Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g03920 | A02 | 1713737 | G | A | synonymous_variant | LOW | c.1140C>T|p.Phe380Phe |
S295 |
2 | BAA02g03920 | A02 | 1713741 | G | A | missense_variant | MODERATE | c.1136C>T|p.Ser379Phe |
S35 |
3 | BAA02g03920 | A02 | 1713956 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.922-1G>A| |
S289 S290 |
4 | BAA02g03920 | A02 | 1714377 | C | T | missense_variant | MODERATE | c.694G>A|p.Gly232Arg |
S130 |
5 | BAA02g03920 | A02 | 1714398 | G | A | missense_variant | MODERATE | c.673C>T|p.Pro225Ser |
S279 |
6 | BAA02g03920 | A02 | 1714512 | C | T | missense_variant | MODERATE | c.638G>A|p.Gly213Glu |
S221 |
7 | BAA02g03920 | A02 | 1714924 | C | T | missense_variant | MODERATE | c.226G>A|p.Asp76Asn |
S193 |
8 | BAA02g03920 | A02 | 1719092 | G | A | upstream_gene_variant | MODIFIER | c.-3943C>T| |
S171 |
9 | BAA02g03920 | A02 | 1719583 | G | A | upstream_gene_variant | MODIFIER | c.-4434C>T| |
S143 |