Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g69130 | A09 | 61836208 | C | T | missense_variant | MODERATE | c.799G>A|p.Asp267Asn |
S239 |
2 | BAA09g69130 | A09 | 61837835 | G | A | synonymous_variant | LOW | c.82C>T|p.Leu28Leu |
S58 |
3 | BAA09g69130 | A09 | 61838419 | C | T | upstream_gene_variant | MODIFIER | c.-274G>A| |
S265 |
4 | BAA09g69130 | A09 | 61839421 | G | A | upstream_gene_variant | MODIFIER | c.-1276C>T| |
S247 |
5 | BAA09g69130 | A09 | 61842142 | C | T | upstream_gene_variant | MODIFIER | c.-3997G>A| |
S122 |
6 | BAA09g69130 | A09 | 61842191 | G | A | upstream_gene_variant | MODIFIER | c.-4046C>T| |
S63 |
7 | BAA09g69130 | A09 | 61842442 | G | A | upstream_gene_variant | MODIFIER | c.-4297C>T| |
S81 |
8 | BAA09g69130 | A09 | 61842601 | C | T | upstream_gene_variant | MODIFIER | c.-4456G>A| |
S219 |