Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g09090 | A09 | 5053701 | G | A | synonymous_variant | LOW | c.852C>T|p.Thr284Thr |
S65 |
2 | BAA09g09090 | A09 | 5053998 | C | T | synonymous_variant | LOW | c.555G>A|p.Gly185Gly |
S148 S210 |
3 | BAA09g09090 | A09 | 5054005 | C | T | missense_variant | MODERATE | c.548G>A|p.Gly183Asp |
S241 |
4 | BAA09g09090 | A09 | 5054059 | C | T | missense_variant | MODERATE | c.494G>A|p.Gly165Glu |
S249 |
5 | BAA09g09090 | A09 | 5054228 | C | T | missense_variant | MODERATE | c.325G>A|p.Glu109Lys |
S109 |
6 | BAA09g09090 | A09 | 5054273 | C | T | missense_variant | MODERATE | c.280G>A|p.Glu94Lys |
S174 S27 |
7 | BAA09g09090 | A09 | 5054283 | G | A | synonymous_variant | LOW | c.270C>T|p.Phe90Phe |
S20 |
8 | BAA09g09090 | A09 | 5056400 | G | A | upstream_gene_variant | MODIFIER | c.-1848C>T| |
S288 |
9 | BAA09g09090 | A09 | 5058426 | A | G | upstream_gene_variant | MODIFIER | c.-3874T>C| |
S296 |