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
|
|