Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g41670 | A02 | 34907612 | C | T | missense_variant | MODERATE | c.1105G>A|p.Val369Ile |
S302 S42 |
2 | BAA02g41670 | A02 | 34907642 | G | A | missense_variant | MODERATE | c.1075C>T|p.Arg359Trp |
S199 |
3 | BAA02g41670 | A02 | 34907883 | G | A | synonymous_variant | LOW | c.834C>T|p.Phe278Phe |
S177 |
4 | BAA02g41670 | A02 | 34908607 | G | A | stop_gained | HIGH | c.187C>T|p.Arg63* |
S251 |
5 | BAA02g41670 | A02 | 34908706 | C | T | missense_variant | MODERATE | c.88G>A|p.Ala30Thr |
S261 |
6 | BAA02g41670 | A02 | 34909415 | G | A | upstream_gene_variant | MODIFIER | c.-622C>T| |
S200 |
7 | BAA02g41670 | A02 | 34910015 | G | A | upstream_gene_variant | MODIFIER | c.-1222C>T| |
S13 |
8 | BAA02g41670 | A02 | 34910768 | G | A | upstream_gene_variant | MODIFIER | c.-1975C>T| |
S251 |
9 | BAA02g41670 | A02 | 34910847 | G | A | upstream_gene_variant | MODIFIER | c.-2054C>T| |
S188 |
10 | BAA02g41670 | A02 | 34911270 | G | A | upstream_gene_variant | MODIFIER | c.-2477C>T| |
S268 |
11 | BAA02g41670 | A02 | 34911343 | C | T | upstream_gene_variant | MODIFIER | c.-2550G>A| |
S139 |
12 | BAA02g41670 | A02 | 34911347 | G | A | upstream_gene_variant | MODIFIER | c.-2554C>T| |
S269 |
13 | BAA02g41670 | A02 | 34912018 | G | A | upstream_gene_variant | MODIFIER | c.-3225C>T| |
S265 |
14 | BAA02g41670 | A02 | 34912589 | T | G | upstream_gene_variant | MODIFIER | c.-3796A>C| |
S220 |
15 | BAA02g41670 | A02 | 34912977 | C | T | upstream_gene_variant | MODIFIER | c.-4184G>A| |
S206 S26 |