| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 25001 | BAA01g17980 | A01 | 8803004 | G | A | synonymous_variant | LOW | c.1002G>A|p.Pro334Pro |
S213 |
| 25002 | BAA01g17980 | A01 | 8803686 | C | T | missense_variant | MODERATE | c.1684C>T|p.Leu562Phe |
S19 |
| 25003 | BAA01g17980 | A01 | 8803752 | G | A | missense_variant | MODERATE | c.1750G>A|p.Glu584Lys |
S298 |
| 25004 | BAA01g17980 | A01 | 8804278 | G | A | missense_variant | MODERATE | c.2276G>A|p.Arg759Lys |
S197 |
| 25005 | BAA01g17980 | A01 | 8804835 | C | T | downstream_gene_variant | MODIFIER | c.*109C>T| |
S51 |
| 25006 | BAA01g17980 | A01 | 8804871 | G | A | downstream_gene_variant | MODIFIER | c.*145G>A| |
S294 |
| 25007 | BAA01g17990 | A01 | 8805471 | G | A | missense_variant | MODERATE | c.1043C>T|p.Pro348Leu |
S94 |
| 25008 | BAA01g17990 | A01 | 8805777 | C | T | missense_variant | MODERATE | c.737G>A|p.Gly246Glu |
S39 |
| 25009 | BAA01g17990 | A01 | 8806480 | C | T | missense_variant | MODERATE | c.34G>A|p.Glu12Lys |
S150 |
| 25010 | BAA01g18000 | A01 | 8807210 | C | T | missense_variant | MODERATE | c.1357G>A|p.Asp453Asn |
S155 S211 |
| 25011 | BAA01g18000 | A01 | 8807296 | G | A | missense_variant | MODERATE | c.1271C>T|p.Pro424Leu |
S159 S243 |
| 25012 | BAA01g17990 | A01 | 8807516 | G | A | upstream_gene_variant | MODIFIER | c.-1003C>T| |
S271 |
| 25013 | BAA01g18000 | A01 | 8807767 | C | T | missense_variant | MODERATE | c.980G>A|p.Arg327Lys |
S185 |
| 25014 | BAA01g17990 | A01 | 8807855 | C | T | upstream_gene_variant | MODIFIER | c.-1342G>A| |
S182 |
| 25015 | BAA01g18000 | A01 | 8807900 | G | A | missense_variant | MODERATE | c.914C>T|p.Ser305Phe |
S239 |
| 25016 | BAA01g17990 | A01 | 8808198 | G | A | upstream_gene_variant | MODIFIER | c.-1685C>T| |
S38 |
| 25017 | BAA01g18000 | A01 | 8808962 | G | A | missense_variant | MODERATE | c.385C>T|p.Leu129Phe |
S152 |
| 25018 | BAA01g17990 | A01 | 8809025 | C | T | upstream_gene_variant | MODIFIER | c.-2512G>A| |
S136 |
| 25019 | BAA01g17990 | A01 | 8810132 | C | T | upstream_gene_variant | MODIFIER | c.-3619G>A| |
S267 |
| 25020 | BAA01g18010 | A01 | 8810832 | C | T | missense_variant | MODERATE | c.425C>T|p.Pro142Leu |
S168 |
| 25021 | BAA01g18010 | A01 | 8810903 | G | A | missense_variant | MODERATE | c.496G>A|p.Val166Met |
S37 |
| 25022 | BAA01g17990 | A01 | 8811207 | G | A | upstream_gene_variant | MODIFIER | c.-4694C>T| |
S157 S163 |
| 25023 | BAA01g18010 | A01 | 8811622 | C | T | synonymous_variant | LOW | c.891C>T|p.Leu297Leu |
S25 |
| 25024 | BAA01g18010 | A01 | 8812621 | G | A | synonymous_variant | LOW | c.1590G>A|p.Arg530Arg |
S168 |
| 25025 | BAA01g18000 | A01 | 8813037 | C | T | upstream_gene_variant | MODIFIER | c.-3259G>A| |
S99 |