Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g11200 | A01 | 5172904 | C | T | missense_variant | MODERATE | c.1393G>A|p.Asp465Asn |
S176 |
2 | BAA01g11200 | A01 | 5173141 | C | T | missense_variant | MODERATE | c.1156G>A|p.Glu386Lys |
S1 S90 |
3 | BAA01g11200 | A01 | 5173508 | C | T | synonymous_variant | LOW | c.789G>A|p.Glu263Glu |
S185 |
4 | BAA01g11200 | A01 | 5173571 | C | T | synonymous_variant | LOW | c.726G>A|p.Gly242Gly |
S135 |
5 | BAA01g11200 | A01 | 5173901 | C | T | synonymous_variant | LOW | c.396G>A|p.Gln132Gln |
S164 |
6 | BAA01g11200 | A01 | 5175860 | G | A | upstream_gene_variant | MODIFIER | c.-1564C>T| |
S63 |
7 | BAA01g11200 | A01 | 5176328 | G | A | upstream_gene_variant | MODIFIER | c.-2032C>T| |
S245 |
8 | BAA01g11200 | A01 | 5177025 | G | A | upstream_gene_variant | MODIFIER | c.-2729C>T| |
S122 |
9 | BAA01g11200 | A01 | 5177707 | C | T | upstream_gene_variant | MODIFIER | c.-3411G>A| |
S69 |
10 | BAA01g11200 | A01 | 5178236 | G | A | upstream_gene_variant | MODIFIER | c.-3940C>T| |
S116 S148 S295 S296 S30 S31 S54 |