Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g18200 | A01 | 8948480 | C | T | splice_region_variant&synonymous_variant | LOW | c.753G>A|p.Glu251Glu |
S19 |
2 | BAA01g18200 | A01 | 8950642 | C | T | missense_variant | MODERATE | c.673G>A|p.Ala225Thr |
S270 |
3 | BAA01g18200 | A01 | 8951911 | C | T | intron_variant | MODIFIER | c.472-1068G>A| |
S148 |
4 | BAA01g18200 | A01 | 8953588 | C | T | missense_variant | MODERATE | c.376G>A|p.Asp126Asn |
S20 |
5 | BAA01g18200 | A01 | 8953713 | G | A | missense_variant | MODERATE | c.251C>T|p.Thr84Ile |
S207 |
6 | BAA01g18200 | A01 | 8953873 | C | T | missense_variant | MODERATE | c.91G>A|p.Glu31Lys |
S256 |
7 | BAA01g18200 | A01 | 8954495 | G | A | upstream_gene_variant | MODIFIER | c.-532C>T| |
S34 |
8 | BAA01g18200 | A01 | 8955537 | G | A | upstream_gene_variant | MODIFIER | c.-1574C>T| |
S5 |
9 | BAA01g18200 | A01 | 8956073 | C | T | upstream_gene_variant | MODIFIER | c.-2110G>A| |
S208 S93 |
10 | BAA01g18200 | A01 | 8956768 | C | T | upstream_gene_variant | MODIFIER | c.-2805G>A| |
S117 |
11 | BAA01g18200 | A01 | 8958589 | C | T | upstream_gene_variant | MODIFIER | c.-4626G>A| |
S289 S290 |
12 | BAA01g18200 | A01 | 8958744 | G | A | upstream_gene_variant | MODIFIER | c.-4781C>T| |
S23 |