Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g08350 | A01 | 3663776 | C | T | synonymous_variant | LOW | c.336C>T|p.Phe112Phe |
S164 |
2 | BAA01g08350 | A01 | 3664335 | G | A | missense_variant | MODERATE | c.682G>A|p.Glu228Lys |
S259 |
3 | BAA01g08350 | A01 | 3664605 | C | T | missense_variant | MODERATE | c.872C>T|p.Thr291Ile |
S53 |
4 | BAA01g08350 | A01 | 3664951 | C | T | synonymous_variant | LOW | c.1132C>T|p.Leu378Leu |
S265 |
5 | BAA01g08350 | A01 | 3665000 | C | T | missense_variant | MODERATE | c.1181C>T|p.Ala394Val |
S8 |
6 | BAA01g08350 | A01 | 3665982 | G | A | missense_variant | MODERATE | c.1769G>A|p.Gly590Glu |
S32 |
7 | BAA01g08350 | A01 | 3665998 | G | A | synonymous_variant | LOW | c.1785G>A|p.Val595Val |
S251 |
8 | BAA01g08350 | A01 | 3666158 | C | T | missense_variant | MODERATE | c.1945C>T|p.His649Tyr |
S25 |
9 | BAA01g08350 | A01 | 3666353 | C | T | missense_variant | MODERATE | c.2140C>T|p.Pro714Ser |
S72 |
10 | BAA01g08350 | A01 | 3666668 | C | T | downstream_gene_variant | MODIFIER | c.*178C>T| |
S99 |
11 | BAA01g08350 | A01 | 3666868 | C | T | downstream_gene_variant | MODIFIER | c.*378C>T| |
S266 |
12 | BAA01g08350 | A01 | 3668162 | C | T | downstream_gene_variant | MODIFIER | c.*1672C>T| |
S68 |
13 | BAA01g08350 | A01 | 3668394 | C | T | downstream_gene_variant | MODIFIER | c.*1904C>T| |
S128 |
14 | BAA01g08350 | A01 | 3668683 | G | A | downstream_gene_variant | MODIFIER | c.*2193G>A| |
S73 |
15 | BAA01g08350 | A01 | 3668715 | C | T | downstream_gene_variant | MODIFIER | c.*2225C>T| |
S189 |