| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 166901 | BAA02g12840 | A02 | 5756277 | G | A | upstream_gene_variant | MODIFIER | c.-3790C>T| |
S118 |
| 166902 | BAA02g12840 | A02 | 5756368 | G | A | upstream_gene_variant | MODIFIER | c.-3881C>T| |
S213 |
| 166903 | BAA02g12870 | A02 | 5758438 | C | T | synonymous_variant | LOW | c.213G>A|p.Glu71Glu |
S16 |
| 166904 | BAA02g12860 | A02 | 5759191 | C | T | upstream_gene_variant | MODIFIER | c.-2927G>A| |
S158 |
| 166905 | BAA02g12860 | A02 | 5759639 | C | T | upstream_gene_variant | MODIFIER | c.-3375G>A| |
S128 |
| 166906 | BAA02g12880 | A02 | 5760208 | C | T | missense_variant | MODERATE | c.2147G>A|p.Gly716Asp |
S112 |
| 166907 | BAA02g12880 | A02 | 5760515 | G | A | missense_variant | MODERATE | c.1840C>T|p.Leu614Phe |
S288 |
| 166908 | BAA02g12880 | A02 | 5761135 | C | T | synonymous_variant | LOW | c.1296G>A|p.Leu432Leu |
S299 |
| 166909 | BAA02g12870 | A02 | 5761387 | C | T | upstream_gene_variant | MODIFIER | c.-2433G>A| |
S130 |
| 166910 | BAA02g12880 | A02 | 5761929 | G | A | missense_variant | MODERATE | c.667C>T|p.Pro223Ser |
S70 |
| 166911 | BAA02g12870 | A02 | 5762638 | G | A | upstream_gene_variant | MODIFIER | c.-3684C>T| |
S36 |
| 166912 | BAA02g12870 | A02 | 5762922 | C | T | upstream_gene_variant | MODIFIER | c.-3968G>A| |
S183 S198 |
| 166913 | BAA02g12870 | A02 | 5763219 | G | A | upstream_gene_variant | MODIFIER | c.-4265C>T| |
S68 |
| 166914 | BAA02g12880 | A02 | 5764735 | G | A | upstream_gene_variant | MODIFIER | c.-1302C>T| |
S209 |
| 166915 | BAA02g12890 | A02 | 5764787 | C | T | missense_variant | MODERATE | c.181G>A|p.Glu61Lys |
S116 S216 S241 S265 S39 |
| 166916 | BAA02g12880 | A02 | 5765135 | C | T | upstream_gene_variant | MODIFIER | c.-1702G>A| |
S270 |
| 166917 | BAA02g12900 | A02 | 5766493 | G | A | synonymous_variant | LOW | c.426G>A|p.Arg142Arg |
S62 |
| 166918 | BAA02g12880 | A02 | 5767105 | G | A | upstream_gene_variant | MODIFIER | c.-3672C>T| |
S238 |
| 166919 | BAA02g12910 | A02 | 5767498 | G | A | missense_variant | MODERATE | c.286C>T|p.Pro96Ser |
S28 |
| 166920 | BAA02g12910 | A02 | 5767555 | C | T | missense_variant | MODERATE | c.229G>A|p.Asp77Asn |
S246 |
| 166921 | BAA02g12910 | A02 | 5767847 | C | T | missense_variant | MODERATE | c.16G>A|p.Asp6Asn |
S40 S49 |
| 166922 | BAA02g12890 | A02 | 5768451 | C | T | upstream_gene_variant | MODIFIER | c.-3341G>A| |
S130 |
| 166923 | BAA02g12890 | A02 | 5768694 | G | A | upstream_gene_variant | MODIFIER | c.-3584C>T| |
S95 |
| 166924 | BAA02g12890 | A02 | 5768992 | G | A | upstream_gene_variant | MODIFIER | c.-3882C>T| |
S286 |
| 166925 | BAA02g12920 | A02 | 5769772 | G | A | missense_variant | MODERATE | c.22G>A|p.Val8Ile |
S150 |