Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g18830 | A05 | 10939432 | G | A | downstream_gene_variant | MODIFIER | c.*1269C>T| |
S13 |
2 | BAA05g18830 | A05 | 10939635 | C | T | downstream_gene_variant | MODIFIER | c.*1066G>A| |
S58 |
3 | BAA05g18830 | A05 | 10939745 | G | A | downstream_gene_variant | MODIFIER | c.*956C>T| |
S157 S163 |
4 | BAA05g18830 | A05 | 10939756 | C | T | downstream_gene_variant | MODIFIER | c.*945G>A| |
S81 S85 |
5 | BAA05g18830 | A05 | 10940549 | G | A | downstream_gene_variant | MODIFIER | c.*152C>T| |
S51 |
6 | BAA05g18830 | A05 | 10941631 | G | A | synonymous_variant | LOW | c.1029C>T|p.Tyr343Tyr |
S3 |
7 | BAA05g18830 | A05 | 10942695 | C | T | missense_variant | MODERATE | c.542G>A|p.Gly181Glu |
S69 |
8 | BAA05g18830 | A05 | 10943254 | C | T | missense_variant | MODERATE | c.277G>A|p.Glu93Lys |
S130 |
9 | BAA05g18830 | A05 | 10943752 | G | A | missense_variant | MODERATE | c.71C>T|p.Ser24Phe |
S292 |
10 | BAA05g18830 | A05 | 10943758 | C | T | missense_variant | MODERATE | c.65G>A|p.Arg22Lys |
S133 |
11 | BAA05g18830 | A05 | 10945090 | C | T | upstream_gene_variant | MODIFIER | c.-1268G>A| |
S118 |
12 | BAA05g18830 | A05 | 10945372 | C | T | upstream_gene_variant | MODIFIER | c.-1550G>A| |
S111 |
13 | BAA05g18830 | A05 | 10945885 | C | T | upstream_gene_variant | MODIFIER | c.-2063G>A| |
S267 |
14 | BAA05g18830 | A05 | 10946378 | C | T | upstream_gene_variant | MODIFIER | c.-2556G>A| |
S36 |
15 | BAA05g18830 | A05 | 10946536 | G | A | upstream_gene_variant | MODIFIER | c.-2714C>T| |
S178 |
16 | BAA05g18830 | A05 | 10947037 | C | T | upstream_gene_variant | MODIFIER | c.-3215G>A| |
S105 S106 |
17 | BAA05g18830 | A05 | 10947189 | G | A | upstream_gene_variant | MODIFIER | c.-3367C>T| |
S302 |
18 | BAA05g18830 | A05 | 10948277 | G | A | upstream_gene_variant | MODIFIER | c.-4455C>T| |
S185 S273 |