Resume of the main outcomes concerning genomic sequence variants (SVs) detected.

Sequence variants key marks reveal by experimental, statistic and in silico analysis. A detailed integrative analysis of nsSVs and their corresponding amino acid changes. The haplotypes corresponds to the frequent haplotypes detected in total samples (frequency >5%). SVs with probably damage effect in protein are in bold text. (%) Percentage. (NA) not applicable. (No) not observed.

序列变异关键标记由实验、统计与计算机模拟（in silico）分析得到。针对非同义序列变异（non-synonymous sequence variants, nsSVs）及其对应氨基酸变化的详细整合分析内容亦包含其中。本次数据集所纳入的单倍型均为在全部样本中检测到的频率高于5%的高频单倍型。对蛋白质存在潜在损伤效应的序列变异（sequence variants, SVs）将以粗体文本标注。符号说明：(%) 代表百分比；(NA) 代表不适用；(No) 代表未观测到。