Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g24230 | A10 | 20038690 | C | T | missense_variant | MODERATE | c.1738G>A|p.Val580Ile |
S25 |
2 | BAA10g24230 | A10 | 20038903 | C | T | missense_variant | MODERATE | c.1525G>A|p.Ala509Thr |
S156 |
3 | BAA10g24230 | A10 | 20039929 | G | A | missense_variant | MODERATE | c.802C>T|p.Arg268Cys |
S279 |
4 | BAA10g24230 | A10 | 20040278 | C | T | missense_variant | MODERATE | c.625G>A|p.Val209Ile |
S157 S163 |
5 | BAA10g24230 | A10 | 20040900 | C | T | missense_variant | MODERATE | c.266G>A|p.Gly89Glu |
S98 |
6 | BAA10g24230 | A10 | 20042696 | A | T | upstream_gene_variant | MODIFIER | c.-1235T>A| |
S153 S213 |
7 | BAA10g24230 | A10 | 20042792 | C | T | upstream_gene_variant | MODIFIER | c.-1331G>A| |
S305 |
8 | BAA10g24230 | A10 | 20043933 | C | T | upstream_gene_variant | MODIFIER | c.-2472G>A| |
S230 |
9 | BAA10g24230 | A10 | 20044607 | C | T | upstream_gene_variant | MODIFIER | c.-3146G>A| |
S238 |
10 | BAA10g24230 | A10 | 20045399 | C | T | upstream_gene_variant | MODIFIER | c.-3938G>A| |
S274 |