| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 158301 | BAA02g05920 | A02 | 2520821 | G | A | upstream_gene_variant | MODIFIER | c.-4526C>T| |
S197 |
| 158302 | BAA02g05920 | A02 | 2520824 | C | T | upstream_gene_variant | MODIFIER | c.-4529G>A| |
S38 |
| 158303 | BAA02g05950 | A02 | 2521462 | C | T | upstream_gene_variant | MODIFIER | c.-62C>T| |
S111 |
| 158304 | BAA02g05950 | A02 | 2523167 | G | A | synonymous_variant | LOW | c.741G>A|p.Glu247Glu |
S283 |
| 158305 | BAA02g05950 | A02 | 2524029 | G | A | missense_variant | MODERATE | c.1463G>A|p.Gly488Glu |
S163 |
| 158306 | BAA02g05940 | A02 | 2524912 | C | T | downstream_gene_variant | MODIFIER | c.*4409C>T| |
S167 |
| 158307 | BAA02g05940 | A02 | 2525369 | G | A | downstream_gene_variant | MODIFIER | c.*4866G>A| |
S308 |
| 158308 | BAA02g05960 | A02 | 2526111 | C | T | missense_variant | MODERATE | c.1406G>A|p.Gly469Asp |
S138 |
| 158309 | BAA02g05950 | A02 | 2527667 | G | A | downstream_gene_variant | MODIFIER | c.*3017G>A| |
S134 |
| 158310 | BAA02g05960 | A02 | 2527735 | C | T | missense_variant | MODERATE | c.526G>A|p.Val176Met |
S306 S308 |
| 158311 | BAA02g05960 | A02 | 2528854 | C | T | upstream_gene_variant | MODIFIER | c.-31G>A| |
S172 |
| 158312 | BAA02g05960 | A02 | 2530258 | C | T | upstream_gene_variant | MODIFIER | c.-1435G>A| |
S221 |
| 158313 | BAA02g05960 | A02 | 2530505 | G | A | upstream_gene_variant | MODIFIER | c.-1682C>T| |
S60 |
| 158314 | BAA02g05960 | A02 | 2530776 | C | T | upstream_gene_variant | MODIFIER | c.-1953G>A| |
S181 |
| 158315 | BAA02g05970 | A02 | 2532351 | C | T | missense_variant | MODERATE | c.1112G>A|p.Arg371Lys |
S180 |
| 158316 | BAA02g05970 | A02 | 2532965 | C | T | stop_gained | HIGH | c.630G>A|p.Trp210* |
S73 |
| 158317 | BAA02g05970 | A02 | 2533420 | G | A | missense_variant | MODERATE | c.175C>T|p.Pro59Ser |
S236 |
| 158318 | BAA02g05970 | A02 | 2533849 | C | T | upstream_gene_variant | MODIFIER | c.-159G>A| |
S179 |
| 158319 | BAA02g05970 | A02 | 2533918 | G | A | upstream_gene_variant | MODIFIER | c.-228C>T| |
S125 |
| 158320 | BAA02g05970 | A02 | 2535438 | G | A | upstream_gene_variant | MODIFIER | c.-1748C>T| |
S171 |
| 158321 | BAA02g05980 | A02 | 2536143 | C | T | missense_variant | MODERATE | c.382G>A|p.Asp128Asn |
S112 |
| 158322 | BAA02g05970 | A02 | 2536645 | G | A | upstream_gene_variant | MODIFIER | c.-2955C>T| |
S177 |
| 158323 | BAA02g05970 | A02 | 2536791 | G | A | upstream_gene_variant | MODIFIER | c.-3101C>T| |
S23 |
| 158324 | BAA02g05980 | A02 | 2538748 | C | T | upstream_gene_variant | MODIFIER | c.-2224G>A| |
S128 S60 |
| 158325 | BAA02g05980 | A02 | 2539563 | C | T | upstream_gene_variant | MODIFIER | c.-3039G>A| |
S85 |