Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g22130 | A03 | 10036227 | C | T | downstream_gene_variant | MODIFIER | c.*2181G>A| |
S158 |
2 | BAA03g22130 | A03 | 10039111 | C | T | missense_variant&splice_region_variant | MODERATE | c.1717G>A|p.Val573Ile |
S19 |
3 | BAA03g22130 | A03 | 10039926 | C | T | synonymous_variant | LOW | c.1326G>A|p.Arg442Arg |
S155 S211 |
4 | BAA03g22130 | A03 | 10040123 | G | A | missense_variant | MODERATE | c.1210C>T|p.Pro404Ser |
S33 |
5 | BAA03g22130 | A03 | 10040957 | G | A | synonymous_variant | LOW | c.654C>T|p.Ile218Ile |
S296 |
6 | BAA03g22130 | A03 | 10040981 | G | A | synonymous_variant | LOW | c.630C>T|p.Asp210Asp |
S95 |
7 | BAA03g22130 | A03 | 10041052 | G | A | synonymous_variant | LOW | c.559C>T|p.Leu187Leu |
S183 |
8 | BAA03g22130 | A03 | 10041089 | C | T | stop_gained | HIGH | c.522G>A|p.Trp174* |
S132 S137 S89 |
9 | BAA03g22130 | A03 | 10043525 | C | T | upstream_gene_variant | MODIFIER | c.-1292G>A| |
S208 S93 |
10 | BAA03g22130 | A03 | 10043544 | C | T | upstream_gene_variant | MODIFIER | c.-1311G>A| |
S177 |
11 | BAA03g22130 | A03 | 10043700 | G | A | upstream_gene_variant | MODIFIER | c.-1467C>T| |
S30 |
12 | BAA03g22130 | A03 | 10044928 | G | A | upstream_gene_variant | MODIFIER | c.-2695C>T| |
S249 |
13 | BAA03g22130 | A03 | 10047019 | G | A | upstream_gene_variant | MODIFIER | c.-4786C>T| |
S206 S26 |