| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g08010 | A10 | 5118976 | C | T | downstream_gene_variant | MODIFIER | c.*4753G>A| |
S139 |
| 2 | BAA10g08010 | A10 | 5119277 | G | A | downstream_gene_variant | MODIFIER | c.*4452C>T| |
S151 S263 |
| 3 | BAA10g08010 | A10 | 5119956 | C | T | downstream_gene_variant | MODIFIER | c.*3773G>A| |
S282 |
| 4 | BAA10g08010 | A10 | 5120448 | G | A | downstream_gene_variant | MODIFIER | c.*3281C>T| |
S245 |
| 5 | BAA10g08010 | A10 | 5120735 | G | A | downstream_gene_variant | MODIFIER | c.*2994C>T| |
S68 |
| 6 | BAA10g08010 | A10 | 5120785 | G | A | downstream_gene_variant | MODIFIER | c.*2944C>T| |
S136 |
| 7 | BAA10g08010 | A10 | 5120997 | G | A | downstream_gene_variant | MODIFIER | c.*2732C>T| |
S66 |
| 8 | BAA10g08010 | A10 | 5121306 | G | A | downstream_gene_variant | MODIFIER | c.*2423C>T| |
S125 |
| 9 | BAA10g08010 | A10 | 5121355 | C | T | downstream_gene_variant | MODIFIER | c.*2374G>A| |
S6 |
| 10 | BAA10g08010 | A10 | 5121359 | C | T | downstream_gene_variant | MODIFIER | c.*2370G>A| |
S199 |
| 11 | BAA10g08010 | A10 | 5121907 | G | A | downstream_gene_variant | MODIFIER | c.*1822C>T| |
S69 |
| 12 | BAA10g08010 | A10 | 5122170 | C | T | downstream_gene_variant | MODIFIER | c.*1559G>A| |
S9 |
| 13 | BAA10g08010 | A10 | 5122543 | G | A | downstream_gene_variant | MODIFIER | c.*1186C>T| |
S186 |
| 14 | BAA10g08010 | A10 | 5122646 | C | T | downstream_gene_variant | MODIFIER | c.*1083G>A| |
S195 |
| 15 | BAA10g08010 | A10 | 5123153 | C | T | downstream_gene_variant | MODIFIER | c.*576G>A| |
S202 |
| 16 | BAA10g08010 | A10 | 5123754 | G | A | missense_variant | MODERATE | c.1745C>T|p.Ala582Val |
S1 S90 |
| 17 | BAA10g08010 | A10 | 5123820 | G | A | missense_variant | MODERATE | c.1679C>T|p.Pro560Leu |
S296 |
| 18 | BAA10g08010 | A10 | 5124230 | G | A | synonymous_variant | LOW | c.1269C>T|p.Ser423Ser |
S262 |
| 19 | BAA10g08010 | A10 | 5125839 | C | T | missense_variant | MODERATE | c.428G>A|p.Gly143Asp |
S40 S49 |
| 20 | BAA10g08010 | A10 | 5126935 | C | T | upstream_gene_variant | MODIFIER | c.-315G>A| |
S104 S52 |
| 21 | BAA10g08010 | A10 | 5128325 | C | T | upstream_gene_variant | MODIFIER | c.-1705G>A| |
S287 |
| 22 | BAA10g08010 | A10 | 5128328 | C | T | upstream_gene_variant | MODIFIER | c.-1708G>A| |
S270 |
| 23 | BAA10g08010 | A10 | 5129072 | C | T | upstream_gene_variant | MODIFIER | c.-2452G>A| |
S10 |
| 24 | BAA10g08010 | A10 | 5129330 | G | A | upstream_gene_variant | MODIFIER | c.-2710C>T| |
S125 |
| 25 | BAA10g08010 | A10 | 5129500 | C | T | upstream_gene_variant | MODIFIER | c.-2880G>A| |
S84 S93 |