Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g41980 | A02 | 35039786 | G | A | missense_variant | MODERATE | c.830C>T|p.Ser277Leu |
S279 |
2 | BAA02g41980 | A02 | 35040102 | C | T | missense_variant | MODERATE | c.514G>A|p.Gly172Arg |
S162 |
3 | BAA02g41980 | A02 | 35040233 | G | A | missense_variant | MODERATE | c.383C>T|p.Pro128Leu |
S84 S93 |
4 | BAA02g41980 | A02 | 35043549 | G | A | upstream_gene_variant | MODIFIER | c.-2934C>T| |
S20 |
5 | BAA02g41980 | A02 | 35043594 | G | A | upstream_gene_variant | MODIFIER | c.-2979C>T| |
S199 |
6 | BAA02g41980 | A02 | 35043686 | C | T | upstream_gene_variant | MODIFIER | c.-3071G>A| |
S152 |
7 | BAA02g41980 | A02 | 35043936 | C | T | upstream_gene_variant | MODIFIER | c.-3321G>A| |
S40 S49 |
8 | BAA02g41980 | A02 | 35044263 | C | T | upstream_gene_variant | MODIFIER | c.-3648G>A| |
S122 |
9 | BAA02g41980 | A02 | 35044309 | G | A | upstream_gene_variant | MODIFIER | c.-3694C>T| |
S228 |
10 | BAA02g41980 | A02 | 35044384 | C | T | upstream_gene_variant | MODIFIER | c.-3769G>A| |
S261 |
11 | BAA02g41980 | A02 | 35044415 | G | A | upstream_gene_variant | MODIFIER | c.-3800C>T| |
S298 |