Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g11450 | A01 | 5300897 | G | A | missense_variant | MODERATE | c.1069C>T|p.Leu357Phe |
S138 |
2 | BAA01g11450 | A01 | 5301662 | G | A | stop_gained | HIGH | c.304C>T|p.Arg102* |
S139 |
3 | BAA01g11450 | A01 | 5301687 | G | A | synonymous_variant | LOW | c.279C>T|p.Ala93Ala |
S9 |
4 | BAA01g11450 | A01 | 5304332 | G | A | upstream_gene_variant | MODIFIER | c.-2367C>T| |
S74 |
5 | BAA01g11450 | A01 | 5305274 | C | T | upstream_gene_variant | MODIFIER | c.-3309G>A| |
S226 |
6 | BAA01g11450 | A01 | 5305310 | C | T | upstream_gene_variant | MODIFIER | c.-3345G>A| |
S249 |
7 | BAA01g11450 | A01 | 5305425 | C | T | upstream_gene_variant | MODIFIER | c.-3460G>A| |
S301 S304 |
8 | BAA01g11450 | A01 | 5306904 | C | T | upstream_gene_variant | MODIFIER | c.-4939G>A| |
S79 S84 |