Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g27360 | A02 | 15379027 | G | A | downstream_gene_variant | MODIFIER | c.*2323C>T| |
S263 |
2 | BAA02g27360 | A02 | 15379229 | C | T | downstream_gene_variant | MODIFIER | c.*2121G>A| |
S127 |
3 | BAA02g27360 | A02 | 15379388 | C | T | downstream_gene_variant | MODIFIER | c.*1962G>A| |
S203 |
4 | BAA02g27360 | A02 | 15380924 | G | A | downstream_gene_variant | MODIFIER | c.*426C>T| |
S125 |
5 | BAA02g27360 | A02 | 15381372 | G | A | missense_variant | MODERATE | c.1226C>T|p.Ala409Val |
S26 |
6 | BAA02g27360 | A02 | 15381726 | G | A | synonymous_variant | LOW | c.1053C>T|p.Leu351Leu |
S37 |
7 | BAA02g27360 | A02 | 15382270 | C | T | missense_variant | MODERATE | c.769G>A|p.Ala257Thr |
S121 |
8 | BAA02g27360 | A02 | 15382274 | G | A | synonymous_variant | LOW | c.765C>T|p.Val255Val |
S80 |
9 | BAA02g27360 | A02 | 15382722 | G | A | missense_variant | MODERATE | c.494C>T|p.Ala165Val |
S209 |
10 | BAA02g27360 | A02 | 15383438 | C | T | synonymous_variant | LOW | c.171G>A|p.Leu57Leu |
S97 |
11 | BAA02g27360 | A02 | 15383877 | G | A | missense_variant | MODERATE | c.49C>T|p.Pro17Ser |
S230 |
12 | BAA02g27360 | A02 | 15387286 | G | A | upstream_gene_variant | MODIFIER | c.-3361C>T| |
S173 |
13 | BAA02g27360 | A02 | 15387436 | C | T | upstream_gene_variant | MODIFIER | c.-3511G>A| |
S242 |
14 | BAA02g27360 | A02 | 15387552 | G | A | upstream_gene_variant | MODIFIER | c.-3627C>T| |
S229 |
15 | BAA02g27360 | A02 | 15388041 | G | A | upstream_gene_variant | MODIFIER | c.-4116C>T| |
S298 |
16 | BAA02g27360 | A02 | 15388175 | C | T | upstream_gene_variant | MODIFIER | c.-4250G>A| |
S163 |