NM_001374353.1(GLI2):c.2939C>G (p.Pro980Arg)
|
rs563818052
|
0.00088
|
NM_001374353.1(GLI2):c.607G>A (p.Ala203Thr)
|
rs147044066
|
0.00088
|
NM_001374353.1(GLI2):c.1080G>A (p.Ser360=)
|
rs149110951
|
0.00073
|
NM_001374353.1(GLI2):c.2251C>T (p.Leu751=)
|
rs200831069
|
0.00033
|
NM_001374353.1(GLI2):c.4506C>T (p.Gly1502=)
|
rs200499325
|
0.00020
|
NM_001374353.1(GLI2):c.132G>A (p.Ala44=)
|
rs145778937
|
0.00017
|
NM_001374353.1(GLI2):c.221A>G (p.His74Arg)
|
rs377700501
|
0.00016
|
NM_001374353.1(GLI2):c.4147G>T (p.Gly1383Cys)
|
rs143914758
|
0.00013
|
NM_001374353.1(GLI2):c.2886G>A (p.Leu962=)
|
rs777165274
|
0.00012
|
NM_001374353.1(GLI2):c.1875C>T (p.His625=)
|
rs372341303
|
0.00007
|
NM_001374353.1(GLI2):c.1120C>T (p.Arg374Cys)
|
rs200076785
|
0.00006
|
NM_001374353.1(GLI2):c.1701T>C (p.His567=)
|
rs370382506
|
0.00005
|
NM_001374353.1(GLI2):c.4241C>T (p.Pro1414Leu)
|
rs749402521
|
0.00005
|
NM_001374353.1(GLI2):c.2006C>T (p.Thr669Met)
|
rs758298657
|
0.00004
|
NM_001374353.1(GLI2):c.2089G>A (p.Ala697Thr)
|
rs553780090
|
0.00004
|
NM_001374353.1(GLI2):c.606C>T (p.Ser202=)
|
rs146181686
|
0.00004
|
NM_001374353.1(GLI2):c.1121G>A (p.Arg374His)
|
rs370220133
|
0.00003
|
NM_001374353.1(GLI2):c.2503G>A (p.Ala835Thr)
|
rs751028726
|
0.00003
|
NM_001374353.1(GLI2):c.4100G>A (p.Arg1367His)
|
rs763852684
|
0.00003
|
NM_001374353.1(GLI2):c.1481C>T (p.Ser494Leu)
|
rs372925840
|
0.00002
|
NM_001374353.1(GLI2):c.2075T>C (p.Leu692Pro)
|
rs781438228
|
0.00002
|
NM_001374353.1(GLI2):c.451G>A (p.Ala151Thr)
|
rs781771721
|
0.00002
|
NM_001374353.1(GLI2):c.196A>G (p.Met66Val)
|
rs768282760
|
0.00001
|
NM_001374353.1(GLI2):c.2208G>A (p.Thr736=)
|
rs372206751
|
0.00001
|
NM_001374353.1(GLI2):c.2690G>A (p.Arg897Gln)
|
rs886054813
|
0.00001
|
NM_001374353.1(GLI2):c.2884C>T (p.Leu962=)
|
rs1345329176
|
0.00001
|
NM_001374353.1(GLI2):c.3066C>T (p.Ala1022=)
|
rs1472557461
|
0.00001
|
NM_001374353.1(GLI2):c.314C>T (p.Pro105Leu)
|
rs370693310
|
0.00001
|
NM_001374353.1(GLI2):c.3784C>A (p.His1262Asn)
|
rs794727100
|
0.00001
|
NM_001374353.1(GLI2):c.765G>A (p.Ser255=)
|
rs200901345
|
0.00001
|
NM_001374353.1(GLI2):c.879C>T (p.Pro293=)
|
rs1318325355
|
0.00001
|
NM_001374353.1(GLI2):c.1125C>T (p.Ser375=)
|
rs1553475192
|
|
NM_001374353.1(GLI2):c.2415C>T (p.Arg805=)
|
rs886044110
|
|
NM_001374353.1(GLI2):c.3037A>G (p.Ser1013Gly)
|
rs1553479006
|
|
NM_001374353.1(GLI2):c.3418C>T (p.Leu1140=)
|
rs141988240
|
|