Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g41380 | A03 | 19392273 | C | T | missense_variant | MODERATE | c.46G>A|p.Glu16Lys |
S2 |
2 | BAA03g41380 | A03 | 19392289 | C | T | synonymous_variant | LOW | c.30G>A|p.Gly10Gly |
S100 |
3 | BAA03g41380 | A03 | 19393041 | C | T | upstream_gene_variant | MODIFIER | c.-723G>A| |
S121 |
4 | BAA03g41380 | A03 | 19393802 | G | A | upstream_gene_variant | MODIFIER | c.-1484C>T| |
S114 |
5 | BAA03g41380 | A03 | 19393990 | G | A | upstream_gene_variant | MODIFIER | c.-1672C>T| |
S168 |
6 | BAA03g41380 | A03 | 19395240 | C | T | upstream_gene_variant | MODIFIER | c.-2922G>A| |
S40 S49 |
7 | BAA03g41380 | A03 | 19395397 | C | T | upstream_gene_variant | MODIFIER | c.-3079G>A| |
S234 |
8 | BAA03g41380 | A03 | 19395821 | C | T | upstream_gene_variant | MODIFIER | c.-3503G>A| |
S263 |
9 | BAA03g41380 | A03 | 19395938 | G | A | upstream_gene_variant | MODIFIER | c.-3620C>T| |
S109 |
10 | BAA03g41380 | A03 | 19396209 | C | T | upstream_gene_variant | MODIFIER | c.-3891G>A| |
S125 |
11 | BAA03g41380 | A03 | 19396368 | C | T | upstream_gene_variant | MODIFIER | c.-4050G>A| |
S159 S224 S243 |
12 | BAA03g41380 | A03 | 19396438 | G | A | upstream_gene_variant | MODIFIER | c.-4120C>T| |
S244 |
13 | BAA03g41380 | A03 | 19396556 | G | A | upstream_gene_variant | MODIFIER | c.-4238C>T| |
S10 |
14 | BAA03g41380 | A03 | 19396692 | C | T | upstream_gene_variant | MODIFIER | c.-4374G>A| |
S8 |
15 | BAA03g41380 | A03 | 19396814 | G | A | upstream_gene_variant | MODIFIER | c.-4496C>T| |
S89 |
16 | BAA03g41380 | A03 | 19397191 | C | T | upstream_gene_variant | MODIFIER | c.-4873G>A| |
S153 S166 S262 S263 |
17 | BAA03g41380 | A03 | 19397221 | C | T | upstream_gene_variant | MODIFIER | c.-4903G>A| |
S293 |
18 | BAA03g41380 | A03 | 19397234 | G | A | upstream_gene_variant | MODIFIER | c.-4916C>T| |
S197 |
19 | BAA03g41380 | A03 | 19397279 | C | T | upstream_gene_variant | MODIFIER | c.-4961G>A| |
S153 |