Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g28700 | A07 | 29761777 | G | A | missense_variant | MODERATE | c.1879C>T|p.Pro627Ser |
S263 |
2 | BAA07g28700 | A07 | 29762117 | C | T | stop_gained | HIGH | c.1539G>A|p.Trp513* |
S58 |
3 | BAA07g28700 | A07 | 29762989 | C | T | missense_variant | MODERATE | c.667G>A|p.Asp223Asn |
S8 |
4 | BAA07g28700 | A07 | 29763512 | C | T | synonymous_variant | LOW | c.144G>A|p.Thr48Thr |
S8 |
5 | BAA07g28700 | A07 | 29763628 | C | T | missense_variant | MODERATE | c.28G>A|p.Ala10Thr |
S276 |
6 | BAA07g28700 | A07 | 29763889 | G | A | upstream_gene_variant | MODIFIER | c.-234C>T| |
S40 S49 |
7 | BAA07g28700 | A07 | 29764115 | C | A | upstream_gene_variant | MODIFIER | c.-460G>T| |
S132 S14 S152 S252 S265 S43 |
8 | BAA07g28700 | A07 | 29766026 | C | T | upstream_gene_variant | MODIFIER | c.-2371G>A| |
S42 |
9 | BAA07g28700 | A07 | 29768623 | G | A | upstream_gene_variant | MODIFIER | c.-4968C>T| |
S240 |