Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g23100 | A02 | 12575300 | G | A | upstream_gene_variant | MODIFIER | c.-3551G>A| |
S61 |
2 | BAA02g23100 | A02 | 12575476 | G | A | upstream_gene_variant | MODIFIER | c.-3375G>A| |
S7 |
3 | BAA02g23100 | A02 | 12575565 | C | T | upstream_gene_variant | MODIFIER | c.-3286C>T| |
S208 |
4 | BAA02g23100 | A02 | 12575620 | G | A | upstream_gene_variant | MODIFIER | c.-3231G>A| |
S59 |
5 | BAA02g23100 | A02 | 12575892 | G | A | upstream_gene_variant | MODIFIER | c.-2959G>A| |
S288 |
6 | BAA02g23100 | A02 | 12577277 | C | T | upstream_gene_variant | MODIFIER | c.-1574C>T| |
S181 |
7 | BAA02g23100 | A02 | 12578697 | C | T | upstream_gene_variant | MODIFIER | c.-154C>T| |
S5 |
8 | BAA02g23100 | A02 | 12579322 | C | T | missense_variant | MODERATE | c.472C>T|p.Pro158Ser |
S192 |
9 | BAA02g23100 | A02 | 12579545 | G | A | intron_variant | MODIFIER | c.482+213G>A| |
S200 |
10 | BAA02g23100 | A02 | 12579700 | G | A | intron_variant | MODIFIER | c.482+368G>A| |
S61 |
11 | BAA02g23100 | A02 | 12579852 | C | T | intron_variant | MODIFIER | c.482+520C>T| |
S289 S290 |
12 | BAA02g23100 | A02 | 12579910 | C | T | intron_variant | MODIFIER | c.482+578C>T| |
S157 S163 |
13 | BAA02g23100 | A02 | 12580209 | C | T | intron_variant | MODIFIER | c.482+877C>T| |
S197 |
14 | BAA02g23100 | A02 | 12580961 | C | T | intron_variant | MODIFIER | c.483-702C>T| |
S94 |
15 | BAA02g23100 | A02 | 12580989 | G | A | intron_variant | MODIFIER | c.483-674G>A| |
S279 |
16 | BAA02g23100 | A02 | 12582147 | G | A | missense_variant | MODERATE | c.967G>A|p.Glu323Lys |
S44 |
17 | BAA02g23100 | A02 | 12582303 | C | T | missense_variant | MODERATE | c.1123C>T|p.Leu375Phe |
S112 |
18 | BAA02g23100 | A02 | 12583290 | G | A | downstream_gene_variant | MODIFIER | c.*505G>A| |
S70 |
19 | BAA02g23100 | A02 | 12583900 | G | A | downstream_gene_variant | MODIFIER | c.*1115G>A| |
S37 |