Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g21270 | A02 | 11396758 | G | A | downstream_gene_variant | MODIFIER | c.*4906C>T| |
S259 |
2 | BAA02g21270 | A02 | 11399687 | A | T | downstream_gene_variant | MODIFIER | c.*1977T>A| |
S146 |
3 | BAA02g21270 | A02 | 11401737 | G | A | missense_variant | MODERATE | c.2258C>T|p.Thr753Ile |
S303 |
4 | BAA02g21270 | A02 | 11401743 | C | T | missense_variant | MODERATE | c.2252G>A|p.Arg751Lys |
S242 |
5 | BAA02g21270 | A02 | 11402450 | G | A | synonymous_variant | LOW | c.1545C>T|p.Val515Val |
S95 |
6 | BAA02g21270 | A02 | 11402519 | G | A | synonymous_variant | LOW | c.1476C>T|p.Phe492Phe |
S59 |
7 | BAA02g21270 | A02 | 11403621 | C | T | synonymous_variant | LOW | c.951G>A|p.Gly317Gly |
S65 |
8 | BAA02g21270 | A02 | 11405255 | G | A | missense_variant | MODERATE | c.431C>T|p.Thr144Met |
S296 |
9 | BAA02g21270 | A02 | 11405281 | C | T | synonymous_variant | LOW | c.405G>A|p.Ser135Ser |
S135 |
10 | BAA02g21270 | A02 | 11406782 | C | T | upstream_gene_variant | MODIFIER | c.-990G>A| |
S244 |
11 | BAA02g21270 | A02 | 11407485 | C | T | upstream_gene_variant | MODIFIER | c.-1693G>A| |
S158 |
12 | BAA02g21270 | A02 | 11408602 | C | T | upstream_gene_variant | MODIFIER | c.-2810G>A| |
S163 |
13 | BAA02g21270 | A02 | 11408609 | C | T | upstream_gene_variant | MODIFIER | c.-2817G>A| |
S63 |
14 | BAA02g21270 | A02 | 11409828 | C | T | upstream_gene_variant | MODIFIER | c.-4036G>A| |
S88 |
15 | BAA02g21270 | A02 | 11410628 | C | T | upstream_gene_variant | MODIFIER | c.-4836G>A| |
S18 |