Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g21790 | A06 | 11776738 | C | T | missense_variant | MODERATE | c.1390G>A|p.Asp464Asn |
S37 |
2 | BAA06g21790 | A06 | 11776745 | C | T | synonymous_variant | LOW | c.1383G>A|p.Gln461Gln |
S261 |
3 | BAA06g21790 | A06 | 11776947 | G | A | missense_variant | MODERATE | c.1181C>T|p.Ala394Val |
S229 |
4 | BAA06g21790 | A06 | 11778206 | G | A | synonymous_variant | LOW | c.675C>T|p.Phe225Phe |
S61 |
5 | BAA06g21790 | A06 | 11779777 | G | A | upstream_gene_variant | MODIFIER | c.-731C>T| |
S130 |