Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g18780 | A08 | 14952291 | C | T | missense_variant | MODERATE | c.23G>A|p.Arg8His |
S86 |
2 | BAA08g18780 | A08 | 14952978 | G | A | upstream_gene_variant | MODIFIER | c.-665C>T| |
S234 |
3 | BAA08g18780 | A08 | 14952998 | A | T | upstream_gene_variant | MODIFIER | c.-685T>A| |
S188 |
4 | BAA08g18780 | A08 | 14953405 | G | A | upstream_gene_variant | MODIFIER | c.-1092C>T| |
S153 |
5 | BAA08g18780 | A08 | 14953916 | C | T | upstream_gene_variant | MODIFIER | c.-1603G>A| |
S197 |
6 | BAA08g18780 | A08 | 14953930 | G | A | upstream_gene_variant | MODIFIER | c.-1617C>T| |
S68 |
7 | BAA08g18780 | A08 | 14956171 | C | T | upstream_gene_variant | MODIFIER | c.-3858G>A| |
S23 |
8 | BAA08g18780 | A08 | 14956424 | G | A | upstream_gene_variant | MODIFIER | c.-4111C>T| |
S5 |
9 | BAA08g18780 | A08 | 14956925 | C | T | upstream_gene_variant | MODIFIER | c.-4612G>A| |
S209 |