NM_014159.7(SETD2):c.5271C>T (p.Leu1757=)
|
rs144825663
|
0.00389
|
NM_014159.7(SETD2):c.2783C>G (p.Thr928Arg)
|
rs72895708
|
0.00228
|
NM_014159.7(SETD2):c.3567C>T (p.Thr1189=)
|
rs140803915
|
0.00131
|
NM_014159.7(SETD2):c.3422C>T (p.Pro1141Leu)
|
rs142723093
|
0.00088
|
NM_014159.7(SETD2):c.1885A>G (p.Lys629Glu)
|
rs145650484
|
0.00047
|
NM_014159.7(SETD2):c.7164C>T (p.Thr2388=)
|
rs144752494
|
0.00047
|
NM_014159.7(SETD2):c.7500C>T (p.Thr2500=)
|
rs148499835
|
0.00036
|
NM_014159.7(SETD2):c.4193T>C (p.Ile1398Thr)
|
rs145732065
|
0.00032
|
NM_014159.7(SETD2):c.6786C>T (p.Pro2262=)
|
rs149552397
|
0.00032
|
NM_014159.7(SETD2):c.1986A>G (p.Gln662=)
|
rs146562413
|
0.00026
|
NM_014159.7(SETD2):c.6455A>G (p.Tyr2152Cys)
|
rs139628048
|
0.00024
|
NM_014159.7(SETD2):c.2096A>G (p.Asp699Gly)
|
rs368132877
|
0.00022
|
NM_014159.7(SETD2):c.1412G>A (p.Arg471Lys)
|
rs191313431
|
0.00021
|
NM_014159.7(SETD2):c.7350+6T>C
|
rs369951554
|
0.00015
|
NM_014159.7(SETD2):c.265C>T (p.Leu89Phe)
|
rs374799616
|
0.00014
|
NM_014159.7(SETD2):c.558G>A (p.Pro186=)
|
rs183095591
|
0.00012
|
NM_014159.7(SETD2):c.2798G>T (p.Gly933Val)
|
rs202209141
|
0.00010
|
NM_014159.7(SETD2):c.2849G>A (p.Arg950His)
|
rs149265978
|
0.00004
|
NM_014159.7(SETD2):c.1914C>T (p.Ser638=)
|
rs1371836213
|
0.00003
|
NM_014159.7(SETD2):c.475A>G (p.Thr159Ala)
|
rs369333306
|
0.00003
|
NM_014159.7(SETD2):c.7239-8C>T
|
rs375557161
|
0.00002
|
NM_014159.7(SETD2):c.3316T>C (p.Leu1106=)
|
rs779666460
|
0.00001
|
NM_014159.7(SETD2):c.4680A>G (p.Lys1560=)
|
rs780684040
|
0.00001
|
NM_014159.7(SETD2):c.2205C>G (p.Thr735=)
|
rs1398507583
|
|
NM_014159.7(SETD2):c.2871A>G (p.Lys957=)
|
|
|
NM_014159.7(SETD2):c.3441G>A (p.Gln1147=)
|
|
|
NM_014159.7(SETD2):c.3458T>C (p.Ile1153Thr)
|
|
|
NM_014159.7(SETD2):c.4137C>T (p.Asp1379=)
|
rs769080716
|
|
NM_014159.7(SETD2):c.4200T>C (p.Asp1400=)
|
|
|
NM_014159.7(SETD2):c.4332G>A (p.Leu1444=)
|
|
|
NM_014159.7(SETD2):c.5322T>C (p.His1774=)
|
|
|
NM_014159.7(SETD2):c.5574T>C (p.Pro1858=)
|
|
|
NM_014159.7(SETD2):c.5872G>C (p.Ala1958Pro)
|
rs377115716
|
|
NM_014159.7(SETD2):c.772A>G (p.Thr258Ala)
|
|
|
NM_014159.7(SETD2):c.985C>A (p.Arg329=)
|
rs372869995
|
|