Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g31970 | A02 | 25998761 | G | A | downstream_gene_variant | MODIFIER | c.*882C>T| |
S182 |
2 | BAA02g31970 | A02 | 26003120 | C | T | missense_variant | MODERATE | c.2267G>A|p.Gly756Glu |
S245 |
3 | BAA02g31970 | A02 | 26003371 | G | A | synonymous_variant | LOW | c.2094C>T|p.Ile698Ile |
S271 |
4 | BAA02g31970 | A02 | 26005263 | G | A | intron_variant | MODIFIER | c.1419+21C>T| |
S303 |
5 | BAA02g31970 | A02 | 26005396 | G | A | missense_variant | MODERATE | c.1307C>T|p.Ser436Phe |
S9 |
6 | BAA02g31970 | A02 | 26005605 | C | T | missense_variant | MODERATE | c.1181G>A|p.Gly394Glu |
S25 |
7 | BAA02g31970 | A02 | 26006164 | G | A | synonymous_variant | LOW | c.771C>T|p.Ser257Ser |
S162 |
8 | BAA02g31970 | A02 | 26006248 | G | T | synonymous_variant | LOW | c.687C>A|p.Val229Val |
S216 |
9 | BAA02g31970 | A02 | 26007309 | G | A | intron_variant | MODIFIER | c.596+379C>T| |
S189 |
10 | BAA02g31970 | A02 | 26007342 | G | A | intron_variant | MODIFIER | c.596+346C>T| |
S153 S213 |
11 | BAA02g31970 | A02 | 26009223 | G | A | upstream_gene_variant | MODIFIER | c.-115C>T| |
S203 |
12 | BAA02g31970 | A02 | 26009260 | C | T | upstream_gene_variant | MODIFIER | c.-152G>A| |
S238 |
13 | BAA02g31970 | A02 | 26009487 | C | T | upstream_gene_variant | MODIFIER | c.-379G>A| |
S256 |
14 | BAA02g31970 | A02 | 26010141 | C | T | upstream_gene_variant | MODIFIER | c.-1033G>A| |
S186 |
15 | BAA02g31970 | A02 | 26010705 | C | T | upstream_gene_variant | MODIFIER | c.-1597G>A| |
S12 |
16 | BAA02g31970 | A02 | 26011790 | C | T | upstream_gene_variant | MODIFIER | c.-2682G>A| |
S61 |
17 | BAA02g31970 | A02 | 26012002 | C | T | upstream_gene_variant | MODIFIER | c.-2894G>A| |
S155 S211 |