Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g56310 | A03 | 27851997 | G | A | missense_variant | MODERATE | c.3991C>T|p.Arg1331Trp |
S112 |
2 | BAA03g56310 | A03 | 27852130 | G | A | synonymous_variant | LOW | c.3858C>T|p.Ile1286Ile |
S294 |
3 | BAA03g56310 | A03 | 27852544 | G | A | synonymous_variant | LOW | c.3444C>T|p.Thr1148Thr |
S298 |
4 | BAA03g56310 | A03 | 27853738 | C | T | synonymous_variant | LOW | c.2250G>A|p.Gly750Gly |
S172 S217 S35 |
5 | BAA03g56310 | A03 | 27854392 | C | T | synonymous_variant | LOW | c.1596G>A|p.Pro532Pro |
S129 |
6 | BAA03g56310 | A03 | 27855026 | G | A | missense_variant | MODERATE | c.962C>T|p.Ser321Phe |
S152 S154 |
7 | BAA03g56310 | A03 | 27855085 | C | T | synonymous_variant | LOW | c.903G>A|p.Gln301Gln |
S80 |
8 | BAA03g56310 | A03 | 27855119 | G | A | missense_variant | MODERATE | c.869C>T|p.Thr290Met |
S283 |
9 | BAA03g56310 | A03 | 27855217 | C | T | synonymous_variant | LOW | c.771G>A|p.Glu257Glu |
S105 S106 |
10 | BAA03g56310 | A03 | 27855860 | C | T | missense_variant | MODERATE | c.128G>A|p.Arg43Lys |
S238 |
11 | BAA03g56310 | A03 | 27855898 | G | A | synonymous_variant | LOW | c.90C>T|p.Phe30Phe |
S210 S225 |
12 | BAA03g56310 | A03 | 27855919 | C | T | synonymous_variant | LOW | c.69G>A|p.Arg23Arg |
S279 |
13 | BAA03g56310 | A03 | 27856262 | C | T | upstream_gene_variant | MODIFIER | c.-275G>A| |
S281 |
14 | BAA03g56310 | A03 | 27856754 | G | A | upstream_gene_variant | MODIFIER | c.-767C>T| |
S295 |
15 | BAA03g56310 | A03 | 27856766 | C | T | upstream_gene_variant | MODIFIER | c.-779G>A| |
S16 |
16 | BAA03g56310 | A03 | 27857121 | G | A | upstream_gene_variant | MODIFIER | c.-1134C>T| |
S297 |
17 | BAA03g56310 | A03 | 27858125 | C | T | upstream_gene_variant | MODIFIER | c.-2138G>A| |
S23 |
18 | BAA03g56310 | A03 | 27858497 | C | T | upstream_gene_variant | MODIFIER | c.-2510G>A| |
S153 |
19 | BAA03g56310 | A03 | 27859181 | G | A | upstream_gene_variant | MODIFIER | c.-3194C>T| |
S276 |