ClinVar Miner

List of variants in gene FOXP1 studied for Inborn genetic diseases

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Gene type:
ClinVar version:
Total variants: 100
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HGVS dbSNP gnomAD frequency
NM_001349338.3(FOXP1):c.1702C>T (p.Pro568Ser) rs147674680 0.00185
NM_001349338.3(FOXP1):c.1709A>G (p.Asn570Ser) rs140161845 0.00140
NM_001349338.3(FOXP1):c.643C>G (p.Pro215Ala) rs146606219 0.00112
NM_001349338.3(FOXP1):c.1413A>G (p.Ala471=) rs144080925 0.00088
NM_001349338.3(FOXP1):c.1825G>A (p.Ala609Thr) rs147537388 0.00062
NM_001349338.3(FOXP1):c.1890-5T>C rs187666567 0.00059
NM_001349338.3(FOXP1):c.1762G>A (p.Ala588Thr) rs202173892 0.00034
NM_001349338.3(FOXP1):c.123G>A (p.Thr41=) rs201155996 0.00030
NM_001349338.3(FOXP1):c.1305C>T (p.Ile435=) rs367624414 0.00020
NM_001349338.3(FOXP1):c.44C>T (p.Ala15Val) rs532329866 0.00018
NM_001349338.3(FOXP1):c.1217C>G (p.Thr406Ser) rs200355554 0.00016
NM_001349338.3(FOXP1):c.1233C>T (p.Thr411=) rs147995584 0.00015
NM_001349338.3(FOXP1):c.936C>T (p.Gly312=) rs61753356 0.00015
NM_001349338.3(FOXP1):c.390C>G (p.Leu130=) rs145868163 0.00011
NM_001349338.3(FOXP1):c.1291A>G (p.Thr431Ala) rs371780146 0.00010
NM_001349338.3(FOXP1):c.1146C>T (p.Pro382=) rs372765119 0.00008
NM_001349338.3(FOXP1):c.1135G>A (p.Ala379Thr) rs149759021 0.00007
NM_001349338.3(FOXP1):c.107G>A (p.Arg36Gln) rs200643313 0.00005
NM_001349338.3(FOXP1):c.1234G>A (p.Ala412Thr) rs200629338 0.00005
NM_001349338.3(FOXP1):c.119A>T (p.Glu40Val) rs765070623 0.00004
NM_001349338.3(FOXP1):c.1359G>A (p.Ala453=) rs766683691 0.00004
NM_001349338.3(FOXP1):c.1383C>T (p.Asn461=) rs372403441 0.00004
NM_001349338.3(FOXP1):c.738C>G (p.Gly246=) rs761092367 0.00004
NM_001349338.3(FOXP1):c.1652+4C>T rs572849158 0.00003
NM_001349338.3(FOXP1):c.169C>G (p.Gln57Glu) rs752141860 0.00003
NM_001349338.3(FOXP1):c.2020G>A (p.Glu674Lys) rs368167189 0.00003
NM_001349338.3(FOXP1):c.794C>G (p.Ser265Cys) rs780997405 0.00003
NM_001349338.3(FOXP1):c.825C>T (p.Ala275=) rs753890873 0.00003
NM_001349338.3(FOXP1):c.1316A>T (p.Tyr439Phe) rs1409656321 0.00002
NM_001349338.3(FOXP1):c.160G>A (p.Ala54Thr) rs758125097 0.00002
NM_001349338.3(FOXP1):c.8A>G (p.Gln3Arg) rs898658081 0.00002
NM_001349338.3(FOXP1):c.113A>G (p.Asn38Ser) rs1330345201 0.00001
NM_001349338.3(FOXP1):c.1193C>T (p.Ala398Val) rs987536405 0.00001
NM_001349338.3(FOXP1):c.122C>T (p.Thr41Met) rs756099573 0.00001
NM_001349338.3(FOXP1):c.135C>A (p.Asp45Glu) rs749307402 0.00001
NM_001349338.3(FOXP1):c.154G>A (p.Ala52Thr) rs1359632401 0.00001
NM_001349338.3(FOXP1):c.161C>T (p.Ala54Val) rs1363644889 0.00001
NM_001349338.3(FOXP1):c.1690G>A (p.Ala564Thr) rs760742879 0.00001
NM_001349338.3(FOXP1):c.1711G>A (p.Ala571Thr) rs769331988 0.00001
NM_001349338.3(FOXP1):c.1785G>C (p.Leu595=) rs1413171367 0.00001
NM_001349338.3(FOXP1):c.1848C>T (p.Asn616=) rs1231630526 0.00001
NM_001349338.3(FOXP1):c.1890-4C>T rs748164903 0.00001
NM_001349338.3(FOXP1):c.1903G>A (p.Val635Ile) rs991506093 0.00001
NM_001349338.3(FOXP1):c.1982T>C (p.Phe661Ser) rs759325225 0.00001
NM_001349338.3(FOXP1):c.267A>C (p.Lys89Asn) rs747077717 0.00001
NM_001349338.3(FOXP1):c.585C>T (p.His195=) rs200803908 0.00001
NM_001349338.3(FOXP1):c.602G>A (p.Arg201His) rs1450448594 0.00001
NM_001349338.3(FOXP1):c.676A>G (p.Thr226Ala) rs1450633154 0.00001
NM_001349338.3(FOXP1):c.840G>C (p.Gln280His) rs375611825 0.00001
NM_001349338.3(FOXP1):c.112A>G (p.Asn38Asp)
NM_001349338.3(FOXP1):c.1146+1G>A rs1559650552
NM_001349338.3(FOXP1):c.114C>T (p.Asn38=) rs1560102007
NM_001349338.3(FOXP1):c.1239_1265dup (p.Leu414_Ser422dup) rs2107316260
NM_001349338.3(FOXP1):c.1240_1241del (p.Leu414fs) rs1064793130
NM_001349338.3(FOXP1):c.1240dup (p.Leu414fs) rs797044652
NM_001349338.3(FOXP1):c.1255C>T (p.Gln419Ter)
NM_001349338.3(FOXP1):c.1256A>G (p.Gln419Arg) rs2037927166
NM_001349338.3(FOXP1):c.1263C>G (p.Pro421=) rs746264001
NM_001349338.3(FOXP1):c.1308C>T (p.Arg436=) rs2037909647
NM_001349338.3(FOXP1):c.1322A>C (p.Asp441Ala)
NM_001349338.3(FOXP1):c.135C>T (p.Asp45=) rs749307402
NM_001349338.3(FOXP1):c.1396CCA[1] (p.Pro467del)
NM_001349338.3(FOXP1):c.1531-9_1534dup rs2036514016
NM_001349338.3(FOXP1):c.1538T>C (p.Val513Ala) rs1553663140
NM_001349338.3(FOXP1):c.153CGCCCA[3] (p.His53_Ala54dup) rs1560101657
NM_001349338.3(FOXP1):c.1541G>A (p.Arg514His) rs797045586
NM_001349338.3(FOXP1):c.1547_1552del (p.Asn516_Leu517del) rs2545050080
NM_001349338.3(FOXP1):c.1549C>T (p.Leu517Phe) rs2107201024
NM_001349338.3(FOXP1):c.1569del (p.Phe523fs) rs2036507371
NM_001349338.3(FOXP1):c.1574G>A (p.Arg525Gln) rs1553663084
NM_001349338.3(FOXP1):c.1615G>C (p.Val539Leu)
NM_001349338.3(FOXP1):c.1616T>A (p.Val539Glu)
NM_001349338.3(FOXP1):c.1631G>A (p.Arg544Gln) rs2036497448
NM_001349338.3(FOXP1):c.1652+5G>A rs794727216
NM_001349338.3(FOXP1):c.1652+5G>C rs794727216
NM_001349338.3(FOXP1):c.1656C>A (p.Asn552Lys) rs2107157001
NM_001349338.3(FOXP1):c.1731G>A (p.Met577Ile) rs2544931449
NM_001349338.3(FOXP1):c.1732G>A (p.Ala578Thr) rs2034696345
NM_001349338.3(FOXP1):c.1739A>G (p.Asn580Ser) rs1038860326
NM_001349338.3(FOXP1):c.1783C>G (p.Leu595Val) rs1292897246
NM_001349338.3(FOXP1):c.180+239G>A
NM_001349338.3(FOXP1):c.180+4C>T rs1404018553
NM_001349338.3(FOXP1):c.1872A>T (p.Arg624Ser) rs2544928204
NM_001349338.3(FOXP1):c.1936G>A (p.Glu646Lys) rs756987886
NM_001349338.3(FOXP1):c.1965C>T (p.Ala655=) rs2544831054
NM_001349338.3(FOXP1):c.227A>G (p.Gln76Arg) rs781246788
NM_001349338.3(FOXP1):c.22G>C (p.Glu8Gln) rs2546770800
NM_001349338.3(FOXP1):c.289G>A (p.Val97Met) rs148369068
NM_001349338.3(FOXP1):c.299C>T (p.Ala100Val) rs2107137232
NM_001349338.3(FOXP1):c.319A>G (p.Ile107Val) rs1440752852
NM_001349338.3(FOXP1):c.399G>A (p.Gln133=) rs2107135008
NM_001349338.3(FOXP1):c.529C>T (p.Gln177Ter) rs1559807265
NM_001349338.3(FOXP1):c.574C>A (p.Gln192Lys) rs1057524732
NM_001349338.3(FOXP1):c.598C>T (p.Gln200Ter) rs1553709919
NM_001349338.3(FOXP1):c.664+6C>T rs552866338
NM_001349338.3(FOXP1):c.713C>T (p.Ala238Val)
NM_001349338.3(FOXP1):c.823G>A (p.Ala275Thr)
NM_001349338.3(FOXP1):c.924C>G (p.Cys308Trp)
NM_001349338.3(FOXP1):c.948G>A (p.Val316=) rs2545542581
NM_001349338.3(FOXP1):c.983A>G (p.Asn328Ser) rs2545413511

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