Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17560 | A02 | 8756222 | G | A | upstream_gene_variant | MODIFIER | c.-747G>A| |
S187 |
2 | BAA02g17560 | A02 | 8756364 | C | T | upstream_gene_variant | MODIFIER | c.-605C>T| |
S75 S81 |
3 | BAA02g17560 | A02 | 8756465 | C | T | upstream_gene_variant | MODIFIER | c.-504C>T| |
S131 |
4 | BAA02g17560 | A02 | 8756480 | G | A | upstream_gene_variant | MODIFIER | c.-489G>A| |
S297 |
5 | BAA02g17560 | A02 | 8756703 | C | T | upstream_gene_variant | MODIFIER | c.-266C>T| |
S216 |
6 | BAA02g17560 | A02 | 8756725 | C | T | upstream_gene_variant | MODIFIER | c.-244C>T| |
S16 |
7 | BAA02g17560 | A02 | 8756757 | G | A | upstream_gene_variant | MODIFIER | c.-212G>A| |
S259 |
8 | BAA02g17560 | A02 | 8757481 | C | T | missense_variant | MODERATE | c.175C>T|p.Pro59Ser |
S160 |
9 | BAA02g17560 | A02 | 8758300 | C | T | missense_variant | MODERATE | c.899C>T|p.Ala300Val |
S107 |
10 | BAA02g17560 | A02 | 8758655 | G | A | synonymous_variant | LOW | c.1254G>A|p.Glu418Glu |
S197 |
11 | BAA02g17560 | A02 | 8759235 | G | A | missense_variant | MODERATE | c.1834G>A|p.Glu612Lys |
S303 |
12 | BAA02g17560 | A02 | 8759898 | G | A | missense_variant | MODERATE | c.2497G>A|p.Glu833Lys |
S247 |
13 | BAA02g17560 | A02 | 8760696 | G | A | missense_variant | MODERATE | c.3295G>A|p.Asp1099Asn |
S279 |
14 | BAA02g17560 | A02 | 8760820 | G | A | missense_variant | MODERATE | c.3419G>A|p.Ser1140Asn |
S4 |
15 | BAA02g17560 | A02 | 8761061 | G | A | synonymous_variant | LOW | c.3660G>A|p.Lys1220Lys |
S217 S248 |