Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g26770 | A02 | 14992725 | G | A | upstream_gene_variant | MODIFIER | c.-4416G>A| |
S91 |
2 | BAA02g26770 | A02 | 14993244 | C | T | upstream_gene_variant | MODIFIER | c.-3897C>T| |
S51 |
3 | BAA02g26770 | A02 | 14994470 | G | A | upstream_gene_variant | MODIFIER | c.-2671G>A| |
S278 |
4 | BAA02g26770 | A02 | 14994891 | C | T | upstream_gene_variant | MODIFIER | c.-2250C>T| |
S53 |
5 | BAA02g26770 | A02 | 14995182 | C | T | upstream_gene_variant | MODIFIER | c.-1959C>T| |
S276 |
6 | BAA02g26770 | A02 | 14995188 | G | A | upstream_gene_variant | MODIFIER | c.-1953G>A| |
S146 |
7 | BAA02g26770 | A02 | 14995428 | G | A | upstream_gene_variant | MODIFIER | c.-1713G>A| |
S37 |
8 | BAA02g26770 | A02 | 14996278 | G | A | upstream_gene_variant | MODIFIER | c.-863G>A| |
S48 |
9 | BAA02g26770 | A02 | 14998370 | G | A | missense_variant | MODERATE | c.532G>A|p.Ala178Thr |
S125 |
10 | BAA02g26770 | A02 | 14998793 | C | T | missense_variant | MODERATE | c.695C>T|p.Pro232Leu |
S78 S83 |
11 | BAA02g26770 | A02 | 14998807 | G | A | missense_variant | MODERATE | c.709G>A|p.Asp237Asn |
S153 S213 |