Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g18220 | A01 | 8958006 | C | T | synonymous_variant | LOW | c.1950G>A|p.Lys650Lys |
S17 |
2 | BAA01g18220 | A01 | 8959439 | G | A | synonymous_variant | LOW | c.1389C>T|p.Arg463Arg |
S278 |
3 | BAA01g18220 | A01 | 8959958 | G | A | missense_variant | MODERATE | c.1112C>T|p.Pro371Leu |
S240 |
4 | BAA01g18220 | A01 | 8960637 | G | A | missense_variant | MODERATE | c.764C>T|p.Pro255Leu |
S96 |
5 | BAA01g18220 | A01 | 8960779 | C | T | splice_donor_variant&intron_variant | HIGH | c.726+1G>A| |
S68 |
6 | BAA01g18220 | A01 | 8961079 | C | T | missense_variant | MODERATE | c.505G>A|p.Ala169Thr |
S277 |
7 | BAA01g18220 | A01 | 8961167 | C | T | synonymous_variant | LOW | c.417G>A|p.Ser139Ser |
S185 |
8 | BAA01g18220 | A01 | 8962212 | G | A | upstream_gene_variant | MODIFIER | c.-77C>T| |
S274 |
9 | BAA01g18220 | A01 | 8962817 | C | T | upstream_gene_variant | MODIFIER | c.-682G>A| |
S255 |
10 | BAA01g18220 | A01 | 8962919 | G | A | upstream_gene_variant | MODIFIER | c.-784C>T| |
S94 |
11 | BAA01g18220 | A01 | 8963211 | G | A | upstream_gene_variant | MODIFIER | c.-1076C>T| |
S203 |
12 | BAA01g18220 | A01 | 8963529 | C | T | upstream_gene_variant | MODIFIER | c.-1394G>A| |
S176 |
13 | BAA01g18220 | A01 | 8963537 | C | T | upstream_gene_variant | MODIFIER | c.-1402G>A| |
S208 S219 |
14 | BAA01g18220 | A01 | 8964694 | C | T | upstream_gene_variant | MODIFIER | c.-2559G>A| |
S128 |
15 | BAA01g18220 | A01 | 8965719 | C | T | upstream_gene_variant | MODIFIER | c.-3584G>A| |
S155 S211 |
16 | BAA01g18220 | A01 | 8965756 | C | T | upstream_gene_variant | MODIFIER | c.-3621G>A| |
S130 |
17 | BAA01g18220 | A01 | 8965861 | C | T | upstream_gene_variant | MODIFIER | c.-3726G>A| |
S230 S94 |