Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g46100 | A01 | 30720442 | C | T | upstream_gene_variant | MODIFIER | c.-3112C>T| |
S294 |
2 | BAA01g46100 | A01 | 30721582 | G | A | upstream_gene_variant | MODIFIER | c.-1972G>A| |
S217 |
3 | BAA01g46100 | A01 | 30722685 | C | T | upstream_gene_variant | MODIFIER | c.-869C>T| |
S35 |
4 | BAA01g46100 | A01 | 30725778 | C | T | intron_variant | MODIFIER | c.871-25C>T| |
S240 |
5 | BAA01g46100 | A01 | 30725977 | G | A | intron_variant | MODIFIER | c.976-45G>A| |
S283 |
6 | BAA01g46100 | A01 | 30727031 | G | A | missense_variant | MODERATE | c.1565G>A|p.Cys522Tyr |
S241 |
7 | BAA01g46100 | A01 | 30727730 | G | A | intron_variant | MODIFIER | c.1708-115G>A| |
S296 |
8 | BAA01g46100 | A01 | 30727854 | C | T | missense_variant | MODERATE | c.1717C>T|p.Leu573Phe |
S281 |
9 | BAA01g46100 | A01 | 30728592 | C | T | downstream_gene_variant | MODIFIER | c.*167C>T| |
S206 S26 |
10 | BAA01g46100 | A01 | 30728902 | C | T | downstream_gene_variant | MODIFIER | c.*477C>T| |
S169 |
11 | BAA01g46100 | A01 | 30729194 | G | A | downstream_gene_variant | MODIFIER | c.*769G>A| |
S189 |
12 | BAA01g46100 | A01 | 30729794 | G | A | downstream_gene_variant | MODIFIER | c.*1369G>A| |
S296 |
13 | BAA01g46100 | A01 | 30730065 | C | T | downstream_gene_variant | MODIFIER | c.*1640C>T| |
S266 |