Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g11200 | A10 | 12831728 | C | T | synonymous_variant | LOW | c.966G>A|p.Ala322Ala |
S162 |
2 | BAA10g11200 | A10 | 12831924 | C | T | missense_variant | MODERATE | c.770G>A|p.Arg257His |
S152 |
3 | BAA10g11200 | A10 | 12831963 | G | A | missense_variant | MODERATE | c.731C>T|p.Thr244Met |
S207 |
4 | BAA10g11200 | A10 | 12832325 | G | A | synonymous_variant | LOW | c.369C>T|p.Arg123Arg |
S181 |
5 | BAA10g11200 | A10 | 12832412 | C | T | synonymous_variant | LOW | c.282G>A|p.Arg94Arg |
S271 |
6 | BAA10g11200 | A10 | 12835976 | C | T | upstream_gene_variant | MODIFIER | c.-3283G>A| |
S190 |
7 | BAA10g11200 | A10 | 12835991 | G | A | upstream_gene_variant | MODIFIER | c.-3298C>T| |
S18 |
8 | BAA10g11200 | A10 | 12836575 | C | T | upstream_gene_variant | MODIFIER | c.-3882G>A| |
S10 |
9 | BAA10g11200 | A10 | 12836893 | G | A | upstream_gene_variant | MODIFIER | c.-4200C>T| |
S284 |