Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g11160 | A04 | 17099031 | G | A | downstream_gene_variant | MODIFIER | c.*3238C>T| |
S259 |
2 | BAA04g11160 | A04 | 17099091 | C | T | downstream_gene_variant | MODIFIER | c.*3178G>A| |
S172 S217 |
3 | BAA04g11160 | A04 | 17102551 | C | T | synonymous_variant | LOW | c.2274G>A|p.Glu758Glu |
S173 |
4 | BAA04g11160 | A04 | 17102566 | G | A | synonymous_variant | LOW | c.2259C>T|p.Val753Val |
S162 |
5 | BAA04g11160 | A04 | 17102669 | G | A | missense_variant | MODERATE | c.2156C>T|p.Thr719Met |
S211 |
6 | BAA04g11160 | A04 | 17103877 | G | A | missense_variant | MODERATE | c.1406C>T|p.Ser469Phe |
S183 S198 |
7 | BAA04g11160 | A04 | 17105040 | G | A | stop_gained | HIGH | c.556C>T|p.Gln186* |
S79 S91 |
8 | BAA04g11160 | A04 | 17105179 | G | A | synonymous_variant | LOW | c.417C>T|p.Ile139Ile |
S208 S219 |
9 | BAA04g11160 | A04 | 17105499 | G | A | missense_variant | MODERATE | c.226C>T|p.Pro76Ser |
S223 |
10 | BAA04g11160 | A04 | 17105624 | C | T | missense_variant | MODERATE | c.101G>A|p.Gly34Glu |
S32 |
11 | BAA04g11160 | A04 | 17105646 | C | T | missense_variant | MODERATE | c.79G>A|p.Ala27Thr |
S224 |
12 | BAA04g11160 | A04 | 17106242 | G | A | upstream_gene_variant | MODIFIER | c.-518C>T| |
S130 |
13 | BAA04g11160 | A04 | 17106372 | G | A | upstream_gene_variant | MODIFIER | c.-648C>T| |
S295 |
14 | BAA04g11160 | A04 | 17106544 | G | A | upstream_gene_variant | MODIFIER | c.-820C>T| |
S151 |
15 | BAA04g11160 | A04 | 17107003 | C | T | upstream_gene_variant | MODIFIER | c.-1279G>A| |
S114 |
16 | BAA04g11160 | A04 | 17107073 | G | A | upstream_gene_variant | MODIFIER | c.-1349C>T| |
S256 |
17 | BAA04g11160 | A04 | 17110412 | G | A | upstream_gene_variant | MODIFIER | c.-4688C>T| |
S262 |
18 | BAA04g11160 | A04 | 17110445 | C | T | upstream_gene_variant | MODIFIER | c.-4721G>A| |
S156 |