Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g46860 | A01 | 31194076 | C | T | missense_variant | MODERATE | c.245G>A|p.Ser82Asn |
S168 |
2 | BAA01g46860 | A01 | 31194210 | C | T | synonymous_variant | LOW | c.111G>A|p.Leu37Leu |
S273 |
3 | BAA01g46860 | A01 | 31194391 | C | T | stop_gained | HIGH | c.6G>A|p.Trp2* |
S44 |
4 | BAA01g46860 | A01 | 31195145 | G | A | upstream_gene_variant | MODIFIER | c.-749C>T| |
S110 |
5 | BAA01g46860 | A01 | 31196282 | C | T | upstream_gene_variant | MODIFIER | c.-1886G>A| |
S133 |
6 | BAA01g46860 | A01 | 31196336 | C | T | upstream_gene_variant | MODIFIER | c.-1940G>A| |
S233 |
7 | BAA01g46860 | A01 | 31198460 | G | A | upstream_gene_variant | MODIFIER | c.-4064C>T| |
S283 |
8 | BAA01g46860 | A01 | 31199199 | C | T | upstream_gene_variant | MODIFIER | c.-4803G>A| |
S192 |
9 | BAA01g46860 | A01 | 31199350 | C | T | upstream_gene_variant | MODIFIER | c.-4954G>A| |
S302 |