Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g03900 | A10 | 1910004 | G | A | missense_variant | MODERATE | c.338C>T|p.Pro113Leu |
S242 |
2 | BAA10g03900 | A10 | 1912299 | C | T | upstream_gene_variant | MODIFIER | c.-372G>A| |
S42 |
3 | BAA10g03900 | A10 | 1912616 | G | A | upstream_gene_variant | MODIFIER | c.-689C>T| |
S124 |
4 | BAA10g03900 | A10 | 1913021 | C | T | upstream_gene_variant | MODIFIER | c.-1094G>A| |
S162 |
5 | BAA10g03900 | A10 | 1913169 | G | A | upstream_gene_variant | MODIFIER | c.-1242C>T| |
S205 |
6 | BAA10g03900 | A10 | 1913255 | G | A | upstream_gene_variant | MODIFIER | c.-1328C>T| |
S33 |
7 | BAA10g03900 | A10 | 1916568 | A | C | upstream_gene_variant | MODIFIER | c.-4641T>G| |
S261 |