Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g26270 | A02 | 14575469 | C | T | upstream_gene_variant | MODIFIER | c.-2513C>T| |
S238 |
2 | BAA02g26270 | A02 | 14575799 | A | C | upstream_gene_variant | MODIFIER | c.-2183A>C| |
S96 |
3 | BAA02g26270 | A02 | 14575993 | G | A | upstream_gene_variant | MODIFIER | c.-1989G>A| |
S38 |
4 | BAA02g26270 | A02 | 14576226 | G | A | upstream_gene_variant | MODIFIER | c.-1756G>A| |
S278 |
5 | BAA02g26270 | A02 | 14576233 | G | A | upstream_gene_variant | MODIFIER | c.-1749G>A| |
S126 |
6 | BAA02g26270 | A02 | 14576764 | G | A | upstream_gene_variant | MODIFIER | c.-1218G>A| |
S251 |
7 | BAA02g26270 | A02 | 14578000 | C | T | missense_variant | MODERATE | c.19C>T|p.Leu7Phe |
S287 |
8 | BAA02g26270 | A02 | 14578007 | C | T | missense_variant | MODERATE | c.26C>T|p.Ser9Phe |
S180 |
9 | BAA02g26270 | A02 | 14578163 | G | A | missense_variant | MODERATE | c.182G>A|p.Arg61His |
S161 |
10 | BAA02g26270 | A02 | 14578202 | C | T | missense_variant | MODERATE | c.221C>T|p.Ser74Phe |
S224 |
11 | BAA02g26270 | A02 | 14578264 | G | A | missense_variant | MODERATE | c.283G>A|p.Gly95Ser |
S56 |
12 | BAA02g26270 | A02 | 14578405 | G | A | downstream_gene_variant | MODIFIER | c.*55G>A| |
S143 |
13 | BAA02g26270 | A02 | 14578904 | G | A | downstream_gene_variant | MODIFIER | c.*554G>A| |
S279 |
14 | BAA02g26270 | A02 | 14579666 | G | A | downstream_gene_variant | MODIFIER | c.*1316G>A| |
S60 |
15 | BAA02g26270 | A02 | 14579919 | G | A | downstream_gene_variant | MODIFIER | c.*1569G>A| |
S125 |