Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g02910 | A04 | 1722772 | G | A | upstream_gene_variant | MODIFIER | c.-101G>A| |
S191 |
2 | BAA04g02910 | A04 | 1723404 | G | A | missense_variant | MODERATE | c.532G>A|p.Asp178Asn |
S286 |
3 | BAA04g02910 | A04 | 1723629 | G | A | missense_variant | MODERATE | c.757G>A|p.Asp253Asn |
S198 |
4 | BAA04g02910 | A04 | 1724243 | G | A | synonymous_variant | LOW | c.1371G>A|p.Gly457Gly |
S146 |
5 | BAA04g02910 | A04 | 1724809 | C | T | missense_variant | MODERATE | c.1937C>T|p.Pro646Leu |
S159 S299 |
6 | BAA04g02910 | A04 | 1725131 | G | A | synonymous_variant | LOW | c.2259G>A|p.Pro753Pro |
S183 S198 |
7 | BAA04g02910 | A04 | 1726571 | G | A | downstream_gene_variant | MODIFIER | c.*1362G>A| |
S162 |
8 | BAA04g02910 | A04 | 1726987 | C | T | downstream_gene_variant | MODIFIER | c.*1778C>T| |
S168 |