Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g16050 | A08 | 13399340 | C | T | missense_variant | MODERATE | c.2419G>A|p.Glu807Lys |
S208 S219 |
2 | BAA08g16050 | A08 | 13399407 | C | T | stop_gained | HIGH | c.2352G>A|p.Trp784* |
S223 |
3 | BAA08g16050 | A08 | 13399760 | G | A | missense_variant | MODERATE | c.2137C>T|p.Pro713Ser |
S67 |
4 | BAA08g16050 | A08 | 13400254 | G | A | missense_variant | MODERATE | c.1814C>T|p.Pro605Leu |
S37 |
5 | BAA08g16050 | A08 | 13401549 | G | A | synonymous_variant | LOW | c.1059C>T|p.Leu353Leu |
S185 |
6 | BAA08g16050 | A08 | 13401829 | G | A | synonymous_variant | LOW | c.946C>T|p.Leu316Leu |
S182 S252 S292 |
7 | BAA08g16050 | A08 | 13402193 | G | A | missense_variant | MODERATE | c.662C>T|p.Thr221Ile |
S65 |
8 | BAA08g16050 | A08 | 13403144 | G | A | synonymous_variant | LOW | c.270C>T|p.Val90Val |
S85 |
9 | BAA08g16050 | A08 | 13404150 | C | T | upstream_gene_variant | MODIFIER | c.-410G>A| |
S67 |
10 | BAA08g16050 | A08 | 13407881 | G | A | upstream_gene_variant | MODIFIER | c.-4141C>T| |
S158 |
11 | BAA08g16050 | A08 | 13408368 | C | T | upstream_gene_variant | MODIFIER | c.-4628G>A| |
S121 |