Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g18140 | A10 | 17120501 | G | A | upstream_gene_variant | MODIFIER | c.-4041G>A| |
S262 |
2 | BAA10g18140 | A10 | 17120558 | C | T | upstream_gene_variant | MODIFIER | c.-3984C>T| |
S12 |
3 | BAA10g18140 | A10 | 17120719 | G | A | upstream_gene_variant | MODIFIER | c.-3823G>A| |
S205 |
4 | BAA10g18140 | A10 | 17120758 | G | A | upstream_gene_variant | MODIFIER | c.-3784G>A| |
S166 |
5 | BAA10g18140 | A10 | 17120896 | G | A | upstream_gene_variant | MODIFIER | c.-3646G>A| |
S226 |
6 | BAA10g18140 | A10 | 17120908 | C | T | upstream_gene_variant | MODIFIER | c.-3634C>T| |
S113 |
7 | BAA10g18140 | A10 | 17121072 | G | A | upstream_gene_variant | MODIFIER | c.-3470G>A| |
S166 |
8 | BAA10g18140 | A10 | 17121694 | C | T | upstream_gene_variant | MODIFIER | c.-2848C>T| |
S210 |
9 | BAA10g18140 | A10 | 17122293 | G | A | upstream_gene_variant | MODIFIER | c.-2249G>A| |
S4 |
10 | BAA10g18140 | A10 | 17123119 | C | T | upstream_gene_variant | MODIFIER | c.-1423C>T| |
S153 S213 |
11 | BAA10g18140 | A10 | 17124874 | C | T | synonymous_variant | LOW | c.333C>T|p.Phe111Phe |
S148 S30 S31 |
12 | BAA10g18140 | A10 | 17125233 | C | T | missense_variant | MODERATE | c.692C>T|p.Thr231Met |
S23 |