Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g62830 | A09 | 59074368 | G | T | upstream_gene_variant | MODIFIER | c.-4858G>T| |
S146 S252 S267 |
2 | BAA09g62830 | A09 | 59074459 | C | T | upstream_gene_variant | MODIFIER | c.-4767C>T| |
S8 |
3 | BAA09g62830 | A09 | 59074701 | G | A | upstream_gene_variant | MODIFIER | c.-4525G>A| |
S181 |
4 | BAA09g62830 | A09 | 59076559 | C | T | upstream_gene_variant | MODIFIER | c.-2667C>T| |
S43 |
5 | BAA09g62830 | A09 | 59079311 | C | T | missense_variant | MODERATE | c.86C>T|p.Pro29Leu |
S176 |
6 | BAA09g62830 | A09 | 59079457 | C | T | missense_variant | MODERATE | c.232C>T|p.Pro78Ser |
S155 |
7 | BAA09g62830 | A09 | 59079476 | C | T | missense_variant | MODERATE | c.251C>T|p.Ser84Phe |
S256 |
8 | BAA09g62830 | A09 | 59079669 | C | T | synonymous_variant | LOW | c.444C>T|p.Ile148Ile |
S215 |
9 | BAA09g62830 | A09 | 59080362 | G | A | missense_variant | MODERATE | c.701G>A|p.Gly234Glu |
S173 |
10 | BAA09g62830 | A09 | 59081210 | C | T | stop_gained | HIGH | c.1549C>T|p.Gln517* |
S18 |
11 | BAA09g62830 | A09 | 59081326 | G | A | synonymous_variant | LOW | c.1665G>A|p.Glu555Glu |
S10 |