| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 52851 | BAA01g29150 | A01 | 18382157 | G | A | upstream_gene_variant | MODIFIER | c.-3237C>T| |
S294 |
| 52852 | BAA01g29150-BAA01g29160 | A01 | 18384560 | C | T | intergenic_region | MODIFIER | n.18384560C>T| |
S150 |
| 52853 | BAA01g29160 | A01 | 18387357 | C | T | downstream_gene_variant | MODIFIER | c.*4342G>A| |
S249 |
| 52854 | BAA01g29160 | A01 | 18389046 | G | A | downstream_gene_variant | MODIFIER | c.*2653C>T| |
S62 |
| 52855 | BAA01g29160 | A01 | 18389793 | C | T | downstream_gene_variant | MODIFIER | c.*1906G>A| |
S139 |
| 52856 | BAA01g29160 | A01 | 18390149 | G | A | downstream_gene_variant | MODIFIER | c.*1550C>T| |
S12 |
| 52857 | BAA01g29160 | A01 | 18390182 | C | T | downstream_gene_variant | MODIFIER | c.*1517G>A| |
S104 S52 |
| 52858 | BAA01g29160 | A01 | 18390404 | G | A | downstream_gene_variant | MODIFIER | c.*1295C>T| |
S263 |
| 52859 | BAA01g29160 | A01 | 18393503 | G | A | synonymous_variant | LOW | c.75C>T|p.Leu25Leu |
S34 |
| 52860 | BAA01g29160 | A01 | 18393528 | G | A | missense_variant | MODERATE | c.50C>T|p.Ser17Phe |
S212 |
| 52861 | BAA01g29160 | A01 | 18394262 | G | A | upstream_gene_variant | MODIFIER | c.-685C>T| |
S169 S173 |
| 52862 | BAA01g29160 | A01 | 18394979 | C | T | upstream_gene_variant | MODIFIER | c.-1402G>A| |
S295 |
| 52863 | BAA01g29160 | A01 | 18395388 | G | A | upstream_gene_variant | MODIFIER | c.-1811C>T| |
S84 S93 |
| 52864 | BAA01g29170 | A01 | 18396044 | G | A | missense_variant | MODERATE | c.3575C>T|p.Ala1192Val |
S7 |
| 52865 | BAA01g29170 | A01 | 18396302 | C | T | missense_variant | MODERATE | c.3317G>A|p.Gly1106Glu |
S255 |
| 52866 | BAA01g29170 | A01 | 18396807 | C | T | synonymous_variant | LOW | c.2901G>A|p.Leu967Leu |
S115 |
| 52867 | BAA01g29170 | A01 | 18396861 | C | T | synonymous_variant | LOW | c.2847G>A|p.Arg949Arg |
S77 S82 |
| 52868 | BAA01g29170 | A01 | 18397097 | C | T | missense_variant | MODERATE | c.2611G>A|p.Glu871Lys |
S177 |
| 52869 | BAA01g29160 | A01 | 18397243 | C | T | upstream_gene_variant | MODIFIER | c.-3666G>A| |
S200 |
| 52870 | BAA01g29160 | A01 | 18397653 | C | T | upstream_gene_variant | MODIFIER | c.-4076G>A| |
S268 |
| 52871 | BAA01g29160 | A01 | 18397910 | C | T | upstream_gene_variant | MODIFIER | c.-4333G>A| |
S256 |
| 52872 | BAA01g29160 | A01 | 18398212 | A | G | upstream_gene_variant | MODIFIER | c.-4635T>C| |
S268 |
| 52873 | BAA01g29160 | A01 | 18398316 | G | A | upstream_gene_variant | MODIFIER | c.-4739C>T| |
S96 |
| 52874 | BAA01g29170 | A01 | 18399094 | G | A | missense_variant | MODERATE | c.2114C>T|p.Ser705Phe |
S60 |
| 52875 | BAA01g29170 | A01 | 18400009 | C | T | intron_variant | MODIFIER | c.1343+29G>A| |
S41 |