Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g17020 | A04 | 21293611 | C | T | downstream_gene_variant | MODIFIER | c.*2557G>A| |
S294 |
2 | BAA04g17020 | A04 | 21295422 | C | T | downstream_gene_variant | MODIFIER | c.*746G>A| |
S296 |
3 | BAA04g17020 | A04 | 21296258 | G | A | synonymous_variant | LOW | c.1716C>T|p.Ile572Ile |
S87 |
4 | BAA04g17020 | A04 | 21296435 | C | T | missense_variant | MODERATE | c.1624G>A|p.Ala542Thr |
S200 |
5 | BAA04g17020 | A04 | 21296578 | G | A | missense_variant | MODERATE | c.1481C>T|p.Ser494Phe |
S256 |
6 | BAA04g17020 | A04 | 21297035 | G | A | synonymous_variant | LOW | c.1095C>T|p.Pro365Pro |
S96 |
7 | BAA04g17020 | A04 | 21297189 | G | A | missense_variant | MODERATE | c.941C>T|p.Ser314Phe |
S133 |
8 | BAA04g17020 | A04 | 21297298 | C | T | missense_variant | MODERATE | c.908G>A|p.Arg303His |
S268 |
9 | BAA04g17020 | A04 | 21297388 | C | T | missense_variant | MODERATE | c.818G>A|p.Gly273Glu |
S1 S90 |
10 | BAA04g17020 | A04 | 21298672 | C | T | missense_variant | MODERATE | c.134G>A|p.Gly45Glu |
S221 |
11 | BAA04g17020 | A04 | 21299192 | C | T | upstream_gene_variant | MODIFIER | c.-387G>A| |
S7 |
12 | BAA04g17020 | A04 | 21299583 | G | A | upstream_gene_variant | MODIFIER | c.-778C>T| |
S174 S27 |
13 | BAA04g17020 | A04 | 21299829 | G | A | upstream_gene_variant | MODIFIER | c.-1024C>T| |
S171 |
14 | BAA04g17020 | A04 | 21301009 | C | T | upstream_gene_variant | MODIFIER | c.-2204G>A| |
S294 |