| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g42050 | A05 | 40000621 | G | A | missense_variant | MODERATE | c.886C>T|p.Pro296Ser |
S229 |
| 2 | BAA05g42050 | A05 | 40000749 | C | T | splice_donor_variant&intron_variant | HIGH | c.843+1G>A| |
S157 S163 |
| 3 | BAA05g42050 | A05 | 40001036 | C | T | synonymous_variant | LOW | c.717G>A|p.Lys239Lys |
S112 |
| 4 | BAA05g42050 | A05 | 40001262 | C | T | missense_variant | MODERATE | c.577G>A|p.Gly193Arg |
S67 |
| 5 | BAA05g42050 | A05 | 40002032 | C | T | missense_variant | MODERATE | c.250G>A|p.Glu84Lys |
S95 |
| 6 | BAA05g42050 | A05 | 40003873 | C | T | upstream_gene_variant | MODIFIER | c.-1235G>A| |
S55 |
| 7 | BAA05g42050 | A05 | 40004164 | C | T | upstream_gene_variant | MODIFIER | c.-1526G>A| |
S162 |
| 8 | BAA05g42050 | A05 | 40004523 | G | A | upstream_gene_variant | MODIFIER | c.-1885C>T| |
S6 |
| 9 | BAA05g42050 | A05 | 40004750 | G | A | upstream_gene_variant | MODIFIER | c.-2112C>T| |
S261 |
| 10 | BAA05g42050 | A05 | 40004921 | G | A | upstream_gene_variant | MODIFIER | c.-2283C>T| |
S87 |
| 11 | BAA05g42050 | A05 | 40005300 | C | T | upstream_gene_variant | MODIFIER | c.-2662G>A| |
S260 |
| 12 | BAA05g42050 | A05 | 40005549 | G | A | upstream_gene_variant | MODIFIER | c.-2911C>T| |
S131 |
| 13 | BAA05g42050 | A05 | 40005582 | G | A | upstream_gene_variant | MODIFIER | c.-2944C>T| |
S289 S290 |
| 14 | BAA05g42050 | A05 | 40005856 | C | T | upstream_gene_variant | MODIFIER | c.-3218G>A| |
S79 S84 |