Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g09990 | A07 | 18917350 | C | T | missense_variant | MODERATE | c.2569G>A|p.Ala857Thr |
S27 |
2 | BAA07g09990 | A07 | 18917569 | C | T | synonymous_variant | LOW | c.2424G>A|p.Gln808Gln |
S270 |
3 | BAA07g09990 | A07 | 18917981 | C | T | missense_variant | MODERATE | c.2012G>A|p.Gly671Asp |
S81 |
4 | BAA07g09990 | A07 | 18918067 | G | A | synonymous_variant | LOW | c.1926C>T|p.Leu642Leu |
S257 |
5 | BAA07g09990 | A07 | 18918105 | G | A | missense_variant | MODERATE | c.1888C>T|p.Pro630Ser |
S44 |
6 | BAA07g09990 | A07 | 18918661 | G | A | missense_variant | MODERATE | c.1451C>T|p.Thr484Met |
S295 |
7 | BAA07g09990 | A07 | 18918977 | G | A | missense_variant | MODERATE | c.1135C>T|p.Leu379Phe |
S199 |
8 | BAA07g09990 | A07 | 18919766 | G | A | missense_variant | MODERATE | c.346C>T|p.Pro116Ser |
S28 |
9 | BAA07g09990 | A07 | 18920116 | C | T | upstream_gene_variant | MODIFIER | c.-5G>A| |
S57 |
10 | BAA07g09990 | A07 | 18920345 | G | A | upstream_gene_variant | MODIFIER | c.-234C>T| |
S117 |
11 | BAA07g09990 | A07 | 18920357 | G | A | upstream_gene_variant | MODIFIER | c.-246C>T| |
S188 |
12 | BAA07g09990 | A07 | 18920452 | G | A | upstream_gene_variant | MODIFIER | c.-341C>T| |
S5 |
13 | BAA07g09990 | A07 | 18920790 | G | A | upstream_gene_variant | MODIFIER | c.-679C>T| |
S61 |
14 | BAA07g09990 | A07 | 18920981 | G | T | upstream_gene_variant | MODIFIER | c.-870C>A| |
S169 |
15 | BAA07g09990 | A07 | 18924392 | C | T | upstream_gene_variant | MODIFIER | c.-4281G>A| |
S164 |
16 | BAA07g09990 | A07 | 18924750 | C | T | upstream_gene_variant | MODIFIER | c.-4639G>A| |
S256 |
17 | BAA07g09990 | A07 | 18924799 | C | T | upstream_gene_variant | MODIFIER | c.-4688G>A| |
S9 |