Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g00940 | A08 | 702500 | C | T | downstream_gene_variant | MODIFIER | c.*4350G>A| |
S179 |
2 | BAA08g00940 | A08 | 707114 | C | T | synonymous_variant | LOW | c.171G>A|p.Gln57Gln |
S226 |
3 | BAA08g00940 | A08 | 708537 | C | T | intron_variant | MODIFIER | c.139-1391G>A| |
S15 S3 |
4 | BAA08g00940 | A08 | 708732 | C | T | intron_variant | MODIFIER | c.139-1586G>A| |
S223 |
5 | BAA08g00940 | A08 | 708778 | G | A | intron_variant | MODIFIER | c.139-1632C>T| |
S199 |
6 | BAA08g00940 | A08 | 708954 | C | T | intron_variant | MODIFIER | c.139-1808G>A| |
S215 |
7 | BAA08g00940 | A08 | 709755 | G | A | intron_variant | MODIFIER | c.139-2609C>T| |
S194 |
8 | BAA08g00940 | A08 | 713522 | G | A | synonymous_variant | LOW | c.9C>T|p.Gly3Gly |
S19 |
9 | BAA08g00940 | A08 | 713973 | T | A | upstream_gene_variant | MODIFIER | c.-443A>T| |
S126 |
10 | BAA08g00940 | A08 | 717403 | C | T | upstream_gene_variant | MODIFIER | c.-3873G>A| |
S138 |
11 | BAA08g00940 | A08 | 717442 | C | T | upstream_gene_variant | MODIFIER | c.-3912G>A| |
S99 |
12 | BAA08g00940 | A08 | 717506 | C | T | upstream_gene_variant | MODIFIER | c.-3976G>A| |
S83 S88 |