NM_001077706.3(ECT2L):c.1579G>A (p.Glu527Lys)
|
rs1529151
|
0.25392
|
NM_001077706.3(ECT2L):c.12C>A (p.Phe4Leu)
|
rs79219465
|
0.01751
|
NM_001077706.3(ECT2L):c.1318T>G (p.Trp440Gly)
|
rs79294486
|
0.01383
|
NM_001077706.3(ECT2L):c.649G>A (p.Val217Met)
|
rs75478555
|
0.01346
|
NM_001077706.3(ECT2L):c.910A>G (p.Met304Val)
|
rs75962473
|
0.01287
|
NM_001077706.3(ECT2L):c.437T>C (p.Ile146Thr)
|
rs76700722
|
0.01264
|
NM_001077706.3(ECT2L):c.145G>A (p.Ala49Thr)
|
rs146769748
|
0.00788
|
NM_001077706.3(ECT2L):c.1780G>A (p.Ala594Thr)
|
rs11968285
|
0.00741
|
NM_001077706.3(ECT2L):c.1579-1G>C
|
rs79069095
|
0.00689
|
NM_001077706.3(ECT2L):c.1709T>C (p.Val570Ala)
|
rs138935097
|
0.00495
|
NM_001077706.3(ECT2L):c.2191C>T (p.His731Tyr)
|
rs144150484
|
0.00412
|
NM_001077706.3(ECT2L):c.272C>T (p.Ser91Phe)
|
rs116211453
|
0.00407
|
NM_001077706.3(ECT2L):c.2180C>T (p.Thr727Ile)
|
rs199701983
|
0.00248
|
NM_001077706.3(ECT2L):c.1145C>A (p.Ala382Asp)
|
rs149517821
|
0.00228
|
NM_001077706.3(ECT2L):c.1135A>T (p.Ser379Cys)
|
rs139396585
|
0.00222
|
NM_001077706.3(ECT2L):c.839A>G (p.Asp280Gly)
|
rs142505459
|
0.00164
|
NM_001077706.3(ECT2L):c.2227C>T (p.Gln743Ter)
|
rs199963616
|
0.00103
|
NM_001077706.3(ECT2L):c.1532C>T (p.Ala511Val)
|
rs202079003
|
0.00014
|
NM_001077706.3(ECT2L):c.2555G>A (p.Arg852Gln)
|
rs371621945
|
0.00009
|
NM_001077706.3(ECT2L):c.1672A>C (p.Ile558Leu)
|
rs375958674
|
0.00006
|
NM_001077706.3(ECT2L):c.2479C>T (p.Arg827Trp)
|
rs539507764
|
0.00005
|
NM_001077706.3(ECT2L):c.1510A>G (p.Ile504Val)
|
rs201270230
|
0.00003
|
NM_001077706.3(ECT2L):c.614G>A (p.Arg205Gln)
|
rs587778245
|
0.00003
|
NM_001077706.3(ECT2L):c.1739A>G (p.Lys580Arg)
|
rs587778240
|
0.00002
|
NM_001077706.3(ECT2L):c.1070-1G>C
|
rs587777937
|
0.00001
|
NM_001077706.3(ECT2L):c.1802C>T (p.Ser601Leu)
|
rs587778241
|
0.00001
|
NM_001077706.3(ECT2L):c.1051G>A (p.Glu351Lys)
|
rs73557274
|
|
NM_001077706.3(ECT2L):c.1672_1674dup (p.Ile558dup)
|
rs587778239
|
|
NM_001077706.3(ECT2L):c.2615G>A (p.Gly872Asp)
|
rs374898524
|
|
NM_001077706.3(ECT2L):c.452A>G (p.His151Arg)
|
rs587778243
|
|
NM_001077706.3(ECT2L):c.713A>C (p.Glu238Ala)
|
rs587778244
|
|
NM_001077706.3(ECT2L):c.958_959inv (p.Val320Thr)
|
|
|