Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g21860 | A01 | 10876980 | G | A | missense_variant | MODERATE | c.2005C>T|p.Pro669Ser |
S251 S297 |
2 | BAA01g21860 | A01 | 10877094 | G | A | missense_variant | MODERATE | c.1891C>T|p.Pro631Ser |
S27 |
3 | BAA01g21860 | A01 | 10877098 | C | T | synonymous_variant | LOW | c.1887G>A|p.Glu629Glu |
S158 |
4 | BAA01g21860 | A01 | 10878228 | C | T | missense_variant | MODERATE | c.757G>A|p.Ala253Thr |
S158 |
5 | BAA01g21860 | A01 | 10878898 | G | A | synonymous_variant | LOW | c.87C>T|p.Thr29Thr |
S174 |
6 | BAA01g21860 | A01 | 10882616 | G | A | upstream_gene_variant | MODIFIER | c.-3632C>T| |
S172 S217 |
7 | BAA01g21860 | A01 | 10882761 | C | T | upstream_gene_variant | MODIFIER | c.-3777G>A| |
S294 |
8 | BAA01g21860 | A01 | 10882925 | C | T | upstream_gene_variant | MODIFIER | c.-3941G>A| |
S192 |
9 | BAA01g21860 | A01 | 10883305 | G | A | upstream_gene_variant | MODIFIER | c.-4321C>T| |
S28 |
10 | BAA01g21860 | A01 | 10883542 | G | A | upstream_gene_variant | MODIFIER | c.-4558C>T| |
S245 |