Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20850 | A10 | 18558886 | C | T | missense_variant | MODERATE | c.1196G>A|p.Gly399Asp |
S125 |
2 | BAA10g20850 | A10 | 18559048 | C | T | missense_variant | MODERATE | c.1034G>A|p.Arg345Lys |
S25 |
3 | BAA10g20850 | A10 | 18559458 | G | A | missense_variant | MODERATE | c.790C>T|p.Leu264Phe |
S67 |
4 | BAA10g20850 | A10 | 18559604 | G | A | missense_variant | MODERATE | c.644C>T|p.Ala215Val |
S25 |
5 | BAA10g20850 | A10 | 18560618 | C | T | upstream_gene_variant | MODIFIER | c.-40G>A| |
S8 |
6 | BAA10g20850 | A10 | 18560890 | G | A | upstream_gene_variant | MODIFIER | c.-312C>T| |
S286 |
7 | BAA10g20850 | A10 | 18561492 | C | T | upstream_gene_variant | MODIFIER | c.-914G>A| |
S152 |
8 | BAA10g20850 | A10 | 18562457 | G | A | upstream_gene_variant | MODIFIER | c.-1879C>T| |
S158 |
9 | BAA10g20850 | A10 | 18563222 | G | A | upstream_gene_variant | MODIFIER | c.-2644C>T| |
S198 |
10 | BAA10g20850 | A10 | 18564007 | C | T | upstream_gene_variant | MODIFIER | c.-3429G>A| |
S114 |
11 | BAA10g20850 | A10 | 18564547 | C | T | upstream_gene_variant | MODIFIER | c.-3969G>A| |
S56 |
12 | BAA10g20850 | A10 | 18565013 | G | A | upstream_gene_variant | MODIFIER | c.-4435C>T| |
S190 S286 S287 |