Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g26800 | A01 | 15092133 | G | A | downstream_gene_variant | MODIFIER | c.*3497C>T| |
S129 |
2 | BAA01g26800 | A01 | 15094009 | G | A | downstream_gene_variant | MODIFIER | c.*1621C>T| |
S280 |
3 | BAA01g26800 | A01 | 15094261 | C | T | downstream_gene_variant | MODIFIER | c.*1369G>A| |
S182 |
4 | BAA01g26800 | A01 | 15094310 | C | T | downstream_gene_variant | MODIFIER | c.*1320G>A| |
S10 |
5 | BAA01g26800 | A01 | 15094401 | G | A | downstream_gene_variant | MODIFIER | c.*1229C>T| |
S202 |
6 | BAA01g26800 | A01 | 15094535 | C | T | downstream_gene_variant | MODIFIER | c.*1095G>A| |
S28 |
7 | BAA01g26800 | A01 | 15095930 | G | A | missense_variant | MODERATE | c.883C>T|p.Leu295Phe |
S180 |
8 | BAA01g26800 | A01 | 15095974 | C | T | missense_variant | MODERATE | c.839G>A|p.Arg280Gln |
S267 |
9 | BAA01g26800 | A01 | 15099026 | C | T | intron_variant | MODIFIER | c.426+140G>A| |
S192 |
10 | BAA01g26800 | A01 | 15102186 | G | A | upstream_gene_variant | MODIFIER | c.-1532C>T| |
S6 |