| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 65301 | BAA01g34180-BAA01g34190 | A01 | 22868250 | C | T | intergenic_region | MODIFIER | n.22868250C>T| |
S284 |
| 65302 | BAA01g34180-BAA01g34190 | A01 | 22869354 | C | T | intergenic_region | MODIFIER | n.22869354C>T| |
S251 |
| 65303 | BAA01g34180-BAA01g34190 | A01 | 22869843 | G | A | intergenic_region | MODIFIER | n.22869843G>A| |
S83 S88 |
| 65304 | BAA01g34180-BAA01g34190 | A01 | 22869857 | G | A | intergenic_region | MODIFIER | n.22869857G>A| |
S61 |
| 65305 | BAA01g34190 | A01 | 22870861 | C | T | downstream_gene_variant | MODIFIER | c.*3997G>A| |
S286 |
| 65306 | BAA01g34190 | A01 | 22872016 | C | T | downstream_gene_variant | MODIFIER | c.*2842G>A| |
S249 |
| 65307 | BAA01g34190 | A01 | 22874556 | C | T | downstream_gene_variant | MODIFIER | c.*302G>A| |
S166 |
| 65308 | BAA01g34190 | A01 | 22874947 | C | T | missense_variant | MODERATE | c.3220G>A|p.Asp1074Asn |
S216 |
| 65309 | BAA01g34190 | A01 | 22874964 | C | T | missense_variant | MODERATE | c.3203G>A|p.Ser1068Asn |
S10 |
| 65310 | BAA01g34190 | A01 | 22876202 | C | T | stop_gained | HIGH | c.3048G>A|p.Trp1016* |
S119 |
| 65311 | BAA01g34190 | A01 | 22876954 | G | A | intron_variant | MODIFIER | c.2443-147C>T| |
S143 |
| 65312 | BAA01g34190 | A01 | 22877117 | G | A | intron_variant | MODIFIER | c.2443-310C>T| |
S129 |
| 65313 | BAA01g34190 | A01 | 22877917 | G | A | missense_variant | MODERATE | c.2167C>T|p.Arg723Cys |
S247 S279 |
| 65314 | BAA01g34190 | A01 | 22878156 | G | A | intron_variant | MODIFIER | c.2074-62C>T| |
S292 |
| 65315 | BAA01g34200 | A01 | 22878322 | C | T | upstream_gene_variant | MODIFIER | c.-4840C>T| |
S234 |
| 65316 | BAA01g34190 | A01 | 22879162 | C | T | missense_variant | MODERATE | c.1921G>A|p.Asp641Asn |
S186 |
| 65317 | BAA01g34190 | A01 | 22879303 | G | A | stop_gained | HIGH | c.1780C>T|p.Gln594* |
S159 S243 |
| 65318 | BAA01g34190 | A01 | 22880383 | C | T | missense_variant | MODERATE | c.1438G>A|p.Ala480Thr |
S183 S198 |
| 65319 | BAA01g34190 | A01 | 22880575 | G | A | missense_variant | MODERATE | c.1268C>T|p.Ser423Phe |
S286 |
| 65320 | BAA01g34200 | A01 | 22880778 | C | T | upstream_gene_variant | MODIFIER | c.-2384C>T| |
S276 |
| 65321 | BAA01g34190 | A01 | 22881487 | G | A | missense_variant | MODERATE | c.548C>T|p.Ser183Phe |
S223 S87 |
| 65322 | BAA01g34190 | A01 | 22881518 | C | T | missense_variant | MODERATE | c.517G>A|p.Val173Met |
S266 |
| 65323 | BAA01g34190 | A01 | 22881618 | G | A | synonymous_variant | LOW | c.417C>T|p.Ser139Ser |
S79 S91 |
| 65324 | BAA01g34190 | A01 | 22882044 | C | A | missense_variant | MODERATE | c.73G>T|p.Asp25Tyr |
S89 |
| 65325 | BAA01g34190 | A01 | 22882782 | C | T | upstream_gene_variant | MODIFIER | c.-666G>A| |
S42 |