Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g40830 | A02 | 34257814 | G | A | synonymous_variant | LOW | c.1596C>T|p.Thr532Thr |
S292 |
2 | BAA02g40830 | A02 | 34257850 | C | T | synonymous_variant | LOW | c.1560G>A|p.Lys520Lys |
S104 S52 |
3 | BAA02g40830 | A02 | 34258079 | G | A | missense_variant | MODERATE | c.1331C>T|p.Ala444Val |
S57 |
4 | BAA02g40830 | A02 | 34258099 | C | T | missense_variant | MODERATE | c.1311G>A|p.Met437Ile |
S295 |
5 | BAA02g40830 | A02 | 34258245 | C | T | missense_variant | MODERATE | c.1165G>A|p.Ala389Thr |
S135 |
6 | BAA02g40830 | A02 | 34258351 | C | T | synonymous_variant | LOW | c.1059G>A|p.Glu353Glu |
S260 |
7 | BAA02g40830 | A02 | 34258518 | C | T | missense_variant | MODERATE | c.892G>A|p.Ala298Thr |
S95 |
8 | BAA02g40830 | A02 | 34258743 | C | T | missense_variant | MODERATE | c.667G>A|p.Ala223Thr |
S170 |
9 | BAA02g40830 | A02 | 34259124 | G | A | synonymous_variant | LOW | c.286C>T|p.Leu96Leu |
S28 |
10 | BAA02g40830 | A02 | 34259735 | G | A | upstream_gene_variant | MODIFIER | c.-326C>T| |
S235 |
11 | BAA02g40830 | A02 | 34261984 | C | T | upstream_gene_variant | MODIFIER | c.-2575G>A| |
S183 S198 |
12 | BAA02g40830 | A02 | 34262284 | G | A | upstream_gene_variant | MODIFIER | c.-2875C>T| |
S107 |
13 | BAA02g40830 | A02 | 34263151 | G | A | upstream_gene_variant | MODIFIER | c.-3742C>T| |
S221 |
14 | BAA02g40830 | A02 | 34263450 | G | T | upstream_gene_variant | MODIFIER | c.-4041C>A| |
S241 |
15 | BAA02g40830 | A02 | 34263591 | G | A | upstream_gene_variant | MODIFIER | c.-4182C>T| |
S126 |