| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g08530 | A10 | 10292732 | C | T | missense_variant | MODERATE | c.1220G>A|p.Gly407Glu |
S44 |
| 2 | BAA10g08530 | A10 | 10294825 | G | A | missense_variant | MODERATE | c.152C>T|p.Thr51Ile |
S134 S88 |
| 3 | BAA10g08530 | A10 | 10295448 | C | T | upstream_gene_variant | MODIFIER | c.-56G>A| |
S244 |
| 4 | BAA10g08530 | A10 | 10295683 | G | A | upstream_gene_variant | MODIFIER | c.-291C>T| |
S280 |
| 5 | BAA10g08530 | A10 | 10296297 | G | A | upstream_gene_variant | MODIFIER | c.-905C>T| |
S13 |
| 6 | BAA10g08530 | A10 | 10296606 | C | T | upstream_gene_variant | MODIFIER | c.-1214G>A| |
S270 |
| 7 | BAA10g08530 | A10 | 10296860 | G | A | upstream_gene_variant | MODIFIER | c.-1468C>T| |
S124 |
| 8 | BAA10g08530 | A10 | 10297074 | G | A | upstream_gene_variant | MODIFIER | c.-1682C>T| |
S207 |
| 9 | BAA10g08530 | A10 | 10297358 | C | T | upstream_gene_variant | MODIFIER | c.-1966G>A| |
S96 |
| 10 | BAA10g08530 | A10 | 10298094 | C | T | upstream_gene_variant | MODIFIER | c.-2702G>A| |
S224 |
| 11 | BAA10g08530 | A10 | 10299321 | C | T | upstream_gene_variant | MODIFIER | c.-3929G>A| |
S269 |
| 12 | BAA10g08530 | A10 | 10299484 | G | A | upstream_gene_variant | MODIFIER | c.-4092C>T| |
S286 |
| 13 | BAA10g08530 | A10 | 10299750 | G | A | upstream_gene_variant | MODIFIER | c.-4358C>T| |
S105 S106 |
| 14 | BAA10g08530 | A10 | 10300038 | C | T | upstream_gene_variant | MODIFIER | c.-4646G>A| |
S183 |
| 15 | BAA10g08530 | A10 | 10300139 | G | A | upstream_gene_variant | MODIFIER | c.-4747C>T| |
S182 |