Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g29700 | A01 | 18775032 | G | A | missense_variant | MODERATE | c.886C>T|p.Pro296Ser |
S51 |
2 | BAA01g29700 | A01 | 18775849 | G | A | intron_variant | MODIFIER | c.476+38C>T| |
S32 |
3 | BAA01g29700 | A01 | 18776187 | C | T | intron_variant | MODIFIER | c.308-37G>A| |
S166 |
4 | BAA01g29700 | A01 | 18776771 | G | A | missense_variant | MODERATE | c.80C>T|p.Thr27Ile |
S129 |
5 | BAA01g29700 | A01 | 18777638 | G | A | upstream_gene_variant | MODIFIER | c.-666C>T| |
S151 |
6 | BAA01g29700 | A01 | 18777893 | G | A | upstream_gene_variant | MODIFIER | c.-921C>T| |
S265 |
7 | BAA01g29700 | A01 | 18778081 | C | T | upstream_gene_variant | MODIFIER | c.-1109G>A| |
S198 |
8 | BAA01g29700 | A01 | 18778206 | C | T | upstream_gene_variant | MODIFIER | c.-1234G>A| |
S26 |
9 | BAA01g29700 | A01 | 18778307 | G | A | upstream_gene_variant | MODIFIER | c.-1335C>T| |
S294 |
10 | BAA01g29700 | A01 | 18778416 | G | A | upstream_gene_variant | MODIFIER | c.-1444C>T| |
S123 |
11 | BAA01g29700 | A01 | 18780436 | G | A | upstream_gene_variant | MODIFIER | c.-3464C>T| |
S283 |
12 | BAA01g29700 | A01 | 18781120 | G | A | upstream_gene_variant | MODIFIER | c.-4148C>T| |
S25 |
13 | BAA01g29700 | A01 | 18781249 | G | A | upstream_gene_variant | MODIFIER | c.-4277C>T| |
S138 |