Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g01070 | A07 | 740693 | C | T | missense_variant | MODERATE | c.265G>A|p.Val89Ile |
S255 |
2 | BAA07g01070 | A07 | 742576 | G | A | upstream_gene_variant | MODIFIER | c.-1056C>T| |
S246 |
3 | BAA07g01070 | A07 | 742660 | G | A | upstream_gene_variant | MODIFIER | c.-1140C>T| |
S192 |
4 | BAA07g01070 | A07 | 742761 | G | A | upstream_gene_variant | MODIFIER | c.-1241C>T| |
S105 S106 |
5 | BAA07g01070 | A07 | 742974 | C | T | upstream_gene_variant | MODIFIER | c.-1454G>A| |
S8 |
6 | BAA07g01070 | A07 | 743438 | C | T | upstream_gene_variant | MODIFIER | c.-1918G>A| |
S197 |
7 | BAA07g01070 | A07 | 744044 | G | A | upstream_gene_variant | MODIFIER | c.-2524C>T| |
S157 S163 |
8 | BAA07g01070 | A07 | 744110 | G | A | upstream_gene_variant | MODIFIER | c.-2590C>T| |
S15 |
9 | BAA07g01070 | A07 | 744386 | G | A | upstream_gene_variant | MODIFIER | c.-2866C>T| |
S134 |
10 | BAA07g01070 | A07 | 744877 | G | A | upstream_gene_variant | MODIFIER | c.-3357C>T| |
S187 |