Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g09190 | A08 | 8403165 | G | A | missense_variant | MODERATE | c.1583C>T|p.Ser528Phe |
S203 |
2 | BAA08g09190 | A08 | 8403698 | C | T | missense_variant | MODERATE | c.1354G>A|p.Gly452Arg |
S44 |
3 | BAA08g09190 | A08 | 8403752 | C | T | missense_variant | MODERATE | c.1300G>A|p.Glu434Lys |
S170 |
4 | BAA08g09190 | A08 | 8403936 | G | A | synonymous_variant | LOW | c.1275C>T|p.Val425Val |
S275 |
5 | BAA08g09190 | A08 | 8404627 | G | A | missense_variant | MODERATE | c.898C>T|p.Pro300Ser |
S223 |
6 | BAA08g09190 | A08 | 8404978 | C | T | missense_variant | MODERATE | c.788G>A|p.Arg263Lys |
S155 |
7 | BAA08g09190 | A08 | 8405028 | C | T | intron_variant | MODIFIER | c.769-31G>A| |
S235 |
8 | BAA08g09190 | A08 | 8406057 | G | A | intron_variant | MODIFIER | c.282+136C>T| |
S53 |
9 | BAA08g09190 | A08 | 8406324 | G | A | intron_variant | MODIFIER | c.189+38C>T| |
S161 |
10 | BAA08g09190 | A08 | 8407194 | C | T | upstream_gene_variant | MODIFIER | c.-644G>A| |
S23 |
11 | BAA08g09190 | A08 | 8407832 | G | A | upstream_gene_variant | MODIFIER | c.-1282C>T| |
S192 |
12 | BAA08g09190 | A08 | 8408937 | C | T | upstream_gene_variant | MODIFIER | c.-2387G>A| |
S54 |
13 | BAA08g09190 | A08 | 8408940 | G | A | upstream_gene_variant | MODIFIER | c.-2390C>T| |
S124 |
14 | BAA08g09190 | A08 | 8409056 | C | T | upstream_gene_variant | MODIFIER | c.-2506G>A| |
S67 |
15 | BAA08g09190 | A08 | 8410717 | G | T | upstream_gene_variant | MODIFIER | c.-4167C>A| |
S267 |
16 | BAA08g09190 | A08 | 8411058 | G | A | upstream_gene_variant | MODIFIER | c.-4508C>T| |
S62 |