Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g14950 | A10 | 15502508 | G | A | missense_variant | MODERATE | c.326G>A|p.Gly109Asp |
S180 |
2 | BAA10g14950 | A10 | 15502660 | C | T | missense_variant | MODERATE | c.478C>T|p.Pro160Ser |
S12 |
3 | BAA10g14950 | A10 | 15502760 | C | T | missense_variant | MODERATE | c.578C>T|p.Ser193Phe |
S168 |
4 | BAA10g14950 | A10 | 15505673 | C | T | downstream_gene_variant | MODIFIER | c.*2840C>T| |
S249 |