Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g37380 | A01 | 24939162 | C | T | splice_region_variant&synonymous_variant | LOW | c.2952G>A|p.Gln984Gln |
S62 |
2 | BAA01g37380 | A01 | 24941191 | G | A | missense_variant | MODERATE | c.1982C>T|p.Ala661Val |
S116 |
3 | BAA01g37380 | A01 | 24942489 | C | T | synonymous_variant | LOW | c.1359G>A|p.Ala453Ala |
S45 |
4 | BAA01g37380 | A01 | 24942591 | C | T | splice_region_variant&intron_variant | LOW | c.1261-4G>A| |
S134 |
5 | BAA01g37380 | A01 | 24943595 | C | T | missense_variant | MODERATE | c.776G>A|p.Arg259His |
S228 |
6 | BAA01g37380 | A01 | 24943895 | G | A | missense_variant | MODERATE | c.604C>T|p.Pro202Ser |
S20 S244 |
7 | BAA01g37380 | A01 | 24946446 | G | A | upstream_gene_variant | MODIFIER | c.-1239C>T| |
S99 |
8 | BAA01g37380 | A01 | 24947003 | G | A | upstream_gene_variant | MODIFIER | c.-1796C>T| |
S218 |
9 | BAA01g37380 | A01 | 24947296 | G | A | upstream_gene_variant | MODIFIER | c.-2089C>T| |
S249 |
10 | BAA01g37380 | A01 | 24947297 | G | A | upstream_gene_variant | MODIFIER | c.-2090C>T| |
S249 |
11 | BAA01g37380 | A01 | 24949005 | G | A | upstream_gene_variant | MODIFIER | c.-3798C>T| |
S45 |
12 | BAA01g37380 | A01 | 24949881 | G | A | upstream_gene_variant | MODIFIER | c.-4674C>T| |
S108 |