Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g21890 | A02 | 11788536 | G | A | downstream_gene_variant | MODIFIER | c.*4750C>T| |
S197 |
2 | BAA02g21890 | A02 | 11788589 | G | A | downstream_gene_variant | MODIFIER | c.*4697C>T| |
S19 |
3 | BAA02g21890 | A02 | 11792120 | G | A | downstream_gene_variant | MODIFIER | c.*1166C>T| |
S37 |
4 | BAA02g21890 | A02 | 11792210 | C | T | downstream_gene_variant | MODIFIER | c.*1076G>A| |
S221 |
5 | BAA02g21890 | A02 | 11792528 | G | A | downstream_gene_variant | MODIFIER | c.*758C>T| |
S235 |
6 | BAA02g21890 | A02 | 11792533 | C | T | downstream_gene_variant | MODIFIER | c.*753G>A| |
S178 |
7 | BAA02g21890 | A02 | 11792546 | C | T | downstream_gene_variant | MODIFIER | c.*740G>A| |
S107 |
8 | BAA02g21890 | A02 | 11792933 | G | A | downstream_gene_variant | MODIFIER | c.*353C>T| |
S48 |
9 | BAA02g21890 | A02 | 11793825 | C | T | missense_variant | MODERATE | c.1006G>A|p.Gly336Arg |
S252 |
10 | BAA02g21890 | A02 | 11793830 | C | T | missense_variant | MODERATE | c.1001G>A|p.Ser334Asn |
S201 |
11 | BAA02g21890 | A02 | 11793858 | C | T | missense_variant | MODERATE | c.973G>A|p.Ala325Thr |
S138 |
12 | BAA02g21890 | A02 | 11794006 | C | T | synonymous_variant | LOW | c.825G>A|p.Gly275Gly |
S240 |
13 | BAA02g21890 | A02 | 11794637 | C | T | missense_variant | MODERATE | c.194G>A|p.Gly65Glu |
S49 |
14 | BAA02g21890 | A02 | 11795070 | G | A | upstream_gene_variant | MODIFIER | c.-240C>T| |
S173 |
15 | BAA02g21890 | A02 | 11795084 | C | T | upstream_gene_variant | MODIFIER | c.-254G>A| |
S51 |
16 | BAA02g21890 | A02 | 11795656 | G | A | upstream_gene_variant | MODIFIER | c.-826C>T| |
S103 |
17 | BAA02g21890 | A02 | 11795663 | C | T | upstream_gene_variant | MODIFIER | c.-833G>A| |
S1 S90 |
18 | BAA02g21890 | A02 | 11796812 | G | A | upstream_gene_variant | MODIFIER | c.-1982C>T| |
S69 |
19 | BAA02g21890 | A02 | 11799043 | G | A | upstream_gene_variant | MODIFIER | c.-4213C>T| |
S148 S30 S31 |
20 | BAA02g21890 | A02 | 11799084 | C | T | upstream_gene_variant | MODIFIER | c.-4254G>A| |
S117 |
21 | BAA02g21890 | A02 | 11799583 | G | A | upstream_gene_variant | MODIFIER | c.-4753C>T| |
S274 |