Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g50800 | A09 | 53498353 | G | A | missense_variant | MODERATE | c.721C>T|p.Pro241Ser |
S15 S3 |
2 | BAA09g50800 | A09 | 53499069 | G | A | synonymous_variant | LOW | c.141C>T|p.Thr47Thr |
S202 |
3 | BAA09g50800 | A09 | 53499667 | G | A | upstream_gene_variant | MODIFIER | c.-458C>T| |
S48 |
4 | BAA09g50800 | A09 | 53500124 | C | T | upstream_gene_variant | MODIFIER | c.-915G>A| |
S223 |
5 | BAA09g50800 | A09 | 53500826 | C | T | upstream_gene_variant | MODIFIER | c.-1617G>A| |
S241 |
6 | BAA09g50800 | A09 | 53503845 | C | T | upstream_gene_variant | MODIFIER | c.-4636G>A| |
S235 |
7 | BAA09g50800 | A09 | 53503934 | C | T | upstream_gene_variant | MODIFIER | c.-4725G>A| |
S56 |