Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g08680 | A10 | 10630199 | G | A | downstream_gene_variant | MODIFIER | c.*2235C>T| |
S75 S81 |
2 | BAA10g08680 | A10 | 10630847 | C | T | downstream_gene_variant | MODIFIER | c.*1587G>A| |
S142 |
3 | BAA10g08680 | A10 | 10631081 | C | T | downstream_gene_variant | MODIFIER | c.*1353G>A| |
S98 |
4 | BAA10g08680 | A10 | 10632650 | C | T | synonymous_variant | LOW | c.1293G>A|p.Leu431Leu |
S272 |
5 | BAA10g08680 | A10 | 10632654 | C | T | missense_variant | MODERATE | c.1289G>A|p.Arg430Lys |
S294 |
6 | BAA10g08680 | A10 | 10632870 | G | A | missense_variant | MODERATE | c.1073C>T|p.Thr358Met |
S292 |
7 | BAA10g08680 | A10 | 10633301 | G | A | synonymous_variant | LOW | c.642C>T|p.Ile214Ile |
S271 |
8 | BAA10g08680 | A10 | 10634647 | C | T | upstream_gene_variant | MODIFIER | c.-362G>A| |
S119 |
9 | BAA10g08680 | A10 | 10635281 | C | T | upstream_gene_variant | MODIFIER | c.-996G>A| |
S294 |
10 | BAA10g08680 | A10 | 10635692 | C | T | upstream_gene_variant | MODIFIER | c.-1407G>A| |
S17 |
11 | BAA10g08680 | A10 | 10636016 | C | T | upstream_gene_variant | MODIFIER | c.-1731G>A| |
S265 |
12 | BAA10g08680 | A10 | 10636049 | C | T | upstream_gene_variant | MODIFIER | c.-1764G>A| |
S256 |
13 | BAA10g08680 | A10 | 10636162 | C | T | upstream_gene_variant | MODIFIER | c.-1877G>A| |
S308 |
14 | BAA10g08680 | A10 | 10636351 | G | A | upstream_gene_variant | MODIFIER | c.-2066C>T| |
S271 |
15 | BAA10g08680 | A10 | 10636635 | C | T | upstream_gene_variant | MODIFIER | c.-2350G>A| |
S244 |
16 | BAA10g08680 | A10 | 10637123 | G | A | upstream_gene_variant | MODIFIER | c.-2838C>T| |
S5 |
17 | BAA10g08680 | A10 | 10638316 | C | T | upstream_gene_variant | MODIFIER | c.-4031G>A| |
S28 |