Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g15150 | A04 | 20017284 | C | T | upstream_gene_variant | MODIFIER | c.-4541C>T| |
S139 |
2 | BAA04g15150 | A04 | 20017324 | C | T | upstream_gene_variant | MODIFIER | c.-4501C>T| |
S167 |
3 | BAA04g15150 | A04 | 20017370 | G | A | upstream_gene_variant | MODIFIER | c.-4455G>A| |
S175 |
4 | BAA04g15150 | A04 | 20020848 | G | A | upstream_gene_variant | MODIFIER | c.-977G>A| |
S237 |
5 | BAA04g15150 | A04 | 20021296 | G | A | upstream_gene_variant | MODIFIER | c.-529G>A| |
S273 |
6 | BAA04g15150 | A04 | 20021397 | G | A | upstream_gene_variant | MODIFIER | c.-428G>A| |
S50 |
7 | BAA04g15150 | A04 | 20022110 | C | T | missense_variant | MODERATE | c.286C>T|p.Pro96Ser |
S267 |
8 | BAA04g15150 | A04 | 20022624 | G | A | missense_variant | MODERATE | c.800G>A|p.Arg267Gln |
S56 |
9 | BAA04g15150 | A04 | 20023062 | G | A | missense_variant | MODERATE | c.1238G>A|p.Arg413Lys |
S237 |
10 | BAA04g15150 | A04 | 20023857 | G | A | downstream_gene_variant | MODIFIER | c.*635G>A| |
S293 |
11 | BAA04g15150 | A04 | 20023952 | C | T | downstream_gene_variant | MODIFIER | c.*730C>T| |
S54 |
12 | BAA04g15150 | A04 | 20024830 | C | T | downstream_gene_variant | MODIFIER | c.*1608C>T| |
S28 |
13 | BAA04g15150 | A04 | 20025026 | G | A | downstream_gene_variant | MODIFIER | c.*1804G>A| |
S1 S228 S244 S90 |
14 | BAA04g15150 | A04 | 20025622 | C | T | downstream_gene_variant | MODIFIER | c.*2400C>T| |
S267 |
15 | BAA04g15150 | A04 | 20025826 | C | T | downstream_gene_variant | MODIFIER | c.*2604C>T| |
S243 S299 |
16 | BAA04g15150 | A04 | 20026324 | C | T | downstream_gene_variant | MODIFIER | c.*3102C>T| |
S32 |
17 | BAA04g15150 | A04 | 20026363 | C | T | downstream_gene_variant | MODIFIER | c.*3141C>T| |
S189 |