Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09880 | A02 | 4350899 | G | A | missense_variant | MODERATE | c.986C>T|p.Ala329Val |
S275 |
2 | BAA02g09880 | A02 | 4352249 | G | A | missense_variant | MODERATE | c.647C>T|p.Pro216Leu |
S165 |
3 | BAA02g09880 | A02 | 4352544 | C | T | splice_region_variant&synonymous_variant | LOW | c.429G>A|p.Arg143Arg |
S200 |
4 | BAA02g09880 | A02 | 4353387 | G | A | upstream_gene_variant | MODIFIER | c.-251C>T| |
S246 |
5 | BAA02g09880 | A02 | 4353927 | T | C | upstream_gene_variant | MODIFIER | c.-791A>G| |
S97 |
6 | BAA02g09880 | A02 | 4354404 | G | A | upstream_gene_variant | MODIFIER | c.-1268C>T| |
S293 |
7 | BAA02g09880 | A02 | 4354505 | G | A | upstream_gene_variant | MODIFIER | c.-1369C>T| |
S5 |
8 | BAA02g09880 | A02 | 4354525 | G | A | upstream_gene_variant | MODIFIER | c.-1389C>T| |
S217 S248 S52 |
9 | BAA02g09880 | A02 | 4354990 | C | T | upstream_gene_variant | MODIFIER | c.-1854G>A| |
S251 |
10 | BAA02g09880 | A02 | 4355135 | G | A | upstream_gene_variant | MODIFIER | c.-1999C>T| |
S274 |
11 | BAA02g09880 | A02 | 4355625 | C | T | upstream_gene_variant | MODIFIER | c.-2489G>A| |
S270 |
12 | BAA02g09880 | A02 | 4356176 | C | T | upstream_gene_variant | MODIFIER | c.-3040G>A| |
S42 |
13 | BAA02g09880 | A02 | 4356485 | C | T | upstream_gene_variant | MODIFIER | c.-3349G>A| |
S8 |
14 | BAA02g09880 | A02 | 4356740 | C | T | upstream_gene_variant | MODIFIER | c.-3604G>A| |
S277 |
15 | BAA02g09880 | A02 | 4356777 | C | T | upstream_gene_variant | MODIFIER | c.-3641G>A| |
S130 |