Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g01490 | A08 | 1108878 | C | T | synonymous_variant | LOW | c.2568G>A|p.Arg856Arg |
S159 |
2 | BAA08g01490 | A08 | 1110598 | G | A | missense_variant | MODERATE | c.1601C>T|p.Ala534Val |
S136 |
3 | BAA08g01490 | A08 | 1110639 | C | T | synonymous_variant | LOW | c.1560G>A|p.Leu520Leu |
S94 |
4 | BAA08g01490 | A08 | 1111318 | C | T | missense_variant | MODERATE | c.881G>A|p.Cys294Tyr |
S180 |
5 | BAA08g01490 | A08 | 1111520 | C | T | missense_variant | MODERATE | c.679G>A|p.Glu227Lys |
S243 S299 |
6 | BAA08g01490 | A08 | 1111716 | C | T | synonymous_variant | LOW | c.483G>A|p.Glu161Glu |
S60 |
7 | BAA08g01490 | A08 | 1112915 | C | T | upstream_gene_variant | MODIFIER | c.-717G>A| |
S289 S290 |
8 | BAA08g01490 | A08 | 1113061 | C | T | upstream_gene_variant | MODIFIER | c.-863G>A| |
S261 |
9 | BAA08g01490 | A08 | 1113514 | C | T | upstream_gene_variant | MODIFIER | c.-1316G>A| |
S118 |
10 | BAA08g01490 | A08 | 1113795 | G | T | upstream_gene_variant | MODIFIER | c.-1597C>A| |
S235 |
11 | BAA08g01490 | A08 | 1113838 | C | T | upstream_gene_variant | MODIFIER | c.-1640G>A| |
S201 |
12 | BAA08g01490 | A08 | 1115109 | C | T | upstream_gene_variant | MODIFIER | c.-2911G>A| |
S296 |
13 | BAA08g01490 | A08 | 1115679 | C | T | upstream_gene_variant | MODIFIER | c.-3481G>A| |
S295 |
14 | BAA08g01490 | A08 | 1116770 | G | A | upstream_gene_variant | MODIFIER | c.-4572C>T| |
S182 |