Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g14660 | A08 | 12459856 | G | A | missense_variant | MODERATE | c.2140C>T|p.Pro714Ser |
S30 |
2 | BAA08g14660 | A08 | 12459909 | G | A | missense_variant | MODERATE | c.2087C>T|p.Ser696Leu |
S16 |
3 | BAA08g14660 | A08 | 12460232 | C | T | synonymous_variant | LOW | c.1764G>A|p.Pro588Pro |
S189 |
4 | BAA08g14660 | A08 | 12462610 | G | A | upstream_gene_variant | MODIFIER | c.-526C>T| |
S130 |
5 | BAA08g14660 | A08 | 12463358 | C | T | upstream_gene_variant | MODIFIER | c.-1274G>A| |
S126 |
6 | BAA08g14660 | A08 | 12464209 | G | A | upstream_gene_variant | MODIFIER | c.-2125C>T| |
S279 |
7 | BAA08g14660 | A08 | 12466115 | G | A | upstream_gene_variant | MODIFIER | c.-4031C>T| |
S266 |