Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g11790 | A01 | 5489569 | C | T | downstream_gene_variant | MODIFIER | c.*561G>A| |
S46 |
2 | BAA01g11790 | A01 | 5489873 | C | T | downstream_gene_variant | MODIFIER | c.*257G>A| |
S2 |
3 | BAA01g11790 | A01 | 5490461 | C | T | synonymous_variant | LOW | c.930G>A|p.Gln310Gln |
S17 S19 |
4 | BAA01g11790 | A01 | 5490473 | C | T | splice_region_variant&synonymous_variant | LOW | c.918G>A|p.Gly306Gly |
S148 S210 S30 S31 |
5 | BAA01g11790 | A01 | 5490496 | C | T | intron_variant | MODIFIER | c.917-22G>A| |
S204 |
6 | BAA01g11790 | A01 | 5490577 | G | A | intron_variant | MODIFIER | c.917-103C>T| |
S45 |
7 | BAA01g11790 | A01 | 5491228 | G | A | missense_variant | MODERATE | c.698C>T|p.Pro233Leu |
S257 |
8 | BAA01g11790 | A01 | 5492203 | G | A | missense_variant | MODERATE | c.290C>T|p.Ser97Phe |
S32 |
9 | BAA01g11790 | A01 | 5492867 | G | A | missense_variant | MODERATE | c.74C>T|p.Pro25Leu |
S54 |
10 | BAA01g11790 | A01 | 5492883 | C | T | missense_variant | MODERATE | c.58G>A|p.Gly20Arg |
S46 |
11 | BAA01g11790 | A01 | 5494706 | G | A | upstream_gene_variant | MODIFIER | c.-1766C>T| |
S114 |
12 | BAA01g11790 | A01 | 5495678 | G | A | upstream_gene_variant | MODIFIER | c.-2738C>T| |
S127 |
13 | BAA01g11790 | A01 | 5496032 | C | T | upstream_gene_variant | MODIFIER | c.-3092G>A| |
S36 |