Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g01390 | A04 | 794893 | G | A | upstream_gene_variant | MODIFIER | c.-4569G>A| |
S159 S188 S243 S276 S298 S299 |
2 | BAA04g01390 | A04 | 795291 | C | T | upstream_gene_variant | MODIFIER | c.-4171C>T| |
S228 |
3 | BAA04g01390 | A04 | 797312 | C | T | upstream_gene_variant | MODIFIER | c.-2150C>T| |
S107 |
4 | BAA04g01390 | A04 | 797527 | C | T | upstream_gene_variant | MODIFIER | c.-1935C>T| |
S2 |
5 | BAA04g01390 | A04 | 799510 | G | A | missense_variant | MODERATE | c.49G>A|p.Val17Ile |
S57 |
6 | BAA04g01390 | A04 | 799746 | G | A | missense_variant | MODERATE | c.197G>A|p.Arg66Lys |
S308 |
7 | BAA04g01390 | A04 | 799747 | G | A | synonymous_variant | LOW | c.198G>A|p.Arg66Arg |
S131 |
8 | BAA04g01390 | A04 | 801623 | G | A | missense_variant | MODERATE | c.755G>A|p.Arg252Lys |
S13 S140 S168 S219 S279 S64 S72 |
9 | BAA04g01390 | A04 | 803152 | T | A | intron_variant | MODIFIER | c.1347+399T>A| |
S148 S30 S31 |
10 | BAA04g01390 | A04 | 804643 | C | T | missense_variant | MODERATE | c.1823C>T|p.Ala608Val |
S294 |