Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g26170 | A09 | 16952430 | C | T | downstream_gene_variant | MODIFIER | c.*1039G>A| |
S231 |
2 | BAA09g26170 | A09 | 16953270 | C | T | downstream_gene_variant | MODIFIER | c.*199G>A| |
S255 |
3 | BAA09g26170 | A09 | 16953685 | G | A | synonymous_variant | LOW | c.414C>T|p.Val138Val |
S38 |
4 | BAA09g26170 | A09 | 16953900 | C | T | missense_variant | MODERATE | c.199G>A|p.Val67Ile |
S182 |
5 | BAA09g26170 | A09 | 16954962 | G | A | upstream_gene_variant | MODIFIER | c.-864C>T| |
S251 |
6 | BAA09g26170 | A09 | 16956093 | G | A | upstream_gene_variant | MODIFIER | c.-1995C>T| |
S223 |
7 | BAA09g26170 | A09 | 16956280 | G | A | upstream_gene_variant | MODIFIER | c.-2182C>T| |
S216 |
8 | BAA09g26170 | A09 | 16956597 | G | A | upstream_gene_variant | MODIFIER | c.-2499C>T| |
S15 |
9 | BAA09g26170 | A09 | 16956890 | C | T | upstream_gene_variant | MODIFIER | c.-2792G>A| |
S35 |
10 | BAA09g26170 | A09 | 16956892 | T | G | upstream_gene_variant | MODIFIER | c.-2794A>C| |
S103 S135 S227 S270 |