Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g22960 | A01 | 11690085 | C | T | upstream_gene_variant | MODIFIER | c.-899C>T| |
S198 |
2 | BAA01g22960 | A01 | 11692739 | C | T | missense_variant | MODERATE | c.451C>T|p.Leu151Phe |
S133 |
3 | BAA01g22960 | A01 | 11693046 | C | T | missense_variant | MODERATE | c.758C>T|p.Ala253Val |
S47 |
4 | BAA01g22960 | A01 | 11693186 | G | A | missense_variant | MODERATE | c.842G>A|p.Gly281Asp |
S199 |
5 | BAA01g22960 | A01 | 11693199 | C | T | synonymous_variant | LOW | c.855C>T|p.Asn285Asn |
S130 |
6 | BAA01g22960 | A01 | 11693282 | G | A | downstream_gene_variant | MODIFIER | c.*65G>A| |
S299 |
7 | BAA01g22960 | A01 | 11695988 | G | A | downstream_gene_variant | MODIFIER | c.*2771G>A| |
S193 |
8 | BAA01g22960 | A01 | 11696033 | G | A | downstream_gene_variant | MODIFIER | c.*2816G>A| |
S129 |
9 | BAA01g22960 | A01 | 11697632 | G | A | downstream_gene_variant | MODIFIER | c.*4415G>A| |
S97 |
10 | BAA01g22960 | A01 | 11697671 | G | A | downstream_gene_variant | MODIFIER | c.*4454G>A| |
S238 |
11 | BAA01g22960 | A01 | 11697825 | G | A | downstream_gene_variant | MODIFIER | c.*4608G>A| |
S255 |