Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g17590 | A10 | 16864151 | G | A | downstream_gene_variant | MODIFIER | c.*2409C>T| |
S134 |
2 | BAA10g17590 | A10 | 16866667 | G | A | missense_variant | MODERATE | c.805C>T|p.Pro269Ser |
S1 S90 |
3 | BAA10g17590 | A10 | 16867961 | C | T | missense_variant | MODERATE | c.125G>A|p.Gly42Glu |
S275 |
4 | BAA10g17590 | A10 | 16867992 | G | A | missense_variant | MODERATE | c.94C>T|p.Pro32Ser |
S228 |
5 | BAA10g17590 | A10 | 16868914 | C | T | upstream_gene_variant | MODIFIER | c.-829G>A| |
S150 |
6 | BAA10g17590 | A10 | 16869135 | G | A | upstream_gene_variant | MODIFIER | c.-1050C>T| |
S63 |
7 | BAA10g17590 | A10 | 16869752 | C | T | upstream_gene_variant | MODIFIER | c.-1667G>A| |
S176 |
8 | BAA10g17590 | A10 | 16870105 | G | A | upstream_gene_variant | MODIFIER | c.-2020C>T| |
S217 |
9 | BAA10g17590 | A10 | 16872229 | G | A | upstream_gene_variant | MODIFIER | c.-4144C>T| |
S236 |
10 | BAA10g17590 | A10 | 16872797 | C | A | upstream_gene_variant | MODIFIER | c.-4712G>T| |
S296 |
11 | BAA10g17590 | A10 | 16872798 | C | A | upstream_gene_variant | MODIFIER | c.-4713G>T| |
S16 |
12 | BAA10g17590 | A10 | 16872852 | C | T | upstream_gene_variant | MODIFIER | c.-4767G>A| |
S37 |
13 | BAA10g17590 | A10 | 16872958 | G | A | upstream_gene_variant | MODIFIER | c.-4873C>T| |
S57 |