Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g19980 | A06 | 10449140 | C | T | downstream_gene_variant | MODIFIER | c.*2775G>A| |
S4 |
2 | BAA06g19980 | A06 | 10452352 | G | A | missense_variant | MODERATE | c.829C>T|p.Leu277Phe |
S133 |
3 | BAA06g19980 | A06 | 10452509 | C | T | missense_variant | MODERATE | c.785G>A|p.Gly262Asp |
S278 |
4 | BAA06g19980 | A06 | 10456196 | G | A | upstream_gene_variant | MODIFIER | c.-1719C>T| |
S179 |
5 | BAA06g19980 | A06 | 10458820 | G | A | upstream_gene_variant | MODIFIER | c.-4343C>T| |
S13 |