Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g20530 | A01 | 10127364 | G | A | upstream_gene_variant | MODIFIER | c.-3966G>A| |
S268 |
2 | BAA01g20530 | A01 | 10128285 | G | A | upstream_gene_variant | MODIFIER | c.-3045G>A| |
S98 |
3 | BAA01g20530 | A01 | 10130319 | G | A | upstream_gene_variant | MODIFIER | c.-1011G>A| |
S149 |
4 | BAA01g20530 | A01 | 10130509 | C | T | upstream_gene_variant | MODIFIER | c.-821C>T| |
S177 |
5 | BAA01g20530 | A01 | 10130781 | C | T | upstream_gene_variant | MODIFIER | c.-549C>T| |
S206 S26 |
6 | BAA01g20530 | A01 | 10130857 | G | A | upstream_gene_variant | MODIFIER | c.-473G>A| |
S155 |
7 | BAA01g20530 | A01 | 10131876 | G | A | missense_variant | MODERATE | c.236G>A|p.Gly79Asp |
S293 |
8 | BAA01g20530 | A01 | 10132253 | C | T | synonymous_variant | LOW | c.411C>T|p.Asn137Asn |
S175 S226 S250 S291 |
9 | BAA01g20530 | A01 | 10132960 | C | T | intron_variant | MODIFIER | c.743+11C>T| |
S151 |
10 | BAA01g20530 | A01 | 10133841 | C | T | downstream_gene_variant | MODIFIER | c.*682C>T| |
S159 S243 |