Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g36990 | A05 | 36771385 | G | A | synonymous_variant | LOW | c.2109C>T|p.Ile703Ile |
S170 |
2 | BAA05g36990 | A05 | 36771714 | C | T | missense_variant | MODERATE | c.1780G>A|p.Gly594Arg |
S56 |
3 | BAA05g36990 | A05 | 36771787 | G | A | synonymous_variant | LOW | c.1707C>T|p.Ala569Ala |
S219 S72 |
4 | BAA05g36990 | A05 | 36772399 | G | A | synonymous_variant | LOW | c.1267C>T|p.Leu423Leu |
S262 |
5 | BAA05g36990 | A05 | 36772926 | C | T | missense_variant | MODERATE | c.826G>A|p.Glu276Lys |
S139 |
6 | BAA05g36990 | A05 | 36772945 | G | A | synonymous_variant | LOW | c.807C>T|p.Phe269Phe |
S281 |
7 | BAA05g36990 | A05 | 36773485 | C | T | synonymous_variant | LOW | c.354G>A|p.Val118Val |
S293 |
8 | BAA05g36990 | A05 | 36773897 | C | T | missense_variant | MODERATE | c.100G>A|p.Glu34Lys |
S162 |
9 | BAA05g36990 | A05 | 36774628 | C | T | upstream_gene_variant | MODIFIER | c.-495G>A| |
S133 |
10 | BAA05g36990 | A05 | 36774662 | C | T | upstream_gene_variant | MODIFIER | c.-529G>A| |
S236 |
11 | BAA05g36990 | A05 | 36775806 | G | A | upstream_gene_variant | MODIFIER | c.-1673C>T| |
S132 S137 |
12 | BAA05g36990 | A05 | 36775844 | C | T | upstream_gene_variant | MODIFIER | c.-1711G>A| |
S12 |
13 | BAA05g36990 | A05 | 36775868 | G | A | upstream_gene_variant | MODIFIER | c.-1735C>T| |
S163 |
14 | BAA05g36990 | A05 | 36777401 | C | T | upstream_gene_variant | MODIFIER | c.-3268G>A| |
S189 |
15 | BAA05g36990 | A05 | 36777495 | G | A | upstream_gene_variant | MODIFIER | c.-3362C>T| |
S116 |
16 | BAA05g36990 | A05 | 36777866 | G | A | upstream_gene_variant | MODIFIER | c.-3733C>T| |
S241 S39 |