Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g00470 | A09 | 483337 | C | T | splice_region_variant&synonymous_variant | LOW | c.1758G>A|p.Glu586Glu |
S278 |
2 | BAA09g00470 | A09 | 483530 | C | T | missense_variant | MODERATE | c.1667G>A|p.Gly556Glu |
S205 |
3 | BAA09g00470 | A09 | 484778 | C | T | synonymous_variant | LOW | c.1140G>A|p.Thr380Thr |
S94 |
4 | BAA09g00470 | A09 | 486071 | G | A | synonymous_variant | LOW | c.573C>T|p.Ile191Ile |
S267 |
5 | BAA09g00470 | A09 | 486362 | C | T | splice_donor_variant&intron_variant | HIGH | c.369+1G>A| |
S234 |
6 | BAA09g00470 | A09 | 486411 | C | T | stop_gained | HIGH | c.321G>A|p.Trp107* |
S172 S217 |
7 | BAA09g00470 | A09 | 486456 | C | T | synonymous_variant | LOW | c.276G>A|p.Arg92Arg |
S177 |
8 | BAA09g00470 | A09 | 487833 | G | C | upstream_gene_variant | MODIFIER | c.-874C>G| |
S280 |
9 | BAA09g00470 | A09 | 487852 | G | A | upstream_gene_variant | MODIFIER | c.-893C>T| |
S80 |
10 | BAA09g00470 | A09 | 488183 | G | A | upstream_gene_variant | MODIFIER | c.-1224C>T| |
S224 |
11 | BAA09g00470 | A09 | 488833 | G | A | upstream_gene_variant | MODIFIER | c.-1874C>T| |
S13 |
12 | BAA09g00470 | A09 | 489645 | C | T | upstream_gene_variant | MODIFIER | c.-2686G>A| |
S57 |
13 | BAA09g00470 | A09 | 490462 | C | T | upstream_gene_variant | MODIFIER | c.-3503G>A| |
S288 |
14 | BAA09g00470 | A09 | 490466 | C | T | upstream_gene_variant | MODIFIER | c.-3507G>A| |
S92 |