| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 181701 | BAA02g20980 | A02 | 11213722 | G | A | upstream_gene_variant | MODIFIER | c.-3370G>A| |
S235 |
| 181702 | BAA02g20980 | A02 | 11213745 | C | T | upstream_gene_variant | MODIFIER | c.-3347C>T| |
S164 |
| 181703 | BAA02g20980 | A02 | 11215640 | C | T | upstream_gene_variant | MODIFIER | c.-1452C>T| |
S152 |
| 181704 | BAA02g20980 | A02 | 11215978 | G | A | upstream_gene_variant | MODIFIER | c.-1114G>A| |
S52 |
| 181705 | BAA02g20990 | A02 | 11218688 | C | T | upstream_gene_variant | MODIFIER | c.-3509C>T| |
S308 |
| 181706 | BAA02g20990 | A02 | 11218817 | G | A | upstream_gene_variant | MODIFIER | c.-3380G>A| |
S269 |
| 181707 | BAA02g20990 | A02 | 11219470 | A | T | upstream_gene_variant | MODIFIER | c.-2727A>T| |
S249 |
| 181708 | BAA02g20990 | A02 | 11220116 | G | A | upstream_gene_variant | MODIFIER | c.-2081G>A| |
S282 |
| 181709 | BAA02g20990 | A02 | 11220476 | G | A | upstream_gene_variant | MODIFIER | c.-1721G>A| |
S297 |
| 181710 | BAA02g20990 | A02 | 11223824 | C | T | missense_variant | MODERATE | c.1091C>T|p.Ser364Phe |
S155 S211 |
| 181711 | BAA02g20980 | A02 | 11224020 | C | T | downstream_gene_variant | MODIFIER | c.*2488C>T| |
S255 |
| 181712 | BAA02g20980 | A02 | 11224025 | G | A | downstream_gene_variant | MODIFIER | c.*2493G>A| |
S148 S210 S30 S31 |
| 181713 | BAA02g20980 | A02 | 11224568 | G | A | downstream_gene_variant | MODIFIER | c.*3036G>A| |
S45 |
| 181714 | BAA02g21000 | A02 | 11225141 | C | T | missense_variant | MODERATE | c.803G>A|p.Gly268Glu |
S112 |
| 181715 | BAA02g21000 | A02 | 11225995 | G | A | missense_variant | MODERATE | c.194C>T|p.Thr65Ile |
S206 S26 |
| 181716 | BAA02g21000 | A02 | 11226170 | C | T | missense_variant | MODERATE | c.19G>A|p.Ala7Thr |
S226 |
| 181717 | BAA02g21000 | A02 | 11226231 | C | T | upstream_gene_variant | MODIFIER | c.-43G>A| |
S221 |
| 181718 | BAA02g21010 | A02 | 11228437 | G | A | missense_variant | MODERATE | c.23C>T|p.Pro8Leu |
S173 |
| 181719 | BAA02g21000 | A02 | 11228652 | C | T | upstream_gene_variant | MODIFIER | c.-2464G>A| |
S270 |
| 181720 | BAA02g21000 | A02 | 11228937 | C | T | upstream_gene_variant | MODIFIER | c.-2749G>A| |
S219 S72 |
| 181721 | BAA02g21000 | A02 | 11229419 | G | A | upstream_gene_variant | MODIFIER | c.-3231C>T| |
S12 |
| 181722 | BAA02g21000 | A02 | 11229463 | C | T | upstream_gene_variant | MODIFIER | c.-3275G>A| |
S249 |
| 181723 | BAA02g21000 | A02 | 11229549 | G | A | upstream_gene_variant | MODIFIER | c.-3361C>T| |
S132 S215 |
| 181724 | BAA02g21000 | A02 | 11231118 | G | A | upstream_gene_variant | MODIFIER | c.-4930C>T| |
S170 |
| 181725 | BAA02g21010 | A02 | 11231422 | G | A | upstream_gene_variant | MODIFIER | c.-2963C>T| |
S85 |