Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g30950 | A02 | 18256097 | C | T | downstream_gene_variant | MODIFIER | c.*377G>A| |
S54 |
2 | BAA02g30950 | A02 | 18257263 | G | A | intron_variant | MODIFIER | c.1501+42C>T| |
S156 |
3 | BAA02g30950 | A02 | 18257364 | C | T | missense_variant | MODERATE | c.1442G>A|p.Gly481Glu |
S183 S198 |
4 | BAA02g30950 | A02 | 18257713 | C | T | synonymous_variant | LOW | c.1167G>A|p.Arg389Arg |
S226 |
5 | BAA02g30950 | A02 | 18258701 | C | T | intron_variant | MODIFIER | c.628-39G>A| |
S140 |
6 | BAA02g30950 | A02 | 18258803 | C | T | splice_region_variant&intron_variant | LOW | c.627+4G>A| |
S40 S49 |
7 | BAA02g30950 | A02 | 18259644 | C | T | stop_gained | HIGH | c.236G>A|p.Trp79* |
S157 S163 |
8 | BAA02g30950 | A02 | 18259871 | G | A | intron_variant | MODIFIER | c.156-54C>T| |
S228 |
9 | BAA02g30950 | A02 | 18260044 | C | T | intron_variant | MODIFIER | c.155+79G>A| |
S75 S81 |
10 | BAA02g30950 | A02 | 18260123 | C | T | missense_variant&splice_region_variant | MODERATE | c.155G>A|p.Arg52His |
S25 |
11 | BAA02g30950 | A02 | 18260886 | G | A | upstream_gene_variant | MODIFIER | c.-609C>T| |
S68 |
12 | BAA02g30950 | A02 | 18261304 | C | T | upstream_gene_variant | MODIFIER | c.-1027G>A| |
S245 |
13 | BAA02g30950 | A02 | 18262059 | C | T | upstream_gene_variant | MODIFIER | c.-1782G>A| |
S66 |
14 | BAA02g30950 | A02 | 18262215 | C | T | upstream_gene_variant | MODIFIER | c.-1938G>A| |
S273 |
15 | BAA02g30950 | A02 | 18262224 | G | A | upstream_gene_variant | MODIFIER | c.-1947C>T| |
S265 |
16 | BAA02g30950 | A02 | 18264347 | G | A | upstream_gene_variant | MODIFIER | c.-4070C>T| |
S268 |
17 | BAA02g30950 | A02 | 18264503 | G | A | upstream_gene_variant | MODIFIER | c.-4226C>T| |
S33 |