Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g29000 | A07 | 29910873 | C | T | upstream_gene_variant | MODIFIER | c.-3059C>T| |
S281 |
2 | BAA07g29000 | A07 | 29913209 | G | A | upstream_gene_variant | MODIFIER | c.-723G>A| |
S267 |
3 | BAA07g29000 | A07 | 29914435 | G | A | missense_variant | MODERATE | c.415G>A|p.Val139Ile |
S170 |
4 | BAA07g29000 | A07 | 29914513 | C | T | synonymous_variant | LOW | c.493C>T|p.Leu165Leu |
S203 |
5 | BAA07g29000 | A07 | 29914638 | C | T | splice_region_variant&intron_variant | LOW | c.545-3C>T| |
S284 |
6 | BAA07g29000 | A07 | 29914711 | C | T | synonymous_variant | LOW | c.615C>T|p.Phe205Phe |
S98 |
7 | BAA07g29000 | A07 | 29914859 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.682-1G>A| |
S287 |
8 | BAA07g29000 | A07 | 29915731 | C | T | downstream_gene_variant | MODIFIER | c.*362C>T| |
S58 |
9 | BAA07g29000 | A07 | 29916219 | C | T | downstream_gene_variant | MODIFIER | c.*850C>T| |
S71 |