| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g07660 | A05 | 3794043 | G | A | upstream_gene_variant | MODIFIER | c.-4728G>A| |
S136 |
| 2 | BAA05g07660 | A05 | 3794548 | G | A | upstream_gene_variant | MODIFIER | c.-4223G>A| |
S219 |
| 3 | BAA05g07660 | A05 | 3795021 | G | A | upstream_gene_variant | MODIFIER | c.-3750G>A| |
S170 |
| 4 | BAA05g07660 | A05 | 3795760 | C | T | upstream_gene_variant | MODIFIER | c.-3011C>T| |
S153 S213 |
| 5 | BAA05g07660 | A05 | 3796171 | G | A | upstream_gene_variant | MODIFIER | c.-2600G>A| |
S233 |
| 6 | BAA05g07660 | A05 | 3796303 | G | A | upstream_gene_variant | MODIFIER | c.-2468G>A| |
S301 S304 |
| 7 | BAA05g07660 | A05 | 3796616 | G | A | upstream_gene_variant | MODIFIER | c.-2155G>A| |
S56 |
| 8 | BAA05g07660 | A05 | 3796641 | C | T | upstream_gene_variant | MODIFIER | c.-2130C>T| |
S262 |
| 9 | BAA05g07660 | A05 | 3797015 | C | T | upstream_gene_variant | MODIFIER | c.-1756C>T| |
S17 |
| 10 | BAA05g07660 | A05 | 3797264 | C | T | upstream_gene_variant | MODIFIER | c.-1507C>T| |
S143 |
| 11 | BAA05g07660 | A05 | 3797524 | G | A | upstream_gene_variant | MODIFIER | c.-1247G>A| |
S264 |
| 12 | BAA05g07660 | A05 | 3797845 | G | A | upstream_gene_variant | MODIFIER | c.-926G>A| |
S278 |
| 13 | BAA05g07660 | A05 | 3798225 | C | T | upstream_gene_variant | MODIFIER | c.-546C>T| |
S100 |
| 14 | BAA05g07660 | A05 | 3798977 | C | T | synonymous_variant | LOW | c.207C>T|p.Cys69Cys |
S247 S266 |
| 15 | BAA05g07660 | A05 | 3799039 | G | A | missense_variant | MODERATE | c.269G>A|p.Gly90Asp |
S125 |
| 16 | BAA05g07660 | A05 | 3799060 | G | A | missense_variant | MODERATE | c.290G>A|p.Gly97Glu |
S122 |
| 17 | BAA05g07660 | A05 | 3799289 | G | A | missense_variant | MODERATE | c.442G>A|p.Gly148Ser |
S46 |
| 18 | BAA05g07660 | A05 | 3800450 | C | T | missense_variant | MODERATE | c.859C>T|p.Pro287Ser |
S228 |
| 19 | BAA05g07660 | A05 | 3805318 | C | T | downstream_gene_variant | MODIFIER | c.*3846C>T| |
S71 |
| 20 | BAA05g07660 | A05 | 3806246 | C | T | downstream_gene_variant | MODIFIER | c.*4774C>T| |
S59 |