Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g47640 | A02 | 38374762 | C | T | upstream_gene_variant | MODIFIER | c.-3118C>T| |
S163 |
2 | BAA02g47640 | A02 | 38375280 | C | T | upstream_gene_variant | MODIFIER | c.-2600C>T| |
S87 |
3 | BAA02g47640 | A02 | 38375294 | G | A | upstream_gene_variant | MODIFIER | c.-2586G>A| |
S50 |
4 | BAA02g47640 | A02 | 38375800 | G | A | upstream_gene_variant | MODIFIER | c.-2080G>A| |
S298 |
5 | BAA02g47640 | A02 | 38375931 | C | T | upstream_gene_variant | MODIFIER | c.-1949C>T| |
S122 |
6 | BAA02g47640 | A02 | 38376892 | G | A | upstream_gene_variant | MODIFIER | c.-988G>A| |
S278 |
7 | BAA02g47640 | A02 | 38379578 | G | A | missense_variant | MODERATE | c.1156G>A|p.Asp386Asn |
S255 |
8 | BAA02g47640 | A02 | 38379926 | G | A | missense_variant | MODERATE | c.1420G>A|p.Val474Met |
S62 |
9 | BAA02g47640 | A02 | 38380335 | G | A | intron_variant | MODIFIER | c.1692-32G>A| |
S266 |
10 | BAA02g47640 | A02 | 38380364 | C | T | splice_region_variant&intron_variant | LOW | c.1692-3C>T| |
S203 S296 |
11 | BAA02g47640 | A02 | 38380521 | G | A | missense_variant | MODERATE | c.1846G>A|p.Glu616Lys |
S150 |
12 | BAA02g47640 | A02 | 38381495 | C | T | downstream_gene_variant | MODIFIER | c.*704C>T| |
S259 |
13 | BAA02g47640 | A02 | 38382173 | G | A | downstream_gene_variant | MODIFIER | c.*1382G>A| |
S223 |