Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19450 | A10 | 17828978 | C | T | missense_variant | MODERATE | c.1195G>A|p.Asp399Asn |
S48 |
2 | BAA10g19450 | A10 | 17830131 | G | A | synonymous_variant | LOW | c.42C>T|p.Ser14Ser |
S272 |
3 | BAA10g19450 | A10 | 17831016 | C | T | upstream_gene_variant | MODIFIER | c.-844G>A| |
S174 S216 S241 S265 |
4 | BAA10g19450 | A10 | 17831349 | C | T | upstream_gene_variant | MODIFIER | c.-1177G>A| |
S92 |
5 | BAA10g19450 | A10 | 17833237 | C | T | upstream_gene_variant | MODIFIER | c.-3065G>A| |
S192 |
6 | BAA10g19450 | A10 | 17833345 | C | T | upstream_gene_variant | MODIFIER | c.-3173G>A| |
S236 |