rs4248158
变体ID
PA166157096
基因 ID
PA30474,PA435
基因符号
LTA,TNF
位置
NC_000006.12:31574756
变异注释计数
1
临床注释计数
0
1-2级临床注释计数
0
指南注释计数
0
标签注释计数
0
同义词
NT_167245.2:g.2822489C>T, NT_167247.1:g.2922239C>T, XM_011548438.1:c.*1063C>T, NM_001159740.2:c.*1063C>T, XM_011548050.1:c.*1063C>T, XM_011548436.1:c.*1063C>T, XM_011548243.1:c.*1063C>T, XM_011547885.1:c.*1063C>T, XM_011547886.1:c.*1063C>T, XM_011547883.1:c.*1063C>T, XM_011547884.1:c.*1063C>T, XM_011548440.1:c.*1063C>T, NT_167249.2:g.2874036C>T, NT_167247.2:g.2916654C>T, NT_167245.1:g.2828074C>T, NG_007462.1:g.4184C>T, NG_007462.1:g.4184=, NT_167249.1:g.2873334C>T, NC_000006.12:g.31574756C>T, NM_000594.3:c.-986C>T, NC_000006.12:g.31574756=, XM_011547887.1:c.*1063C>T, NT_167248.1:g.2836171C>T, NC_000006.11:g.31542533C>T, rs115177064, 115177064, NT_113891.3:g.3052043C>T, NG_012010.1:g.7658C>T, XM_011548439.1:c.*1063C>T, NM_000595.3:c.*1063C>T, XM_011547653.1:c.*1063C>T, XM_011548242.1:c.*1063C>T, NT_167246.1:g.2885417C>T, XM_011548051.1:c.*1063C>T, XM_011548437.1:c.*1063C>T, NT_167246.2:g.2879797C>T, XM_011547250.1:c.*1063C>T, rs4248158, NT_167248.2:g.2830575C>T, NT_113891.2:g.3052149C>T, 4248158, XM_011547654.1:c.*1063C>T, XM_011514614.1:c.*1063C>T, XM_011514615.1:c.*1063C>T, XM_011514616.1:c.*1063C>T, NC_000006.11:g.31542533=, NG_012010.1:g.7658=, XM_011514617.1:c.*1063C>T, XM_011514618.1:c.*1063C>T
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