Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10050 | A02 | 4433108 | G | A | synonymous_variant | LOW | c.24G>A|p.Ala8Ala |
S110 |
2 | BAA02g10050 | A02 | 4433472 | G | A | synonymous_variant | LOW | c.285G>A|p.Gln95Gln |
S259 |
3 | BAA02g10050 | A02 | 4433584 | G | A | missense_variant | MODERATE | c.397G>A|p.Asp133Asn |
S61 |
4 | BAA02g10050 | A02 | 4434256 | G | A | synonymous_variant | LOW | c.831G>A|p.Gln277Gln |
S60 |
5 | BAA02g10050 | A02 | 4434686 | C | T | missense_variant | MODERATE | c.1105C>T|p.Arg369Cys |
S71 |
6 | BAA02g10050 | A02 | 4435258 | G | A | splice_donor_variant&intron_variant | HIGH | c.1416+1G>A| |
S43 |
7 | BAA02g10050 | A02 | 4435450 | G | A | splice_region_variant&intron_variant | LOW | c.1530+5G>A| |
S35 |
8 | BAA02g10050 | A02 | 4435666 | C | T | missense_variant | MODERATE | c.1669C>T|p.Leu557Phe |
S204 |
9 | BAA02g10050 | A02 | 4437871 | G | A | downstream_gene_variant | MODIFIER | c.*164G>A| |
S148 S210 S30 S31 |
10 | BAA02g10050 | A02 | 4438020 | C | T | downstream_gene_variant | MODIFIER | c.*313C>T| |
S185 |
11 | BAA02g10050 | A02 | 4439021 | C | T | downstream_gene_variant | MODIFIER | c.*1314C>T| |
S280 |