Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g02460 | A10 | 1198648 | G | A | missense_variant | MODERATE | c.805C>T|p.Arg269Cys |
S59 |
2 | BAA10g02460 | A10 | 1199359 | G | A | missense_variant | MODERATE | c.454C>T|p.Pro152Ser |
S120 |
3 | BAA10g02460 | A10 | 1199667 | C | T | missense_variant | MODERATE | c.262G>A|p.Glu88Lys |
S188 |
4 | BAA10g02460 | A10 | 1203149 | C | T | upstream_gene_variant | MODIFIER | c.-3141G>A| |
S89 |
5 | BAA10g02460 | A10 | 1203899 | G | A | upstream_gene_variant | MODIFIER | c.-3891C>T| |
S212 |
6 | BAA10g02460 | A10 | 1204209 | G | A | upstream_gene_variant | MODIFIER | c.-4201C>T| |
S97 |