Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g19640 | A08 | 15419285 | G | A | upstream_gene_variant | MODIFIER | c.-91G>A| |
S221 |
2 | BAA08g19640 | A08 | 15420919 | C | T | missense_variant | MODERATE | c.1000C>T|p.Leu334Phe |
S60 |
3 | BAA08g19640 | A08 | 15421003 | C | T | missense_variant | MODERATE | c.1084C>T|p.Leu362Phe |
S186 |
4 | BAA08g19640 | A08 | 15421167 | G | A | synonymous_variant | LOW | c.1248G>A|p.Thr416Thr |
S96 |
5 | BAA08g19640 | A08 | 15421762 | C | T | missense_variant | MODERATE | c.1843C>T|p.Leu615Phe |
S169 |
6 | BAA08g19640 | A08 | 15421842 | G | A | synonymous_variant | LOW | c.1923G>A|p.Glu641Glu |
S61 |
7 | BAA08g19640 | A08 | 15422424 | G | A | synonymous_variant | LOW | c.2505G>A|p.Glu835Glu |
S246 |
8 | BAA08g19640 | A08 | 15422893 | G | A | missense_variant | MODERATE | c.2974G>A|p.Ala992Thr |
S32 |