ClinVar Miner

List of variants in gene FOXP2 reported as likely benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 9
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HGVS dbSNP gnomAD frequency
NM_014491.4(FOXP2):c.50A>T (p.Gln17Leu) rs201649896 0.00034
NM_014491.4(FOXP2):c.*2302G>A rs192272516 0.00021
NM_014491.4(FOXP2):c.*832A>C rs769641895 0.00010
NM_014491.4(FOXP2):c.*2017del rs377464931 0.00009
NM_014491.4(FOXP2):c.1569G>A (p.Arg523=) rs376776032 0.00005
NM_014491.4(FOXP2):c.2103C>T (p.Asp701=) rs559347815 0.00005
NM_014491.4(FOXP2):c.*188CTT[5] rs770516756
NM_014491.4(FOXP2):c.*3279_*3280dup rs777898958
NM_014491.4(FOXP2):c.510ACA[4] (p.Gln191del) rs398124272

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