Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01080 | A02 | 500076 | C | T | upstream_gene_variant | MODIFIER | c.-4746C>T| |
S201 |
2 | BAA02g01080 | A02 | 500486 | G | A | upstream_gene_variant | MODIFIER | c.-4336G>A| |
S289 S290 |
3 | BAA02g01080 | A02 | 501003 | C | T | upstream_gene_variant | MODIFIER | c.-3819C>T| |
S15 S3 |
4 | BAA02g01080 | A02 | 502179 | G | A | upstream_gene_variant | MODIFIER | c.-2643G>A| |
S122 |
5 | BAA02g01080 | A02 | 502423 | C | T | upstream_gene_variant | MODIFIER | c.-2399C>T| |
S243 S299 |
6 | BAA02g01080 | A02 | 504876 | G | A | missense_variant | MODERATE | c.55G>A|p.Gly19Ser |
S202 |
7 | BAA02g01080 | A02 | 505016 | G | A | synonymous_variant | LOW | c.195G>A|p.Gln65Gln |
S221 |
8 | BAA02g01080 | A02 | 507149 | G | A | missense_variant | MODERATE | c.1186G>A|p.Gly396Ser |
S148 S210 S30 S31 |
9 | BAA02g01080 | A02 | 507602 | C | T | synonymous_variant | LOW | c.1639C>T|p.Leu547Leu |
S172 S217 |
10 | BAA02g01080 | A02 | 509204 | G | A | downstream_gene_variant | MODIFIER | c.*1552G>A| |
S129 |
11 | BAA02g01080 | A02 | 509457 | C | T | downstream_gene_variant | MODIFIER | c.*1805C>T| |
S2 |
12 | BAA02g01080 | A02 | 510730 | C | T | downstream_gene_variant | MODIFIER | c.*3078C>T| |
S117 |
13 | BAA02g01080 | A02 | 511090 | C | T | downstream_gene_variant | MODIFIER | c.*3438C>T| |
S2 |