Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g26160 | A10 | 20862439 | C | T | missense_variant | MODERATE | c.1187G>A|p.Gly396Glu |
S196 |
2 | BAA10g26160 | A10 | 20862599 | G | A | stop_gained | HIGH | c.1027C>T|p.Gln343* |
S269 |
3 | BAA10g26160 | A10 | 20863974 | G | A | missense_variant | MODERATE | c.136C>T|p.Leu46Phe |
S80 |
4 | BAA10g26160 | A10 | 20865404 | G | A | upstream_gene_variant | MODIFIER | c.-974C>T| |
S303 |
5 | BAA10g26160 | A10 | 20867861 | C | T | upstream_gene_variant | MODIFIER | c.-3431G>A| |
S115 |
6 | BAA10g26160 | A10 | 20868362 | G | A | upstream_gene_variant | MODIFIER | c.-3932C>T| |
S252 |
7 | BAA10g26160 | A10 | 20869158 | G | A | upstream_gene_variant | MODIFIER | c.-4728C>T| |
S7 |