Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g27630 | A02 | 15551465 | G | A | upstream_gene_variant | MODIFIER | c.-4830G>A| |
S168 |
2 | BAA02g27630 | A02 | 15551563 | C | T | upstream_gene_variant | MODIFIER | c.-4732C>T| |
S8 |
3 | BAA02g27630 | A02 | 15552128 | C | T | upstream_gene_variant | MODIFIER | c.-4167C>T| |
S218 |
4 | BAA02g27630 | A02 | 15552695 | G | A | upstream_gene_variant | MODIFIER | c.-3600G>A| |
S251 |
5 | BAA02g27630 | A02 | 15553057 | C | T | upstream_gene_variant | MODIFIER | c.-3238C>T| |
S206 |
6 | BAA02g27630 | A02 | 15553949 | C | T | upstream_gene_variant | MODIFIER | c.-2346C>T| |
S245 |
7 | BAA02g27630 | A02 | 15555104 | G | A | upstream_gene_variant | MODIFIER | c.-1191G>A| |
S111 |
8 | BAA02g27630 | A02 | 15555798 | C | T | upstream_gene_variant | MODIFIER | c.-497C>T| |
S160 |
9 | BAA02g27630 | A02 | 15556711 | G | A | missense_variant | MODERATE | c.341G>A|p.Gly114Glu |
S150 |
10 | BAA02g27630 | A02 | 15557184 | C | T | missense_variant | MODERATE | c.641C>T|p.Ala214Val |
S262 |
11 | BAA02g27630 | A02 | 15558424 | C | T | downstream_gene_variant | MODIFIER | c.*579C>T| |
S296 |
12 | BAA02g27630 | A02 | 15559039 | G | A | downstream_gene_variant | MODIFIER | c.*1194G>A| |
S272 |
13 | BAA02g27630 | A02 | 15560473 | C | T | downstream_gene_variant | MODIFIER | c.*2628C>T| |
S216 |