Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g09640 | A08 | 8763332 | G | A | missense_variant | MODERATE | c.1724C>T|p.Ser575Phe |
S19 S25 |
2 | BAA08g09640 | A08 | 8764580 | C | T | splice_region_variant&intron_variant | LOW | c.1087-7G>A| |
S123 |
3 | BAA08g09640 | A08 | 8764799 | C | T | splice_region_variant&synonymous_variant | LOW | c.990G>A|p.Lys330Lys |
S226 |
4 | BAA08g09640 | A08 | 8765754 | C | T | missense_variant | MODERATE | c.355G>A|p.Gly119Arg |
S113 |
5 | BAA08g09640 | A08 | 8766200 | G | A | missense_variant | MODERATE | c.89C>T|p.Ser30Phe |
S61 |
6 | BAA08g09640 | A08 | 8767107 | C | T | upstream_gene_variant | MODIFIER | c.-819G>A| |
S301 S304 |
7 | BAA08g09640 | A08 | 8768301 | G | A | upstream_gene_variant | MODIFIER | c.-2013C>T| |
S274 |
8 | BAA08g09640 | A08 | 8768331 | C | T | upstream_gene_variant | MODIFIER | c.-2043G>A| |
S261 |