Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g07480 | A02 | 3206183 | C | T | synonymous_variant | LOW | c.2559G>A|p.Lys853Lys |
S159 S188 S299 |
2 | BAA02g07480 | A02 | 3209202 | G | A | synonymous_variant | LOW | c.1932C>T|p.Ser644Ser |
S207 S280 |
3 | BAA02g07480 | A02 | 3209257 | G | A | missense_variant | MODERATE | c.1877C>T|p.Ala626Val |
S80 |
4 | BAA02g07480 | A02 | 3209571 | G | A | intron_variant | MODIFIER | c.1773+40C>T| |
S225 |
5 | BAA02g07480 | A02 | 3209694 | C | T | missense_variant | MODERATE | c.1690G>A|p.Val564Ile |
S174 |
6 | BAA02g07480 | A02 | 3209899 | G | A | missense_variant | MODERATE | c.1616C>T|p.Ser539Phe |
S132 |
7 | BAA02g07480 | A02 | 3210119 | G | A | intron_variant | MODIFIER | c.1415-19C>T| |
S269 |
8 | BAA02g07480 | A02 | 3211488 | C | T | splice_region_variant&synonymous_variant | LOW | c.891G>A|p.Thr297Thr |
S299 |
9 | BAA02g07480 | A02 | 3211855 | G | A | missense_variant | MODERATE | c.524C>T|p.Ser175Phe |
S107 |
10 | BAA02g07480 | A02 | 3213671 | G | A | upstream_gene_variant | MODIFIER | c.-462C>T| |
S34 |
11 | BAA02g07480 | A02 | 3214166 | G | A | upstream_gene_variant | MODIFIER | c.-957C>T| |
S144 S173 |
12 | BAA02g07480 | A02 | 3214610 | T | A | upstream_gene_variant | MODIFIER | c.-1401A>T| |
S100 |
13 | BAA02g07480 | A02 | 3214633 | C | T | upstream_gene_variant | MODIFIER | c.-1424G>A| |
S284 |
14 | BAA02g07480 | A02 | 3215306 | C | T | upstream_gene_variant | MODIFIER | c.-2097G>A| |
S277 |
15 | BAA02g07480 | A02 | 3215989 | G | A | upstream_gene_variant | MODIFIER | c.-2780C>T| |
S168 |
16 | BAA02g07480 | A02 | 3216313 | G | A | upstream_gene_variant | MODIFIER | c.-3104C>T| |
S153 S257 S263 |
17 | BAA02g07480 | A02 | 3217212 | C | T | upstream_gene_variant | MODIFIER | c.-4003G>A| |
S263 |
18 | BAA02g07480 | A02 | 3217364 | C | T | upstream_gene_variant | MODIFIER | c.-4155G>A| |
S276 |