Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g01350 | A01 | 583938 | G | A | upstream_gene_variant | MODIFIER | c.-4039G>A| |
S204 |
2 | BAA01g01350 | A01 | 585340 | G | A | upstream_gene_variant | MODIFIER | c.-2637G>A| |
S6 |
3 | BAA01g01350 | A01 | 586050 | C | A | upstream_gene_variant | MODIFIER | c.-1927C>A| |
S297 |
4 | BAA01g01350 | A01 | 586184 | G | A | upstream_gene_variant | MODIFIER | c.-1793G>A| |
S181 |
5 | BAA01g01350 | A01 | 586593 | C | T | upstream_gene_variant | MODIFIER | c.-1384C>T| |
S206 S26 |
6 | BAA01g01350 | A01 | 586602 | C | T | upstream_gene_variant | MODIFIER | c.-1375C>T| |
S62 |
7 | BAA01g01350 | A01 | 587438 | G | A | upstream_gene_variant | MODIFIER | c.-539G>A| |
S178 |
8 | BAA01g01350 | A01 | 588446 | G | A | intron_variant | MODIFIER | c.267-43G>A| |
S169 |
9 | BAA01g01350 | A01 | 588845 | C | T | missense_variant | MODERATE | c.623C>T|p.Ser208Leu |
S130 |
10 | BAA01g01350 | A01 | 588990 | C | T | synonymous_variant | LOW | c.768C>T|p.Ala256Ala |
S148 S210 S30 S31 |
11 | BAA01g01350 | A01 | 590455 | C | T | downstream_gene_variant | MODIFIER | c.*1315C>T| |
S20 |
12 | BAA01g01350 | A01 | 590849 | C | T | downstream_gene_variant | MODIFIER | c.*1709C>T| |
S79 S84 |
13 | BAA01g01350 | A01 | 591310 | G | A | downstream_gene_variant | MODIFIER | c.*2170G>A| |
S188 |
14 | BAA01g01350 | A01 | 592592 | C | T | downstream_gene_variant | MODIFIER | c.*3452C>T| |
S74 |
15 | BAA01g01350 | A01 | 593678 | G | A | downstream_gene_variant | MODIFIER | c.*4538G>A| |
S197 |