Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g00900 | A09 | 674794 | C | T | missense_variant | MODERATE | c.1814G>A|p.Gly605Glu |
S133 |
2 | BAA09g00900 | A09 | 678802 | C | T | synonymous_variant | LOW | c.318G>A|p.Glu106Glu |
S250 |
3 | BAA09g00900 | A09 | 679663 | G | A | upstream_gene_variant | MODIFIER | c.-348C>T| |
S79 S84 |
4 | BAA09g00900 | A09 | 682694 | G | A | upstream_gene_variant | MODIFIER | c.-3379C>T| |
S7 |
5 | BAA09g00900 | A09 | 682723 | C | T | upstream_gene_variant | MODIFIER | c.-3408G>A| |
S305 |
6 | BAA09g00900 | A09 | 683048 | C | T | upstream_gene_variant | MODIFIER | c.-3733G>A| |
S70 |
7 | BAA09g00900 | A09 | 683923 | G | A | upstream_gene_variant | MODIFIER | c.-4608C>T| |
S167 |