| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g14840 | A08 | 12565122 | C | T | downstream_gene_variant | MODIFIER | c.*1168G>A| |
S53 |
| 2 | BAA08g14840 | A08 | 12565303 | C | T | downstream_gene_variant | MODIFIER | c.*987G>A| |
S126 |
| 3 | BAA08g14840 | A08 | 12566763 | G | A | missense_variant | MODERATE | c.1906C>T|p.Leu636Phe |
S13 |
| 4 | BAA08g14840 | A08 | 12566849 | G | A | missense_variant | MODERATE | c.1820C>T|p.Ser607Phe |
S117 |
| 5 | BAA08g14840 | A08 | 12567382 | G | C | splice_region_variant&intron_variant | LOW | c.1723-3C>G| |
S202 |
| 6 | BAA08g14840 | A08 | 12567682 | G | A | missense_variant | MODERATE | c.1510C>T|p.Leu504Phe |
S109 |
| 7 | BAA08g14840 | A08 | 12568660 | C | T | intron_variant | MODIFIER | c.615-83G>A| |
S122 |
| 8 | BAA08g14840 | A08 | 12568806 | C | T | intron_variant | MODIFIER | c.615-229G>A| |
S276 |
| 9 | BAA08g14840 | A08 | 12568880 | C | T | intron_variant | MODIFIER | c.615-303G>A| |
S36 |
| 10 | BAA08g14840 | A08 | 12570714 | C | T | missense_variant | MODERATE | c.506G>A|p.Gly169Glu |
S36 |
| 11 | BAA08g14840 | A08 | 12571004 | G | A | synonymous_variant | LOW | c.216C>T|p.Val72Val |
S286 |
| 12 | BAA08g14840 | A08 | 12571158 | C | T | missense_variant | MODERATE | c.62G>A|p.Arg21Gln |
S277 |
| 13 | BAA08g14840 | A08 | 12571894 | C | T | upstream_gene_variant | MODIFIER | c.-675G>A| |
S60 |
| 14 | BAA08g14840 | A08 | 12571963 | C | T | upstream_gene_variant | MODIFIER | c.-744G>A| |
S207 |
| 15 | BAA08g14840 | A08 | 12572137 | G | A | upstream_gene_variant | MODIFIER | c.-918C>T| |
S95 |
| 16 | BAA08g14840 | A08 | 12572630 | G | A | upstream_gene_variant | MODIFIER | c.-1411C>T| |
S188 |
| 17 | BAA08g14840 | A08 | 12574739 | C | T | upstream_gene_variant | MODIFIER | c.-3520G>A| |
S237 |
| 18 | BAA08g14840 | A08 | 12574777 | C | T | upstream_gene_variant | MODIFIER | c.-3558G>A| |
S123 |
| 19 | BAA08g14840 | A08 | 12575371 | C | T | upstream_gene_variant | MODIFIER | c.-4152G>A| |
S236 |