NM_001099922.3(ALG13):c.3093A>G (p.Gln1031=)
|
rs372260338
|
0.00065
|
NM_001099922.3(ALG13):c.2796A>T (p.Pro932=)
|
rs748742452
|
0.00058
|
NM_001099922.3(ALG13):c.371A>G (p.Tyr124Cys)
|
rs145518377
|
0.00035
|
NM_001099922.3(ALG13):c.3008A>G (p.Tyr1003Cys)
|
rs201055779
|
0.00024
|
NM_001099922.3(ALG13):c.383+1033G>A
|
rs772039609
|
0.00017
|
NM_001099922.3(ALG13):c.2802T>A (p.Pro934=)
|
rs865879266
|
0.00014
|
NM_001099922.3(ALG13):c.1313C>A (p.Thr438Lys)
|
rs367783946
|
0.00013
|
NM_001099922.3(ALG13):c.975T>G (p.Thr325=)
|
rs767735916
|
0.00008
|
NM_001099922.3(ALG13):c.108A>G (p.Arg36=)
|
rs769838471
|
0.00005
|
NM_001099922.3(ALG13):c.1377C>G (p.Ala459=)
|
rs368020541
|
0.00005
|
NM_001099922.3(ALG13):c.2805T>A (p.Pro935=)
|
rs754346057
|
0.00005
|
NM_001099922.3(ALG13):c.3240A>G (p.Pro1080=)
|
rs773452673
|
0.00005
|
NM_001099922.3(ALG13):c.1947G>A (p.Pro649=)
|
rs758659441
|
0.00001
|
NM_001099922.3(ALG13):c.2372G>A (p.Arg791Gln)
|
rs374290658
|
0.00001
|
NM_001099922.3(ALG13):c.2974-5T>C
|
rs776113182
|
0.00001
|
NM_001099922.3(ALG13):c.426T>C (p.Ala142=)
|
rs759472632
|
0.00001
|
NM_001099922.3(ALG13):c.486T>C (p.Phe162=)
|
rs751015058
|
0.00001
|
NM_001099922.3(ALG13):c.1228T>C (p.Tyr410His)
|
|
|
NM_001099922.3(ALG13):c.128G>A (p.Arg43Lys)
|
rs1057519175
|
|
NM_001099922.3(ALG13):c.1438C>G (p.Leu480Val)
|
rs2148165155
|
|
NM_001099922.3(ALG13):c.1883A>G (p.His628Arg)
|
|
|
NM_001099922.3(ALG13):c.2008A>G (p.Met670Val)
|
|
|
NM_001099922.3(ALG13):c.2143T>C (p.Tyr715His)
|
|
|
NM_001099922.3(ALG13):c.2191A>G (p.Thr731Ala)
|
|
|
NM_001099922.3(ALG13):c.2291A>G (p.Tyr764Cys)
|
|
|
NM_001099922.3(ALG13):c.2352T>A (p.Asn784Lys)
|
rs1602753116
|
|
NM_001099922.3(ALG13):c.2380GAA[1] (p.Glu795del)
|
rs772766102
|
|
NM_001099922.3(ALG13):c.2754ACC[10] (p.Pro941_Pro945del)
|
rs750710267
|
|
NM_001099922.3(ALG13):c.2754ACC[14] (p.Pro945del)
|
rs750710267
|
|
NM_001099922.3(ALG13):c.2763A>C (p.Pro921=)
|
rs1602887961
|
|
NM_001099922.3(ALG13):c.2775A>C (p.Pro925=)
|
rs1285221362
|
|
NM_001099922.3(ALG13):c.2793A>T (p.Pro931=)
|
|
|
NM_001099922.3(ALG13):c.320A>G (p.Asn107Ser)
|
rs398122394
|
|
NM_001099922.3(ALG13):c.383+2827A>C
|
|
|
NM_001099922.3(ALG13):c.912A>C (p.Arg304Ser)
|
|
|