Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g66520 | A09 | 60752056 | G | A | upstream_gene_variant | MODIFIER | c.-3409G>A| |
S276 |
2 | BAA09g66520 | A09 | 60753163 | G | A | upstream_gene_variant | MODIFIER | c.-2302G>A| |
S277 |
3 | BAA09g66520 | A09 | 60754569 | C | T | upstream_gene_variant | MODIFIER | c.-896C>T| |
S176 |
4 | BAA09g66520 | A09 | 60754624 | G | A | upstream_gene_variant | MODIFIER | c.-841G>A| |
S70 |
5 | BAA09g66520 | A09 | 60754841 | C | T | upstream_gene_variant | MODIFIER | c.-624C>T| |
S125 |
6 | BAA09g66520 | A09 | 60755110 | G | A | upstream_gene_variant | MODIFIER | c.-355G>A| |
S57 |
7 | BAA09g66520 | A09 | 60755570 | G | A | missense_variant | MODERATE | c.106G>A|p.Glu36Lys |
S45 |
8 | BAA09g66520 | A09 | 60756355 | C | T | missense_variant | MODERATE | c.287C>T|p.Thr96Ile |
S35 |
9 | BAA09g66520 | A09 | 60756999 | C | T | synonymous_variant | LOW | c.849C>T|p.Val283Val |
S186 |
10 | BAA09g66520 | A09 | 60757049 | C | T | missense_variant | MODERATE | c.899C>T|p.Pro300Leu |
S245 |
11 | BAA09g66520 | A09 | 60757088 | G | A | missense_variant | MODERATE | c.938G>A|p.Arg313His |
S284 |