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=)
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NM_001349338.3(FOXP1):c.2032_2033del (p.Ter678ThrextTer?)
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rs1575650113
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NM_001349338.3(FOXP1):c.2033G>A (p.Ter678=)
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NM_001349338.3(FOXP1):c.246A>G (p.Lys82=)
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NM_001349338.3(FOXP1):c.270A>G (p.Gln90=)
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NM_001349338.3(FOXP1):c.282+15T>G
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NM_001349338.3(FOXP1):c.282+18T>C
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NM_001349338.3(FOXP1):c.283-14C>T
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NM_001349338.3(FOXP1):c.283-18C>A
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NM_001349338.3(FOXP1):c.283-4C>T
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NM_001349338.3(FOXP1):c.29A>G (p.Lys10Arg)
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NM_001349338.3(FOXP1):c.300T>A (p.Ala100=)
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NM_001349338.3(FOXP1):c.333A>G (p.Gln111=)
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NM_001349338.3(FOXP1):c.354A>G (p.Gln118=)
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NM_001349338.3(FOXP1):c.366C>T (p.Ser122=)
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NM_001349338.3(FOXP1):c.378C>G (p.Leu126=)
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NM_001349338.3(FOXP1):c.384T>C (p.Val128=)
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NM_001349338.3(FOXP1):c.420+10C>A
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NM_001349338.3(FOXP1):c.420+10C>T
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NM_001349338.3(FOXP1):c.420+9C>T
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NM_001349338.3(FOXP1):c.421-15C>T
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NM_001349338.3(FOXP1):c.421-20G>A
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NM_001349338.3(FOXP1):c.421-4G>A
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NM_001349338.3(FOXP1):c.421-5T>C
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NM_001349338.3(FOXP1):c.421-9C>G
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NM_001349338.3(FOXP1):c.490G>T (p.Ala164Ser)
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NM_001349338.3(FOXP1):c.497A>T (p.Lys166Ile)
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NM_001349338.3(FOXP1):c.501G>A (p.Gln167=)
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NM_001349338.3(FOXP1):c.510+13C>T
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NM_001349338.3(FOXP1):c.510+14A>G
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NM_001349338.3(FOXP1):c.510+17T>G
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NM_001349338.3(FOXP1):c.511-12G>A
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NM_001349338.3(FOXP1):c.511-16T>A
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NM_001349338.3(FOXP1):c.511-18del
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NM_001349338.3(FOXP1):c.511-7C>G
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NM_001349338.3(FOXP1):c.516G>A (p.Gln172=)
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NM_001349338.3(FOXP1):c.51G>A (p.Gln17=)
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NM_001349338.3(FOXP1):c.525T>C (p.Ala175=)
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NM_001349338.3(FOXP1):c.528C>T (p.Thr176=)
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NM_001349338.3(FOXP1):c.582G>A (p.Gln194=)
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NM_001349338.3(FOXP1):c.585C>T (p.His195=)
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NM_001349338.3(FOXP1):c.588C>G (p.Leu196=)
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NM_001349338.3(FOXP1):c.606A>G (p.Gln202=)
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NM_001349338.3(FOXP1):c.611T>A (p.Leu204His)
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NM_001349338.3(FOXP1):c.615G>C (p.Leu205=)
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NM_001349338.3(FOXP1):c.628G>A (p.Gly210Arg)
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NM_001349338.3(FOXP1):c.653C>A (p.Pro218His)
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NM_001349338.3(FOXP1):c.664+17C>G
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NM_001349338.3(FOXP1):c.664+7G>A
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NM_001349338.3(FOXP1):c.665-17C>T
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NM_001349338.3(FOXP1):c.665-5T>C
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NM_001349338.3(FOXP1):c.665-7_665-4del
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rs1453915867
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NM_001349338.3(FOXP1):c.684G>A (p.Leu228=)
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NM_001349338.3(FOXP1):c.728A>G (p.Glu243Gly)
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NM_001349338.3(FOXP1):c.741C>T (p.Asn247=)
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NM_001349338.3(FOXP1):c.768G>A (p.Thr256=)
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NM_001349338.3(FOXP1):c.772T>C (p.Cys258Arg)
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NM_001349338.3(FOXP1):c.786T>C (p.Ser262=)
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NM_001349338.3(FOXP1):c.78A>G (p.Leu26=)
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NM_001349338.3(FOXP1):c.795C>T (p.Ser265=)
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NM_001349338.3(FOXP1):c.813G>A (p.Met271Ile)
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NM_001349338.3(FOXP1):c.825C>T (p.Ala275=)
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NM_001349338.3(FOXP1):c.834T>C (p.Asn278=)
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NM_001349338.3(FOXP1):c.843C>T (p.Leu281=)
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NM_001349338.3(FOXP1):c.869+17G>T
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NM_001349338.3(FOXP1):c.869+943G>C
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NM_001349338.3(FOXP1):c.870-14G>A
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NM_001349338.3(FOXP1):c.879T>C (p.His293=)
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NM_001349338.3(FOXP1):c.87C>T (p.Cys29=)
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NM_001349338.3(FOXP1):c.885G>A (p.Glu295=)
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NM_001349338.3(FOXP1):c.892C>T (p.His298Tyr)
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NM_001349338.3(FOXP1):c.909T>C (p.Tyr303=)
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NM_001349338.3(FOXP1):c.90C>T (p.Gly30=)
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NM_001349338.3(FOXP1):c.915T>C (p.His305=)
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NM_001349338.3(FOXP1):c.918T>C (p.Gly306=)
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NM_001349338.3(FOXP1):c.927G>C (p.Lys309Asn)
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NM_001349338.3(FOXP1):c.945A>C (p.Ala315=)
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NM_001349338.3(FOXP1):c.960C>T (p.Phe320=)
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NM_001349338.3(FOXP1):c.963A>G (p.Gln321=)
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NM_001349338.3(FOXP1):c.966A>T (p.Ser322=)
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NM_001349338.3(FOXP1):c.974+16T>C
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NM_001349338.3(FOXP1):c.975-18T>G
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NM_001349338.3(FOXP1):c.975-6T>C
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rs1576028816
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NM_001349338.3(FOXP1):c.996G>A (p.Ala332=)
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