Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g10210 | A05 | 5184446 | G | A | missense_variant | MODERATE | c.2174C>T|p.Ala725Val |
S306 S308 |
2 | BAA05g10210 | A05 | 5184519 | C | T | missense_variant | MODERATE | c.2101G>A|p.Glu701Lys |
S292 |
3 | BAA05g10210 | A05 | 5185484 | C | T | missense_variant | MODERATE | c.1580G>A|p.Gly527Asp |
S256 |
4 | BAA05g10210 | A05 | 5188269 | G | A | missense_variant | MODERATE | c.821C>T|p.Ala274Val |
S238 |
5 | BAA05g10210 | A05 | 5188388 | C | T | synonymous_variant | LOW | c.702G>A|p.Glu234Glu |
S100 |
6 | BAA05g10210 | A05 | 5188402 | G | A | missense_variant | MODERATE | c.688C>T|p.Pro230Ser |
S111 |
7 | BAA05g10210 | A05 | 5188643 | G | A | synonymous_variant | LOW | c.447C>T|p.Phe149Phe |
S296 |
8 | BAA05g10210 | A05 | 5188879 | G | A | missense_variant | MODERATE | c.211C>T|p.Pro71Ser |
S85 |
9 | BAA05g10210 | A05 | 5188915 | G | A | synonymous_variant | LOW | c.175C>T|p.Leu59Leu |
S41 |
10 | BAA05g10210 | A05 | 5189600 | G | A | upstream_gene_variant | MODIFIER | c.-511C>T| |
S283 |
11 | BAA05g10210 | A05 | 5189783 | G | A | upstream_gene_variant | MODIFIER | c.-694C>T| |
S85 |
12 | BAA05g10210 | A05 | 5190407 | G | A | upstream_gene_variant | MODIFIER | c.-1318C>T| |
S134 |
13 | BAA05g10210 | A05 | 5190838 | C | T | upstream_gene_variant | MODIFIER | c.-1749G>A| |
S19 |
14 | BAA05g10210 | A05 | 5190840 | G | A | upstream_gene_variant | MODIFIER | c.-1751C>T| |
S274 |
15 | BAA05g10210 | A05 | 5190859 | C | T | upstream_gene_variant | MODIFIER | c.-1770G>A| |
S50 |
16 | BAA05g10210 | A05 | 5190912 | G | A | upstream_gene_variant | MODIFIER | c.-1823C>T| |
S126 S192 |
17 | BAA05g10210 | A05 | 5190960 | G | A | upstream_gene_variant | MODIFIER | c.-1871C>T| |
S150 |
18 | BAA05g10210 | A05 | 5192042 | C | T | upstream_gene_variant | MODIFIER | c.-2953G>A| |
S243 |