Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g23250 | A01 | 11897405 | C | T | upstream_gene_variant | MODIFIER | c.-4301C>T| |
S166 |
2 | BAA01g23250 | A01 | 11897728 | C | T | upstream_gene_variant | MODIFIER | c.-3978C>T| |
S200 |
3 | BAA01g23250 | A01 | 11898611 | G | A | upstream_gene_variant | MODIFIER | c.-3095G>A| |
S292 |
4 | BAA01g23250 | A01 | 11902252 | G | A | synonymous_variant | LOW | c.264G>A|p.Lys88Lys |
S274 |
5 | BAA01g23250 | A01 | 11902999 | C | T | missense_variant | MODERATE | c.724C>T|p.Pro242Ser |
S256 |
6 | BAA01g23250 | A01 | 11904594 | A | G | missense_variant | MODERATE | c.1382A>G|p.Asp461Gly |
S113 S115 S121 S122 S23 S266 S297 S55 S9 |
7 | BAA01g23250 | A01 | 11904787 | C | T | synonymous_variant | LOW | c.1458C>T|p.Leu486Leu |
S39 |
8 | BAA01g23250 | A01 | 11904822 | C | T | missense_variant | MODERATE | c.1493C>T|p.Pro498Leu |
S295 |