Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g21240 | A02 | 11376880 | C | T | missense_variant | MODERATE | c.449G>A|p.Arg150Lys |
S221 |
2 | BAA02g21240 | A02 | 11377151 | G | A | missense_variant | MODERATE | c.178C>T|p.Pro60Ser |
S133 |
3 | BAA02g21240 | A02 | 11377378 | G | A | upstream_gene_variant | MODIFIER | c.-50C>T| |
S148 |
4 | BAA02g21240 | A02 | 11377853 | G | A | upstream_gene_variant | MODIFIER | c.-525C>T| |
S59 |
5 | BAA02g21240 | A02 | 11378002 | G | A | upstream_gene_variant | MODIFIER | c.-674C>T| |
S256 |
6 | BAA02g21240 | A02 | 11378666 | C | T | upstream_gene_variant | MODIFIER | c.-1338G>A| |
S262 |
7 | BAA02g21240 | A02 | 11378945 | C | T | upstream_gene_variant | MODIFIER | c.-1617G>A| |
S130 |
8 | BAA02g21240 | A02 | 11379608 | C | T | upstream_gene_variant | MODIFIER | c.-2280G>A| |
S53 |
9 | BAA02g21240 | A02 | 11380683 | G | A | upstream_gene_variant | MODIFIER | c.-3355C>T| |
S206 S26 |
10 | BAA02g21240 | A02 | 11381729 | C | A | upstream_gene_variant | MODIFIER | c.-4401G>T| |
S134 |
11 | BAA02g21240 | A02 | 11381820 | C | T | upstream_gene_variant | MODIFIER | c.-4492G>A| |
S178 |
12 | BAA02g21240 | A02 | 11382012 | G | A | upstream_gene_variant | MODIFIER | c.-4684C>T| |
S44 |