| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g12620 | A10 | 14012097 | C | T | downstream_gene_variant | MODIFIER | c.*1474G>A| |
S176 |
| 2 | BAA10g12620 | A10 | 14012710 | C | T | downstream_gene_variant | MODIFIER | c.*861G>A| |
S259 |
| 3 | BAA10g12620 | A10 | 14012805 | G | A | downstream_gene_variant | MODIFIER | c.*766C>T| |
S28 |
| 4 | BAA10g12620 | A10 | 14013344 | G | A | downstream_gene_variant | MODIFIER | c.*227C>T| |
S216 |
| 5 | BAA10g12620 | A10 | 14013605 | G | A | missense_variant | MODERATE | c.308C>T|p.Ser103Leu |
S289 |
| 6 | BAA10g12620 | A10 | 14013616 | G | A | synonymous_variant | LOW | c.297C>T|p.Leu99Leu |
S148 S210 S30 S31 |
| 7 | BAA10g12620 | A10 | 14013717 | C | T | missense_variant | MODERATE | c.196G>A|p.Gly66Arg |
S80 |
| 8 | BAA10g12620 | A10 | 14014854 | C | T | upstream_gene_variant | MODIFIER | c.-942G>A| |
S259 |
| 9 | BAA10g12620 | A10 | 14014865 | C | T | upstream_gene_variant | MODIFIER | c.-953G>A| |
S249 |
| 10 | BAA10g12620 | A10 | 14015684 | C | T | upstream_gene_variant | MODIFIER | c.-1772G>A| |
S162 |
| 11 | BAA10g12620 | A10 | 14016273 | G | A | upstream_gene_variant | MODIFIER | c.-2361C>T| |
S27 |
| 12 | BAA10g12620 | A10 | 14016899 | G | A | upstream_gene_variant | MODIFIER | c.-2987C>T| |
S1 S157 S163 S90 |
| 13 | BAA10g12620 | A10 | 14018788 | G | A | upstream_gene_variant | MODIFIER | c.-4876C>T| |
S216 |
| 14 | BAA10g12620 | A10 | 14018811 | C | T | upstream_gene_variant | MODIFIER | c.-4899G>A| |
S239 |