Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g57200 | A09 | 56566861 | G | A | upstream_gene_variant | MODIFIER | c.-924G>A| |
S177 |
2 | BAA09g57200 | A09 | 56571703 | C | T | synonymous_variant | LOW | c.978C>T|p.Val326Val |
S35 |
3 | BAA09g57200 | A09 | 56571762 | C | T | missense_variant | MODERATE | c.1037C>T|p.Ala346Val |
S294 |
4 | BAA09g57200 | A09 | 56571951 | C | T | missense_variant | MODERATE | c.1105C>T|p.Leu369Phe |
S208 S93 |
5 | BAA09g57200 | A09 | 56572371 | G | A | stop_gained | HIGH | c.1332G>A|p.Trp444* |
S4 |
6 | BAA09g57200 | A09 | 56572424 | C | T | missense_variant&splice_region_variant | MODERATE | c.1385C>T|p.Pro462Leu |
S293 |
7 | BAA09g57200 | A09 | 56573164 | C | T | synonymous_variant | LOW | c.1762C>T|p.Leu588Leu |
S217 |
8 | BAA09g57200 | A09 | 56573508 | C | A | downstream_gene_variant | MODIFIER | c.*78C>A| |
S122 S192 S208 S229 S237 S263 S301 S49 |
9 | BAA09g57200 | A09 | 56573687 | C | T | downstream_gene_variant | MODIFIER | c.*257C>T| |
S94 |
10 | BAA09g57200 | A09 | 56575650 | G | A | downstream_gene_variant | MODIFIER | c.*2220G>A| |
S38 |
11 | BAA09g57200 | A09 | 56576542 | C | T | downstream_gene_variant | MODIFIER | c.*3112C>T| |
S200 S261 S303 |