Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g21530 | A08 | 16293841 | G | A | upstream_gene_variant | MODIFIER | c.-129G>A| |
S286 |
2 | BAA08g21530 | A08 | 16294288 | C | T | missense_variant | MODERATE | c.241C>T|p.Leu81Phe |
S28 |
3 | BAA08g21530 | A08 | 16294310 | G | A | missense_variant | MODERATE | c.263G>A|p.Arg88His |
S165 |
4 | BAA08g21530 | A08 | 16296002 | G | A | missense_variant | MODERATE | c.1100G>A|p.Gly367Glu |
S32 |
5 | BAA08g21530 | A08 | 16297044 | C | T | missense_variant | MODERATE | c.1688C>T|p.Ser563Phe |
S211 S227 |
6 | BAA08g21530 | A08 | 16297115 | G | A | missense_variant | MODERATE | c.1759G>A|p.Val587Ile |
S221 S229 |
7 | BAA08g21530 | A08 | 16297710 | C | T | synonymous_variant | LOW | c.2079C>T|p.Ile693Ile |
S36 |
8 | BAA08g21530 | A08 | 16297906 | G | A | synonymous_variant | LOW | c.2202G>A|p.Leu734Leu |
S257 |
9 | BAA08g21530 | A08 | 16299404 | G | A | missense_variant | MODERATE | c.3064G>A|p.Val1022Ile |
S266 |
10 | BAA08g21530 | A08 | 16299986 | C | T | downstream_gene_variant | MODIFIER | c.*499C>T| |
S144 |