| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA03g66080 | A03 | 40359820 | C | T | downstream_gene_variant | MODIFIER | c.*836G>A| |
S289 S290 |
| 2 | BAA03g66080 | A03 | 40360180 | C | T | downstream_gene_variant | MODIFIER | c.*476G>A| |
S237 |
| 3 | BAA03g66080 | A03 | 40360297 | C | T | downstream_gene_variant | MODIFIER | c.*359G>A| |
S184 |
| 4 | BAA03g66080 | A03 | 40360703 | C | T | missense_variant | MODERATE | c.1441G>A|p.Glu481Lys |
S246 |
| 5 | BAA03g66080 | A03 | 40360777 | C | T | missense_variant | MODERATE | c.1367G>A|p.Ser456Asn |
S228 |
| 6 | BAA03g66080 | A03 | 40360801 | C | T | missense_variant | MODERATE | c.1343G>A|p.Gly448Glu |
S144 |
| 7 | BAA03g66080 | A03 | 40360994 | C | T | missense_variant | MODERATE | c.1150G>A|p.Glu384Lys |
S162 |
| 8 | BAA03g66080 | A03 | 40361443 | C | T | missense_variant | MODERATE | c.790G>A|p.Val264Ile |
S61 |
| 9 | BAA03g66080 | A03 | 40362345 | G | A | intron_variant | MODIFIER | c.226-63C>T| |
S136 |
| 10 | BAA03g66080 | A03 | 40362436 | C | T | intron_variant | MODIFIER | c.225+101G>A| |
S202 |
| 11 | BAA03g66080 | A03 | 40362445 | C | T | intron_variant | MODIFIER | c.225+92G>A| |
S244 |
| 12 | BAA03g66080 | A03 | 40363430 | C | T | upstream_gene_variant | MODIFIER | c.-669G>A| |
S95 |
| 13 | BAA03g66080 | A03 | 40364292 | G | A | upstream_gene_variant | MODIFIER | c.-1531C>T| |
S56 |
| 14 | BAA03g66080 | A03 | 40365436 | G | A | upstream_gene_variant | MODIFIER | c.-2675C>T| |
S136 |
| 15 | BAA03g66080 | A03 | 40366343 | G | A | upstream_gene_variant | MODIFIER | c.-3582C>T| |
S209 |
| 16 | BAA03g66080 | A03 | 40366705 | G | A | upstream_gene_variant | MODIFIER | c.-3944C>T| |
S280 |
| 17 | BAA03g66080 | A03 | 40366921 | G | A | upstream_gene_variant | MODIFIER | c.-4160C>T| |
S183 S198 |