Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g15790 | A10 | 16006597 | G | A | missense_variant | MODERATE | c.503C>T|p.Ser168Phe |
S286 |
2 | BAA10g15790 | A10 | 16007418 | C | T | upstream_gene_variant | MODIFIER | c.-52G>A| |
S190 |
3 | BAA10g15790 | A10 | 16007523 | G | A | upstream_gene_variant | MODIFIER | c.-157C>T| |
S178 |
4 | BAA10g15790 | A10 | 16008045 | C | T | upstream_gene_variant | MODIFIER | c.-679G>A| |
S296 |
5 | BAA10g15790 | A10 | 16008279 | G | A | upstream_gene_variant | MODIFIER | c.-913C>T| |
S209 |
6 | BAA10g15790 | A10 | 16008757 | C | T | upstream_gene_variant | MODIFIER | c.-1391G>A| |
S156 |
7 | BAA10g15790 | A10 | 16010602 | G | A | upstream_gene_variant | MODIFIER | c.-3236C>T| |
S71 |
8 | BAA10g15790 | A10 | 16011407 | G | A | upstream_gene_variant | MODIFIER | c.-4041C>T| |
S134 |
9 | BAA10g15790 | A10 | 16012280 | G | A | upstream_gene_variant | MODIFIER | c.-4914C>T| |
S180 |