Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g29290 | A10 | 22097829 | C | T | upstream_gene_variant | MODIFIER | c.-4691C>T| |
S130 |
2 | BAA10g29290 | A10 | 22099151 | G | A | upstream_gene_variant | MODIFIER | c.-3369G>A| |
S240 |
3 | BAA10g29290 | A10 | 22102965 | C | T | missense_variant | MODERATE | c.113C>T|p.Ser38Phe |
S104 S52 |
4 | BAA10g29290 | A10 | 22103325 | C | T | missense_variant | MODERATE | c.473C>T|p.Pro158Leu |
S247 |
5 | BAA10g29290 | A10 | 22103448 | C | T | missense_variant | MODERATE | c.596C>T|p.Ala199Val |
S221 |
6 | BAA10g29290 | A10 | 22103467 | G | A | synonymous_variant | LOW | c.615G>A|p.Leu205Leu |
S223 |
7 | BAA10g29290 | A10 | 22103570 | G | A | missense_variant | MODERATE | c.718G>A|p.Glu240Lys |
S286 |
8 | BAA10g29290 | A10 | 22103703 | G | A | stop_gained | HIGH | c.851G>A|p.Trp284* |
S219 |
9 | BAA10g29290 | A10 | 22104280 | C | T | synonymous_variant | LOW | c.1428C>T|p.Arg476Arg |
S211 |