Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g38880 | A05 | 38067370 | C | T | missense_variant | MODERATE | c.1732G>A|p.Val578Ile |
S173 |
2 | BAA05g38880 | A05 | 38068824 | C | T | splice_region_variant&intron_variant | LOW | c.843+5G>A| |
S67 |
3 | BAA05g38880 | A05 | 38069809 | C | T | synonymous_variant | LOW | c.288G>A|p.Gly96Gly |
S71 |
4 | BAA05g38880 | A05 | 38070022 | C | T | missense_variant | MODERATE | c.152G>A|p.Arg51Gln |
S89 |
5 | BAA05g38880 | A05 | 38070147 | C | T | missense_variant | MODERATE | c.92G>A|p.Gly31Glu |
S216 |
6 | BAA05g38880 | A05 | 38070152 | G | A | synonymous_variant | LOW | c.87C>T|p.Ile29Ile |
S208 S219 |
7 | BAA05g38880 | A05 | 38070841 | G | A | upstream_gene_variant | MODIFIER | c.-525C>T| |
S259 |
8 | BAA05g38880 | A05 | 38072320 | C | T | upstream_gene_variant | MODIFIER | c.-2004G>A| |
S169 |