Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g28990 | A04 | 28323482 | C | T | missense_variant | MODERATE | c.556G>A|p.Val186Met |
S40 S49 |
2 | BAA04g28990 | A04 | 28323517 | C | T | missense_variant | MODERATE | c.521G>A|p.Gly174Asp |
S176 |
3 | BAA04g28990 | A04 | 28323677 | C | T | missense_variant | MODERATE | c.361G>A|p.Asp121Asn |
S167 |
4 | BAA04g28990 | A04 | 28323845 | C | T | missense_variant | MODERATE | c.193G>A|p.Ala65Thr |
S238 |
5 | BAA04g28990 | A04 | 28324935 | G | A | upstream_gene_variant | MODIFIER | c.-67C>T| |
S211 S227 |
6 | BAA04g28990 | A04 | 28325327 | G | A | upstream_gene_variant | MODIFIER | c.-459C>T| |
S261 |
7 | BAA04g28990 | A04 | 28326687 | C | T | upstream_gene_variant | MODIFIER | c.-1819G>A| |
S28 |
8 | BAA04g28990 | A04 | 28329530 | C | T | upstream_gene_variant | MODIFIER | c.-4662G>A| |
S156 |
9 | BAA04g28990 | A04 | 28329582 | G | A | upstream_gene_variant | MODIFIER | c.-4714C>T| |
S162 |
10 | BAA04g28990 | A04 | 28329669 | C | T | upstream_gene_variant | MODIFIER | c.-4801G>A| |
S122 |