Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g65660 | A03 | 39936319 | C | T | upstream_gene_variant | MODIFIER | c.-4945C>T| |
S59 |
2 | BAA03g65660 | A03 | 39936394 | G | A | upstream_gene_variant | MODIFIER | c.-4870G>A| |
S58 |
3 | BAA03g65660 | A03 | 39941368 | C | T | synonymous_variant | LOW | c.105C>T|p.Asp35Asp |
S15 S3 |
4 | BAA03g65660 | A03 | 39941383 | G | A | synonymous_variant | LOW | c.120G>A|p.Thr40Thr |
S194 |
5 | BAA03g65660 | A03 | 39941681 | C | T | missense_variant | MODERATE | c.418C>T|p.Leu140Phe |
S298 |
6 | BAA03g65660 | A03 | 39942075 | G | A | downstream_gene_variant | MODIFIER | c.*134G>A| |
S77 S82 |
7 | BAA03g65660 | A03 | 39942080 | G | A | downstream_gene_variant | MODIFIER | c.*139G>A| |
S60 |
8 | BAA03g65660 | A03 | 39942151 | C | T | downstream_gene_variant | MODIFIER | c.*210C>T| |
S212 |
9 | BAA03g65660 | A03 | 39942712 | C | T | downstream_gene_variant | MODIFIER | c.*771C>T| |
S30 S31 |
10 | BAA03g65660 | A03 | 39942733 | C | T | downstream_gene_variant | MODIFIER | c.*792C>T| |
S131 |
11 | BAA03g65660 | A03 | 39943599 | C | T | downstream_gene_variant | MODIFIER | c.*1658C>T| |
S172 |
12 | BAA03g65660 | A03 | 39943651 | C | T | downstream_gene_variant | MODIFIER | c.*1710C>T| |
S274 |
13 | BAA03g65660 | A03 | 39943982 | G | C | downstream_gene_variant | MODIFIER | c.*2041G>C| |
S273 |
14 | BAA03g65660 | A03 | 39946129 | C | T | downstream_gene_variant | MODIFIER | c.*4188C>T| |
S45 |
15 | BAA03g65660 | A03 | 39946203 | G | A | downstream_gene_variant | MODIFIER | c.*4262G>A| |
S40 S49 |