Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g22980 | A07 | 27059753 | G | A | upstream_gene_variant | MODIFIER | c.-588G>A| |
S113 |
2 | BAA07g22980 | A07 | 27060459 | C | T | intron_variant | MODIFIER | c.50-37C>T| |
S8 |
3 | BAA07g22980 | A07 | 27060508 | C | T | missense_variant | MODERATE | c.62C>T|p.Thr21Ile |
S3 |
4 | BAA07g22980 | A07 | 27060873 | C | T | intron_variant | MODIFIER | c.204-50C>T| |
S58 |
5 | BAA07g22980 | A07 | 27063170 | G | A | missense_variant | MODERATE | c.1129G>A|p.Asp377Asn |
S180 |
6 | BAA07g22980 | A07 | 27063950 | G | A | downstream_gene_variant | MODIFIER | c.*582G>A| |
S97 |
7 | BAA07g22980 | A07 | 27066155 | C | T | downstream_gene_variant | MODIFIER | c.*2787C>T| |
S179 |
8 | BAA07g22980 | A07 | 27066862 | C | T | downstream_gene_variant | MODIFIER | c.*3494C>T| |
S169 |
9 | BAA07g22980 | A07 | 27066876 | G | A | downstream_gene_variant | MODIFIER | c.*3508G>A| |
S278 |
10 | BAA07g22980 | A07 | 27067311 | C | T | downstream_gene_variant | MODIFIER | c.*3943C>T| |
S170 |