Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g15800 | A01 | 7669756 | C | T | upstream_gene_variant | MODIFIER | c.-3953C>T| |
S250 |
2 | BAA01g15800 | A01 | 7671262 | C | T | upstream_gene_variant | MODIFIER | c.-2447C>T| |
S210 S225 |
3 | BAA01g15800 | A01 | 7672003 | G | A | upstream_gene_variant | MODIFIER | c.-1706G>A| |
S13 |
4 | BAA01g15800 | A01 | 7672025 | C | T | upstream_gene_variant | MODIFIER | c.-1684C>T| |
S230 |
5 | BAA01g15800 | A01 | 7673815 | C | T | missense_variant | MODERATE | c.107C>T|p.Pro36Leu |
S296 |
6 | BAA01g15800 | A01 | 7673983 | G | A | missense_variant | MODERATE | c.275G>A|p.Gly92Asp |
S142 |
7 | BAA01g15800 | A01 | 7674125 | C | A | synonymous_variant | LOW | c.417C>A|p.Pro139Pro |
S66 |
8 | BAA01g15800 | A01 | 7675828 | C | T | missense_variant | MODERATE | c.1373C>T|p.Pro458Leu |
S286 |
9 | BAA01g15800 | A01 | 7677020 | C | T | missense_variant | MODERATE | c.1781C>T|p.Pro594Leu |
S302 |
10 | BAA01g15800 | A01 | 7677398 | C | T | missense_variant | MODERATE | c.2044C>T|p.Arg682Cys |
S112 |
11 | BAA01g15800 | A01 | 7678263 | C | T | synonymous_variant | LOW | c.2772C>T|p.His924His |
S213 |
12 | BAA01g15800 | A01 | 7681030 | C | T | downstream_gene_variant | MODIFIER | c.*2740C>T| |
S65 |
13 | BAA01g15800 | A01 | 7682312 | C | T | downstream_gene_variant | MODIFIER | c.*4022C>T| |
S100 |