Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g22170 | A10 | 19203491 | G | A | upstream_gene_variant | MODIFIER | c.-1172G>A| |
S3 |
2 | BAA10g22170 | A10 | 19204332 | G | A | upstream_gene_variant | MODIFIER | c.-331G>A| |
S76 |
3 | BAA10g22170 | A10 | 19204973 | C | T | missense_variant | MODERATE | c.139C>T|p.Pro47Ser |
S14 |