Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g35730 | A09 | 44075806 | C | T | upstream_gene_variant | MODIFIER | c.-2621C>T| |
S192 |
2 | BAA09g35730 | A09 | 44075816 | C | T | upstream_gene_variant | MODIFIER | c.-2611C>T| |
S278 |
3 | BAA09g35730 | A09 | 44076256 | A | G | upstream_gene_variant | MODIFIER | c.-2171A>G| |
S67 |
4 | BAA09g35730 | A09 | 44077069 | G | A | upstream_gene_variant | MODIFIER | c.-1358G>A| |
S130 |
5 | BAA09g35730 | A09 | 44077261 | C | T | upstream_gene_variant | MODIFIER | c.-1166C>T| |
S302 |
6 | BAA09g35730 | A09 | 44077445 | G | A | upstream_gene_variant | MODIFIER | c.-982G>A| |
S189 |
7 | BAA09g35730 | A09 | 44077812 | G | A | upstream_gene_variant | MODIFIER | c.-615G>A| |
S45 |
8 | BAA09g35730 | A09 | 44078393 | C | T | upstream_gene_variant | MODIFIER | c.-34C>T| |
S36 |
9 | BAA09g35730 | A09 | 44078395 | C | T | upstream_gene_variant | MODIFIER | c.-32C>T| |
S50 |
10 | BAA09g35730 | A09 | 44079130 | G | A | missense_variant | MODERATE | c.173G>A|p.Arg58Gln |
S148 S210 |
11 | BAA09g35730 | A09 | 44081674 | C | T | downstream_gene_variant | MODIFIER | c.*1478C>T| |
S159 S243 S299 |
12 | BAA09g35730 | A09 | 44081986 | G | A | downstream_gene_variant | MODIFIER | c.*1790G>A| |
S59 |
13 | BAA09g35730 | A09 | 44083099 | C | T | downstream_gene_variant | MODIFIER | c.*2903C>T| |
S108 |
14 | BAA09g35730 | A09 | 44083581 | G | A | downstream_gene_variant | MODIFIER | c.*3385G>A| |
S210 S225 |
15 | BAA09g35730 | A09 | 44083950 | C | T | downstream_gene_variant | MODIFIER | c.*3754C>T| |
S249 S43 |
16 | BAA09g35730 | A09 | 44084458 | C | T | downstream_gene_variant | MODIFIER | c.*4262C>T| |
S14 |
17 | BAA09g35730 | A09 | 44085097 | C | T | downstream_gene_variant | MODIFIER | c.*4901C>T| |
S240 |