Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g36100 | A09 | 44423495 | C | T | upstream_gene_variant | MODIFIER | c.-3570C>T| |
S113 |
2 | BAA09g36100 | A09 | 44425727 | T | C | upstream_gene_variant | MODIFIER | c.-1338T>C| |
S275 |
3 | BAA09g36100 | A09 | 44426087 | G | A | upstream_gene_variant | MODIFIER | c.-978G>A| |
S297 |
4 | BAA09g36100 | A09 | 44426579 | C | T | upstream_gene_variant | MODIFIER | c.-486C>T| |
S13 S278 S279 |
5 | BAA09g36100 | A09 | 44426902 | G | A | upstream_gene_variant | MODIFIER | c.-163G>A| |
S134 |
6 | BAA09g36100 | A09 | 44427029 | C | T | upstream_gene_variant | MODIFIER | c.-36C>T| |
S160 |
7 | BAA09g36100 | A09 | 44427190 | C | T | synonymous_variant | LOW | c.126C>T|p.Ser42Ser |
S234 |
8 | BAA09g36100 | A09 | 44429290 | G | A | synonymous_variant | LOW | c.1251G>A|p.Arg417Arg |
S202 |
9 | BAA09g36100 | A09 | 44429686 | C | T | missense_variant | MODERATE | c.1555C>T|p.Leu519Phe |
S135 |
10 | BAA09g36100 | A09 | 44429955 | C | T | missense_variant | MODERATE | c.1726C>T|p.Leu576Phe |
S302 |
11 | BAA09g36100 | A09 | 44430726 | G | A | downstream_gene_variant | MODIFIER | c.*52G>A| |
S196 |
12 | BAA09g36100 | A09 | 44431180 | C | T | downstream_gene_variant | MODIFIER | c.*506C>T| |
S80 |
13 | BAA09g36100 | A09 | 44431410 | G | A | downstream_gene_variant | MODIFIER | c.*736G>A| |
S157 |