Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g27400 | A02 | 15416883 | C | T | missense_variant | MODERATE | c.964G>A|p.Gly322Ser |
S183 S198 |
2 | BAA02g27400 | A02 | 15416970 | C | T | missense_variant | MODERATE | c.877G>A|p.Asp293Asn |
S81 S85 |
3 | BAA02g27400 | A02 | 15416974 | G | A | synonymous_variant | LOW | c.873C>T|p.Ile291Ile |
S119 |
4 | BAA02g27400 | A02 | 15417021 | C | T | intron_variant | MODIFIER | c.853-27G>A| |
S124 S15 |
5 | BAA02g27400 | A02 | 15417163 | G | A | missense_variant | MODERATE | c.752C>T|p.Ala251Val |
S10 |
6 | BAA02g27400 | A02 | 15417179 | C | T | missense_variant | MODERATE | c.736G>A|p.Asp246Asn |
S78 S83 |
7 | BAA02g27400 | A02 | 15417699 | G | A | synonymous_variant | LOW | c.216C>T|p.Thr72Thr |
S70 |
8 | BAA02g27400 | A02 | 15418370 | G | A | synonymous_variant | LOW | c.57C>T|p.Ser19Ser |
S91 |
9 | BAA02g27400 | A02 | 15418540 | G | A | upstream_gene_variant | MODIFIER | c.-114C>T| |
S187 |
10 | BAA02g27400 | A02 | 15418879 | C | T | upstream_gene_variant | MODIFIER | c.-453G>A| |
S260 |
11 | BAA02g27400 | A02 | 15419156 | G | A | upstream_gene_variant | MODIFIER | c.-730C>T| |
S261 |
12 | BAA02g27400 | A02 | 15419311 | C | T | upstream_gene_variant | MODIFIER | c.-885G>A| |
S255 |
13 | BAA02g27400 | A02 | 15420317 | G | A | upstream_gene_variant | MODIFIER | c.-1891C>T| |
S68 |
14 | BAA02g27400 | A02 | 15421738 | G | A | upstream_gene_variant | MODIFIER | c.-3312C>T| |
S38 |