Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g41920 | A01 | 27880516 | G | A | downstream_gene_variant | MODIFIER | c.*3049C>T| |
S225 S73 |
2 | BAA01g41920 | A01 | 27880708 | G | A | downstream_gene_variant | MODIFIER | c.*2857C>T| |
S176 |
3 | BAA01g41920 | A01 | 27880728 | G | A | downstream_gene_variant | MODIFIER | c.*2837C>T| |
S244 |
4 | BAA01g41920 | A01 | 27880845 | G | A | downstream_gene_variant | MODIFIER | c.*2720C>T| |
S225 |
5 | BAA01g41920 | A01 | 27881105 | G | A | downstream_gene_variant | MODIFIER | c.*2460C>T| |
S268 |
6 | BAA01g41920 | A01 | 27881590 | C | T | downstream_gene_variant | MODIFIER | c.*1975G>A| |
S40 S49 |
7 | BAA01g41920 | A01 | 27883901 | G | A | synonymous_variant | LOW | c.2454C>T|p.Phe818Phe |
S140 S219 S279 S72 |
8 | BAA01g41920 | A01 | 27884074 | G | A | synonymous_variant | LOW | c.2281C>T|p.Leu761Leu |
S268 |
9 | BAA01g41920 | A01 | 27884185 | C | T | missense_variant | MODERATE | c.2170G>A|p.Val724Met |
S288 |
10 | BAA01g41920 | A01 | 27884284 | C | T | missense_variant | MODERATE | c.2071G>A|p.Asp691Asn |
S59 |
11 | BAA01g41920 | A01 | 27885155 | C | T | synonymous_variant | LOW | c.1200G>A|p.Lys400Lys |
S183 |
12 | BAA01g41920 | A01 | 27886276 | C | T | missense_variant | MODERATE | c.79G>A|p.Asp27Asn |
S54 |
13 | BAA01g41920 | A01 | 27888573 | G | A | upstream_gene_variant | MODIFIER | c.-2219C>T| |
S175 |
14 | BAA01g41920 | A01 | 27890882 | G | A | upstream_gene_variant | MODIFIER | c.-4528C>T| |
S173 |
15 | BAA01g41920 | A01 | 27891060 | C | T | upstream_gene_variant | MODIFIER | c.-4706G>A| |
S47 |
16 | BAA01g41920 | A01 | 27891344 | C | T | upstream_gene_variant | MODIFIER | c.-4990G>A| |
S206 S26 |