ClinVar Miner

List of variants in gene FOXP1 reported as likely benign

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 68
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HGVS dbSNP
NM_032682.5(FOXP1):c.*1043T>A rs577920948
NM_032682.5(FOXP1):c.*1189A>G rs555165294
NM_032682.5(FOXP1):c.*1296C>T rs528918208
NM_032682.5(FOXP1):c.*1352_*1355dup rs144583656
NM_032682.5(FOXP1):c.*1536G>A rs573286093
NM_032682.5(FOXP1):c.*1536G>T rs573286093
NM_032682.5(FOXP1):c.*2092dup rs573886345
NM_032682.5(FOXP1):c.*2157G>A rs548853878
NM_032682.5(FOXP1):c.*222C>T rs537642111
NM_032682.5(FOXP1):c.*2302A>T rs566280510
NM_032682.5(FOXP1):c.*2337G>C rs532852561
NM_032682.5(FOXP1):c.*2575C>T rs528887649
NM_032682.5(FOXP1):c.*2682A>G rs138967615
NM_032682.5(FOXP1):c.*2826A>G rs537308827
NM_032682.5(FOXP1):c.*2942A>G rs189826792
NM_032682.5(FOXP1):c.*3413T>C rs185295985
NM_032682.5(FOXP1):c.*3608dup rs533607618
NM_032682.5(FOXP1):c.*3685G>A rs114680316
NM_032682.5(FOXP1):c.*3693G>A rs145083026
NM_032682.5(FOXP1):c.*3818C>T rs149064360
NM_032682.5(FOXP1):c.*39A>G rs376179029
NM_032682.5(FOXP1):c.*4076C>A rs11914627
NM_032682.5(FOXP1):c.*4349_*4353TTTTG[4] rs57959417
NM_032682.5(FOXP1):c.*4411G>A rs193042825
NM_032682.5(FOXP1):c.*4515C>T rs189112133
NM_032682.5(FOXP1):c.*665G>A rs549807296
NM_032682.5(FOXP1):c.*827G>A rs568661192
NM_032682.5(FOXP1):c.*974G>A rs777481567
NM_032682.5(FOXP1):c.-112C>T rs536195899
NM_032682.5(FOXP1):c.-208C>G rs188855280
NM_032682.5(FOXP1):c.-297-14T>C rs144952829
NM_032682.5(FOXP1):c.-385C>T rs576720632
NM_032682.5(FOXP1):c.-425A>G rs1499893
NM_032682.5(FOXP1):c.-542delG rs534653828
NM_032682.5(FOXP1):c.1146+19C>G rs140060227
NM_032682.5(FOXP1):c.114C>T (p.Asn38=) rs1560102007
NM_032682.5(FOXP1):c.1183G>A (p.Ala395Thr)
NM_032682.5(FOXP1):c.1217C>G (p.Thr406Ser) rs200355554
NM_032682.5(FOXP1):c.1233C>T (p.Thr411=) rs147995584
NM_032682.5(FOXP1):c.123G>A (p.Thr41=)
NM_032682.5(FOXP1):c.126G>A (p.Pro42=) rs762082081
NM_032682.5(FOXP1):c.1328A>G (p.Tyr443Cys) rs727503936
NM_032682.5(FOXP1):c.135C>T (p.Asp45=)
NM_032682.5(FOXP1):c.1413A>G (p.Ala471=) rs144080925
NM_032682.5(FOXP1):c.154G>A (p.Ala52Thr) rs1359632401
NM_032682.5(FOXP1):c.1652+403A>G rs76145927
NM_032682.5(FOXP1):c.1652+4C>T
NM_032682.5(FOXP1):c.169C>G (p.Gln57Glu) rs752141860
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.1722+12G>A rs150547886
NM_032682.5(FOXP1):c.1762G>A (p.Ala588Thr) rs202173892
NM_032682.5(FOXP1):c.181-13T>G rs139264797
NM_032682.5(FOXP1):c.1825G>A (p.Ala609Thr)
NM_032682.5(FOXP1):c.1848C>T (p.Asn616=) rs1231630526
NM_032682.5(FOXP1):c.1888G>T (p.Val630Leu)
NM_032682.5(FOXP1):c.1890-5T>C rs187666567
NM_032682.5(FOXP1):c.301A>G (p.Met101Val) rs564508875
NM_032682.5(FOXP1):c.306G>A (p.Met102Ile) rs749611196
NM_032682.5(FOXP1):c.44C>T (p.Ala15Val) rs532329866
NM_032682.5(FOXP1):c.63C>T (p.Gly21=) rs376702675
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=)
NM_032682.5(FOXP1):c.855T>G (p.Thr285=) rs141007926
NM_032682.5(FOXP1):c.936C>T (p.Gly312=) rs61753356
NM_032682.5(FOXP1):c.975-14A>G rs201374957
NM_032682.5(FOXP1):c.98G>C (p.Arg33Pro) rs587780339

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