rs59421388
变体ID
PA166156171
基因 ID
PA128
基因符号
CYP2D6
位置
NC_000022.11:42127608
变异注释计数
23
临床注释计数
7
1-2级临床注释计数
7
指南注释计数
0
标签注释计数
0
同义词
NC_000022.10:g.42523610=, XM_005278354.1:c.712G>A, XM_011529968.1:c.1012G>A, XP_011528269.1:p.Val338Met, XM_011529966.1:c.1012G>A, XM_011529967.1:c.1012G>A, XP_011528274.1:p.Thr290=, NG_008376.3:g.7384G>A, NW_004504305.1:g.49935C>T, XP_011528272.1:p.Val287Met, NG_008376.3:g.7384=, NC_000022.10:g.42523610C>T, NG_008376.4:g.8203G>A, XM_005278353.1:c.868G>A, XM_011529972.1:c.870G>A, NG_008376.4:g.8203=, NC_000022.11:g.42127608=, XP_011546052.1:p.Val290Met, XM_011547750.1:c.868G>A, XP_011528270.1:p.Val338Met, NW_009646208.1:g.13174C>T, XM_011529970.1:c.859G>A, XP_011546053.1:p.Val266Met, NM_001025161.2:c.859G>A, NP_000097.3:p.Val338=, rs59421388, XM_011547751.1:c.796G>A, XM_011529971.1:c.868G>A, XM_005278354.3:c.712G>A, XP_005278410.1:p.Val290Met, NT_187682.1:g.49949C>T, XP_011528268.1:p.Val338Met, XM_011548819.1:c.*118G>A, NM_000106.5:c.1012G>A, NP_000097.3:p.Val338Met, XM_011529969.1:c.868G>A, XP_005278411.1:p.Val238Met, 59421388, XP_011528271.1:p.Val290Met, NP_001020332.2:p.Val287Met, NC_000022.11:g.42127608C>T, XM_011547541.1:c.*118G>A, XP_011528273.1:p.Val290Met, XR_952745.1:n.2027G>A
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