| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA06g05160 | A06 | 2898419 | C | T | upstream_gene_variant | MODIFIER | c.-3623C>T| |
S238 |
| 2 | BAA06g05160 | A06 | 2898940 | C | T | upstream_gene_variant | MODIFIER | c.-3102C>T| |
S279 |
| 3 | BAA06g05160 | A06 | 2899011 | A | G | upstream_gene_variant | MODIFIER | c.-3031A>G| |
S255 |
| 4 | BAA06g05160 | A06 | 2902410 | C | T | synonymous_variant | LOW | c.297C>T|p.Phe99Phe |
S228 |
| 5 | BAA06g05160 | A06 | 2902722 | G | A | synonymous_variant | LOW | c.609G>A|p.Ala203Ala |
S234 S51 |
| 6 | BAA06g05160 | A06 | 2902918 | G | A | missense_variant | MODERATE | c.805G>A|p.Asp269Asn |
S115 |
| 7 | BAA06g05160 | A06 | 2906305 | C | T | missense_variant | MODERATE | c.3152C>T|p.Thr1051Ile |
S202 |
| 8 | BAA06g05160 | A06 | 2906573 | C | T | synonymous_variant | LOW | c.3420C>T|p.Ile1140Ile |
S287 |
| 9 | BAA06g05160 | A06 | 2906866 | C | T | missense_variant | MODERATE | c.3713C>T|p.Thr1238Ile |
S23 |
| 10 | BAA06g05160 | A06 | 2910185 | G | A | downstream_gene_variant | MODIFIER | c.*3036G>A| |
S165 |
| 11 | BAA06g05160 | A06 | 2911014 | C | T | downstream_gene_variant | MODIFIER | c.*3865C>T| |
S134 |