| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g36230 | A02 | 31074039 | C | T | missense_variant | MODERATE | c.1969G>A|p.Glu657Lys |
S16 |
| 2 | BAA02g36230 | A02 | 31074862 | C | A | missense_variant&splice_region_variant | MODERATE | c.1221G>T|p.Leu407Phe |
S15 S3 |
| 3 | BAA02g36230 | A02 | 31076643 | C | T | upstream_gene_variant | MODIFIER | c.-475G>A| |
S171 |
| 4 | BAA02g36230 | A02 | 31076681 | C | T | upstream_gene_variant | MODIFIER | c.-513G>A| |
S301 S304 |
| 5 | BAA02g36230 | A02 | 31077145 | G | A | upstream_gene_variant | MODIFIER | c.-977C>T| |
S293 |
| 6 | BAA02g36230 | A02 | 31077402 | C | T | upstream_gene_variant | MODIFIER | c.-1234G>A| |
S100 |
| 7 | BAA02g36230 | A02 | 31077626 | G | A | upstream_gene_variant | MODIFIER | c.-1458C>T| |
S80 |
| 8 | BAA02g36230 | A02 | 31077664 | G | A | upstream_gene_variant | MODIFIER | c.-1496C>T| |
S185 |
| 9 | BAA02g36230 | A02 | 31078634 | C | T | upstream_gene_variant | MODIFIER | c.-2466G>A| |
S277 |
| 10 | BAA02g36230 | A02 | 31079154 | A | T | upstream_gene_variant | MODIFIER | c.-2986T>A| |
S261 |
| 11 | BAA02g36230 | A02 | 31079287 | G | A | upstream_gene_variant | MODIFIER | c.-3119C>T| |
S94 |
| 12 | BAA02g36230 | A02 | 31079800 | G | A | upstream_gene_variant | MODIFIER | c.-3632C>T| |
S4 |
| 13 | BAA02g36230 | A02 | 31080101 | G | A | upstream_gene_variant | MODIFIER | c.-3933C>T| |
S1 |
| 14 | BAA02g36230 | A02 | 31080756 | C | T | upstream_gene_variant | MODIFIER | c.-4588G>A| |
S289 S290 |