Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g06840 | A02 | 2925225 | C | T | missense_variant | MODERATE | c.3262G>A|p.Gly1088Ser |
S66 |
2 | BAA02g06840 | A02 | 2927584 | G | A | missense_variant | MODERATE | c.1796C>T|p.Pro599Leu |
S206 S26 |
3 | BAA02g06840 | A02 | 2929156 | C | T | missense_variant | MODERATE | c.802G>A|p.Glu268Lys |
S226 |
4 | BAA02g06840 | A02 | 2929325 | C | T | splice_region_variant&intron_variant | LOW | c.640-7G>A| |
S13 |
5 | BAA02g06840 | A02 | 2929829 | C | T | intron_variant | MODIFIER | c.531+51G>A| |
S46 |
6 | BAA02g06840 | A02 | 2930006 | C | T | synonymous_variant | LOW | c.405G>A|p.Lys135Lys |
S245 |
7 | BAA02g06840 | A02 | 2930341 | C | T | intron_variant | MODIFIER | c.352+85G>A| |
S13 |
8 | BAA02g06840 | A02 | 2930796 | C | T | missense_variant | MODERATE | c.110G>A|p.Arg37His |
S242 |
9 | BAA02g06840 | A02 | 2930966 | C | T | upstream_gene_variant | MODIFIER | c.-61G>A| |
S37 |
10 | BAA02g06840 | A02 | 2933005 | G | A | upstream_gene_variant | MODIFIER | c.-2100C>T| |
S211 |
11 | BAA02g06840 | A02 | 2933618 | C | T | upstream_gene_variant | MODIFIER | c.-2713G>A| |
S142 |
12 | BAA02g06840 | A02 | 2933997 | T | C | upstream_gene_variant | MODIFIER | c.-3092A>G| |
S185 |
13 | BAA02g06840 | A02 | 2934150 | G | A | upstream_gene_variant | MODIFIER | c.-3245C>T| |
S17 |
14 | BAA02g06840 | A02 | 2934769 | C | T | upstream_gene_variant | MODIFIER | c.-3864G>A| |
S240 |
15 | BAA02g06840 | A02 | 2935588 | C | T | upstream_gene_variant | MODIFIER | c.-4683G>A| |
S257 |