Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g16950 | A09 | 10073503 | C | T | upstream_gene_variant | MODIFIER | c.-2021C>T| |
S256 |
2 | BAA09g16950 | A09 | 10073719 | G | A | upstream_gene_variant | MODIFIER | c.-1805G>A| |
S260 |
3 | BAA09g16950 | A09 | 10074085 | C | T | upstream_gene_variant | MODIFIER | c.-1439C>T| |
S84 S93 |
4 | BAA09g16950 | A09 | 10074088 | C | T | upstream_gene_variant | MODIFIER | c.-1436C>T| |
S50 |
5 | BAA09g16950 | A09 | 10074941 | A | T | upstream_gene_variant | MODIFIER | c.-583A>T| |
S262 |
6 | BAA09g16950 | A09 | 10075264 | G | A | upstream_gene_variant | MODIFIER | c.-260G>A| |
S63 |
7 | BAA09g16950 | A09 | 10075707 | C | T | missense_variant | MODERATE | c.184C>T|p.Pro62Ser |
S293 |
8 | BAA09g16950 | A09 | 10076144 | G | A | synonymous_variant | LOW | c.621G>A|p.Ser207Ser |
|
9 | BAA09g16950 | A09 | 10076741 | C | T | missense_variant | MODERATE | c.929C>T|p.Ala310Val |
S64 |