Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g43670 | A06 | 28068641 | A | G | upstream_gene_variant | MODIFIER | c.-4697A>G| |
S204 |
2 | BAA06g43670 | A06 | 28068752 | C | T | upstream_gene_variant | MODIFIER | c.-4586C>T| |
S80 |
3 | BAA06g43670 | A06 | 28069626 | C | T | upstream_gene_variant | MODIFIER | c.-3712C>T| |
S150 |
4 | BAA06g43670 | A06 | 28070475 | C | T | upstream_gene_variant | MODIFIER | c.-2863C>T| |
S165 |
5 | BAA06g43670 | A06 | 28070480 | G | A | upstream_gene_variant | MODIFIER | c.-2858G>A| |
S210 |
6 | BAA06g43670 | A06 | 28071568 | C | T | upstream_gene_variant | MODIFIER | c.-1770C>T| |
S39 |
7 | BAA06g43670 | A06 | 28073362 | C | A | missense_variant | MODERATE | c.25C>A|p.Pro9Thr |
S111 |
8 | BAA06g43670 | A06 | 28073917 | C | T | missense_variant | MODERATE | c.292C>T|p.His98Tyr |
S246 |
9 | BAA06g43670 | A06 | 28076014 | C | T | synonymous_variant | LOW | c.1584C>T|p.Cys528Cys |
S51 |
10 | BAA06g43670 | A06 | 28076701 | C | T | downstream_gene_variant | MODIFIER | c.*654C>T| |
S30 S31 |