| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 174951 | BAA02g17600 | A02 | 8778760 | G | A | downstream_gene_variant | MODIFIER | c.*1565G>A| |
S155 S211 |
| 174952 | BAA02g17610 | A02 | 8780604 | C | T | upstream_gene_variant | MODIFIER | c.-482G>A| |
S66 |
| 174953 | BAA02g17620 | A02 | 8781607 | C | T | missense_variant | MODERATE | c.1162G>A|p.Gly388Arg |
S244 |
| 174954 | BAA02g17620 | A02 | 8781819 | G | A | missense_variant | MODERATE | c.1022C>T|p.Ser341Phe |
S274 |
| 174955 | BAA02g17610 | A02 | 8782245 | G | A | upstream_gene_variant | MODIFIER | c.-2123C>T| |
S263 |
| 174956 | BAA02g17610 | A02 | 8783458 | C | T | upstream_gene_variant | MODIFIER | c.-3336G>A| |
S42 |
| 174957 | BAA02g17610 | A02 | 8783490 | C | T | upstream_gene_variant | MODIFIER | c.-3368G>A| |
S78 S83 |
| 174958 | BAA02g17630 | A02 | 8786645 | G | A | downstream_gene_variant | MODIFIER | c.*2833C>T| |
S69 |
| 174959 | BAA02g17630 | A02 | 8786734 | C | T | downstream_gene_variant | MODIFIER | c.*2744G>A| |
S152 |
| 174960 | BAA02g17630 | A02 | 8786743 | T | G | downstream_gene_variant | MODIFIER | c.*2735A>C| |
S186 |
| 174961 | BAA02g17620 | A02 | 8787380 | G | A | missense_variant&splice_region_variant | MODERATE | c.443C>T|p.Ala148Val |
S140 |
| 174962 | BAA02g17620 | A02 | 8787668 | G | A | missense_variant | MODERATE | c.356C>T|p.Thr119Ile |
S236 |
| 174963 | BAA02g17620 | A02 | 8788232 | T | C | upstream_gene_variant | MODIFIER | c.-209A>G| |
S276 |
| 174964 | BAA02g17620 | A02 | 8788282 | G | A | upstream_gene_variant | MODIFIER | c.-259C>T| |
S182 |
| 174965 | BAA02g17620 | A02 | 8788397 | C | T | upstream_gene_variant | MODIFIER | c.-374G>A| |
S88 |
| 174966 | BAA02g17620 | A02 | 8788698 | C | T | upstream_gene_variant | MODIFIER | c.-675G>A| |
S139 |
| 174967 | BAA02g17620 | A02 | 8788703 | C | T | upstream_gene_variant | MODIFIER | c.-680G>A| |
S13 |
| 174968 | BAA02g17620 | A02 | 8789106 | C | T | upstream_gene_variant | MODIFIER | c.-1083G>A| |
S179 |
| 174969 | BAA02g17620 | A02 | 8791399 | G | A | upstream_gene_variant | MODIFIER | c.-3376C>T| |
S259 |
| 174970 | BAA02g17620 | A02 | 8791741 | C | T | upstream_gene_variant | MODIFIER | c.-3718G>A| |
S236 |
| 174971 | BAA02g17640 | A02 | 8792252 | C | T | synonymous_variant | LOW | c.105G>A|p.Lys35Lys |
S174 S27 |
| 174972 | BAA02g17620 | A02 | 8792447 | G | A | upstream_gene_variant | MODIFIER | c.-4424C>T| |
S159 S243 |
| 174973 | BAA02g17620 | A02 | 8792746 | G | A | upstream_gene_variant | MODIFIER | c.-4723C>T| |
S162 |
| 174974 | BAA02g17620 | A02 | 8792871 | T | A | upstream_gene_variant | MODIFIER | c.-4848A>T| |
S113 S117 S120 S122 S23 S266 S55 S9 |
| 174975 | BAA02g17620 | A02 | 8792883 | C | T | upstream_gene_variant | MODIFIER | c.-4860G>A| |
S186 |