Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g01030 | A04 | 598310 | C | G | downstream_gene_variant | MODIFIER | c.*1416G>C| |
S252 |
2 | BAA04g01030 | A04 | 598540 | C | A | downstream_gene_variant | MODIFIER | c.*1186G>T| |
S264 |
3 | BAA04g01030 | A04 | 599129 | C | T | downstream_gene_variant | MODIFIER | c.*597G>A| |
S41 |
4 | BAA04g01030 | A04 | 599906 | G | A | synonymous_variant | LOW | c.1758C>T|p.Asp586Asp |
S261 |
5 | BAA04g01030 | A04 | 600481 | C | T | splice_donor_variant&intron_variant | HIGH | c.1527+1G>A| |
S295 |
6 | BAA04g01030 | A04 | 600683 | G | T | synonymous_variant | LOW | c.1326C>A|p.Val442Val |
S114 S123 S256 S270 |
7 | BAA04g01030 | A04 | 600801 | C | T | missense_variant | MODERATE | c.1208G>A|p.Gly403Glu |
S132 S137 S215 S89 |
8 | BAA04g01030 | A04 | 600951 | C | T | intron_variant | MODIFIER | c.1111-53G>A| |
S8 |
9 | BAA04g01030 | A04 | 601200 | G | A | missense_variant | MODERATE | c.1055C>T|p.Ser352Phe |
S150 |
10 | BAA04g01030 | A04 | 601514 | G | A | synonymous_variant | LOW | c.837C>T|p.His279His |
S133 |
11 | BAA04g01030 | A04 | 605994 | C | T | upstream_gene_variant | MODIFIER | c.-3644G>A| |
S55 |