Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g15080 | A01 | 7181320 | G | A | upstream_gene_variant | MODIFIER | c.-4604G>A| |
S171 |
2 | BAA01g15080 | A01 | 7186194 | C | T | missense_variant | MODERATE | c.271C>T|p.Leu91Phe |
S179 |
3 | BAA01g15080 | A01 | 7186569 | C | T | synonymous_variant | LOW | c.646C>T|p.Leu216Leu |
S67 |
4 | BAA01g15080 | A01 | 7189762 | G | A | missense_variant | MODERATE | c.1469G>A|p.Arg490Lys |
S217 S248 |
5 | BAA01g15080 | A01 | 7190892 | C | T | intron_variant | MODIFIER | c.2153+33C>T| |
S9 |
6 | BAA01g15080 | A01 | 7192951 | C | T | synonymous_variant | LOW | c.2295C>T|p.Thr765Thr |
S296 |
7 | BAA01g15080 | A01 | 7192970 | G | A | missense_variant | MODERATE | c.2314G>A|p.Ala772Thr |
S237 |
8 | BAA01g15080 | A01 | 7197511 | G | A | downstream_gene_variant | MODIFIER | c.*1759G>A| |
S163 |
9 | BAA01g15080 | A01 | 7199267 | C | T | downstream_gene_variant | MODIFIER | c.*3515C>T| |
S192 S252 |
10 | BAA01g15080 | A01 | 7199325 | G | A | downstream_gene_variant | MODIFIER | c.*3573G>A| |
S259 |