Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g02170 | A10 | 1028461 | C | T | missense_variant | MODERATE | c.233G>A|p.Gly78Asp |
S270 |
2 | BAA10g02170 | A10 | 1028708 | C | T | missense_variant | MODERATE | c.68G>A|p.Ser23Asn |
S308 |
3 | BAA10g02170 | A10 | 1030843 | G | T | upstream_gene_variant | MODIFIER | c.-2068C>A| |
S289 |
4 | BAA10g02170 | A10 | 1031068 | G | A | upstream_gene_variant | MODIFIER | c.-2293C>T| |
S251 |
5 | BAA10g02170 | A10 | 1031369 | C | T | upstream_gene_variant | MODIFIER | c.-2594G>A| |
S256 |