Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g45070 | A01 | 30048550 | C | T | upstream_gene_variant | MODIFIER | c.-2606C>T| |
S65 |
2 | BAA01g45070 | A01 | 30051501 | G | A | missense_variant | MODERATE | c.224G>A|p.Arg75Lys |
S15 S3 |
3 | BAA01g45070 | A01 | 30051814 | G | A | missense_variant | MODERATE | c.382G>A|p.Ala128Thr |
S15 |
4 | BAA01g45070 | A01 | 30052040 | C | T | synonymous_variant | LOW | c.525C>T|p.Ala175Ala |
S288 |
5 | BAA01g45070 | A01 | 30052079 | C | T | synonymous_variant | LOW | c.564C>T|p.Ser188Ser |
S281 |
6 | BAA01g45070 | A01 | 30052303 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.704-1G>A| |
S250 |
7 | BAA01g45070 | A01 | 30054195 | C | T | missense_variant | MODERATE | c.1192C>T|p.Pro398Ser |
S219 S301 S72 |
8 | BAA01g45070 | A01 | 30054333 | G | A | missense_variant | MODERATE | c.1330G>A|p.Glu444Lys |
S172 S217 |
9 | BAA01g45070 | A01 | 30054494 | G | A | synonymous_variant | LOW | c.1491G>A|p.Lys497Lys |
S33 |