Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g05070 | A08 | 3767794 | C | T | downstream_gene_variant | MODIFIER | c.*4801G>A| |
S226 |
2 | BAA08g05070 | A08 | 3768364 | G | A | downstream_gene_variant | MODIFIER | c.*4231C>T| |
S146 |
3 | BAA08g05070 | A08 | 3768970 | C | T | downstream_gene_variant | MODIFIER | c.*3625G>A| |
S252 |
4 | BAA08g05070 | A08 | 3769451 | C | T | downstream_gene_variant | MODIFIER | c.*3144G>A| |
S223 |
5 | BAA08g05070 | A08 | 3770142 | C | T | downstream_gene_variant | MODIFIER | c.*2453G>A| |
S162 |
6 | BAA08g05070 | A08 | 3772504 | A | C | downstream_gene_variant | MODIFIER | c.*91T>G| |
S168 |
7 | BAA08g05070 | A08 | 3773508 | C | T | intron_variant | MODIFIER | c.342-310G>A| |
S44 |
8 | BAA08g05070 | A08 | 3773877 | C | T | intron_variant | MODIFIER | c.342-679G>A| |
S76 |
9 | BAA08g05070 | A08 | 3774642 | C | T | intron_variant | MODIFIER | c.341+973G>A| |
S132 S137 S89 |
10 | BAA08g05070 | A08 | 3775070 | C | T | intron_variant | MODIFIER | c.341+545G>A| |
S148 S210 |
11 | BAA08g05070 | A08 | 3775742 | G | A | missense_variant | MODERATE | c.214C>T|p.Leu72Phe |
S190 |
12 | BAA08g05070 | A08 | 3776405 | C | T | upstream_gene_variant | MODIFIER | c.-450G>A| |
S295 |
13 | BAA08g05070 | A08 | 3776806 | G | A | upstream_gene_variant | MODIFIER | c.-851C>T| |
S191 |
14 | BAA08g05070 | A08 | 3778117 | C | T | upstream_gene_variant | MODIFIER | c.-2162G>A| |
S23 |
15 | BAA08g05070 | A08 | 3779799 | G | A | upstream_gene_variant | MODIFIER | c.-3844C>T| |
S234 S41 |