NM_000053.4(ATP7B):c.3369G>A (p.Pro1123=)
|
rs61733679
|
0.00362
|
NM_000053.4(ATP7B):c.1607T>C (p.Val536Ala)
|
rs138427376
|
0.00342
|
NM_000053.4(ATP7B):c.2175G>A (p.Arg725=)
|
rs61733684
|
0.00329
|
NM_000053.4(ATP7B):c.2355+13T>G
|
rs139211339
|
0.00293
|
NM_000053.4(ATP7B):c.1707+29dup
|
rs113829533
|
0.00273
|
NM_000053.4(ATP7B):c.1620C>T (p.Leu540=)
|
rs145798966
|
0.00150
|
NM_000053.4(ATP7B):c.1278C>T (p.Val426=)
|
rs143556945
|
0.00135
|
NM_000053.4(ATP7B):c.1375G>T (p.Val459Leu)
|
rs183044693
|
0.00080
|
NM_000053.4(ATP7B):c.3405A>G (p.Ala1135=)
|
rs373081328
|
0.00078
|
NM_000053.4(ATP7B):c.3324C>T (p.Asn1108=)
|
rs372456815
|
0.00029
|
NM_000053.4(ATP7B):c.3105C>T (p.Gly1035=)
|
rs200324179
|
0.00022
|
NM_000053.4(ATP7B):c.2859C>T (p.Tyr953=)
|
rs762782389
|
0.00017
|
NM_000053.4(ATP7B):c.1839C>T (p.Ile613=)
|
rs370476756
|
0.00011
|
NM_000053.4(ATP7B):c.3396C>T (p.Ser1132=)
|
rs370947152
|
0.00011
|
NM_000053.4(ATP7B):c.4162G>A (p.Ala1388Thr)
|
rs745866259
|
0.00010
|
NM_000053.4(ATP7B):c.2028C>T (p.Asn676=)
|
rs764441090
|
0.00009
|
NM_000053.4(ATP7B):c.4251A>G (p.Thr1417=)
|
rs546721020
|
0.00006
|
NM_000053.4(ATP7B):c.2310C>G (p.Leu770=)
|
rs398123136
|
0.00005
|
NM_000053.4(ATP7B):c.3885C>T (p.Ala1295=)
|
rs200597654
|
0.00004
|
NM_000053.4(ATP7B):c.993C>T (p.Ala331=)
|
rs377294197
|
0.00003
|
NM_000053.4(ATP7B):c.1122C>G (p.Val374=)
|
rs201254466
|
0.00002
|
NM_000053.4(ATP7B):c.15G>A (p.Glu5=)
|
rs751634415
|
0.00001
|
NM_000053.4(ATP7B):c.2436T>C (p.Asn812=)
|
rs533967323
|
0.00001
|
NM_000053.4(ATP7B):c.2490C>T (p.Ile830=)
|
rs759213674
|
0.00001
|
NM_000053.4(ATP7B):c.2985C>T (p.Val995=)
|
rs758641148
|
0.00001
|
NM_000053.4(ATP7B):c.3291G>A (p.Val1097=)
|
rs766632973
|
0.00001
|
NM_000053.4(ATP7B):c.4110C>T (p.Ser1370=)
|
rs779979628
|
0.00001
|
NM_000053.4(ATP7B):c.4272T>C (p.Tyr1424=)
|
rs780613139
|
0.00001
|
NM_000053.4(ATP7B):c.4338C>T (p.Asp1446=)
|
rs760661082
|
0.00001
|
NM_000053.4(ATP7B):c.618T>C (p.Phe206=)
|
rs764353593
|
0.00001
|
NM_000053.4(ATP7B):c.-396C>G
|
rs145371060
|
|
NM_000053.4(ATP7B):c.1164G>A (p.Gln388=)
|
rs2140070526
|
|
NM_000053.4(ATP7B):c.1762A>C (p.Arg588=)
|
rs1566559391
|
|
NM_000053.4(ATP7B):c.2976C>A (p.Pro992=)
|
rs746358240
|
|
NM_000053.4(ATP7B):c.2997C>G (p.Thr999=)
|
rs199581971
|
|
NM_000053.4(ATP7B):c.540C>T (p.Asn180=)
|
rs537892210
|
|
NM_000053.4(ATP7B):c.879G>A (p.Glu293=)
|
rs1593789326
|
|