Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g01190 | A04 | 683070 | C | T | missense_variant | MODERATE | c.269G>A|p.Arg90Gln |
S95 |
2 | BAA04g01190 | A04 | 683917 | C | T | upstream_gene_variant | MODIFIER | c.-205G>A| |
S97 |
3 | BAA04g01190 | A04 | 683934 | C | T | upstream_gene_variant | MODIFIER | c.-222G>A| |
S301 |
4 | BAA04g01190 | A04 | 683965 | G | A | upstream_gene_variant | MODIFIER | c.-253C>T| |
S177 |
5 | BAA04g01190 | A04 | 684902 | C | T | upstream_gene_variant | MODIFIER | c.-1190G>A| |
S89 |
6 | BAA04g01190 | A04 | 685489 | G | A | upstream_gene_variant | MODIFIER | c.-1777C>T| |
S66 |
7 | BAA04g01190 | A04 | 685678 | G | A | upstream_gene_variant | MODIFIER | c.-1966C>T| |
S203 |
8 | BAA04g01190 | A04 | 685773 | G | A | upstream_gene_variant | MODIFIER | c.-2061C>T| |
S266 |
9 | BAA04g01190 | A04 | 686386 | C | T | upstream_gene_variant | MODIFIER | c.-2674G>A| |
S204 |
10 | BAA04g01190 | A04 | 687272 | G | A | upstream_gene_variant | MODIFIER | c.-3560C>T| |
S225 |
11 | BAA04g01190 | A04 | 688028 | C | T | upstream_gene_variant | MODIFIER | c.-4316G>A| |
S296 |