Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g21170 | A09 | 13195726 | C | T | missense_variant | MODERATE | c.2188G>A|p.Glu730Lys |
S116 |
2 | BAA09g21170 | A09 | 13195984 | G | A | missense_variant | MODERATE | c.1930C>T|p.Pro644Ser |
S203 |
3 | BAA09g21170 | A09 | 13196744 | C | T | missense_variant | MODERATE | c.1346G>A|p.Arg449Lys |
S120 |
4 | BAA09g21170 | A09 | 13197021 | C | T | missense_variant | MODERATE | c.1069G>A|p.Val357Ile |
S228 |
5 | BAA09g21170 | A09 | 13197515 | G | A | missense_variant | MODERATE | c.575C>T|p.Thr192Ile |
S66 |
6 | BAA09g21170 | A09 | 13199901 | G | A | upstream_gene_variant | MODIFIER | c.-1663C>T| |
S174 S241 S27 S39 |
7 | BAA09g21170 | A09 | 13200087 | C | T | upstream_gene_variant | MODIFIER | c.-1849G>A| |
S273 |
8 | BAA09g21170 | A09 | 13201240 | G | A | upstream_gene_variant | MODIFIER | c.-3002C>T| |
S162 |
9 | BAA09g21170 | A09 | 13201571 | G | A | upstream_gene_variant | MODIFIER | c.-3333C>T| |
S178 |
10 | BAA09g21170 | A09 | 13202229 | G | A | upstream_gene_variant | MODIFIER | c.-3991C>T| |
S268 |
11 | BAA09g21170 | A09 | 13202395 | T | A | upstream_gene_variant | MODIFIER | c.-4157A>T| |
S279 |