Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g18060 | A09 | 10831849 | G | A | upstream_gene_variant | MODIFIER | c.-4981G>A| |
S73 |
2 | BAA09g18060 | A09 | 10832231 | C | T | upstream_gene_variant | MODIFIER | c.-4599C>T| |
S289 S290 |
3 | BAA09g18060 | A09 | 10832521 | G | A | upstream_gene_variant | MODIFIER | c.-4309G>A| |
S153 |
4 | BAA09g18060 | A09 | 10833017 | G | A | upstream_gene_variant | MODIFIER | c.-3813G>A| |
S249 |
5 | BAA09g18060 | A09 | 10833197 | C | T | upstream_gene_variant | MODIFIER | c.-3633C>T| |
S109 |
6 | BAA09g18060 | A09 | 10835719 | C | T | upstream_gene_variant | MODIFIER | c.-1111C>T| |
S255 |
7 | BAA09g18060 | A09 | 10835734 | G | A | upstream_gene_variant | MODIFIER | c.-1096G>A| |
S191 |
8 | BAA09g18060 | A09 | 10836608 | G | A | upstream_gene_variant | MODIFIER | c.-222G>A| |
S238 |
9 | BAA09g18060 | A09 | 10837899 | G | A | synonymous_variant | LOW | c.594G>A|p.Gly198Gly |
S308 |
10 | BAA09g18060 | A09 | 10838314 | G | A | splice_region_variant&intron_variant | LOW | c.817-6G>A| |
S289 |
11 | BAA09g18060 | A09 | 10839060 | G | A | missense_variant | MODERATE | c.1405G>A|p.Ala469Thr |
S80 |
12 | BAA09g18060 | A09 | 10840051 | C | T | downstream_gene_variant | MODIFIER | c.*785C>T| |
S58 |
13 | BAA09g18060 | A09 | 10840120 | C | T | downstream_gene_variant | MODIFIER | c.*854C>T| |
S278 |
14 | BAA09g18060 | A09 | 10840943 | C | T | downstream_gene_variant | MODIFIER | c.*1677C>T| |
S13 S278 S279 |
15 | BAA09g18060 | A09 | 10840944 | G | A | downstream_gene_variant | MODIFIER | c.*1678G>A| |
S170 |