Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11900 | A02 | 5373640 | G | A | upstream_gene_variant | MODIFIER | c.-2742G>A| |
S225 |
2 | BAA02g11900 | A02 | 5373731 | C | T | upstream_gene_variant | MODIFIER | c.-2651C>T| |
S6 |
3 | BAA02g11900 | A02 | 5374252 | G | A | upstream_gene_variant | MODIFIER | c.-2130G>A| |
S291 |
4 | BAA02g11900 | A02 | 5376132 | G | A | upstream_gene_variant | MODIFIER | c.-250G>A| |
S41 |
5 | BAA02g11900 | A02 | 5376968 | G | A | intron_variant | MODIFIER | c.306-12G>A| |
S223 |
6 | BAA02g11900 | A02 | 5377297 | G | A | missense_variant | MODERATE | c.623G>A|p.Gly208Glu |
S81 |
7 | BAA02g11900 | A02 | 5377802 | G | A | downstream_gene_variant | MODIFIER | c.*372G>A| |
S197 |
8 | BAA02g11900 | A02 | 5379109 | C | T | downstream_gene_variant | MODIFIER | c.*1679C>T| |
S216 S265 S39 |
9 | BAA02g11900 | A02 | 5380549 | G | A | downstream_gene_variant | MODIFIER | c.*3119G>A| |
S136 |
10 | BAA02g11900 | A02 | 5380619 | G | A | downstream_gene_variant | MODIFIER | c.*3189G>A| |
S79 S91 |