Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g39700 | A06 | 25869434 | G | A | synonymous_variant | LOW | c.858G>A|p.Lys286Lys |
S292 |
2 | BAA06g39700 | A06 | 25869861 | G | T | missense_variant | MODERATE | c.1285G>T|p.Ala429Ser |
S196 |
3 | BAA06g39700 | A06 | 25869877 | C | T | missense_variant | MODERATE | c.1301C>T|p.Ser434Phe |
S167 |
4 | BAA06g39700 | A06 | 25870077 | C | T | missense_variant | MODERATE | c.1501C>T|p.Pro501Ser |
S128 |
5 | BAA06g39700 | A06 | 25870294 | G | A | missense_variant | MODERATE | c.1718G>A|p.Arg573Lys |
S175 |
6 | BAA06g39700 | A06 | 25870777 | C | T | missense_variant | MODERATE | c.2201C>T|p.Thr734Met |
S176 |
7 | BAA06g39700 | A06 | 25871376 | G | A | missense_variant | MODERATE | c.2800G>A|p.Ala934Thr |
S19 |
8 | BAA06g39700 | A06 | 25871750 | G | A | intron_variant | MODIFIER | c.3122+52G>A| |
S131 |