| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g09910 | A08 | 8981477 | C | T | downstream_gene_variant | MODIFIER | c.*4257G>A| |
S181 |
| 2 | BAA08g09910 | A08 | 8981480 | C | T | downstream_gene_variant | MODIFIER | c.*4254G>A| |
S284 |
| 3 | BAA08g09910 | A08 | 8982902 | C | T | downstream_gene_variant | MODIFIER | c.*2832G>A| |
S259 |
| 4 | BAA08g09910 | A08 | 8982956 | C | T | downstream_gene_variant | MODIFIER | c.*2778G>A| |
S171 |
| 5 | BAA08g09910 | A08 | 8983396 | G | A | downstream_gene_variant | MODIFIER | c.*2338C>T| |
S249 |
| 6 | BAA08g09910 | A08 | 8983482 | C | T | downstream_gene_variant | MODIFIER | c.*2252G>A| |
S278 |
| 7 | BAA08g09910 | A08 | 8983490 | G | A | downstream_gene_variant | MODIFIER | c.*2244C>T| |
S119 |
| 8 | BAA08g09910 | A08 | 8983568 | G | A | downstream_gene_variant | MODIFIER | c.*2166C>T| |
S19 |
| 9 | BAA08g09910 | A08 | 8984573 | G | A | downstream_gene_variant | MODIFIER | c.*1161C>T| |
S78 |
| 10 | BAA08g09910 | A08 | 8984585 | G | A | downstream_gene_variant | MODIFIER | c.*1149C>T| |
S2 |
| 11 | BAA08g09910 | A08 | 8985831 | C | T | missense_variant | MODERATE | c.1250G>A|p.Arg417Lys |
S70 |
| 12 | BAA08g09910 | A08 | 8986136 | G | A | synonymous_variant | LOW | c.945C>T|p.Tyr315Tyr |
S165 |
| 13 | BAA08g09910 | A08 | 8986297 | C | T | missense_variant | MODERATE | c.784G>A|p.Glu262Lys |
S284 |
| 14 | BAA08g09910 | A08 | 8987870 | C | T | intron_variant | MODIFIER | c.703-1492G>A| |
S162 |
| 15 | BAA08g09910 | A08 | 8989316 | G | A | intron_variant | MODIFIER | c.702+650C>T| |
S32 |
| 16 | BAA08g09910 | A08 | 8989642 | C | T | intron_variant | MODIFIER | c.702+324G>A| |
S59 |
| 17 | BAA08g09910 | A08 | 8989722 | C | T | intron_variant | MODIFIER | c.702+244G>A| |
S177 |
| 18 | BAA08g09910 | A08 | 8989857 | G | A | intron_variant | MODIFIER | c.702+109C>T| |
S236 |
| 19 | BAA08g09910 | A08 | 8990329 | C | T | intron_variant | MODIFIER | c.457-118G>A| |
S132 S137 S89 |
| 20 | BAA08g09910 | A08 | 8991012 | C | T | intron_variant | MODIFIER | c.456+433G>A| |
S302 |
| 21 | BAA08g09910 | A08 | 8991528 | C | T | missense_variant | MODERATE | c.373G>A|p.Glu125Lys |
S60 |
| 22 | BAA08g09910 | A08 | 8993112 | G | A | upstream_gene_variant | MODIFIER | c.-1212C>T| |
S249 |