| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 75701 | BAA01g39860 | A01 | 26475036 | G | A | downstream_gene_variant | MODIFIER | c.*955C>T| |
S199 |
| 75702 | BAA01g39860 | A01 | 26475186 | C | T | downstream_gene_variant | MODIFIER | c.*805G>A| |
S158 |
| 75703 | BAA01g39860 | A01 | 26475572 | G | A | downstream_gene_variant | MODIFIER | c.*419C>T| |
S38 |
| 75704 | BAA01g39860 | A01 | 26476611 | G | A | missense_variant | MODERATE | c.163C>T|p.Pro55Ser |
S298 |
| 75705 | BAA01g39860 | A01 | 26477209 | C | T | upstream_gene_variant | MODIFIER | c.-436G>A| |
S81 |
| 75706 | BAA01g39860 | A01 | 26478058 | C | T | upstream_gene_variant | MODIFIER | c.-1285G>A| |
S157 |
| 75707 | BAA01g39860 | A01 | 26478295 | G | A | upstream_gene_variant | MODIFIER | c.-1522C>T| |
S138 |
| 75708 | BAA01g39860 | A01 | 26479693 | C | T | upstream_gene_variant | MODIFIER | c.-2920G>A| |
S32 |
| 75709 | BAA01g39860 | A01 | 26480063 | G | A | upstream_gene_variant | MODIFIER | c.-3290C>T| |
S287 |
| 75710 | BAA01g39860 | A01 | 26480362 | G | A | upstream_gene_variant | MODIFIER | c.-3589C>T| |
S86 |
| 75711 | BAA01g39860 | A01 | 26480784 | C | T | upstream_gene_variant | MODIFIER | c.-4011G>A| |
S131 |
| 75712 | BAA01g39860 | A01 | 26481046 | G | A | upstream_gene_variant | MODIFIER | c.-4273C>T| |
S5 |
| 75713 | BAA01g39860 | A01 | 26481414 | C | T | upstream_gene_variant | MODIFIER | c.-4641G>A| |
S41 |
| 75714 | BAA01g39860 | A01 | 26481537 | T | A | upstream_gene_variant | MODIFIER | c.-4764A>T| |
S12 |
| 75715 | BAA01g39860-BAA01g39870 | A01 | 26483089 | G | A | intergenic_region | MODIFIER | n.26483089G>A| |
S257 |
| 75716 | BAA01g39870 | A01 | 26484082 | C | A | upstream_gene_variant | MODIFIER | c.-4155C>A| |
S11 |
| 75717 | BAA01g39870 | A01 | 26484628 | C | T | upstream_gene_variant | MODIFIER | c.-3609C>T| |
S184 |
| 75718 | BAA01g39870 | A01 | 26486042 | C | T | upstream_gene_variant | MODIFIER | c.-2195C>T| |
S28 |
| 75719 | BAA01g39870 | A01 | 26487317 | C | T | upstream_gene_variant | MODIFIER | c.-920C>T| |
S231 |
| 75720 | BAA01g39870 | A01 | 26487775 | G | A | upstream_gene_variant | MODIFIER | c.-462G>A| |
S79 S91 |
| 75721 | BAA01g39880 | A01 | 26488586 | C | T | downstream_gene_variant | MODIFIER | c.*4898G>A| |
S242 |
| 75722 | BAA01g39880 | A01 | 26488691 | C | T | downstream_gene_variant | MODIFIER | c.*4793G>A| |
S247 |
| 75723 | BAA01g39880 | A01 | 26489013 | G | A | downstream_gene_variant | MODIFIER | c.*4471C>T| |
S152 |
| 75724 | BAA01g39880 | A01 | 26489168 | G | A | downstream_gene_variant | MODIFIER | c.*4316C>T| |
S86 |
| 75725 | BAA01g39870 | A01 | 26489826 | G | A | synonymous_variant | LOW | c.195G>A|p.Leu65Leu |
S221 |