Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g11550 | A01 | 5345970 | C | T | upstream_gene_variant | MODIFIER | c.-994C>T| |
S210 S225 |
2 | BAA01g11550 | A01 | 5346263 | C | T | upstream_gene_variant | MODIFIER | c.-701C>T| |
S66 |
3 | BAA01g11550 | A01 | 5346361 | C | T | upstream_gene_variant | MODIFIER | c.-603C>T| |
S202 |
4 | BAA01g11550 | A01 | 5346423 | C | T | upstream_gene_variant | MODIFIER | c.-541C>T| |
S1 |
5 | BAA01g11550 | A01 | 5346709 | C | T | upstream_gene_variant | MODIFIER | c.-255C>T| |
S18 |
6 | BAA01g11550 | A01 | 5347008 | C | T | synonymous_variant | LOW | c.45C>T|p.Val15Val |
S295 |
7 | BAA01g11550 | A01 | 5347380 | C | T | synonymous_variant | LOW | c.417C>T|p.Ser139Ser |
S270 |
8 | BAA01g11550 | A01 | 5347456 | C | T | missense_variant | MODERATE | c.493C>T|p.Leu165Phe |
S53 |
9 | BAA01g11550 | A01 | 5347458 | C | T | synonymous_variant | LOW | c.495C>T|p.Leu165Leu |
S61 |
10 | BAA01g11550 | A01 | 5347633 | G | A | missense_variant | MODERATE | c.670G>A|p.Val224Ile |
S157 S163 |
11 | BAA01g11550 | A01 | 5353335 | G | A | downstream_gene_variant | MODIFIER | c.*4797G>A| |
S9 |