| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA06g22740 | A06 | 12674146 | C | T | upstream_gene_variant | MODIFIER | c.-4930C>T| |
S37 |
| 2 | BAA06g22740 | A06 | 12675126 | C | T | upstream_gene_variant | MODIFIER | c.-3950C>T| |
S279 |
| 3 | BAA06g22740 | A06 | 12675191 | C | T | upstream_gene_variant | MODIFIER | c.-3885C>T| |
S37 |
| 4 | BAA06g22740 | A06 | 12675466 | G | A | upstream_gene_variant | MODIFIER | c.-3610G>A| |
S11 |
| 5 | BAA06g22740 | A06 | 12675499 | C | T | upstream_gene_variant | MODIFIER | c.-3577C>T| |
S179 |
| 6 | BAA06g22740 | A06 | 12675928 | G | A | upstream_gene_variant | MODIFIER | c.-3148G>A| |
S123 |
| 7 | BAA06g22740 | A06 | 12676115 | C | T | upstream_gene_variant | MODIFIER | c.-2961C>T| |
S242 |
| 8 | BAA06g22740 | A06 | 12676557 | C | T | upstream_gene_variant | MODIFIER | c.-2519C>T| |
S121 |
| 9 | BAA06g22740 | A06 | 12678768 | C | T | upstream_gene_variant | MODIFIER | c.-308C>T| |
S266 |
| 10 | BAA06g22740 | A06 | 12678954 | C | T | upstream_gene_variant | MODIFIER | c.-122C>T| |
S174 |
| 11 | BAA06g22740 | A06 | 12679206 | G | A | missense_variant | MODERATE | c.131G>A|p.Gly44Asp |
S130 |
| 12 | BAA06g22740 | A06 | 12679461 | C | T | missense_variant | MODERATE | c.386C>T|p.Pro129Leu |
S56 |
| 13 | BAA06g22740 | A06 | 12680105 | T | C | synonymous_variant | LOW | c.804T>C|p.Gly268Gly |
S157 S163 |
| 14 | BAA06g22740 | A06 | 12680117 | C | T | synonymous_variant | LOW | c.816C>T|p.Gly272Gly |
S10 |
| 15 | BAA06g22740 | A06 | 12680229 | C | T | missense_variant | MODERATE | c.928C>T|p.Arg310Cys |
S159 S243 |
| 16 | BAA06g22740 | A06 | 12680316 | T | C | intron_variant | MODIFIER | c.958-32T>C| |
S267 S268 |
| 17 | BAA06g22740 | A06 | 12680712 | C | T | intron_variant | MODIFIER | c.1132-73C>T| |
S124 |
| 18 | BAA06g22740 | A06 | 12681853 | G | A | intron_variant | MODIFIER | c.1491+215G>A| |
S280 |
| 19 | BAA06g22740 | A06 | 12681911 | C | T | intron_variant | MODIFIER | c.1492-192C>T| |
S17 |
| 20 | BAA06g22740 | A06 | 12683959 | C | T | missense_variant | MODERATE | c.2111C>T|p.Pro704Leu |
S245 |
| 21 | BAA06g22740 | A06 | 12684022 | G | A | intron_variant | MODIFIER | c.2151+23G>A| |
S3 |
| 22 | BAA06g22740 | A06 | 12685060 | C | T | missense_variant | MODERATE | c.2675C>T|p.Ser892Leu |
S171 |
| 23 | BAA06g22740 | A06 | 12685447 | G | A | intron_variant | MODIFIER | c.2928+32G>A| |
S261 |
| 24 | BAA06g22740 | A06 | 12686777 | A | T | downstream_gene_variant | MODIFIER | c.*869A>T| |
S79 S84 |