Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g28910 | A10 | 21973532 | C | T | missense_variant | MODERATE | c.601G>A|p.Val201Ile |
S11 |
2 | BAA10g28910 | A10 | 21973535 | A | C | missense_variant | MODERATE | c.598T>G|p.Leu200Val |
S17 S232 S246 S262 |
3 | BAA10g28910 | A10 | 21973940 | C | T | missense_variant | MODERATE | c.193G>A|p.Asp65Asn |
S11 |
4 | BAA10g28910 | A10 | 21974610 | G | A | upstream_gene_variant | MODIFIER | c.-478C>T| |
S126 |
5 | BAA10g28910 | A10 | 21974669 | G | A | upstream_gene_variant | MODIFIER | c.-537C>T| |
S262 |
6 | BAA10g28910 | A10 | 21975103 | G | A | upstream_gene_variant | MODIFIER | c.-971C>T| |
S184 |
7 | BAA10g28910 | A10 | 21977492 | G | A | upstream_gene_variant | MODIFIER | c.-3360C>T| |
S85 |