Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g14080 | A10 | 14943820 | C | T | missense_variant | MODERATE | c.382G>A|p.Val128Ile |
S244 |
2 | BAA10g14080 | A10 | 14944013 | G | A | synonymous_variant | LOW | c.189C>T|p.His63His |
S128 |
3 | BAA10g14080 | A10 | 14944127 | G | A | synonymous_variant | LOW | c.75C>T|p.Ser25Ser |
S263 |
4 | BAA10g14080 | A10 | 14944217 | G | A | upstream_gene_variant | MODIFIER | c.-16C>T| |
S198 |
5 | BAA10g14080 | A10 | 14945726 | C | T | upstream_gene_variant | MODIFIER | c.-1525G>A| |
S6 |
6 | BAA10g14080 | A10 | 14946772 | C | T | upstream_gene_variant | MODIFIER | c.-2571G>A| |
S244 |
7 | BAA10g14080 | A10 | 14947276 | C | T | upstream_gene_variant | MODIFIER | c.-3075G>A| |
S63 |
8 | BAA10g14080 | A10 | 14947448 | G | A | upstream_gene_variant | MODIFIER | c.-3247C>T| |
S129 |
9 | BAA10g14080 | A10 | 14947683 | G | A | upstream_gene_variant | MODIFIER | c.-3482C>T| |
S293 |
10 | BAA10g14080 | A10 | 14947811 | C | T | upstream_gene_variant | MODIFIER | c.-3610G>A| |
S187 |