ClinVar Miner

List of variants in gene FOXP1 reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 291
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HGVS dbSNP gnomAD frequency
NM_001349338.3(FOXP1):c.510+108T>C rs4555486 0.01117
NM_001349338.3(FOXP1):c.511-248G>C rs11914321 0.01024
NM_001349338.3(FOXP1):c.181-262T>C rs79522164 0.00948
NM_001349338.3(FOXP1):c.181-29G>A rs113050068 0.00886
NM_001349338.3(FOXP1):c.1722+179C>T rs111425991 0.00812
NM_001349338.3(FOXP1):c.282+211T>C rs115531620 0.00743
NM_001349338.3(FOXP1):c.180+289C>T rs141808088 0.00725
NM_001349338.3(FOXP1):c.869+134G>A rs145314293 0.00530
NM_001349338.3(FOXP1):c.1652+839C>G rs184390493 0.00455
NM_001349338.3(FOXP1):c.1890-137G>A rs139747537 0.00429
NM_001349338.3(FOXP1):c.1062+265G>A rs374214924 0.00399
NM_001349338.3(FOXP1):c.1722+63A>G rs189960519 0.00376
NM_001349338.3(FOXP1):c.-11-71A>T rs144226924 0.00316
NM_001349338.3(FOXP1):c.1652+403A>G rs76145927 0.00298
NM_001349338.3(FOXP1):c.1428+173A>G rs140116317 0.00274
NM_001349338.3(FOXP1):c.181-18423_181-18422insC rs1553753128 0.00262
NM_001349338.3(FOXP1):c.1146+19C>G rs140060227 0.00228
NM_001349338.3(FOXP1):c.181-13T>G rs139264797 0.00220
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 0.00118
NM_001349338.3(FOXP1):c.1413A>G (p.Ala471=) rs144080925 0.00088
NM_001349338.3(FOXP1):c.1825G>A (p.Ala609Thr) rs147537388 0.00067
NM_001349338.3(FOXP1):c.1890-5T>C rs187666567 0.00059
NM_001349338.3(FOXP1):c.123G>A (p.Thr41=) rs201155996 0.00030
NM_001349338.3(FOXP1):c.855T>G (p.Thr285=) rs141007926 0.00029
NM_001349338.3(FOXP1):c.1722+15C>T rs370356350 0.00025
NM_001349338.3(FOXP1):c.1217C>G (p.Thr406Ser) rs200355554 0.00016
NM_001349338.3(FOXP1):c.936C>T (p.Gly312=) rs61753356 0.00016
NM_001349338.3(FOXP1):c.44C>T (p.Ala15Val) rs532329866 0.00015
NM_001349338.3(FOXP1):c.13T>C (p.Ser5Pro) rs762898505 0.00012
NM_001349338.3(FOXP1):c.390C>G (p.Leu130=) rs145868163 0.00011
NM_001349338.3(FOXP1):c.1531-6C>T rs767129660 0.00009
NM_001349338.3(FOXP1):c.1135G>A (p.Ala379Thr) rs149759021 0.00008
NM_001349338.3(FOXP1):c.627C>T (p.Pro209=) rs557318477 0.00008
NM_001349338.3(FOXP1):c.216G>A (p.Gln72=) rs144347581 0.00006
NM_001349338.3(FOXP1):c.107G>A (p.Arg36Gln) rs200643313 0.00005
NM_001349338.3(FOXP1):c.1652+12A>G rs981139510 0.00005
NM_001349338.3(FOXP1):c.63C>T (p.Gly21=) rs376702675 0.00005
NM_001349338.3(FOXP1):c.1149G>A (p.Leu383=) rs372657299 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.450A>G (p.Gln150=) rs1433777499 0.00004
NM_001349338.3(FOXP1):c.738C>G (p.Gly246=) rs761092367 0.00004
NM_001349338.3(FOXP1):c.888C>T (p.His296=) rs144274165 0.00004
NM_001349338.3(FOXP1):c.1344G>A (p.Ser448=) rs143503790 0.00003
NM_001349338.3(FOXP1):c.1764T>C (p.Ala588=) rs765482675 0.00003
NM_001349338.3(FOXP1):c.1902C>T (p.His634=) rs749771909 0.00003
NM_001349338.3(FOXP1):c.288C>T (p.Pro96=) rs528713688 0.00003
NM_001349338.3(FOXP1):c.699A>G (p.Lys233=) rs944917133 0.00003
NM_001349338.3(FOXP1):c.1768A>G (p.Met590Val) rs201446635 0.00002
NM_001349338.3(FOXP1):c.316G>A (p.Val106Ile) rs755709669 0.00002
NM_001349338.3(FOXP1):c.8A>G (p.Gln3Arg) rs898658081 0.00002
NM_001349338.3(FOXP1):c.1155G>A (p.Leu385=) rs368920983 0.00001
NM_001349338.3(FOXP1):c.1641A>G (p.Gln547=) rs886058864 0.00001
NM_001349338.3(FOXP1):c.1652+4C>T rs572849158 0.00001
NM_001349338.3(FOXP1):c.1890-4C>T rs748164903 0.00001
NM_001349338.3(FOXP1):c.1964C>T (p.Ala655Val) rs762475508 0.00001
NM_001349338.3(FOXP1):c.321C>T (p.Ile107=) rs747108471 0.00001
NM_001349338.3(FOXP1):c.444A>G (p.Lys148=) rs763673991 0.00001
NM_001349338.3(FOXP1):c.665-19T>C rs1430014504 0.00001
NM_001349338.3(FOXP1):c.665-7G>T rs773950156 0.00001
NM_001349338.3(FOXP1):c.79C>T (p.Leu27=) rs374005944 0.00001
NM_001349338.3(FOXP1):c.*1669dup rs886058842
NM_001349338.3(FOXP1):c.*3192del rs535202716
NM_001349338.3(FOXP1):c.*3391TG[10] rs143202281
NM_001349338.3(FOXP1):c.1002C>T (p.Asp334=)
NM_001349338.3(FOXP1):c.1038G>A (p.Gln346=)
NM_001349338.3(FOXP1):c.105G>A (p.Gly35=)
NM_001349338.3(FOXP1):c.1062+128ATTTT[14] rs59993750
NM_001349338.3(FOXP1):c.1062+128ATTTT[15] rs59993750
NM_001349338.3(FOXP1):c.1062+128ATTTT[9] rs59993750
NM_001349338.3(FOXP1):c.1062+14del
NM_001349338.3(FOXP1):c.1063-5G>A
NM_001349338.3(FOXP1):c.1063-8C>T
NM_001349338.3(FOXP1):c.1086G>A (p.Leu362=)
NM_001349338.3(FOXP1):c.108G>A (p.Arg36=)
NM_001349338.3(FOXP1):c.1092C>T (p.Ala364=)
NM_001349338.3(FOXP1):c.1104C>T (p.His368=)
NM_001349338.3(FOXP1):c.1116G>A (p.Lys372=)
NM_001349338.3(FOXP1):c.1128C>T (p.Pro376=)
NM_001349338.3(FOXP1):c.1134C>T (p.Ala378=)
NM_001349338.3(FOXP1):c.1146+10_1146+12del rs199543140
NM_001349338.3(FOXP1):c.1146+12dup
NM_001349338.3(FOXP1):c.1146+13C>A
NM_001349338.3(FOXP1):c.1146+13C>G
NM_001349338.3(FOXP1):c.1146+18_1146+20del
NM_001349338.3(FOXP1):c.1146+19C>T
NM_001349338.3(FOXP1):c.1146C>T (p.Pro382=)
NM_001349338.3(FOXP1):c.1147-10T>C
NM_001349338.3(FOXP1):c.1147-11T>C
NM_001349338.3(FOXP1):c.1147-13T>C
NM_001349338.3(FOXP1):c.1147-16_1147-12dup
NM_001349338.3(FOXP1):c.1147-16_1147-14del
NM_001349338.3(FOXP1):c.1147-17T>C
NM_001349338.3(FOXP1):c.1147-20C>T
NM_001349338.3(FOXP1):c.1147-9T>C
NM_001349338.3(FOXP1):c.114C>T (p.Asn38=) rs1560102007
NM_001349338.3(FOXP1):c.1152T>C (p.Asn384=)
NM_001349338.3(FOXP1):c.1158A>G (p.Val386=)
NM_001349338.3(FOXP1):c.1158A>T (p.Val386=)
NM_001349338.3(FOXP1):c.1162A>T (p.Ser388Cys)
NM_001349338.3(FOXP1):c.1167C>T (p.Val389=)
NM_001349338.3(FOXP1):c.1176C>A (p.Ser392=)
NM_001349338.3(FOXP1):c.1176C>T (p.Ser392=)
NM_001349338.3(FOXP1):c.1182C>T (p.Ser394=)
NM_001349338.3(FOXP1):c.1188G>A (p.Ser396=)
NM_001349338.3(FOXP1):c.1193C>T (p.Ala398Val)
NM_001349338.3(FOXP1):c.1221A>G (p.Pro407=)
NM_001349338.3(FOXP1):c.1236C>T (p.Ala412=)
NM_001349338.3(FOXP1):c.1239C>G (p.Pro413=)
NM_001349338.3(FOXP1):c.1248C>G (p.Pro416=)
NM_001349338.3(FOXP1):c.1248C>T (p.Pro416=)
NM_001349338.3(FOXP1):c.1249G>A (p.Val417Ile)
NM_001349338.3(FOXP1):c.1254C>A (p.Thr418=)
NM_001349338.3(FOXP1):c.126G>A (p.Pro42=) rs762082081
NM_001349338.3(FOXP1):c.1293G>A (p.Thr431=)
NM_001349338.3(FOXP1):c.1293G>C (p.Thr431=)
NM_001349338.3(FOXP1):c.129C>A (p.Ala43=)
NM_001349338.3(FOXP1):c.129C>T (p.Ala43=)
NM_001349338.3(FOXP1):c.1308C>T (p.Arg436=)
NM_001349338.3(FOXP1):c.1311G>A (p.Arg437=)
NM_001349338.3(FOXP1):c.1314G>C (p.Arg438=)
NM_001349338.3(FOXP1):c.1335G>A (p.Val445=)
NM_001349338.3(FOXP1):c.1338C>T (p.Pro446=)
NM_001349338.3(FOXP1):c.1343C>T (p.Ser448Leu)
NM_001349338.3(FOXP1):c.1348+14C>G
NM_001349338.3(FOXP1):c.1348+14C>T
NM_001349338.3(FOXP1):c.1348+15T>G rs2107313157
NM_001349338.3(FOXP1):c.1348+19G>C
NM_001349338.3(FOXP1):c.1349-17C>T
NM_001349338.3(FOXP1):c.1349-20G>T
NM_001349338.3(FOXP1):c.1384G>A (p.Ala462Thr)
NM_001349338.3(FOXP1):c.1386A>T (p.Ala462=)
NM_001349338.3(FOXP1):c.138C>T (p.Ile46=)
NM_001349338.3(FOXP1):c.1398A>G (p.Pro466=)
NM_001349338.3(FOXP1):c.141G>A (p.Gly47=)
NM_001349338.3(FOXP1):c.1428+10_1428+13del
NM_001349338.3(FOXP1):c.1428+11A>C
NM_001349338.3(FOXP1):c.1428+15C>T
NM_001349338.3(FOXP1):c.1428+16A>G
NM_001349338.3(FOXP1):c.1428+17G>A
NM_001349338.3(FOXP1):c.1428+20T>C
NM_001349338.3(FOXP1):c.1428+3A>G
NM_001349338.3(FOXP1):c.1428+8A>G rs1575803895
NM_001349338.3(FOXP1):c.1428+9_1428+12del
NM_001349338.3(FOXP1):c.151C>T (p.Leu51Phe)
NM_001349338.3(FOXP1):c.1531-18_1531-15dup rs754225912
NM_001349338.3(FOXP1):c.1531-7G>A
NM_001349338.3(FOXP1):c.153C>T (p.Leu51=)
NM_001349338.3(FOXP1):c.1584C>T (p.Asn528=)
NM_001349338.3(FOXP1):c.1590A>G (p.Lys530=)
NM_001349338.3(FOXP1):c.1596A>G (p.Ala532=)
NM_001349338.3(FOXP1):c.1599A>G (p.Val533=)
NM_001349338.3(FOXP1):c.159C>T (p.His53=)
NM_001349338.3(FOXP1):c.162C>T (p.Ala54=)
NM_001349338.3(FOXP1):c.1652+515C>T
NM_001349338.3(FOXP1):c.1652+540G>A
NM_001349338.3(FOXP1):c.1653-17A>C
NM_001349338.3(FOXP1):c.1653-17A>G
NM_001349338.3(FOXP1):c.1677G>A (p.Met559Ile)
NM_001349338.3(FOXP1):c.1681A>G (p.Ser561Gly)
NM_001349338.3(FOXP1):c.1686C>T (p.Ser562=)
NM_001349338.3(FOXP1):c.1689C>T (p.His563=)
NM_001349338.3(FOXP1):c.1690G>A (p.Ala564Thr)
NM_001349338.3(FOXP1):c.1701A>G (p.Thr567=)
NM_001349338.3(FOXP1):c.1709_1722+10dup
NM_001349338.3(FOXP1):c.171G>A (p.Gln57=)
NM_001349338.3(FOXP1):c.1722+11C>T
NM_001349338.3(FOXP1):c.1722+20C>T
NM_001349338.3(FOXP1):c.1722+6A>T
NM_001349338.3(FOXP1):c.1723-14T>G
NM_001349338.3(FOXP1):c.1740T>C (p.Asn580=)
NM_001349338.3(FOXP1):c.174G>A (p.Gln58=)
NM_001349338.3(FOXP1):c.1761C>T (p.Thr587=)
NM_001349338.3(FOXP1):c.1785G>C (p.Leu595=)
NM_001349338.3(FOXP1):c.180+13G>T
NM_001349338.3(FOXP1):c.180+18C>G
NM_001349338.3(FOXP1):c.180+230T>C
NM_001349338.3(FOXP1):c.180+7G>T
NM_001349338.3(FOXP1):c.1800C>T (p.Ser600=)
NM_001349338.3(FOXP1):c.1801G>A (p.Ala601Thr)
NM_001349338.3(FOXP1):c.1803A>T (p.Ala601=) rs2034678143
NM_001349338.3(FOXP1):c.1808G>A (p.Arg603Gln)
NM_001349338.3(FOXP1):c.181-14G>A
NM_001349338.3(FOXP1):c.181-16T>C
NM_001349338.3(FOXP1):c.181-7C>T
NM_001349338.3(FOXP1):c.1816C>T (p.Leu606=)
NM_001349338.3(FOXP1):c.1821C>T (p.Asn607=)
NM_001349338.3(FOXP1):c.1826C>T (p.Ala609Val)
NM_001349338.3(FOXP1):c.1831G>A (p.Glu611Lys)
NM_001349338.3(FOXP1):c.1833G>T (p.Glu611Asp)
NM_001349338.3(FOXP1):c.1848C>T (p.Asn616=) rs1231630526
NM_001349338.3(FOXP1):c.184C>T (p.Leu62Phe) rs538443416
NM_001349338.3(FOXP1):c.1889+11T>C
NM_001349338.3(FOXP1):c.1889+7A>G
NM_001349338.3(FOXP1):c.1889+8T>C
NM_001349338.3(FOXP1):c.1890-10T>A
NM_001349338.3(FOXP1):c.1890-16T>C
NM_001349338.3(FOXP1):c.1890-8_1890-5dup rs2106859245
NM_001349338.3(FOXP1):c.1896T>A (p.Pro632=)
NM_001349338.3(FOXP1):c.1968C>T (p.Asn656=)
NM_001349338.3(FOXP1):c.1977A>G (p.Pro659=)
NM_001349338.3(FOXP1):c.1989T>C (p.His663=)
NM_001349338.3(FOXP1):c.2001C>T (p.Tyr667=)
NM_001349338.3(FOXP1):c.2022G>A (p.Glu674=)
NM_001349338.3(FOXP1):c.2024A>G (p.Asp675Gly)
NM_001349338.3(FOXP1):c.2031G>A (p.Glu677=)
NM_001349338.3(FOXP1):c.2032_2033del (p.Ter678ThrextTer?) rs1575650113
NM_001349338.3(FOXP1):c.2033G>A (p.Ter678=)
NM_001349338.3(FOXP1):c.246A>G (p.Lys82=)
NM_001349338.3(FOXP1):c.270A>G (p.Gln90=)
NM_001349338.3(FOXP1):c.282+15T>G
NM_001349338.3(FOXP1):c.282+18T>C
NM_001349338.3(FOXP1):c.283-14C>T
NM_001349338.3(FOXP1):c.283-18C>A
NM_001349338.3(FOXP1):c.283-4C>T
NM_001349338.3(FOXP1):c.29A>G (p.Lys10Arg)
NM_001349338.3(FOXP1):c.300T>A (p.Ala100=)
NM_001349338.3(FOXP1):c.333A>G (p.Gln111=)
NM_001349338.3(FOXP1):c.354A>G (p.Gln118=)
NM_001349338.3(FOXP1):c.366C>T (p.Ser122=)
NM_001349338.3(FOXP1):c.378C>G (p.Leu126=)
NM_001349338.3(FOXP1):c.384T>C (p.Val128=)
NM_001349338.3(FOXP1):c.420+10C>A
NM_001349338.3(FOXP1):c.420+10C>T
NM_001349338.3(FOXP1):c.420+9C>T
NM_001349338.3(FOXP1):c.421-15C>T
NM_001349338.3(FOXP1):c.421-20G>A
NM_001349338.3(FOXP1):c.421-4G>A
NM_001349338.3(FOXP1):c.421-5T>C
NM_001349338.3(FOXP1):c.421-9C>G
NM_001349338.3(FOXP1):c.490G>T (p.Ala164Ser)
NM_001349338.3(FOXP1):c.497A>T (p.Lys166Ile)
NM_001349338.3(FOXP1):c.501G>A (p.Gln167=)
NM_001349338.3(FOXP1):c.510+13C>T
NM_001349338.3(FOXP1):c.510+14A>G
NM_001349338.3(FOXP1):c.510+17T>G
NM_001349338.3(FOXP1):c.511-12G>A
NM_001349338.3(FOXP1):c.511-16T>A
NM_001349338.3(FOXP1):c.511-18del
NM_001349338.3(FOXP1):c.511-7C>G
NM_001349338.3(FOXP1):c.516G>A (p.Gln172=)
NM_001349338.3(FOXP1):c.51G>A (p.Gln17=)
NM_001349338.3(FOXP1):c.525T>C (p.Ala175=)
NM_001349338.3(FOXP1):c.528C>T (p.Thr176=)
NM_001349338.3(FOXP1):c.582G>A (p.Gln194=)
NM_001349338.3(FOXP1):c.585C>T (p.His195=)
NM_001349338.3(FOXP1):c.588C>G (p.Leu196=)
NM_001349338.3(FOXP1):c.606A>G (p.Gln202=)
NM_001349338.3(FOXP1):c.611T>A (p.Leu204His)
NM_001349338.3(FOXP1):c.615G>C (p.Leu205=)
NM_001349338.3(FOXP1):c.628G>A (p.Gly210Arg)
NM_001349338.3(FOXP1):c.653C>A (p.Pro218His)
NM_001349338.3(FOXP1):c.664+17C>G
NM_001349338.3(FOXP1):c.664+7G>A
NM_001349338.3(FOXP1):c.665-17C>T
NM_001349338.3(FOXP1):c.665-5T>C
NM_001349338.3(FOXP1):c.665-7_665-4del rs1453915867
NM_001349338.3(FOXP1):c.684G>A (p.Leu228=)
NM_001349338.3(FOXP1):c.728A>G (p.Glu243Gly)
NM_001349338.3(FOXP1):c.741C>T (p.Asn247=)
NM_001349338.3(FOXP1):c.768G>A (p.Thr256=)
NM_001349338.3(FOXP1):c.772T>C (p.Cys258Arg)
NM_001349338.3(FOXP1):c.786T>C (p.Ser262=)
NM_001349338.3(FOXP1):c.78A>G (p.Leu26=)
NM_001349338.3(FOXP1):c.795C>T (p.Ser265=)
NM_001349338.3(FOXP1):c.813G>A (p.Met271Ile)
NM_001349338.3(FOXP1):c.825C>T (p.Ala275=)
NM_001349338.3(FOXP1):c.834T>C (p.Asn278=)
NM_001349338.3(FOXP1):c.843C>T (p.Leu281=)
NM_001349338.3(FOXP1):c.869+17G>T
NM_001349338.3(FOXP1):c.869+943G>C
NM_001349338.3(FOXP1):c.870-14G>A
NM_001349338.3(FOXP1):c.879T>C (p.His293=)
NM_001349338.3(FOXP1):c.87C>T (p.Cys29=)
NM_001349338.3(FOXP1):c.885G>A (p.Glu295=)
NM_001349338.3(FOXP1):c.892C>T (p.His298Tyr)
NM_001349338.3(FOXP1):c.909T>C (p.Tyr303=)
NM_001349338.3(FOXP1):c.90C>T (p.Gly30=)
NM_001349338.3(FOXP1):c.915T>C (p.His305=)
NM_001349338.3(FOXP1):c.918T>C (p.Gly306=)
NM_001349338.3(FOXP1):c.927G>C (p.Lys309Asn)
NM_001349338.3(FOXP1):c.945A>C (p.Ala315=)
NM_001349338.3(FOXP1):c.960C>T (p.Phe320=)
NM_001349338.3(FOXP1):c.963A>G (p.Gln321=)
NM_001349338.3(FOXP1):c.966A>T (p.Ser322=)
NM_001349338.3(FOXP1):c.974+16T>C
NM_001349338.3(FOXP1):c.975-18T>G
NM_001349338.3(FOXP1):c.975-6T>C rs1576028816
NM_001349338.3(FOXP1):c.996G>A (p.Ala332=)

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