Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g66930 | A09 | 60917426 | G | A | missense_variant | MODERATE | c.820C>T|p.Leu274Phe |
S280 |
2 | BAA09g66930 | A09 | 60918448 | G | T | upstream_gene_variant | MODIFIER | c.-203C>A| |
S194 |
3 | BAA09g66930 | A09 | 60918597 | A | G | upstream_gene_variant | MODIFIER | c.-352T>C| |
S291 S297 |
4 | BAA09g66930 | A09 | 60918638 | G | A | upstream_gene_variant | MODIFIER | c.-393C>T| |
S252 |
5 | BAA09g66930 | A09 | 60918692 | G | A | upstream_gene_variant | MODIFIER | c.-447C>T| |
S133 |
6 | BAA09g66930 | A09 | 60919010 | G | A | upstream_gene_variant | MODIFIER | c.-765C>T| |
S107 |
7 | BAA09g66930 | A09 | 60919019 | C | T | upstream_gene_variant | MODIFIER | c.-774G>A| |
S262 |
8 | BAA09g66930 | A09 | 60919360 | G | A | upstream_gene_variant | MODIFIER | c.-1115C>T| |
S135 |
9 | BAA09g66930 | A09 | 60919577 | C | T | upstream_gene_variant | MODIFIER | c.-1332G>A| |
S250 |
10 | BAA09g66930 | A09 | 60920072 | C | T | upstream_gene_variant | MODIFIER | c.-1827G>A| |
S296 |
11 | BAA09g66930 | A09 | 60920515 | A | T | upstream_gene_variant | MODIFIER | c.-2270T>A| |
S200 |
12 | BAA09g66930 | A09 | 60920718 | C | T | upstream_gene_variant | MODIFIER | c.-2473G>A| |
S170 |
13 | BAA09g66930 | A09 | 60921129 | G | A | upstream_gene_variant | MODIFIER | c.-2884C>T| |
S128 S280 |
14 | BAA09g66930 | A09 | 60922545 | C | T | upstream_gene_variant | MODIFIER | c.-4300G>A| |
S153 S213 |
15 | BAA09g66930 | A09 | 60922644 | G | A | upstream_gene_variant | MODIFIER | c.-4399C>T| |
S225 |
16 | BAA09g66930 | A09 | 60922886 | G | A | upstream_gene_variant | MODIFIER | c.-4641C>T| |
S174 |
17 | BAA09g66930 | A09 | 60923151 | T | C | upstream_gene_variant | MODIFIER | c.-4906A>G| |
S13 S140 S278 S64 |