| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 165051 | BAA02g11340 | A02 | 5121224 | G | A | missense_variant | MODERATE | c.649G>A|p.Val217Ile |
S136 |
| 165052 | BAA02g11340 | A02 | 5121295 | G | A | synonymous_variant | LOW | c.720G>A|p.Glu240Glu |
S28 |
| 165053 | BAA02g11340 | A02 | 5121646 | G | A | synonymous_variant | LOW | c.1071G>A|p.Arg357Arg |
S136 |
| 165054 | BAA02g11340 | A02 | 5121788 | C | T | synonymous_variant | LOW | c.1213C>T|p.Leu405Leu |
S108 |
| 165055 | BAA02g11330 | A02 | 5122855 | G | A | upstream_gene_variant | MODIFIER | c.-2794C>T| |
S95 |
| 165056 | BAA02g11350 | A02 | 5122982 | C | T | splice_region_variant&synonymous_variant | LOW | c.3645G>A|p.Glu1215Glu |
S233 |
| 165057 | BAA02g11350 | A02 | 5123628 | G | A | synonymous_variant | LOW | c.3264C>T|p.Arg1088Arg |
S37 |
| 165058 | BAA02g11330 | A02 | 5124047 | G | A | upstream_gene_variant | MODIFIER | c.-3986C>T| |
S193 |
| 165059 | BAA02g11350 | A02 | 5124989 | C | T | missense_variant | MODERATE | c.2425G>A|p.Asp809Asn |
S195 |
| 165060 | BAA02g11360 | A02 | 5125740 | G | A | upstream_gene_variant | MODIFIER | c.-4859G>A| |
S120 S209 |
| 165061 | BAA02g11360 | A02 | 5126343 | C | T | upstream_gene_variant | MODIFIER | c.-4256C>T| |
S18 |
| 165062 | BAA02g11360 | A02 | 5126992 | C | T | upstream_gene_variant | MODIFIER | c.-3607C>T| |
S66 |
| 165063 | BAA02g11360 | A02 | 5127379 | G | A | upstream_gene_variant | MODIFIER | c.-3220G>A| |
S109 |
| 165064 | BAA02g11360 | A02 | 5127877 | G | A | upstream_gene_variant | MODIFIER | c.-2722G>A| |
S231 |
| 165065 | BAA02g11350 | A02 | 5128715 | G | A | synonymous_variant | LOW | c.771C>T|p.Cys257Cys |
S13 |
| 165066 | BAA02g11360 | A02 | 5128913 | G | A | upstream_gene_variant | MODIFIER | c.-1686G>A| |
S264 |
| 165067 | BAA02g11350 | A02 | 5128965 | C | T | missense_variant | MODERATE | c.692G>A|p.Arg231Lys |
S267 |
| 165068 | BAA02g11350 | A02 | 5129787 | G | A | missense_variant | MODERATE | c.202C>T|p.Pro68Ser |
S303 |
| 165069 | BAA02g11350 | A02 | 5129922 | G | A | synonymous_variant | LOW | c.150C>T|p.Tyr50Tyr |
S12 |
| 165070 | BAA02g11350 | A02 | 5129969 | C | T | missense_variant | MODERATE | c.103G>A|p.Glu35Lys |
S8 |
| 165071 | BAA02g11350 | A02 | 5129981 | G | A | missense_variant | MODERATE | c.91C>T|p.Leu31Phe |
S36 |
| 165072 | BAA02g11350 | A02 | 5130272 | G | A | upstream_gene_variant | MODIFIER | c.-115C>T| |
S303 |
| 165073 | BAA02g11360 | A02 | 5130845 | G | A | missense_variant | MODERATE | c.247G>A|p.Glu83Lys |
S105 S106 |
| 165074 | BAA02g11360 | A02 | 5131000 | G | A | synonymous_variant | LOW | c.402G>A|p.Lys134Lys |
S153 S213 |
| 165075 | BAA02g11350 | A02 | 5131326 | G | A | upstream_gene_variant | MODIFIER | c.-1169C>T| |
S69 |