| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID | 
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g40820 | A07 | 36052946 | G | A | upstream_gene_variant | MODIFIER | c.-83G>A| | S33 | 
| 2 | BAA07g40820 | A07 | 36053290 | C | T | intron_variant | MODIFIER | c.55-123C>T| | S159 S243 | 
| 3 | BAA07g40820 | A07 | 36053336 | G | A | intron_variant | MODIFIER | c.55-77G>A| | S163 | 
| 4 | BAA07g40820 | A07 | 36053526 | C | T | intron_variant | MODIFIER | c.141+27C>T| | S179 | 
| 5 | BAA07g40820 | A07 | 36053733 | G | A | intron_variant | MODIFIER | c.232-53G>A| | S231 | 
| 6 | BAA07g40820 | A07 | 36054283 | C | T | intron_variant | MODIFIER | c.438+203C>T| | S252 | 
| 7 | BAA07g40820 | A07 | 36055040 | C | T | missense_variant | MODERATE | c.479C>T|p.Ser160Phe | S124 | 
| 8 | BAA07g40820 | A07 | 36055294 | G | A | missense_variant | MODERATE | c.733G>A|p.Val245Ile | S296 | 
| 9 | BAA07g40820 | A07 | 36055723 | C | T | missense_variant | MODERATE | c.1162C>T|p.His388Tyr | S79 S91 | 
| 10 | BAA07g40820 | A07 | 36056184 | G | A | synonymous_variant | LOW | c.1623G>A|p.Ala541Ala | S289 S290 | 
| 11 | BAA07g40820 | A07 | 36056650 | G | A | missense_variant | MODERATE | c.2089G>A|p.Gly697Arg | S69 | 
| 12 | BAA07g40820 | A07 | 36056877 | C | T | synonymous_variant | LOW | c.2316C>T|p.Ser772Ser | S190 | 
| 13 | BAA07g40820 | A07 | 36057987 | C | T | missense_variant | MODERATE | c.2827C>T|p.Pro943Ser | S19 | 
| 14 | BAA07g40820 | A07 | 36058353 | G | A | missense_variant | MODERATE | c.3115G>A|p.Glu1039Lys | S17 | 
| 15 | BAA07g40820 | A07 | 36058648 | C | T | downstream_gene_variant | MODIFIER | c.*185C>T| | S177 | 
| 16 | BAA07g40820 | A07 | 36058829 | C | T | downstream_gene_variant | MODIFIER | c.*366C>T| | S165 | 
| 17 | BAA07g40820 | A07 | 36059056 | C | T | downstream_gene_variant | MODIFIER | c.*593C>T| | S168 |