NM_175875.5(SIX5):c.1903C>T (p.Pro635Ser)
|
rs2014576
|
0.43324
|
NM_000503.6(EYA1):c.639+39T>G
|
rs3779747
|
0.39091
|
NM_000503.6(EYA1):c.1755T>C (p.His585=)
|
rs10103397
|
0.35033
|
NM_000503.6(EYA1):c.1699-23A>G
|
rs10090382
|
0.34966
|
NM_175875.5(SIX5):c.2077G>A (p.Val693Met)
|
rs2341097
|
0.33126
|
NM_001372066.1(TFAP2A):c.1032-44T>A
|
rs303048
|
0.31435
|
NM_000503.6(EYA1):c.1476-21G>T
|
rs3735935
|
0.30839
|
NM_000503.6(EYA1):c.1278C>T (p.Gly426=)
|
rs4738118
|
0.13734
|
NM_000503.6(EYA1):c.813A>G (p.Thr271=)
|
rs1445398
|
0.08547
|
NM_000503.6(EYA1):c.58C>G (p.Pro20Ala)
|
rs1445404
|
0.05809
|
NM_000503.6(EYA1):c.556+18G>T
|
rs113694988
|
0.02938
|
NM_000503.6(EYA1):c.1597+18T>C
|
rs76259565
|
0.02609
|
NM_000503.6(EYA1):c.1699-3C>T
|
rs117149407
|
0.01158
|
NM_000503.6(EYA1):c.840C>A (p.Ile280=)
|
rs55972891
|
0.00286
|
NM_000503.6(EYA1):c.1200-11C>A
|
rs181457812
|
0.00176
|
NM_000503.6(EYA1):c.321T>C (p.Ala107=)
|
rs112282055
|
0.00162
|
NM_000503.6(EYA1):c.744G>A (p.Thr248=)
|
rs10098224
|
0.00124
|
NM_000503.6(EYA1):c.1141-15T>G
|
rs186249248
|
0.00103
|
NM_000503.6(EYA1):c.1199+13G>T
|
rs200345478
|
0.00096
|
NM_000503.6(EYA1):c.782C>T (p.Pro261Leu)
|
rs77825059
|
0.00069
|
NM_000503.6(EYA1):c.648G>A (p.Pro216=)
|
rs148973681
|
0.00067
|
NM_000503.6(EYA1):c.557-11T>A
|
rs201752432
|
0.00056
|
NM_000503.6(EYA1):c.1699-8T>C
|
rs201537030
|
0.00048
|
NM_000503.6(EYA1):c.35G>A (p.Arg12His)
|
rs74720958
|
0.00035
|
NM_000503.6(EYA1):c.966+4C>T
|
rs139429307
|
0.00032
|
NM_000503.6(EYA1):c.1734G>A (p.Ser578=)
|
rs770876882
|
0.00027
|
NM_000503.6(EYA1):c.1185C>T (p.Asn395=)
|
rs372488542
|
0.00016
|
NM_000503.6(EYA1):c.783G>A (p.Pro261=)
|
rs146648560
|
0.00013
|
NM_000503.6(EYA1):c.1377T>A (p.Ala459=)
|
rs112593082
|
0.00007
|
NM_000503.6(EYA1):c.65G>A (p.Gly22Asp)
|
rs727503049
|
0.00005
|
NM_000503.6(EYA1):c.49A>G (p.Ser17Gly)
|
rs747231434
|
0.00002
|
NM_000503.6(EYA1):c.1276G>A (p.Gly426Ser)
|
rs121909199
|
0.00001
|
NM_000503.6(EYA1):c.923G>A (p.Arg308Gln)
|
rs369822742
|
0.00001
|
NM_000503.6(EYA1):c.121G>C (p.Glu41Gln)
|
rs561111097
|
|
NM_000503.6(EYA1):c.147C>T (p.Ser49=)
|
|
|
NM_000503.6(EYA1):c.1598-15A>G
|
rs372286227
|
|
NM_000503.6(EYA1):c.1598-19ATTT[3]
|
|
|
NM_000503.6(EYA1):c.702G>A (p.Pro234=)
|
|
|
NM_175875.5(SIX5):c.1666C>G (p.Leu556Val)
|
rs2014377
|
|