Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g10770 | A01 | 4958146 | C | T | upstream_gene_variant | MODIFIER | c.-3124C>T| |
S136 |
2 | BAA01g10770 | A01 | 4959087 | C | T | upstream_gene_variant | MODIFIER | c.-2183C>T| |
S130 |
3 | BAA01g10770 | A01 | 4959853 | G | A | upstream_gene_variant | MODIFIER | c.-1417G>A| |
S216 |
4 | BAA01g10770 | A01 | 4959957 | G | A | upstream_gene_variant | MODIFIER | c.-1313G>A| |
S229 |
5 | BAA01g10770 | A01 | 4961966 | G | A | missense_variant | MODERATE | c.697G>A|p.Gly233Arg |
S226 |
6 | BAA01g10770 | A01 | 4962000 | C | T | missense_variant | MODERATE | c.731C>T|p.Ser244Phe |
S155 S211 |
7 | BAA01g10770 | A01 | 4963872 | C | T | downstream_gene_variant | MODIFIER | c.*1469C>T| |
S47 |
8 | BAA01g10770 | A01 | 4963892 | G | A | downstream_gene_variant | MODIFIER | c.*1489G>A| |
S191 |
9 | BAA01g10770 | A01 | 4966216 | G | A | downstream_gene_variant | MODIFIER | c.*3813G>A| |
S263 |
10 | BAA01g10770 | A01 | 4966930 | C | T | downstream_gene_variant | MODIFIER | c.*4527C>T| |
S221 |
11 | BAA01g10770 | A01 | 4966969 | C | T | downstream_gene_variant | MODIFIER | c.*4566C>T| |
S185 |