| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA03g56390 | A03 | 27888886 | C | T | upstream_gene_variant | MODIFIER | c.-3737C>T| |
S75 S81 |
| 2 | BAA03g56390 | A03 | 27889497 | G | A | upstream_gene_variant | MODIFIER | c.-3126G>A| |
S18 |
| 3 | BAA03g56390 | A03 | 27890925 | C | T | upstream_gene_variant | MODIFIER | c.-1698C>T| |
S179 |
| 4 | BAA03g56390 | A03 | 27890947 | C | T | upstream_gene_variant | MODIFIER | c.-1676C>T| |
S35 |
| 5 | BAA03g56390 | A03 | 27892633 | T | G | missense_variant | MODERATE | c.11T>G|p.Leu4Trp |
S113 |
| 6 | BAA03g56390 | A03 | 27892691 | C | T | synonymous_variant | LOW | c.69C>T|p.Asp23Asp |
S158 |
| 7 | BAA03g56390 | A03 | 27892735 | C | T | missense_variant | MODERATE | c.113C>T|p.Ser38Phe |
S33 |
| 8 | BAA03g56390 | A03 | 27892945 | G | A | missense_variant | MODERATE | c.323G>A|p.Arg108His |
S56 |
| 9 | BAA03g56390 | A03 | 27893359 | G | A | missense_variant | MODERATE | c.662G>A|p.Arg221Gln |
S165 |
| 10 | BAA03g56390 | A03 | 27893397 | C | T | missense_variant | MODERATE | c.700C>T|p.His234Tyr |
S107 |
| 11 | BAA03g56390 | A03 | 27893682 | G | A | splice_region_variant&intron_variant | LOW | c.981+4G>A| |
S296 |
| 12 | BAA03g56390 | A03 | 27897273 | C | T | downstream_gene_variant | MODIFIER | c.*3127C>T| |
S47 |
| 13 | BAA03g56390 | A03 | 27897837 | G | A | downstream_gene_variant | MODIFIER | c.*3691G>A| |
S134 |
| 14 | BAA03g56390 | A03 | 27898135 | G | A | downstream_gene_variant | MODIFIER | c.*3989G>A| |
S167 |
| 15 | BAA03g56390 | A03 | 27898457 | G | A | downstream_gene_variant | MODIFIER | c.*4311G>A| |
S170 |
| 16 | BAA03g56390 | A03 | 27898510 | C | T | downstream_gene_variant | MODIFIER | c.*4364C>T| |
S59 |