Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g41960 | A09 | 48515357 | C | T | downstream_gene_variant | MODIFIER | c.*4928G>A| |
S280 |
2 | BAA09g41960 | A09 | 48515819 | G | A | downstream_gene_variant | MODIFIER | c.*4466C>T| |
S265 |
3 | BAA09g41960 | A09 | 48520329 | C | T | missense_variant | MODERATE | c.1087G>A|p.Gly363Ser |
S20 |
4 | BAA09g41960 | A09 | 48520534 | G | T | missense_variant | MODERATE | c.882C>A|p.Phe294Leu |
S134 |
5 | BAA09g41960 | A09 | 48520564 | G | A | synonymous_variant | LOW | c.852C>T|p.Thr284Thr |
S124 |
6 | BAA09g41960 | A09 | 48522422 | C | T | upstream_gene_variant | MODIFIER | c.-1007G>A| |
S294 |
7 | BAA09g41960 | A09 | 48523171 | G | A | upstream_gene_variant | MODIFIER | c.-1756C>T| |
S239 |
8 | BAA09g41960 | A09 | 48524895 | G | A | upstream_gene_variant | MODIFIER | c.-3480C>T| |
S291 |
9 | BAA09g41960 | A09 | 48525047 | G | A | upstream_gene_variant | MODIFIER | c.-3632C>T| |
S172 |