Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g19240 | A01 | 9450729 | C | T | upstream_gene_variant | MODIFIER | c.-4851C>T| |
S168 |
2 | BAA01g19240 | A01 | 9450877 | C | T | upstream_gene_variant | MODIFIER | c.-4703C>T| |
S184 |
3 | BAA01g19240 | A01 | 9450963 | G | A | upstream_gene_variant | MODIFIER | c.-4617G>A| |
S117 |
4 | BAA01g19240 | A01 | 9452241 | C | T | upstream_gene_variant | MODIFIER | c.-3339C>T| |
S18 |
5 | BAA01g19240 | A01 | 9452462 | C | T | upstream_gene_variant | MODIFIER | c.-3118C>T| |
S50 |
6 | BAA01g19240 | A01 | 9453326 | C | T | upstream_gene_variant | MODIFIER | c.-2254C>T| |
S216 |
7 | BAA01g19240 | A01 | 9453683 | C | T | upstream_gene_variant | MODIFIER | c.-1897C>T| |
S256 |
8 | BAA01g19240 | A01 | 9453716 | G | A | upstream_gene_variant | MODIFIER | c.-1864G>A| |
S257 |
9 | BAA01g19240 | A01 | 9454742 | C | T | upstream_gene_variant | MODIFIER | c.-838C>T| |
S138 |
10 | BAA01g19240 | A01 | 9455942 | C | T | intron_variant | MODIFIER | c.326+37C>T| |
S273 |
11 | BAA01g19240 | A01 | 9456193 | G | A | missense_variant | MODERATE | c.341G>A|p.Gly114Asp |
S107 |
12 | BAA01g19240 | A01 | 9457867 | C | T | synonymous_variant | LOW | c.1662C>T|p.Phe554Phe |
S166 S167 S263 |
13 | BAA01g19240 | A01 | 9458865 | C | T | downstream_gene_variant | MODIFIER | c.*821C>T| |
S107 |
14 | BAA01g19240 | A01 | 9459531 | G | A | downstream_gene_variant | MODIFIER | c.*1487G>A| |
S59 |
15 | BAA01g19240 | A01 | 9460271 | C | T | downstream_gene_variant | MODIFIER | c.*2227C>T| |
S10 |
16 | BAA01g19240 | A01 | 9461960 | C | T | downstream_gene_variant | MODIFIER | c.*3916C>T| |
S51 |
17 | BAA01g19240 | A01 | 9462430 | C | T | downstream_gene_variant | MODIFIER | c.*4386C>T| |
S166 |
18 | BAA01g19240 | A01 | 9462634 | C | T | downstream_gene_variant | MODIFIER | c.*4590C>T| |
S158 |