Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g17090 | A04 | 21332526 | C | T | downstream_gene_variant | MODIFIER | c.*4564G>A| |
S68 |
2 | BAA04g17090 | A04 | 21338619 | G | A | missense_variant | MODERATE | c.3566C>T|p.Ser1189Phe |
S75 S81 |
3 | BAA04g17090 | A04 | 21338781 | G | A | missense_variant | MODERATE | c.3479C>T|p.Ala1160Val |
S177 |
4 | BAA04g17090 | A04 | 21339213 | C | T | missense_variant | MODERATE | c.3229G>A|p.Glu1077Lys |
S200 S239 |
5 | BAA04g17090 | A04 | 21339254 | G | A | missense_variant | MODERATE | c.3188C>T|p.Thr1063Ile |
S85 |
6 | BAA04g17090 | A04 | 21340121 | C | T | missense_variant | MODERATE | c.2518G>A|p.Glu840Lys |
S268 |
7 | BAA04g17090 | A04 | 21340782 | C | T | synonymous_variant | LOW | c.1857G>A|p.Lys619Lys |
S178 |
8 | BAA04g17090 | A04 | 21340810 | G | A | missense_variant | MODERATE | c.1829C>T|p.Pro610Leu |
S219 S72 |
9 | BAA04g17090 | A04 | 21340964 | C | T | missense_variant | MODERATE | c.1675G>A|p.Gly559Arg |
S297 |
10 | BAA04g17090 | A04 | 21341265 | G | A | synonymous_variant | LOW | c.1374C>T|p.Phe458Phe |
S219 S72 |
11 | BAA04g17090 | A04 | 21342173 | C | T | missense_variant | MODERATE | c.466G>A|p.Asp156Asn |
S221 |
12 | BAA04g17090 | A04 | 21342305 | C | T | missense_variant | MODERATE | c.334G>A|p.Val112Met |
S243 S299 |
13 | BAA04g17090 | A04 | 21342328 | C | T | missense_variant | MODERATE | c.311G>A|p.Gly104Glu |
S23 |
14 | BAA04g17090 | A04 | 21342363 | C | T | synonymous_variant | LOW | c.276G>A|p.Arg92Arg |
S115 |
15 | BAA04g17090 | A04 | 21343191 | G | A | upstream_gene_variant | MODIFIER | c.-553C>T| |
S186 |
16 | BAA04g17090 | A04 | 21343471 | G | A | upstream_gene_variant | MODIFIER | c.-833C>T| |
S259 |
17 | BAA04g17090 | A04 | 21344158 | G | A | upstream_gene_variant | MODIFIER | c.-1520C>T| |
S58 |
18 | BAA04g17090 | A04 | 21344211 | G | A | upstream_gene_variant | MODIFIER | c.-1573C>T| |
S59 |
19 | BAA04g17090 | A04 | 21345500 | C | T | upstream_gene_variant | MODIFIER | c.-2862G>A| |
S130 |