Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g29170 | A10 | 22058974 | G | A | missense_variant | MODERATE | c.1082C>T|p.Pro361Leu |
S173 |
2 | BAA10g29170 | A10 | 22060451 | G | A | missense_variant | MODERATE | c.232C>T|p.Pro78Ser |
S112 |
3 | BAA10g29170 | A10 | 22061109 | G | A | upstream_gene_variant | MODIFIER | c.-427C>T| |
S267 |
4 | BAA10g29170 | A10 | 22061559 | C | T | upstream_gene_variant | MODIFIER | c.-877G>A| |
S251 |
5 | BAA10g29170 | A10 | 22063416 | C | T | upstream_gene_variant | MODIFIER | c.-2734G>A| |
S28 |
6 | BAA10g29170 | A10 | 22063954 | C | T | upstream_gene_variant | MODIFIER | c.-3272G>A| |
S229 |