| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g20490 | A07 | 25717169 | G | A | upstream_gene_variant | MODIFIER | c.-4486G>A| |
S73 S91 |
| 2 | BAA07g20490 | A07 | 25717418 | G | A | upstream_gene_variant | MODIFIER | c.-4237G>A| |
S231 |
| 3 | BAA07g20490 | A07 | 25718511 | G | A | upstream_gene_variant | MODIFIER | c.-3144G>A| |
S259 |
| 4 | BAA07g20490 | A07 | 25719028 | A | T | upstream_gene_variant | MODIFIER | c.-2627A>T| |
S154 |
| 5 | BAA07g20490 | A07 | 25719029 | G | A | upstream_gene_variant | MODIFIER | c.-2626G>A| |
S264 |
| 6 | BAA07g20490 | A07 | 25721150 | C | T | upstream_gene_variant | MODIFIER | c.-505C>T| |
S61 |
| 7 | BAA07g20490 | A07 | 25721982 | C | T | missense_variant | MODERATE | c.328C>T|p.Arg110Cys |
S297 |
| 8 | BAA07g20490 | A07 | 25722244 | G | A | missense_variant | MODERATE | c.590G>A|p.Gly197Glu |
S223 |
| 9 | BAA07g20490 | A07 | 25722542 | A | T | missense_variant | MODERATE | c.888A>T|p.Arg296Ser |
S155 S211 |
| 10 | BAA07g20490 | A07 | 25723853 | G | A | missense_variant | MODERATE | c.2126G>A|p.Gly709Asp |
S157 S163 |