Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g28790 | A01 | 18086907 | C | T | upstream_gene_variant | MODIFIER | c.-1868C>T| |
S118 |
2 | BAA01g28790 | A01 | 18087239 | G | A | upstream_gene_variant | MODIFIER | c.-1536G>A| |
S268 |
3 | BAA01g28790 | A01 | 18087352 | C | T | upstream_gene_variant | MODIFIER | c.-1423C>T| |
S37 |
4 | BAA01g28790 | A01 | 18088326 | G | A | upstream_gene_variant | MODIFIER | c.-449G>A| |
S105 S106 |
5 | BAA01g28790 | A01 | 18088376 | G | A | upstream_gene_variant | MODIFIER | c.-399G>A| |
S13 |
6 | BAA01g28790 | A01 | 18088754 | C | T | upstream_gene_variant | MODIFIER | c.-21C>T| |
S146 |
7 | BAA01g28790 | A01 | 18088937 | C | T | intron_variant | MODIFIER | c.94-36C>T| |
S156 |
8 | BAA01g28790 | A01 | 18088979 | G | A | missense_variant | MODERATE | c.100G>A|p.Asp34Asn |
S181 |
9 | BAA01g28790 | A01 | 18089302 | C | T | synonymous_variant | LOW | c.325C>T|p.Leu109Leu |
S293 |
10 | BAA01g28790 | A01 | 18089637 | G | A | downstream_gene_variant | MODIFIER | c.*171G>A| |
S155 S211 |
11 | BAA01g28790 | A01 | 18089777 | G | A | downstream_gene_variant | MODIFIER | c.*311G>A| |
S292 |
12 | BAA01g28790 | A01 | 18090263 | C | G | downstream_gene_variant | MODIFIER | c.*797C>G| |
S155 S211 |
13 | BAA01g28790 | A01 | 18090576 | G | A | downstream_gene_variant | MODIFIER | c.*1110G>A| |
S190 |
14 | BAA01g28790 | A01 | 18094102 | C | T | downstream_gene_variant | MODIFIER | c.*4636C>T| |
S77 S82 |
15 | BAA01g28790 | A01 | 18094149 | C | T | downstream_gene_variant | MODIFIER | c.*4683C>T| |
S113 |
16 | BAA01g28790 | A01 | 18094162 | C | T | downstream_gene_variant | MODIFIER | c.*4696C>T| |
S134 |