Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g02590 | A08 | 1820785 | C | T | missense_variant | MODERATE | c.1966G>A|p.Glu656Lys |
S243 S299 |
2 | BAA08g02590 | A08 | 1821038 | C | G | synonymous_variant | LOW | c.1713G>C|p.Val571Val |
S153 |
3 | BAA08g02590 | A08 | 1821471 | G | A | missense_variant | MODERATE | c.1345C>T|p.Leu449Phe |
S188 |
4 | BAA08g02590 | A08 | 1822131 | G | A | stop_gained | HIGH | c.685C>T|p.Gln229* |
S259 |
5 | BAA08g02590 | A08 | 1822182 | C | T | missense_variant | MODERATE | c.634G>A|p.Gly212Arg |
S134 |
6 | BAA08g02590 | A08 | 1822837 | G | A | missense_variant | MODERATE | c.56C>T|p.Ser19Phe |
S115 |
7 | BAA08g02590 | A08 | 1827347 | G | A | upstream_gene_variant | MODIFIER | c.-4455C>T| |
S188 |