Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g29820 | A02 | 17143521 | C | T | missense_variant | MODERATE | c.832G>A|p.Asp278Asn |
S124 |
2 | BAA02g29820 | A02 | 17143974 | G | A | splice_region_variant&intron_variant | LOW | c.434+8C>T| |
S232 |
3 | BAA02g29820 | A02 | 17144268 | C | T | missense_variant | MODERATE | c.148G>A|p.Asp50Asn |
S114 |
4 | BAA02g29820 | A02 | 17147522 | C | T | upstream_gene_variant | MODIFIER | c.-3107G>A| |
S152 |
5 | BAA02g29820 | A02 | 17147737 | G | A | upstream_gene_variant | MODIFIER | c.-3322C>T| |
S10 |