Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g13770 | A08 | 11911586 | G | A | upstream_gene_variant | MODIFIER | c.-4882G>A| |
S32 |
2 | BAA08g13770 | A08 | 11912106 | C | T | upstream_gene_variant | MODIFIER | c.-4362C>T| |
S243 S299 |
3 | BAA08g13770 | A08 | 11916649 | A | T | missense_variant | MODERATE | c.160A>T|p.Thr54Ser |
S45 |
4 | BAA08g13770 | A08 | 11917860 | C | A | downstream_gene_variant | MODIFIER | c.*622C>A| |
S209 |
5 | BAA08g13770 | A08 | 11918165 | G | A | downstream_gene_variant | MODIFIER | c.*927G>A| |
S61 |
6 | BAA08g13770 | A08 | 11918172 | C | T | downstream_gene_variant | MODIFIER | c.*934C>T| |
S305 |
7 | BAA08g13770 | A08 | 11918622 | C | T | downstream_gene_variant | MODIFIER | c.*1384C>T| |
S297 S45 |
8 | BAA08g13770 | A08 | 11918741 | G | A | downstream_gene_variant | MODIFIER | c.*1503G>A| |
S13 |
9 | BAA08g13770 | A08 | 11919008 | C | T | downstream_gene_variant | MODIFIER | c.*1770C>T| |
S271 |
10 | BAA08g13770 | A08 | 11920603 | C | T | downstream_gene_variant | MODIFIER | c.*3365C>T| |
S189 |