Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g29190 | A07 | 30006112 | G | A | missense_variant | MODERATE | c.1276C>T|p.Pro426Ser |
S208 S219 |
2 | BAA07g29190 | A07 | 30006386 | C | T | synonymous_variant | LOW | c.1002G>A|p.Arg334Arg |
S136 |
3 | BAA07g29190 | A07 | 30006907 | G | A | synonymous_variant | LOW | c.579C>T|p.Ile193Ile |
S292 |
4 | BAA07g29190 | A07 | 30007739 | C | T | splice_region_variant&intron_variant | LOW | c.127+5G>A| |
S86 |
5 | BAA07g29190 | A07 | 30010511 | G | A | upstream_gene_variant | MODIFIER | c.-2641C>T| |
S263 |
6 | BAA07g29190 | A07 | 30010588 | G | A | upstream_gene_variant | MODIFIER | c.-2718C>T| |
S134 |
7 | BAA07g29190 | A07 | 30011261 | A | T | upstream_gene_variant | MODIFIER | c.-3391T>A| |
S127 |
8 | BAA07g29190 | A07 | 30011715 | G | A | upstream_gene_variant | MODIFIER | c.-3845C>T| |
S60 |