Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g01400 | A10 | 693110 | G | A | upstream_gene_variant | MODIFIER | c.-4446G>A| |
S219 |
2 | BAA10g01400 | A10 | 695033 | G | A | upstream_gene_variant | MODIFIER | c.-2523G>A| |
S284 |
3 | BAA10g01400 | A10 | 695888 | G | A | upstream_gene_variant | MODIFIER | c.-1668G>A| |
S201 |
4 | BAA10g01400 | A10 | 699109 | G | A | missense_variant | MODERATE | c.607G>A|p.Gly203Ser |
S279 |
5 | BAA10g01400 | A10 | 699128 | C | T | missense_variant | MODERATE | c.626C>T|p.Thr209Ile |
S210 |
6 | BAA10g01400 | A10 | 701303 | G | A | downstream_gene_variant | MODIFIER | c.*1666G>A| |
S18 |
7 | BAA10g01400 | A10 | 702386 | G | A | downstream_gene_variant | MODIFIER | c.*2749G>A| |
S293 |