Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g33260 | A07 | 32269983 | G | A | missense_variant | MODERATE | c.172G>A|p.Val58Ile |
S139 |
2 | BAA07g33260 | A07 | 32270179 | A | C | missense_variant | MODERATE | c.368A>C|p.Asn123Thr |
S236 S306 S32 S72 S87 |
3 | BAA07g33260 | A07 | 32270562 | G | A | synonymous_variant | LOW | c.669G>A|p.Arg223Arg |
S115 |
4 | BAA07g33260 | A07 | 32272571 | C | T | missense_variant | MODERATE | c.1459C>T|p.Leu487Phe |
S103 |
5 | BAA07g33260 | A07 | 32274042 | C | T | downstream_gene_variant | MODIFIER | c.*1376C>T| |
S169 |
6 | BAA07g33260 | A07 | 32274195 | T | C | downstream_gene_variant | MODIFIER | c.*1529T>C| |
S198 |
7 | BAA07g33260 | A07 | 32274326 | C | T | downstream_gene_variant | MODIFIER | c.*1660C>T| |
S38 |
8 | BAA07g33260 | A07 | 32276452 | C | T | downstream_gene_variant | MODIFIER | c.*3786C>T| |
S260 |