Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g29990 | A02 | 17289155 | C | T | downstream_gene_variant | MODIFIER | c.*2190G>A| |
S195 |
2 | BAA02g29990 | A02 | 17289282 | G | A | downstream_gene_variant | MODIFIER | c.*2063C>T| |
S143 |
3 | BAA02g29990 | A02 | 17290038 | C | T | downstream_gene_variant | MODIFIER | c.*1307G>A| |
S178 |
4 | BAA02g29990 | A02 | 17290165 | C | T | downstream_gene_variant | MODIFIER | c.*1180G>A| |
S138 |
5 | BAA02g29990 | A02 | 17290479 | G | A | downstream_gene_variant | MODIFIER | c.*866C>T| |
S28 |
6 | BAA02g29990 | A02 | 17293774 | G | A | missense_variant | MODERATE | c.980C>T|p.Ser327Phe |
S60 |
7 | BAA02g29990 | A02 | 17294540 | G | A | missense_variant | MODERATE | c.358C>T|p.Arg120Cys |
S211 S227 |
8 | BAA02g29990 | A02 | 17294638 | G | A | missense_variant | MODERATE | c.260C>T|p.Ala87Val |
S19 |
9 | BAA02g29990 | A02 | 17294799 | G | A | synonymous_variant | LOW | c.99C>T|p.Ser33Ser |
S116 |
10 | BAA02g29990 | A02 | 17295119 | C | T | upstream_gene_variant | MODIFIER | c.-222G>A| |
S11 |
11 | BAA02g29990 | A02 | 17295650 | G | A | upstream_gene_variant | MODIFIER | c.-753C>T| |
S23 |
12 | BAA02g29990 | A02 | 17296032 | G | A | upstream_gene_variant | MODIFIER | c.-1135C>T| |
S56 |
13 | BAA02g29990 | A02 | 17297035 | G | A | upstream_gene_variant | MODIFIER | c.-2138C>T| |
S80 |
14 | BAA02g29990 | A02 | 17297439 | C | T | upstream_gene_variant | MODIFIER | c.-2542G>A| |
S241 |
15 | BAA02g29990 | A02 | 17297684 | C | T | upstream_gene_variant | MODIFIER | c.-2787G>A| |
S219 S72 |
16 | BAA02g29990 | A02 | 17298214 | T | C | upstream_gene_variant | MODIFIER | c.-3317A>G| |
S172 S217 |
17 | BAA02g29990 | A02 | 17298865 | G | A | upstream_gene_variant | MODIFIER | c.-3968C>T| |
S186 |
18 | BAA02g29990 | A02 | 17299451 | C | T | upstream_gene_variant | MODIFIER | c.-4554G>A| |
S44 |