Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g00040 | A05 | 11722 | C | T | synonymous_variant | LOW | c.705G>A|p.Pro235Pro |
S286 |
2 | BAA05g00040 | A05 | 12569 | C | T | synonymous_variant | LOW | c.321G>A|p.Arg107Arg |
S267 |
3 | BAA05g00040 | A05 | 12665 | C | T | synonymous_variant | LOW | c.225G>A|p.Arg75Arg |
S262 |
4 | BAA05g00040 | A05 | 12789 | C | T | missense_variant | MODERATE | c.166G>A|p.Glu56Lys |
S179 |
5 | BAA05g00040 | A05 | 14062 | G | A | upstream_gene_variant | MODIFIER | c.-1041C>T| |
S88 |
6 | BAA05g00040 | A05 | 14211 | C | T | upstream_gene_variant | MODIFIER | c.-1190G>A| |
S10 |
7 | BAA05g00040 | A05 | 14245 | C | T | upstream_gene_variant | MODIFIER | c.-1224G>A| |
S203 |
8 | BAA05g00040 | A05 | 14353 | C | T | upstream_gene_variant | MODIFIER | c.-1332G>A| |
S197 |
9 | BAA05g00040 | A05 | 14369 | G | A | upstream_gene_variant | MODIFIER | c.-1348C>T| |
S177 |
10 | BAA05g00040 | A05 | 14385 | A | T | upstream_gene_variant | MODIFIER | c.-1364T>A| |
S85 |
11 | BAA05g00040 | A05 | 14486 | G | A | upstream_gene_variant | MODIFIER | c.-1465C>T| |
S192 |
12 | BAA05g00040 | A05 | 14741 | G | A | upstream_gene_variant | MODIFIER | c.-1720C>T| |
S104 S52 |
13 | BAA05g00040 | A05 | 15306 | C | T | upstream_gene_variant | MODIFIER | c.-2285G>A| |
S36 |
14 | BAA05g00040 | A05 | 16385 | G | A | upstream_gene_variant | MODIFIER | c.-3364C>T| |
S25 |
15 | BAA05g00040 | A05 | 16417 | C | T | upstream_gene_variant | MODIFIER | c.-3396G>A| |
S189 |
16 | BAA05g00040 | A05 | 16530 | C | T | upstream_gene_variant | MODIFIER | c.-3509G>A| |
S57 |
17 | BAA05g00040 | A05 | 16956 | C | T | upstream_gene_variant | MODIFIER | c.-3935G>A| |
S112 |
18 | BAA05g00040 | A05 | 17504 | G | C | upstream_gene_variant | MODIFIER | c.-4483C>G| |
S57 |
19 | BAA05g00040 | A05 | 17744 | C | T | upstream_gene_variant | MODIFIER | c.-4723G>A| |
S172 S217 |
20 | BAA05g00040 | A05 | 17877 | C | T | upstream_gene_variant | MODIFIER | c.-4856G>A| |
S54 |