Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g00230 | A07 | 104660 | C | T | upstream_gene_variant | MODIFIER | c.-1518C>T| |
S284 |
2 | BAA07g00230 | A07 | 105259 | C | T | upstream_gene_variant | MODIFIER | c.-919C>T| |
S59 |
3 | BAA07g00230 | A07 | 105908 | G | A | upstream_gene_variant | MODIFIER | c.-270G>A| |
S216 |
4 | BAA07g00230 | A07 | 106137 | G | A | upstream_gene_variant | MODIFIER | c.-41G>A| |
S156 |
5 | BAA07g00230 | A07 | 106424 | C | T | missense_variant | MODERATE | c.247C>T|p.Arg83Cys |
S192 |
6 | BAA07g00230 | A07 | 107194 | G | A | missense_variant | MODERATE | c.688G>A|p.Ala230Thr |
S296 |
7 | BAA07g00230 | A07 | 107848 | G | A | missense_variant | MODERATE | c.1183G>A|p.Ala395Thr |
S96 |
8 | BAA07g00230 | A07 | 110980 | C | T | downstream_gene_variant | MODIFIER | c.*2890C>T| |
S250 |
9 | BAA07g00230 | A07 | 111700 | C | T | downstream_gene_variant | MODIFIER | c.*3610C>T| |
S261 |
10 | BAA07g00230 | A07 | 112233 | C | T | downstream_gene_variant | MODIFIER | c.*4143C>T| |
S238 |