| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 74301 | BAA01g39040 | A01 | 25992195 | C | T | upstream_gene_variant | MODIFIER | c.-2074G>A| |
S32 |
| 74302 | BAA01g39040 | A01 | 25992197 | G | A | upstream_gene_variant | MODIFIER | c.-2076C>T| |
S283 |
| 74303 | BAA01g39040 | A01 | 25992573 | C | T | upstream_gene_variant | MODIFIER | c.-2452G>A| |
S113 |
| 74304 | BAA01g39040 | A01 | 25993434 | G | A | upstream_gene_variant | MODIFIER | c.-3313C>T| |
S280 |
| 74305 | BAA01g39040 | A01 | 25993932 | C | T | upstream_gene_variant | MODIFIER | c.-3811G>A| |
S273 |
| 74306 | BAA01g39040 | A01 | 25994122 | C | T | upstream_gene_variant | MODIFIER | c.-4001G>A| |
S198 |
| 74307 | BAA01g39050 | A01 | 25994407 | C | T | missense_variant | MODERATE | c.145C>T|p.Leu49Phe |
S272 |
| 74308 | BAA01g39060 | A01 | 25995286 | G | A | downstream_gene_variant | MODIFIER | c.*1544C>T| |
S105 S106 |
| 74309 | BAA01g39060 | A01 | 25996912 | C | T | missense_variant | MODERATE | c.332G>A|p.Arg111Gln |
S293 |
| 74310 | BAA01g39060 | A01 | 25998381 | C | T | upstream_gene_variant | MODIFIER | c.-1060G>A| |
S90 |
| 74311 | BAA01g39060 | A01 | 25998454 | G | A | upstream_gene_variant | MODIFIER | c.-1133C>T| |
S260 |
| 74312 | BAA01g39060 | A01 | 25998972 | G | A | upstream_gene_variant | MODIFIER | c.-1651C>T| |
S181 |
| 74313 | BAA01g39060 | A01 | 25999584 | G | A | upstream_gene_variant | MODIFIER | c.-2263C>T| |
S163 |
| 74314 | BAA01g39080 | A01 | 26000416 | C | T | missense_variant | MODERATE | c.2155G>A|p.Val719Ile |
S289 S290 |
| 74315 | BAA01g39080 | A01 | 26000518 | G | A | stop_gained | HIGH | c.2053C>T|p.Gln685* |
S125 |
| 74316 | BAA01g39070 | A01 | 26002737 | C | T | upstream_gene_variant | MODIFIER | c.-3855G>A| |
S204 |
| 74317 | BAA01g39080 | A01 | 26004207 | C | T | missense_variant | MODERATE | c.791G>A|p.Gly264Glu |
S89 |
| 74318 | BAA01g39080 | A01 | 26005355 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.270-1G>A| |
S43 |
| 74319 | BAA01g39080 | A01 | 26006725 | G | A | intron_variant | MODIFIER | c.269+16C>T| |
S229 |
| 74320 | BAA01g39080 | A01 | 26009023 | G | A | upstream_gene_variant | MODIFIER | c.-1935C>T| |
S117 |
| 74321 | BAA01g39080 | A01 | 26009127 | G | A | upstream_gene_variant | MODIFIER | c.-2039C>T| |
S70 |
| 74322 | BAA01g39080 | A01 | 26009983 | G | A | upstream_gene_variant | MODIFIER | c.-2895C>T| |
S226 |
| 74323 | BAA01g39080 | A01 | 26010115 | C | T | upstream_gene_variant | MODIFIER | c.-3027G>A| |
S11 |
| 74324 | BAA01g39080 | A01 | 26011515 | C | T | upstream_gene_variant | MODIFIER | c.-4427G>A| |
S54 |
| 74325 | BAA01g39080 | A01 | 26011825 | C | T | upstream_gene_variant | MODIFIER | c.-4737G>A| |
S266 |