Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g06010 | A08 | 4711545 | C | T | upstream_gene_variant | MODIFIER | c.-4384C>T| |
S247 |
2 | BAA08g06010 | A08 | 4711669 | G | A | upstream_gene_variant | MODIFIER | c.-4260G>A| |
S51 |
3 | BAA08g06010 | A08 | 4712041 | C | T | upstream_gene_variant | MODIFIER | c.-3888C>T| |
S140 |
4 | BAA08g06010 | A08 | 4712109 | C | T | upstream_gene_variant | MODIFIER | c.-3820C>T| |
S268 |
5 | BAA08g06010 | A08 | 4712335 | G | A | upstream_gene_variant | MODIFIER | c.-3594G>A| |
S32 |
6 | BAA08g06010 | A08 | 4712512 | G | A | upstream_gene_variant | MODIFIER | c.-3417G>A| |
S146 |
7 | BAA08g06010 | A08 | 4714505 | G | A | upstream_gene_variant | MODIFIER | c.-1424G>A| |
S73 |
8 | BAA08g06010 | A08 | 4715798 | C | T | upstream_gene_variant | MODIFIER | c.-131C>T| |
S152 |
9 | BAA08g06010 | A08 | 4716010 | G | A | missense_variant&splice_region_variant | MODERATE | c.82G>A|p.Gly28Ser |
S32 |
10 | BAA08g06010 | A08 | 4716470 | C | T | missense_variant | MODERATE | c.239C>T|p.Ser80Phe |
S48 |