Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g34460 | A05 | 35663097 | G | A | missense_variant | MODERATE | c.3749C>T|p.Ser1250Phe |
S212 |
2 | BAA05g34460 | A05 | 35663228 | G | A | synonymous_variant | LOW | c.3618C>T|p.Phe1206Phe |
S199 |
3 | BAA05g34460 | A05 | 35664870 | C | T | missense_variant | MODERATE | c.3221G>A|p.Arg1074Lys |
S142 |
4 | BAA05g34460 | A05 | 35665141 | C | T | missense_variant | MODERATE | c.2950G>A|p.Ala984Thr |
S100 |
5 | BAA05g34460 | A05 | 35665685 | C | T | stop_gained | HIGH | c.2406G>A|p.Trp802* |
S297 |
6 | BAA05g34460 | A05 | 35666714 | G | A | synonymous_variant | LOW | c.1569C>T|p.Arg523Arg |
S245 |
7 | BAA05g34460 | A05 | 35666918 | G | A | missense_variant | MODERATE | c.1432C>T|p.Pro478Ser |
S124 |
8 | BAA05g34460 | A05 | 35667584 | C | T | missense_variant | MODERATE | c.766G>A|p.Ala256Thr |
S169 |
9 | BAA05g34460 | A05 | 35667856 | C | T | missense_variant | MODERATE | c.494G>A|p.Gly165Glu |
S297 |
10 | BAA05g34460 | A05 | 35667958 | G | A | missense_variant | MODERATE | c.392C>T|p.Thr131Met |
S107 |
11 | BAA05g34460 | A05 | 35669980 | G | A | upstream_gene_variant | MODIFIER | c.-1631C>T| |
S25 |
12 | BAA05g34460 | A05 | 35671973 | C | T | upstream_gene_variant | MODIFIER | c.-3624G>A| |
S294 |
13 | BAA05g34460 | A05 | 35672894 | C | T | upstream_gene_variant | MODIFIER | c.-4545G>A| |
S53 |