Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17710 | A02 | 8815822 | C | T | upstream_gene_variant | MODIFIER | c.-2096C>T| |
S233 |
2 | BAA02g17710 | A02 | 8815859 | G | A | upstream_gene_variant | MODIFIER | c.-2059G>A| |
S45 |
3 | BAA02g17710 | A02 | 8815929 | C | T | upstream_gene_variant | MODIFIER | c.-1989C>T| |
S105 S106 |
4 | BAA02g17710 | A02 | 8817426 | C | T | upstream_gene_variant | MODIFIER | c.-492C>T| |
S277 |
5 | BAA02g17710 | A02 | 8818048 | C | T | splice_region_variant&intron_variant | LOW | c.124+7C>T| |
S216 |
6 | BAA02g17710 | A02 | 8818723 | C | T | missense_variant | MODERATE | c.401C>T|p.Ser134Phe |
S186 |
7 | BAA02g17710 | A02 | 8818829 | G | A | missense_variant | MODERATE | c.430G>A|p.Ala144Thr |
S207 |
8 | BAA02g17710 | A02 | 8818841 | G | A | missense_variant | MODERATE | c.442G>A|p.Gly148Arg |
S260 |
9 | BAA02g17710 | A02 | 8820962 | C | T | missense_variant | MODERATE | c.875C>T|p.Pro292Leu |
S233 |
10 | BAA02g17710 | A02 | 8824243 | C | T | downstream_gene_variant | MODIFIER | c.*3178C>T| |
S164 |
11 | BAA02g17710 | A02 | 8825741 | G | A | downstream_gene_variant | MODIFIER | c.*4676G>A| |
S140 |