Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g06130 | A10 | 3167833 | G | A | upstream_gene_variant | MODIFIER | c.-4978G>A| |
S274 |
2 | BAA10g06130 | A10 | 3169408 | G | A | upstream_gene_variant | MODIFIER | c.-3403G>A| |
S223 |
3 | BAA10g06130 | A10 | 3170943 | G | A | upstream_gene_variant | MODIFIER | c.-1868G>A| |
S138 |
4 | BAA10g06130 | A10 | 3171184 | C | T | upstream_gene_variant | MODIFIER | c.-1627C>T| |
S244 |
5 | BAA10g06130 | A10 | 3171902 | C | T | upstream_gene_variant | MODIFIER | c.-909C>T| |
S53 S81 S92 |
6 | BAA10g06130 | A10 | 3172501 | C | T | upstream_gene_variant | MODIFIER | c.-310C>T| |
S193 |
7 | BAA10g06130 | A10 | 3173014 | C | T | synonymous_variant | LOW | c.204C>T|p.Leu68Leu |
S208 S93 |
8 | BAA10g06130 | A10 | 3173587 | C | T | synonymous_variant | LOW | c.777C>T|p.Ala259Ala |
S297 |
9 | BAA10g06130 | A10 | 3175362 | G | A | missense_variant | MODERATE | c.1519G>A|p.Ala507Thr |
S221 |
10 | BAA10g06130 | A10 | 3175755 | C | T | downstream_gene_variant | MODIFIER | c.*367C>T| |
S287 |
11 | BAA10g06130 | A10 | 3177565 | G | A | downstream_gene_variant | MODIFIER | c.*2177G>A| |
S203 |