Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01640 | A02 | 731500 | G | A | missense_variant | MODERATE | c.1550C>T|p.Ser517Phe |
S235 |
2 | BAA02g01640 | A02 | 732820 | C | T | missense_variant | MODERATE | c.230G>A|p.Arg77His |
S6 S70 |
3 | BAA02g01640 | A02 | 732931 | C | T | intron_variant | MODIFIER | c.221-102G>A| |
S181 |
4 | BAA02g01640 | A02 | 733032 | C | T | intron_variant | MODIFIER | c.220+148G>A| |
S46 |
5 | BAA02g01640 | A02 | 733350 | G | A | intron_variant | MODIFIER | c.128-78C>T| |
S174 |
6 | BAA02g01640 | A02 | 733911 | C | T | intron_variant | MODIFIER | c.127+427G>A| |
S292 |
7 | BAA02g01640 | A02 | 734005 | C | T | intron_variant | MODIFIER | c.127+333G>A| |
S200 |
8 | BAA02g01640 | A02 | 734514 | G | A | upstream_gene_variant | MODIFIER | c.-50C>T| |
S197 |
9 | BAA02g01640 | A02 | 735173 | C | T | upstream_gene_variant | MODIFIER | c.-709G>A| |
S255 |
10 | BAA02g01640 | A02 | 736923 | C | T | upstream_gene_variant | MODIFIER | c.-2459G>A| |
S183 S198 |