Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g01700 | A01 | 757943 | C | T | downstream_gene_variant | MODIFIER | c.*1661G>A| |
S171 |
2 | BAA01g01700 | A01 | 758071 | C | T | downstream_gene_variant | MODIFIER | c.*1533G>A| |
S38 |
3 | BAA01g01700 | A01 | 759749 | G | A | missense_variant | MODERATE | c.1619C>T|p.Ala540Val |
S209 |
4 | BAA01g01700 | A01 | 759776 | C | T | missense_variant | MODERATE | c.1592G>A|p.Gly531Asp |
S18 |
5 | BAA01g01700 | A01 | 760459 | C | T | synonymous_variant | LOW | c.909G>A|p.Lys303Lys |
S208 S219 |
6 | BAA01g01700 | A01 | 761267 | C | T | intron_variant | MODIFIER | c.312-97G>A| |
S152 |
7 | BAA01g01700 | A01 | 761433 | G | A | missense_variant | MODERATE | c.265C>T|p.Arg89Cys |
S303 |
8 | BAA01g01700 | A01 | 762783 | G | A | upstream_gene_variant | MODIFIER | c.-1086C>T| |
S73 S91 |
9 | BAA01g01700 | A01 | 765611 | G | A | upstream_gene_variant | MODIFIER | c.-3914C>T| |
S177 |