Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g29080 | A02 | 16574864 | C | T | upstream_gene_variant | MODIFIER | c.-1576C>T| |
S172 S217 |
2 | BAA02g29080 | A02 | 16575154 | G | A | upstream_gene_variant | MODIFIER | c.-1286G>A| |
S188 |
3 | BAA02g29080 | A02 | 16575537 | G | A | upstream_gene_variant | MODIFIER | c.-903G>A| |
S205 |
4 | BAA02g29080 | A02 | 16575605 | C | T | upstream_gene_variant | MODIFIER | c.-835C>T| |
S293 |
5 | BAA02g29080 | A02 | 16575745 | G | A | upstream_gene_variant | MODIFIER | c.-695G>A| |
S132 S137 S215 |
6 | BAA02g29080 | A02 | 16576040 | C | T | upstream_gene_variant | MODIFIER | c.-400C>T| |
S119 |
7 | BAA02g29080 | A02 | 16576112 | G | A | upstream_gene_variant | MODIFIER | c.-328G>A| |
S5 |
8 | BAA02g29080 | A02 | 16576297 | A | G | upstream_gene_variant | MODIFIER | c.-143A>G| |
S217 |
9 | BAA02g29080 | A02 | 16576450 | C | T | missense_variant | MODERATE | c.11C>T|p.Ser4Phe |
S42 |