Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g06020 | A08 | 4717452 | C | T | missense_variant | MODERATE | c.776G>A|p.Arg259Lys |
S210 |
2 | BAA08g06020 | A08 | 4718142 | G | A | missense_variant | MODERATE | c.442C>T|p.Pro148Ser |
S178 |
3 | BAA08g06020 | A08 | 4718908 | C | T | synonymous_variant | LOW | c.78G>A|p.Lys26Lys |
S47 |
4 | BAA08g06020 | A08 | 4720027 | G | A | upstream_gene_variant | MODIFIER | c.-1042C>T| |
S273 |
5 | BAA08g06020 | A08 | 4720456 | G | A | upstream_gene_variant | MODIFIER | c.-1471C>T| |
S85 |
6 | BAA08g06020 | A08 | 4721001 | G | A | upstream_gene_variant | MODIFIER | c.-2016C>T| |
S148 |
7 | BAA08g06020 | A08 | 4721093 | C | T | upstream_gene_variant | MODIFIER | c.-2108G>A| |
S255 |
8 | BAA08g06020 | A08 | 4722001 | C | T | upstream_gene_variant | MODIFIER | c.-3016G>A| |
S4 |
9 | BAA08g06020 | A08 | 4722955 | G | A | upstream_gene_variant | MODIFIER | c.-3970C>T| |
S69 |
10 | BAA08g06020 | A08 | 4723086 | C | T | upstream_gene_variant | MODIFIER | c.-4101G>A| |
S281 |
11 | BAA08g06020 | A08 | 4723096 | G | A | upstream_gene_variant | MODIFIER | c.-4111C>T| |
S200 |
12 | BAA08g06020 | A08 | 4723309 | G | A | upstream_gene_variant | MODIFIER | c.-4324C>T| |
S11 |