| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 134851 | BAA10g20910 | A10 | 18596105 | G | A | synonymous_variant | LOW | c.486C>T|p.Asp162Asp |
S245 |
| 134852 | BAA10g20910 | A10 | 18598027 | C | T | upstream_gene_variant | MODIFIER | c.-758G>A| |
S84 S93 |
| 134853 | BAA10g20910 | A10 | 18598057 | C | T | upstream_gene_variant | MODIFIER | c.-788G>A| |
S114 S180 |
| 134854 | BAA10g20910 | A10 | 18598852 | C | T | upstream_gene_variant | MODIFIER | c.-1583G>A| |
S142 |
| 134855 | BAA10g20910 | A10 | 18599784 | G | A | upstream_gene_variant | MODIFIER | c.-2515C>T| |
S62 |
| 134856 | BAA10g20910 | A10 | 18599987 | G | A | upstream_gene_variant | MODIFIER | c.-2718C>T| |
S113 |
| 134857 | BAA10g20910 | A10 | 18600344 | C | T | upstream_gene_variant | MODIFIER | c.-3075G>A| |
S103 |
| 134858 | BAA10g20910 | A10 | 18600377 | C | T | upstream_gene_variant | MODIFIER | c.-3108G>A| |
S68 |
| 134859 | BAA10g20930 | A10 | 18604893 | C | T | upstream_gene_variant | MODIFIER | c.-1904C>T| |
S115 |
| 134860 | BAA10g20930 | A10 | 18606256 | G | A | upstream_gene_variant | MODIFIER | c.-541G>A| |
S94 |
| 134861 | BAA10g20930 | A10 | 18606497 | G | A | upstream_gene_variant | MODIFIER | c.-300G>A| |
S1 |
| 134862 | BAA10g20930 | A10 | 18606718 | G | A | upstream_gene_variant | MODIFIER | c.-79G>A| |
S298 |
| 134863 | BAA10g20930 | A10 | 18606771 | C | T | upstream_gene_variant | MODIFIER | c.-26C>T| |
S255 |
| 134864 | BAA10g20930 | A10 | 18606890 | G | A | missense_variant | MODERATE | c.94G>A|p.Glu32Lys |
S216 |
| 134865 | BAA10g20920 | A10 | 18606995 | C | T | downstream_gene_variant | MODIFIER | c.*2144C>T| |
S133 |
| 134866 | BAA10g20930 | A10 | 18607908 | G | A | missense_variant | MODERATE | c.574G>A|p.Glu192Lys |
S71 |
| 134867 | BAA10g20920 | A10 | 18608189 | C | T | downstream_gene_variant | MODIFIER | c.*3338C>T| |
S199 |
| 134868 | BAA10g20930 | A10 | 18610403 | G | A | missense_variant | MODERATE | c.889G>A|p.Ala297Thr |
S82 S92 |
| 134869 | BAA10g20940 | A10 | 18612177 | C | T | synonymous_variant | LOW | c.1830G>A|p.Glu610Glu |
S266 |
| 134870 | BAA10g20940 | A10 | 18613476 | C | T | synonymous_variant | LOW | c.873G>A|p.Arg291Arg |
S187 |
| 134871 | BAA10g20940 | A10 | 18613806 | C | T | synonymous_variant | LOW | c.543G>A|p.Leu181Leu |
S70 |
| 134872 | BAA10g20940 | A10 | 18615093 | G | A | upstream_gene_variant | MODIFIER | c.-745C>T| |
S279 |
| 134873 | BAA10g20940 | A10 | 18615193 | G | A | upstream_gene_variant | MODIFIER | c.-845C>T| |
S32 |
| 134874 | BAA10g20940 | A10 | 18616059 | C | T | upstream_gene_variant | MODIFIER | c.-1711G>A| |
S84 S93 |
| 134875 | BAA10g20950 | A10 | 18616829 | C | T | missense_variant | MODERATE | c.1954G>A|p.Gly652Arg |
S78 |