Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g13970 | A06 | 6898897 | G | A | upstream_gene_variant | MODIFIER | c.-4446G>A| |
S299 |
2 | BAA06g13970 | A06 | 6900015 | G | A | upstream_gene_variant | MODIFIER | c.-3328G>A| |
S173 |
3 | BAA06g13970 | A06 | 6900530 | C | T | upstream_gene_variant | MODIFIER | c.-2813C>T| |
S178 |
4 | BAA06g13970 | A06 | 6900781 | C | T | upstream_gene_variant | MODIFIER | c.-2562C>T| |
S142 |
5 | BAA06g13970 | A06 | 6901026 | C | T | upstream_gene_variant | MODIFIER | c.-2317C>T| |
S187 |
6 | BAA06g13970 | A06 | 6901032 | G | A | upstream_gene_variant | MODIFIER | c.-2311G>A| |
S40 S49 |
7 | BAA06g13970 | A06 | 6901293 | C | T | upstream_gene_variant | MODIFIER | c.-2050C>T| |
S301 S304 |
8 | BAA06g13970 | A06 | 6901493 | C | T | upstream_gene_variant | MODIFIER | c.-1850C>T| |
S4 |
9 | BAA06g13970 | A06 | 6903639 | C | T | synonymous_variant | LOW | c.297C>T|p.Phe99Phe |
S165 |
10 | BAA06g13970 | A06 | 6903674 | C | T | missense_variant | MODERATE | c.332C>T|p.Ser111Phe |
S188 |