| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g42340 | A09 | 48776855 | A | T | downstream_gene_variant | MODIFIER | c.*1996T>A| |
S151 S153 S157 S166 S167 S236 S257 S262 S263 |
| 2 | BAA09g42340 | A09 | 48777094 | C | T | downstream_gene_variant | MODIFIER | c.*1757G>A| |
S58 |
| 3 | BAA09g42340 | A09 | 48777675 | G | A | downstream_gene_variant | MODIFIER | c.*1176C>T| |
S166 |
| 4 | BAA09g42340 | A09 | 48778873 | G | A | missense_variant | MODERATE | c.1121C>T|p.Ala374Val |
S262 |
| 5 | BAA09g42340 | A09 | 48779413 | G | A | missense_variant | MODERATE | c.736C>T|p.Arg246Cys |
S189 |
| 6 | BAA09g42340 | A09 | 48779618 | C | T | synonymous_variant | LOW | c.531G>A|p.Gln177Gln |
S30 S31 |
| 7 | BAA09g42340 | A09 | 48780199 | C | T | intron_variant | MODIFIER | c.343-21G>A| |
S297 |
| 8 | BAA09g42340 | A09 | 48780451 | C | T | missense_variant | MODERATE | c.232G>A|p.Ala78Thr |
S292 |
| 9 | BAA09g42340 | A09 | 48780507 | C | T | intron_variant | MODIFIER | c.196-20G>A| |
S96 |
| 10 | BAA09g42340 | A09 | 48781813 | C | T | upstream_gene_variant | MODIFIER | c.-798G>A| |
S36 |
| 11 | BAA09g42340 | A09 | 48781845 | C | T | upstream_gene_variant | MODIFIER | c.-830G>A| |
S136 |
| 12 | BAA09g42340 | A09 | 48782015 | C | T | upstream_gene_variant | MODIFIER | c.-1000G>A| |
S32 |
| 13 | BAA09g42340 | A09 | 48782282 | C | T | upstream_gene_variant | MODIFIER | c.-1267G>A| |
S278 |
| 14 | BAA09g42340 | A09 | 48782434 | G | A | upstream_gene_variant | MODIFIER | c.-1419C>T| |
S15 S3 |
| 15 | BAA09g42340 | A09 | 48783118 | G | A | upstream_gene_variant | MODIFIER | c.-2103C>T| |
S288 |
| 16 | BAA09g42340 | A09 | 48784643 | G | A | upstream_gene_variant | MODIFIER | c.-3628C>T| |
S284 |