| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 167051 | BAA02g12990 | A02 | 5805168 | C | T | upstream_gene_variant | MODIFIER | c.-697C>T| |
S261 |
| 167052 | BAA02g12990 | A02 | 5805362 | G | A | upstream_gene_variant | MODIFIER | c.-503G>A| |
S269 |
| 167053 | BAA02g12990 | A02 | 5805989 | G | A | missense_variant&splice_region_variant | MODERATE | c.17G>A|p.Gly6Glu |
S176 |
| 167054 | BAA02g12990 | A02 | 5806610 | G | A | missense_variant | MODERATE | c.466G>A|p.Val156Ile |
S53 |
| 167055 | BAA02g13010 | A02 | 5807029 | T | C | upstream_gene_variant | MODIFIER | c.-4656T>C| |
S187 |
| 167056 | BAA02g13010 | A02 | 5807262 | C | T | upstream_gene_variant | MODIFIER | c.-4423C>T| |
S127 |
| 167057 | BAA02g13000 | A02 | 5808025 | G | A | missense_variant | MODERATE | c.2776C>T|p.Arg926Trp |
S231 |
| 167058 | BAA02g13000 | A02 | 5808565 | C | T | missense_variant | MODERATE | c.2236G>A|p.Asp746Asn |
S139 |
| 167059 | BAA02g13000 | A02 | 5808855 | C | T | missense_variant | MODERATE | c.1946G>A|p.Arg649Lys |
S179 |
| 167060 | BAA02g13000 | A02 | 5808945 | C | T | missense_variant | MODERATE | c.1856G>A|p.Gly619Glu |
S58 |
| 167061 | BAA02g13000 | A02 | 5809026 | G | A | missense_variant | MODERATE | c.1775C>T|p.Ala592Val |
S282 |
| 167062 | BAA02g13000 | A02 | 5809123 | G | A | missense_variant | MODERATE | c.1678C>T|p.Leu560Phe |
S263 |
| 167063 | BAA02g13000 | A02 | 5809204 | C | T | missense_variant | MODERATE | c.1597G>A|p.Gly533Arg |
S25 |
| 167064 | BAA02g13000 | A02 | 5809438 | C | T | missense_variant | MODERATE | c.1363G>A|p.Glu455Lys |
S124 |
| 167065 | BAA02g13000 | A02 | 5809693 | C | T | missense_variant | MODERATE | c.1207G>A|p.Asp403Asn |
S224 |
| 167066 | BAA02g13000 | A02 | 5810231 | C | T | missense_variant | MODERATE | c.742G>A|p.Glu248Lys |
S13 |
| 167067 | BAA02g13000 | A02 | 5810427 | C | T | synonymous_variant | LOW | c.546G>A|p.Thr182Thr |
S276 |
| 167068 | BAA02g13000 | A02 | 5810891 | C | T | missense_variant | MODERATE | c.82G>A|p.Ala28Thr |
S186 |
| 167069 | BAA02g13000 | A02 | 5811649 | G | A | upstream_gene_variant | MODIFIER | c.-677C>T| |
S271 |
| 167070 | BAA02g13000 | A02 | 5811656 | C | T | upstream_gene_variant | MODIFIER | c.-684G>A| |
S224 |
| 167071 | BAA02g13010 | A02 | 5811693 | G | A | stop_gained | HIGH | c.9G>A|p.Trp3* |
S166 |
| 167072 | BAA02g13010 | A02 | 5811696 | G | A | synonymous_variant | LOW | c.12G>A|p.Arg4Arg |
S187 |
| 167073 | BAA02g13010 | A02 | 5811729 | A | C | missense_variant | MODERATE | c.45A>C|p.Gln15His |
S184 S223 S263 |
| 167074 | BAA02g13010 | A02 | 5811741 | G | A | missense_variant | MODERATE | c.57G>A|p.Met19Ile |
S139 |
| 167075 | BAA02g13000 | A02 | 5812159 | G | A | upstream_gene_variant | MODIFIER | c.-1187C>T| |
S193 |