Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g11830 | A01 | 5523263 | G | A | downstream_gene_variant | MODIFIER | c.*3738C>T| |
S60 |
2 | BAA01g11830 | A01 | 5523475 | C | T | downstream_gene_variant | MODIFIER | c.*3526G>A| |
S287 |
3 | BAA01g11830 | A01 | 5523831 | C | T | downstream_gene_variant | MODIFIER | c.*3170G>A| |
S226 |
4 | BAA01g11830 | A01 | 5527336 | C | T | missense_variant | MODERATE | c.1147G>A|p.Asp383Asn |
S112 |
5 | BAA01g11830 | A01 | 5527788 | G | A | missense_variant | MODERATE | c.695C>T|p.Ala232Val |
S67 |
6 | BAA01g11830 | A01 | 5527938 | G | A | missense_variant | MODERATE | c.545C>T|p.Thr182Met |
S271 |
7 | BAA01g11830 | A01 | 5528036 | A | C | missense_variant | MODERATE | c.447T>G|p.His149Gln |
S263 |
8 | BAA01g11830 | A01 | 5528089 | G | A | stop_gained | HIGH | c.394C>T|p.Gln132* |
S190 |
9 | BAA01g11830 | A01 | 5528500 | C | T | upstream_gene_variant | MODIFIER | c.-18G>A| |
S150 |
10 | BAA01g11830 | A01 | 5529649 | C | T | upstream_gene_variant | MODIFIER | c.-1167G>A| |
S202 |
11 | BAA01g11830 | A01 | 5529705 | C | T | upstream_gene_variant | MODIFIER | c.-1223G>A| |
S230 |
12 | BAA01g11830 | A01 | 5529927 | C | T | upstream_gene_variant | MODIFIER | c.-1445G>A| |
S113 |