Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g21290 | A10 | 18774615 | G | A | missense_variant | MODERATE | c.38G>A|p.Arg13Lys |
S162 |
2 | BAA10g21290 | A10 | 18774972 | C | T | missense_variant | MODERATE | c.395C>T|p.Pro132Leu |
S91 |
3 | BAA10g21290 | A10 | 18774998 | C | T | missense_variant | MODERATE | c.421C>T|p.Leu141Phe |
S115 |
4 | BAA10g21290 | A10 | 18775426 | C | T | synonymous_variant | LOW | c.849C>T|p.Leu283Leu |
S103 S25 |
5 | BAA10g21290 | A10 | 18778864 | C | T | downstream_gene_variant | MODIFIER | c.*3163C>T| |
S281 |