Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g11980 | A08 | 10532475 | G | A | missense_variant | MODERATE | c.295G>A|p.Gly99Arg |
S165 |
2 | BAA08g11980 | A08 | 10532697 | G | A | splice_region_variant&synonymous_variant | LOW | c.432G>A|p.Gly144Gly |
S267 |
3 | BAA08g11980 | A08 | 10532735 | G | A | stop_gained | HIGH | c.470G>A|p.Trp157* |
S20 |
4 | BAA08g11980 | A08 | 10533168 | G | A | missense_variant | MODERATE | c.700G>A|p.Val234Ile |
S229 |
5 | BAA08g11980 | A08 | 10533250 | G | A | splice_region_variant&intron_variant | LOW | c.777+5G>A| |
S181 |
6 | BAA08g11980 | A08 | 10533331 | C | T | missense_variant | MODERATE | c.782C>T|p.Ser261Phe |
S256 |
7 | BAA08g11980 | A08 | 10535794 | G | A | downstream_gene_variant | MODIFIER | c.*2137G>A| |
S238 |
8 | BAA08g11980 | A08 | 10536273 | C | T | downstream_gene_variant | MODIFIER | c.*2616C>T| |
S268 |
9 | BAA08g11980 | A08 | 10536391 | G | A | downstream_gene_variant | MODIFIER | c.*2734G>A| |
S13 |
10 | BAA08g11980 | A08 | 10536520 | A | G | downstream_gene_variant | MODIFIER | c.*2863A>G| |
S93 |