Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g43590 | A09 | 49671402 | C | T | upstream_gene_variant | MODIFIER | c.-1804C>T| |
S36 |
2 | BAA09g43590 | A09 | 49671794 | C | T | upstream_gene_variant | MODIFIER | c.-1412C>T| |
S245 |
3 | BAA09g43590 | A09 | 49677948 | C | T | intron_variant | MODIFIER | c.2642-670C>T| |
S135 |
4 | BAA09g43590 | A09 | 49678620 | C | T | missense_variant&splice_region_variant | MODERATE | c.2644C>T|p.Leu882Phe |
S170 |
5 | BAA09g43590 | A09 | 49678757 | G | A | intron_variant | MODIFIER | c.2713-52G>A| |
S174 S216 S265 S27 |
6 | BAA09g43590 | A09 | 49679028 | G | A | missense_variant | MODERATE | c.2836G>A|p.Val946Ile |
S81 S85 |
7 | BAA09g43590 | A09 | 49680785 | C | T | downstream_gene_variant | MODIFIER | c.*1722C>T| |
S132 S137 S215 |
8 | BAA09g43590 | A09 | 49680841 | C | T | downstream_gene_variant | MODIFIER | c.*1778C>T| |
S96 |
9 | BAA09g43590 | A09 | 49681595 | C | T | downstream_gene_variant | MODIFIER | c.*2532C>T| |
S20 |
10 | BAA09g43590 | A09 | 49682838 | G | A | downstream_gene_variant | MODIFIER | c.*3775G>A| |
S55 |
11 | BAA09g43590 | A09 | 49683431 | C | T | downstream_gene_variant | MODIFIER | c.*4368C>T| |
S302 |