Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g17080 | A04 | 21326110 | G | A | downstream_gene_variant | MODIFIER | c.*4174C>T| |
S59 |
2 | BAA04g17080 | A04 | 21331432 | C | T | intron_variant | MODIFIER | c.704-454G>A| |
S82 S92 |
3 | BAA04g17080 | A04 | 21331906 | G | A | intron_variant | MODIFIER | c.704-928C>T| |
S286 |
4 | BAA04g17080 | A04 | 21333602 | C | T | missense_variant | MODERATE | c.436G>A|p.Glu146Lys |
S113 |
5 | BAA04g17080 | A04 | 21333731 | C | T | missense_variant | MODERATE | c.307G>A|p.Val103Met |
S252 |
6 | BAA04g17080 | A04 | 21333739 | C | T | missense_variant | MODERATE | c.299G>A|p.Gly100Glu |
S140 S168 S64 |
7 | BAA04g17080 | A04 | 21333820 | G | A | missense_variant | MODERATE | c.218C>T|p.Thr73Ile |
S293 |
8 | BAA04g17080 | A04 | 21334261 | C | T | upstream_gene_variant | MODIFIER | c.-146G>A| |
S137 |
9 | BAA04g17080 | A04 | 21335423 | C | T | upstream_gene_variant | MODIFIER | c.-1308G>A| |
S247 |
10 | BAA04g17080 | A04 | 21335555 | C | T | upstream_gene_variant | MODIFIER | c.-1440G>A| |
S44 |
11 | BAA04g17080 | A04 | 21335642 | G | A | upstream_gene_variant | MODIFIER | c.-1527C>T| |
S263 |
12 | BAA04g17080 | A04 | 21335807 | C | T | upstream_gene_variant | MODIFIER | c.-1692G>A| |
S10 |
13 | BAA04g17080 | A04 | 21336607 | G | A | upstream_gene_variant | MODIFIER | c.-2492C>T| |
S104 S52 |
14 | BAA04g17080 | A04 | 21337056 | C | T | upstream_gene_variant | MODIFIER | c.-2941G>A| |
S79 |
15 | BAA04g17080 | A04 | 21337295 | C | T | upstream_gene_variant | MODIFIER | c.-3180G>A| |
S212 |