Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g18450 | A10 | 17252946 | C | T | missense_variant | MODERATE | c.1363G>A|p.Asp455Asn |
S260 |
2 | BAA10g18450 | A10 | 17254095 | G | A | synonymous_variant | LOW | c.768C>T|p.Phe256Phe |
S32 |
3 | BAA10g18450 | A10 | 17257714 | C | T | upstream_gene_variant | MODIFIER | c.-2600G>A| |
S160 |
4 | BAA10g18450 | A10 | 17258926 | C | T | upstream_gene_variant | MODIFIER | c.-3812G>A| |
S20 |
5 | BAA10g18450 | A10 | 17259184 | C | T | upstream_gene_variant | MODIFIER | c.-4070G>A| |
S211 |