| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g19830 | A10 | 18051962 | C | T | downstream_gene_variant | MODIFIER | c.*4172G>A| |
S168 |
| 2 | BAA10g19830 | A10 | 18051983 | C | T | downstream_gene_variant | MODIFIER | c.*4151G>A| |
S308 |
| 3 | BAA10g19830 | A10 | 18056311 | G | A | synonymous_variant | LOW | c.1008C>T|p.Ile336Ile |
S74 |
| 4 | BAA10g19830 | A10 | 18056623 | C | T | synonymous_variant | LOW | c.696G>A|p.Leu232Leu |
S19 |
| 5 | BAA10g19830 | A10 | 18057147 | C | T | missense_variant | MODERATE | c.281G>A|p.Arg94Lys |
S51 |
| 6 | BAA10g19830 | A10 | 18057155 | G | A | synonymous_variant | LOW | c.273C>T|p.His91His |
S79 S84 |
| 7 | BAA10g19830 | A10 | 18059142 | G | A | upstream_gene_variant | MODIFIER | c.-1715C>T| |
S280 |
| 8 | BAA10g19830 | A10 | 18059459 | G | A | upstream_gene_variant | MODIFIER | c.-2032C>T| |
S4 |
| 9 | BAA10g19830 | A10 | 18059482 | C | T | upstream_gene_variant | MODIFIER | c.-2055G>A| |
S30 S31 |
| 10 | BAA10g19830 | A10 | 18059582 | G | A | upstream_gene_variant | MODIFIER | c.-2155C>T| |
S66 |
| 11 | BAA10g19830 | A10 | 18059601 | G | A | upstream_gene_variant | MODIFIER | c.-2174C>T| |
S16 |
| 12 | BAA10g19830 | A10 | 18060885 | G | A | upstream_gene_variant | MODIFIER | c.-3458C>T| |
S79 S84 |
| 13 | BAA10g19830 | A10 | 18061494 | G | A | upstream_gene_variant | MODIFIER | c.-4067C>T| |
S192 |
| 14 | BAA10g19830 | A10 | 18061534 | G | A | upstream_gene_variant | MODIFIER | c.-4107C>T| |
S241 |
| 15 | BAA10g19830 | A10 | 18062328 | G | A | upstream_gene_variant | MODIFIER | c.-4901C>T| |
S262 |