Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g02450 | A10 | 1197182 | C | T | missense_variant | MODERATE | c.280G>A|p.Glu94Lys |
S194 |
2 | BAA10g02450 | A10 | 1197329 | C | T | splice_region_variant&intron_variant | LOW | c.267+5G>A| |
S235 |
3 | BAA10g02450 | A10 | 1197358 | C | T | synonymous_variant | LOW | c.243G>A|p.Arg81Arg |
S146 |
4 | BAA10g02450 | A10 | 1201410 | G | A | upstream_gene_variant | MODIFIER | c.-3740C>T| |
S50 |
5 | BAA10g02450 | A10 | 1201895 | C | T | upstream_gene_variant | MODIFIER | c.-4225G>A| |
S265 |
6 | BAA10g02450 | A10 | 1202319 | G | A | upstream_gene_variant | MODIFIER | c.-4649C>T| |
S209 |