NM_000124.4(ERCC6):c.3637A>G (p.Arg1213Gly)
|
rs2228527
|
0.19565
|
NM_000124.4(ERCC6):c.3289A>G (p.Met1097Val)
|
rs2228526
|
0.19072
|
NM_000124.4(ERCC6):c.4238A>G (p.Gln1413Arg)
|
rs2228529
|
0.18890
|
NM_000124.4(ERCC6):c.528A>G (p.Arg176=)
|
rs4253027
|
0.01480
|
NM_000124.4(ERCC6):c.3010C>T (p.Leu1004=)
|
rs2274097
|
0.00466
|
NM_000124.4(ERCC6):c.4065T>G (p.Asp1355Glu)
|
rs34917815
|
0.00246
|
NM_000124.4(ERCC6):c.2403C>T (p.Ala801=)
|
rs114896216
|
0.00234
|
NM_000124.4(ERCC6):c.3745G>A (p.Asp1249Asn)
|
rs114234514
|
0.00234
|
NM_000124.4(ERCC6):c.1996C>T (p.Arg666Cys)
|
rs61760163
|
0.00179
|
NM_000124.4(ERCC6):c.3122A>C (p.Gln1041Pro)
|
rs139007661
|
0.00179
|
NM_000124.4(ERCC6):c.4223A>C (p.Glu1408Ala)
|
rs61760167
|
0.00154
|
NM_000124.4(ERCC6):c.2096C>T (p.Thr699Met)
|
rs55698015
|
0.00142
|
NM_000124.4(ERCC6):c.3061A>G (p.Ile1021Val)
|
rs41562713
|
0.00127
|
NM_000124.4(ERCC6):c.2124C>T (p.Ser708=)
|
rs114832108
|
0.00090
|
NM_000124.4(ERCC6):c.2479C>T (p.Leu827=)
|
rs115875661
|
0.00087
|
NM_000124.4(ERCC6):c.3650T>G (p.Phe1217Cys)
|
rs61760166
|
0.00084
|
NM_000124.4(ERCC6):c.3719G>T (p.Ser1240Ile)
|
rs142219494
|
0.00082
|
NM_000124.4(ERCC6):c.2391C>T (p.Ser797=)
|
rs142641602
|
0.00031
|
NM_000124.4(ERCC6):c.3862C>T (p.Arg1288Ter)
|
rs185142838
|
0.00025
|
NM_000124.4(ERCC6):c.438C>T (p.Ser146=)
|
rs138756386
|
0.00025
|
NM_000124.4(ERCC6):c.670C>T (p.Leu224Phe)
|
rs150935953
|
0.00025
|
NM_000124.4(ERCC6):c.2048G>A (p.Arg683Gln)
|
rs148845653
|
0.00020
|
NM_000124.4(ERCC6):c.1659G>T (p.Lys553Asn)
|
rs116373975
|
0.00013
|
NM_000124.4(ERCC6):c.3581A>G (p.Glu1194Gly)
|
rs114479292
|
0.00009
|
NM_000124.4(ERCC6):c.4143C>T (p.Ser1381=)
|
rs375921453
|
0.00008
|
NM_000124.4(ERCC6):c.3643G>A (p.Ala1215Thr)
|
rs377041857
|
0.00003
|
NM_000124.4(ERCC6):c.1452C>T (p.Asp484=)
|
rs762734699
|
0.00001
|
NM_000124.4(ERCC6):c.1526+1G>T
|
rs371739894
|
0.00001
|
NM_000124.4(ERCC6):c.1888T>C (p.Leu630=)
|
rs747204355
|
0.00001
|
NM_000124.4(ERCC6):c.813C>T (p.Phe271=)
|
rs764319566
|
0.00001
|
NM_000124.4(ERCC6):c.2058G>C (p.Trp686Cys)
|
rs751292948
|
|
NM_000124.4(ERCC6):c.2287-4G>A
|
rs375617750
|
|
NM_000124.4(ERCC6):c.3284C>G (p.Pro1095Arg)
|
rs4253208
|
|
NM_000124.4(ERCC6):c.3634T>A (p.Cys1212Ser)
|
rs886042655
|
|
NM_000124.4(ERCC6):c.3636C>T (p.Cys1212=)
|
rs886047033
|
|
NM_000124.4(ERCC6):c.4066G>A (p.Gly1356Ser)
|
rs574272317
|
|
NM_000124.4(ERCC6):c.4096G>A (p.Val1366Ile)
|
rs745758957
|
|