Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g22100 | A09 | 13812405 | G | A | missense_variant | MODERATE | c.1373C>T|p.Ser458Leu |
S80 |
2 | BAA09g22100 | A09 | 13815211 | G | A | intron_variant | MODIFIER | c.1223+163C>T| |
S209 |
3 | BAA09g22100 | A09 | 13817475 | G | A | upstream_gene_variant | MODIFIER | c.-116C>T| |
S151 S166 S167 S257 S262 |
4 | BAA09g22100 | A09 | 13817726 | C | T | upstream_gene_variant | MODIFIER | c.-367G>A| |
S296 |
5 | BAA09g22100 | A09 | 13818181 | C | T | upstream_gene_variant | MODIFIER | c.-822G>A| |
S107 |
6 | BAA09g22100 | A09 | 13818452 | G | A | upstream_gene_variant | MODIFIER | c.-1093C>T| |
S80 |
7 | BAA09g22100 | A09 | 13819027 | C | T | upstream_gene_variant | MODIFIER | c.-1668G>A| |
S293 |
8 | BAA09g22100 | A09 | 13819223 | C | T | upstream_gene_variant | MODIFIER | c.-1864G>A| |
S282 |
9 | BAA09g22100 | A09 | 13819717 | G | A | upstream_gene_variant | MODIFIER | c.-2358C>T| |
S175 |