Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g26880 | A05 | 31399661 | G | A | upstream_gene_variant | MODIFIER | c.-2067G>A| |
S308 |
2 | BAA05g26880 | A05 | 31400568 | G | A | upstream_gene_variant | MODIFIER | c.-1160G>A| |
S40 S49 |
3 | BAA05g26880 | A05 | 31400758 | G | A | upstream_gene_variant | MODIFIER | c.-970G>A| |
S134 |
4 | BAA05g26880 | A05 | 31401871 | C | T | synonymous_variant | LOW | c.144C>T|p.Tyr48Tyr |
S286 |
5 | BAA05g26880 | A05 | 31402178 | C | T | missense_variant | MODERATE | c.451C>T|p.Pro151Ser |
S287 |
6 | BAA05g26880 | A05 | 31402460 | C | A | missense_variant | MODERATE | c.733C>A|p.Leu245Ile |
S37 |
7 | BAA05g26880 | A05 | 31402522 | G | A | synonymous_variant | LOW | c.795G>A|p.Leu265Leu |
S54 |
8 | BAA05g26880 | A05 | 31402956 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1121-1G>A| |
S12 |
9 | BAA05g26880 | A05 | 31404622 | C | T | downstream_gene_variant | MODIFIER | c.*1634C>T| |
S213 |
10 | BAA05g26880 | A05 | 31405093 | C | T | downstream_gene_variant | MODIFIER | c.*2105C>T| |
S297 |
11 | BAA05g26880 | A05 | 31405234 | C | T | downstream_gene_variant | MODIFIER | c.*2246C>T| |
S292 |
12 | BAA05g26880 | A05 | 31405271 | C | T | downstream_gene_variant | MODIFIER | c.*2283C>T| |
S226 |