Miner

List of variants in gene FOXP1 studied for History of neurodevelopmental disorder

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Gene type:
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Total variants: 21
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HGVS dbSNP
NM_032682.5(FOXP1):c.107G>A (p.Arg36Gln)
NM_032682.5(FOXP1):c.114C>T (p.Asn38=) rs1560102007
NM_032682.5(FOXP1):c.123G>A (p.Thr41=)
NM_032682.5(FOXP1):c.135C>T (p.Asp45=)
NM_032682.5(FOXP1):c.1413A>G (p.Ala471=) rs144080925
NM_032682.5(FOXP1):c.153_158CGCCCA[3] (p.His53_Ala54dup) rs1560101657
NM_032682.5(FOXP1):c.154G>A (p.Ala52Thr) rs1359632401
NM_032682.5(FOXP1):c.1652+4C>T
NM_032682.5(FOXP1):c.1702C>T (p.Pro568Ser) rs147674680
NM_032682.5(FOXP1):c.1709A>G (p.Asn570Ser) rs140161845
NM_032682.5(FOXP1):c.1762G>A (p.Ala588Thr) rs202173892
NM_032682.5(FOXP1):c.1825G>A (p.Ala609Thr)
NM_032682.5(FOXP1):c.1848C>T (p.Asn616=) rs1231630526
NM_032682.5(FOXP1):c.1890-4C>T
NM_032682.5(FOXP1):c.1890-5T>C rs187666567
NM_032682.5(FOXP1):c.1936G>A (p.Glu646Lys)
NM_032682.5(FOXP1):c.319A>G (p.Ile107Val) rs1440752852
NM_032682.5(FOXP1):c.44C>T (p.Ala15Val) rs532329866
NM_032682.5(FOXP1):c.643C>G (p.Pro215Ala) rs146606219
NM_032682.5(FOXP1):c.676A>G (p.Thr226Ala) rs1450633154
NM_032682.5(FOXP1):c.738C>G (p.Gly246=)

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