Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44980 | A02 | 36949921 | G | A | upstream_gene_variant | MODIFIER | c.-3976G>A| |
S176 |
2 | BAA02g44980 | A02 | 36950255 | G | A | upstream_gene_variant | MODIFIER | c.-3642G>A| |
S187 |
3 | BAA02g44980 | A02 | 36951553 | C | T | upstream_gene_variant | MODIFIER | c.-2344C>T| |
S15 |
4 | BAA02g44980 | A02 | 36952164 | G | A | upstream_gene_variant | MODIFIER | c.-1733G>A| |
S203 |
5 | BAA02g44980 | A02 | 36952855 | G | A | upstream_gene_variant | MODIFIER | c.-1042G>A| |
S53 |
6 | BAA02g44980 | A02 | 36953801 | G | A | upstream_gene_variant | MODIFIER | c.-96G>A| |
S186 |
7 | BAA02g44980 | A02 | 36953949 | C | T | missense_variant | MODERATE | c.53C>T|p.Thr18Ile |
S187 |
8 | BAA02g44980 | A02 | 36954056 | C | T | intron_variant | MODIFIER | c.133+27C>T| |
S75 S81 |
9 | BAA02g44980 | A02 | 36955046 | C | T | missense_variant | MODERATE | c.635C>T|p.Ser212Phe |
S260 |
10 | BAA02g44980 | A02 | 36956017 | C | T | downstream_gene_variant | MODIFIER | c.*763C>T| |
S128 |
11 | BAA02g44980 | A02 | 36956952 | G | A | downstream_gene_variant | MODIFIER | c.*1698G>A| |
S264 |
12 | BAA02g44980 | A02 | 36956990 | G | A | downstream_gene_variant | MODIFIER | c.*1736G>A| |
S247 |
13 | BAA02g44980 | A02 | 36958938 | G | A | downstream_gene_variant | MODIFIER | c.*3684G>A| |
S265 |
14 | BAA02g44980 | A02 | 36960131 | G | A | downstream_gene_variant | MODIFIER | c.*4877G>A| |
S238 |