| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g29620 | A08 | 20272926 | C | T | upstream_gene_variant | MODIFIER | c.-3944C>T| |
S205 |
| 2 | BAA08g29620 | A08 | 20273320 | C | T | upstream_gene_variant | MODIFIER | c.-3550C>T| |
S132 S137 S89 |
| 3 | BAA08g29620 | A08 | 20274325 | G | A | upstream_gene_variant | MODIFIER | c.-2545G>A| |
S260 |
| 4 | BAA08g29620 | A08 | 20274345 | C | T | upstream_gene_variant | MODIFIER | c.-2525C>T| |
S171 |
| 5 | BAA08g29620 | A08 | 20274402 | C | T | upstream_gene_variant | MODIFIER | c.-2468C>T| |
S83 S88 |
| 6 | BAA08g29620 | A08 | 20276304 | C | T | upstream_gene_variant | MODIFIER | c.-566C>T| |
S276 |
| 7 | BAA08g29620 | A08 | 20277110 | C | T | missense_variant | MODERATE | c.241C>T|p.Pro81Ser |
S210 S225 |
| 8 | BAA08g29620 | A08 | 20277578 | C | T | missense_variant | MODERATE | c.709C>T|p.Pro237Ser |
S167 |
| 9 | BAA08g29620 | A08 | 20278127 | G | A | missense_variant&splice_region_variant | MODERATE | c.1171G>A|p.Gly391Arg |
S246 |
| 10 | BAA08g29620 | A08 | 20278209 | G | A | missense_variant&splice_region_variant | MODERATE | c.1172G>A|p.Gly391Glu |
S30 S31 |
| 11 | BAA08g29620 | A08 | 20278397 | G | A | splice_region_variant&intron_variant | LOW | c.1274-4G>A| |
S259 |