Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g21400 | A08 | 16227421 | G | A | upstream_gene_variant | MODIFIER | c.-2751G>A| |
S130 S69 |
2 | BAA08g21400 | A08 | 16227863 | G | A | upstream_gene_variant | MODIFIER | c.-2309G>A| |
S100 |
3 | BAA08g21400 | A08 | 16230277 | C | T | synonymous_variant | LOW | c.106C>T|p.Leu36Leu |
S135 |
4 | BAA08g21400 | A08 | 16231822 | G | A | synonymous_variant | LOW | c.528G>A|p.Lys176Lys |
S305 |
5 | BAA08g21400 | A08 | 16231904 | C | T | missense_variant | MODERATE | c.610C>T|p.Pro204Ser |
S13 S168 S219 S72 |
6 | BAA08g21400 | A08 | 16233162 | G | A | missense_variant | MODERATE | c.1765G>A|p.Ala589Thr |
S10 |
7 | BAA08g21400 | A08 | 16233511 | C | T | missense_variant | MODERATE | c.2035C>T|p.Leu679Phe |
S33 |
8 | BAA08g21400 | A08 | 16233643 | C | T | missense_variant | MODERATE | c.2167C>T|p.Leu723Phe |
S168 |
9 | BAA08g21400 | A08 | 16234200 | G | A | synonymous_variant | LOW | c.2724G>A|p.Leu908Leu |
S274 |
10 | BAA08g21400 | A08 | 16234447 | G | A | missense_variant&splice_region_variant | MODERATE | c.2887G>A|p.Gly963Arg |
S42 |
11 | BAA08g21400 | A08 | 16234946 | G | A | missense_variant | MODERATE | c.3386G>A|p.Arg1129Lys |
S116 |
12 | BAA08g21400 | A08 | 16239851 | G | A | downstream_gene_variant | MODIFIER | c.*4778G>A| |
S96 |