Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g35050 | A02 | 30136397 | C | T | downstream_gene_variant | MODIFIER | c.*1584G>A| |
S124 |
2 | BAA02g35050 | A02 | 30136985 | C | T | downstream_gene_variant | MODIFIER | c.*996G>A| |
S15 S3 |
3 | BAA02g35050 | A02 | 30137126 | G | A | downstream_gene_variant | MODIFIER | c.*855C>T| |
S200 |
4 | BAA02g35050 | A02 | 30138673 | G | A | synonymous_variant | LOW | c.1137C>T|p.Ile379Ile |
S174 |
5 | BAA02g35050 | A02 | 30139019 | G | A | missense_variant | MODERATE | c.974C>T|p.Pro325Leu |
S20 |
6 | BAA02g35050 | A02 | 30139069 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.925-1G>A| |
S263 |
7 | BAA02g35050 | A02 | 30139494 | C | T | intron_variant | MODIFIER | c.762+12G>A| |
S262 |
8 | BAA02g35050 | A02 | 30139765 | C | T | missense_variant | MODERATE | c.503G>A|p.Arg168Lys |
S16 |
9 | BAA02g35050 | A02 | 30139970 | G | A | missense_variant | MODERATE | c.298C>T|p.Leu100Phe |
S175 |
10 | BAA02g35050 | A02 | 30140304 | C | A | upstream_gene_variant | MODIFIER | c.-37G>T| |
S70 |
11 | BAA02g35050 | A02 | 30140506 | G | A | upstream_gene_variant | MODIFIER | c.-239C>T| |
S26 |
12 | BAA02g35050 | A02 | 30141246 | C | T | upstream_gene_variant | MODIFIER | c.-979G>A| |
S202 |
13 | BAA02g35050 | A02 | 30142146 | T | C | upstream_gene_variant | MODIFIER | c.-1879A>G| |
S163 |
14 | BAA02g35050 | A02 | 30142156 | G | A | upstream_gene_variant | MODIFIER | c.-1889C>T| |
S156 |