ClinVar Miner

List of variants in gene FOXP1 reported as benign

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Gene type:
ClinVar version:
Total variants: 19
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HGVS dbSNP
GRCh37/hg19 3p13(chr3:71383767-71397385)x1
GRCh37/hg19 3p13(chr3:71505403-71509083)x3
GRCh37/hg19 3p13(chr3:71631606-71652888)x1
NM_032682.5(FOXP1):c.*1037C>A rs1053797
NM_032682.5(FOXP1):c.*1125dup rs199626546
NM_032682.5(FOXP1):c.*1409T>C rs17008063
NM_032682.5(FOXP1):c.*3175dup rs202105915
NM_032682.5(FOXP1):c.*3676dup rs35502550
NM_032682.5(FOXP1):c.*56dup rs112773801
NM_032682.5(FOXP1):c.*923_*928dup rs145455295
NM_032682.5(FOXP1):c.-91G>A rs17008544
NM_032682.5(FOXP1):c.1146+10_1146+12delGAT rs199543140
NM_032682.5(FOXP1):c.1147-19G>A rs75214049
NM_032682.5(FOXP1):c.1413A>G (p.Ala471=) rs144080925
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.1889+20C>A rs7638391
NM_032682.5(FOXP1):c.1890-15G>T rs7639736
NM_032682.5(FOXP1):c.1890-5T>C rs187666567

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