Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g16980 | A02 | 8418950 | C | T | downstream_gene_variant | MODIFIER | c.*1830G>A| |
S6 |
2 | BAA02g16980 | A02 | 8419056 | C | T | downstream_gene_variant | MODIFIER | c.*1724G>A| |
S233 |
3 | BAA02g16980 | A02 | 8419652 | G | A | downstream_gene_variant | MODIFIER | c.*1128C>T| |
S238 |
4 | BAA02g16980 | A02 | 8419671 | G | A | downstream_gene_variant | MODIFIER | c.*1109C>T| |
S256 |
5 | BAA02g16980 | A02 | 8420124 | A | T | downstream_gene_variant | MODIFIER | c.*656T>A| |
S153 S213 |
6 | BAA02g16980 | A02 | 8420369 | C | T | downstream_gene_variant | MODIFIER | c.*411G>A| |
S175 |
7 | BAA02g16980 | A02 | 8421537 | G | A | intron_variant | MODIFIER | c.774+41C>T| |
S279 |
8 | BAA02g16980 | A02 | 8421612 | C | T | missense_variant | MODERATE | c.740G>A|p.Cys247Tyr |
S39 |
9 | BAA02g16980 | A02 | 8422319 | C | T | missense_variant | MODERATE | c.388G>A|p.Glu130Lys |
S111 |
10 | BAA02g16980 | A02 | 8422461 | G | A | intron_variant | MODIFIER | c.277-31C>T| |
S259 |
11 | BAA02g16980 | A02 | 8422567 | G | A | missense_variant | MODERATE | c.220C>T|p.Pro74Ser |
S290 |
12 | BAA02g16980 | A02 | 8423022 | G | A | upstream_gene_variant | MODIFIER | c.-236C>T| |
S99 |
13 | BAA02g16980 | A02 | 8424072 | G | A | upstream_gene_variant | MODIFIER | c.-1286C>T| |
S294 |
14 | BAA02g16980 | A02 | 8425292 | C | T | upstream_gene_variant | MODIFIER | c.-2506G>A| |
S13 |
15 | BAA02g16980 | A02 | 8426349 | C | T | upstream_gene_variant | MODIFIER | c.-3563G>A| |
S264 |