| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g21590 | A07 | 26265721 | C | T | upstream_gene_variant | MODIFIER | c.-2784C>T| |
S265 |
| 2 | BAA07g21590 | A07 | 26266443 | G | A | upstream_gene_variant | MODIFIER | c.-2062G>A| |
S271 |
| 3 | BAA07g21590 | A07 | 26266837 | G | A | upstream_gene_variant | MODIFIER | c.-1668G>A| |
S124 |
| 4 | BAA07g21590 | A07 | 26267171 | C | T | upstream_gene_variant | MODIFIER | c.-1334C>T| |
S90 |
| 5 | BAA07g21590 | A07 | 26267793 | G | A | upstream_gene_variant | MODIFIER | c.-712G>A| |
S182 |
| 6 | BAA07g21590 | A07 | 26268888 | G | A | synonymous_variant | LOW | c.384G>A|p.Gln128Gln |
S157 S163 |
| 7 | BAA07g21590 | A07 | 26269126 | C | T | missense_variant | MODERATE | c.622C>T|p.His208Tyr |
S59 |
| 8 | BAA07g21590 | A07 | 26269178 | C | T | missense_variant | MODERATE | c.674C>T|p.Pro225Leu |
S292 S303 |
| 9 | BAA07g21590 | A07 | 26269992 | G | A | synonymous_variant | LOW | c.1488G>A|p.Arg496Arg |
S39 |
| 10 | BAA07g21590 | A07 | 26270245 | C | T | missense_variant | MODERATE | c.1741C>T|p.Pro581Ser |
S245 S81 |
| 11 | BAA07g21590 | A07 | 26270601 | C | T | synonymous_variant | LOW | c.2025C>T|p.Asp675Asp |
S297 |
| 12 | BAA07g21590 | A07 | 26271035 | C | T | missense_variant | MODERATE | c.2315C>T|p.Pro772Leu |
S143 |
| 13 | BAA07g21590 | A07 | 26271400 | C | T | synonymous_variant | LOW | c.2529C>T|p.Asn843Asn |
S144 |
| 14 | BAA07g21590 | A07 | 26271885 | G | A | synonymous_variant | LOW | c.2853G>A|p.Ala951Ala |
S16 |
| 15 | BAA07g21590 | A07 | 26272715 | G | A | downstream_gene_variant | MODIFIER | c.*632G>A| |
S231 |
| 16 | BAA07g21590 | A07 | 26273045 | C | A | downstream_gene_variant | MODIFIER | c.*962C>A| |
S48 |
| 17 | BAA07g21590 | A07 | 26274612 | C | T | downstream_gene_variant | MODIFIER | c.*2529C>T| |
S13 S140 S168 S219 S278 S279 S72 |