Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAS13g00120 | Scaffold13 | 4349651 | C | T | upstream_gene_variant | MODIFIER | c.-1868C>T| |
S308 |
2 | BAS13g00120 | Scaffold13 | 4349743 | G | A | upstream_gene_variant | MODIFIER | c.-1776G>A| |
S51 |
3 | BAS13g00120 | Scaffold13 | 4350085 | C | T | upstream_gene_variant | MODIFIER | c.-1434C>T| |
S135 |
4 | BAS13g00120 | Scaffold13 | 4351549 | C | T | missense_variant | MODERATE | c.31C>T|p.Leu11Phe |
S221 |
5 | BAS13g00120 | Scaffold13 | 4353297 | G | A | downstream_gene_variant | MODIFIER | c.*1068G>A| |
S202 |
6 | BAS13g00120 | Scaffold13 | 4353451 | C | T | downstream_gene_variant | MODIFIER | c.*1222C>T| |
S12 |
7 | BAS13g00120 | Scaffold13 | 4353946 | G | A | downstream_gene_variant | MODIFIER | c.*1717G>A| |
S79 S91 |
8 | BAS13g00120 | Scaffold13 | 4354106 | G | A | downstream_gene_variant | MODIFIER | c.*1877G>A| |
S162 |
9 | BAS13g00120 | Scaffold13 | 4354335 | G | A | downstream_gene_variant | MODIFIER | c.*2106G>A| |
S205 |
10 | BAS13g00120 | Scaffold13 | 4354455 | G | A | downstream_gene_variant | MODIFIER | c.*2226G>A| |
S180 |
11 | BAS13g00120 | Scaffold13 | 4354891 | G | A | downstream_gene_variant | MODIFIER | c.*2662G>A| |
S173 |
12 | BAS13g00120 | Scaffold13 | 4355123 | C | T | downstream_gene_variant | MODIFIER | c.*2894C>T| |
S146 |
13 | BAS13g00120 | Scaffold13 | 4355410 | G | A | downstream_gene_variant | MODIFIER | c.*3181G>A| |
S244 |
14 | BAS13g00120 | Scaffold13 | 4355514 | G | A | downstream_gene_variant | MODIFIER | c.*3285G>A| |
S35 |
15 | BAS13g00120 | Scaffold13 | 4356156 | G | A | downstream_gene_variant | MODIFIER | c.*3927G>A| |
S97 |
16 | BAS13g00120 | Scaffold13 | 4356263 | G | A | downstream_gene_variant | MODIFIER | c.*4034G>A| |
S115 |
17 | BAS13g00120 | Scaffold13 | 4356720 | G | A | downstream_gene_variant | MODIFIER | c.*4491G>A| |
S153 |