Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g01660 | A05 | 956531 | C | T | missense_variant | MODERATE | c.799G>A|p.Val267Ile |
S162 |
2 | BAA05g01660 | A05 | 957528 | C | T | missense_variant | MODERATE | c.88G>A|p.Asp30Asn |
S159 S243 S299 |
3 | BAA05g01660 | A05 | 957712 | G | A | upstream_gene_variant | MODIFIER | c.-97C>T| |
S33 |
4 | BAA05g01660 | A05 | 957893 | G | A | upstream_gene_variant | MODIFIER | c.-278C>T| |
S32 |
5 | BAA05g01660 | A05 | 959932 | C | T | upstream_gene_variant | MODIFIER | c.-2317G>A| |
S94 |
6 | BAA05g01660 | A05 | 960144 | C | T | upstream_gene_variant | MODIFIER | c.-2529G>A| |
S182 |
7 | BAA05g01660 | A05 | 962579 | G | A | upstream_gene_variant | MODIFIER | c.-4964C>T| |
S296 |