| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g10660 | A08 | 9565371 | C | T | downstream_gene_variant | MODIFIER | c.*4587G>A| |
S70 |
| 2 | BAA08g10660 | A08 | 9565615 | C | T | downstream_gene_variant | MODIFIER | c.*4343G>A| |
S6 |
| 3 | BAA08g10660 | A08 | 9568812 | C | T | downstream_gene_variant | MODIFIER | c.*1146G>A| |
S243 S299 |
| 4 | BAA08g10660 | A08 | 9569068 | C | T | downstream_gene_variant | MODIFIER | c.*890G>A| |
S157 S163 |
| 5 | BAA08g10660 | A08 | 9569719 | C | T | downstream_gene_variant | MODIFIER | c.*239G>A| |
S243 S299 |
| 6 | BAA08g10660 | A08 | 9570110 | C | T | missense_variant | MODERATE | c.379G>A|p.Ala127Thr |
S67 |
| 7 | BAA08g10660 | A08 | 9570263 | G | A | synonymous_variant | LOW | c.310C>T|p.Leu104Leu |
S297 |
| 8 | BAA08g10660 | A08 | 9570296 | C | T | missense_variant | MODERATE | c.277G>A|p.Ala93Thr |
S205 |
| 9 | BAA08g10660 | A08 | 9571056 | G | A | intron_variant | MODIFIER | c.242-725C>T| |
S94 |
| 10 | BAA08g10660 | A08 | 9571249 | G | T | intron_variant | MODIFIER | c.242-918C>A| |
S131 |
| 11 | BAA08g10660 | A08 | 9573297 | G | A | missense_variant | MODERATE | c.52C>T|p.Pro18Ser |
S158 |
| 12 | BAA08g10660 | A08 | 9573319 | C | T | synonymous_variant | LOW | c.30G>A|p.Leu10Leu |
S12 |
| 13 | BAA08g10660 | A08 | 9573463 | G | A | upstream_gene_variant | MODIFIER | c.-115C>T| |
S128 |
| 14 | BAA08g10660 | A08 | 9574140 | C | T | upstream_gene_variant | MODIFIER | c.-792G>A| |
S295 |
| 15 | BAA08g10660 | A08 | 9574381 | G | A | upstream_gene_variant | MODIFIER | c.-1033C>T| |
S257 |
| 16 | BAA08g10660 | A08 | 9575245 | C | T | upstream_gene_variant | MODIFIER | c.-1897G>A| |
S277 |
| 17 | BAA08g10660 | A08 | 9575350 | C | T | upstream_gene_variant | MODIFIER | c.-2002G>A| |
S293 |
| 18 | BAA08g10660 | A08 | 9575799 | C | T | upstream_gene_variant | MODIFIER | c.-2451G>A| |
S185 |
| 19 | BAA08g10660 | A08 | 9576160 | C | T | upstream_gene_variant | MODIFIER | c.-2812G>A| |
S47 |
| 20 | BAA08g10660 | A08 | 9576280 | C | T | upstream_gene_variant | MODIFIER | c.-2932G>A| |
S203 |
| 21 | BAA08g10660 | A08 | 9576560 | C | T | upstream_gene_variant | MODIFIER | c.-3212G>A| |
S38 |
| 22 | BAA08g10660 | A08 | 9577934 | G | A | upstream_gene_variant | MODIFIER | c.-4586C>T| |
S117 |