ClinVar Miner

List of variants in gene FOXP2 reported as uncertain significance for childhood apraxia of speech

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 78
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HGVS dbSNP gnomAD frequency
NM_014491.4(FOXP2):c.-170T>C rs117662905 0.00086
NM_014491.4(FOXP2):c.*2922T>G rs544333798 0.00060
NM_014491.4(FOXP2):c.-335A>G rs531957198 0.00049
NM_014491.4(FOXP2):c.*1868T>C rs760021288 0.00041
NM_014491.4(FOXP2):c.*319A>G rs141343189 0.00031
NM_014491.4(FOXP2):c.*3749C>A rs188138100 0.00025
NM_014491.4(FOXP2):c.*3643T>C rs536004145 0.00019
NM_014491.4(FOXP2):c.*2029A>G rs769993562 0.00017
NM_014491.4(FOXP2):c.*366G>A rs745872209 0.00015
NM_014491.4(FOXP2):c.*1947C>T rs777110115 0.00013
NM_014491.4(FOXP2):c.*1524C>T rs537398392 0.00011
NM_014491.4(FOXP2):c.*208T>C rs745705171 0.00011
NM_014491.4(FOXP2):c.598-1G>C rs752704782 0.00009
NM_014491.4(FOXP2):c.*2489A>C rs886061930 0.00008
NM_014491.4(FOXP2):c.1264C>T (p.Pro422Ser) rs751931499 0.00006
NM_014491.4(FOXP2):c.*1598G>A rs753075964 0.00004
NM_014491.4(FOXP2):c.*1826G>A rs771404418 0.00003
NM_014491.4(FOXP2):c.*1964C>T rs762401218 0.00003
NM_014491.4(FOXP2):c.*2558A>G rs886061931 0.00003
NM_014491.4(FOXP2):c.-293C>T rs773664240 0.00003
NM_014491.4(FOXP2):c.1856G>A (p.Ser619Asn) rs757373725 0.00003
NM_014491.4(FOXP2):c.258+15661C>T rs1339286790 0.00003
NM_014491.4(FOXP2):c.*1210A>G rs886061927 0.00002
NM_014491.4(FOXP2):c.*3235T>C rs886061934 0.00002
NM_014491.4(FOXP2):c.*388G>A rs750669536 0.00002
NM_014491.4(FOXP2):c.892T>G (p.Ser298Ala) rs138374374 0.00002
NM_014491.4(FOXP2):c.*107A>G rs763037482 0.00001
NM_014491.4(FOXP2):c.*1222G>C rs1319688291 0.00001
NM_014491.4(FOXP2):c.*1675C>A rs886061928 0.00001
NM_014491.4(FOXP2):c.*1701A>C rs886061929 0.00001
NM_014491.4(FOXP2):c.*285T>C rs886061923 0.00001
NM_014491.4(FOXP2):c.*3220A>C rs886061933 0.00001
NM_014491.4(FOXP2):c.*3608A>G rs886061936 0.00001
NM_014491.4(FOXP2):c.*3736C>A rs886061937 0.00001
NM_014491.4(FOXP2):c.*956G>A rs886061926 0.00001
NM_014491.4(FOXP2):c.-16G>A rs886061914 0.00001
NM_014491.4(FOXP2):c.-290A>C rs1166508172 0.00001
NM_014491.4(FOXP2):c.124T>C (p.Ser42Pro) rs942638508 0.00001
NM_014491.4(FOXP2):c.1344C>T (p.Thr448=) rs1283357982 0.00001
NM_014491.4(FOXP2):c.1352C>T (p.Thr451Met) rs199776572 0.00001
NM_014491.4(FOXP2):c.1789A>C (p.Asn597His) rs766476648 0.00001
NM_014491.4(FOXP2):c.342T>C (p.Ser114=) rs886061915 0.00001
NM_014491.4(FOXP2):c.52A>G (p.Asn18Asp) rs763263115 0.00001
NM_014491.4(FOXP2):c.*1415A>T rs1808658457
NM_014491.4(FOXP2):c.*1585T>C rs1808664980
NM_014491.4(FOXP2):c.*203_*204del rs886061918
NM_014491.4(FOXP2):c.*219_*220del rs398005924
NM_014491.4(FOXP2):c.*220del rs398005924
NM_014491.4(FOXP2):c.*2261T>C rs1808704401
NM_014491.4(FOXP2):c.*2449A>G rs1808712530
NM_014491.4(FOXP2):c.*260dup rs752684219
NM_014491.4(FOXP2):c.*2970T>A rs886061932
NM_014491.4(FOXP2):c.*3414G>C rs1036408992
NM_014491.4(FOXP2):c.*449_*451del rs886061924
NM_014491.4(FOXP2):c.*686A>G rs1808616479
NM_014491.4(FOXP2):c.*708T>G rs886061925
NM_014491.4(FOXP2):c.*96A>G rs765304609
NM_014491.4(FOXP2):c.-222C>A rs761418050
NM_014491.4(FOXP2):c.11A>G (p.Glu4Gly) rs1793857952
NM_014491.4(FOXP2):c.1276G>T (p.Val426Leu)
NM_014491.4(FOXP2):c.131T>C (p.Val44Ala) rs1283187808
NM_014491.4(FOXP2):c.1462T>G (p.Ser488Ala) rs201320940
NM_014491.4(FOXP2):c.1657C>T (p.Arg553Cys)
NM_014491.4(FOXP2):c.165G>A (p.Gln55=) rs766616577
NM_014491.4(FOXP2):c.1661A>G (p.His554Arg)
NM_014491.4(FOXP2):c.1770-4dup rs398005923
NM_014491.4(FOXP2):c.1794A>G (p.Ile598Met)
NM_014491.4(FOXP2):c.183A>G (p.Ala61=) rs747126499
NM_014491.4(FOXP2):c.199C>G (p.Gln67Glu) rs759949520
NM_014491.4(FOXP2):c.258+13C>G rs1799294727
NM_014491.4(FOXP2):c.258+36173G>A rs747951230
NM_014491.4(FOXP2):c.361C>T (p.Leu121Phe)
NM_014491.4(FOXP2):c.447G>C (p.Gln149His) rs1804788563
NM_014491.4(FOXP2):c.693G>T (p.Gln231His)
NM_014491.4(FOXP2):c.774A>G (p.Gln258=)
NM_014491.4(FOXP2):c.962C>T (p.Ser321Phe) rs944127085
NM_014491.4(FOXP2):c.988A>T (p.Ser330Cys) rs886061916
NM_014491.4(FOXP2):c.989+6T>A rs1805599792

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