List of variants in gene FOXP1 reported as pathogenic by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001349338.3(FOXP1):c.1396C>A (p.Pro466Thr)	rs1057518926
NM_001349338.3(FOXP1):c.1409A>G (p.Tyr470Cys)	rs769448730
NM_001349338.3(FOXP1):c.1541G>A (p.Arg514His)	rs797045586
NM_001349338.3(FOXP1):c.214C>T (p.Gln72Ter)	rs2107748579
NM_001349338.3(FOXP1):c.508G>T (p.Glu170Ter)
NM_001349338.3(FOXP1):c.972delA (p.Lys325fs)

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