Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g64530 | A09 | 59867462 | G | A | synonymous_variant | LOW | c.1437C>T|p.Ile479Ile |
S71 |
2 | BAA09g64530 | A09 | 59867727 | C | T | missense_variant | MODERATE | c.1172G>A|p.Gly391Asp |
S62 |
3 | BAA09g64530 | A09 | 59867926 | G | A | missense_variant | MODERATE | c.973C>T|p.Leu325Phe |
S274 |
4 | BAA09g64530 | A09 | 59868103 | C | T | missense_variant | MODERATE | c.796G>A|p.Glu266Lys |
S153 S213 |
5 | BAA09g64530 | A09 | 59868468 | G | A | missense_variant | MODERATE | c.431C>T|p.Thr144Met |
S262 |
6 | BAA09g64530 | A09 | 59869958 | C | T | upstream_gene_variant | MODIFIER | c.-1060G>A| |
S163 |
7 | BAA09g64530 | A09 | 59870008 | C | T | upstream_gene_variant | MODIFIER | c.-1110G>A| |
S136 |
8 | BAA09g64530 | A09 | 59871444 | C | T | upstream_gene_variant | MODIFIER | c.-2546G>A| |
S242 |
9 | BAA09g64530 | A09 | 59871579 | G | A | upstream_gene_variant | MODIFIER | c.-2681C>T| |
S111 |
10 | BAA09g64530 | A09 | 59872922 | C | T | upstream_gene_variant | MODIFIER | c.-4024G>A| |
S219 S72 |