Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g02160 | A10 | 1026223 | C | T | missense_variant | MODERATE | c.11C>T|p.Ser4Phe |
S157 |
2 | BAA10g02160 | A10 | 1026838 | C | T | missense_variant | MODERATE | c.626C>T|p.Pro209Leu |
S135 |
3 | BAA10g02160 | A10 | 1026947 | C | T | synonymous_variant | LOW | c.735C>T|p.Leu245Leu |
S73 |
4 | BAA10g02160 | A10 | 1027509 | G | A | downstream_gene_variant | MODIFIER | c.*109G>A| |
S301 S304 |
5 | BAA10g02160 | A10 | 1027705 | G | A | downstream_gene_variant | MODIFIER | c.*305G>A| |
S280 |
6 | BAA10g02160 | A10 | 1028041 | G | A | downstream_gene_variant | MODIFIER | c.*641G>A| |
S18 |