Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g00520 | A05 | 291596 | C | T | missense_variant | MODERATE | c.1621G>A|p.Asp541Asn |
S153 S213 |
2 | BAA05g00520 | A05 | 292047 | G | A | synonymous_variant | LOW | c.1170C>T|p.Tyr390Tyr |
S6 |
3 | BAA05g00520 | A05 | 292279 | C | T | missense_variant | MODERATE | c.938G>A|p.Arg313Lys |
S73 S91 |
4 | BAA05g00520 | A05 | 292363 | G | A | missense_variant | MODERATE | c.854C>T|p.Ser285Phe |
S45 |
5 | BAA05g00520 | A05 | 292403 | G | A | missense_variant | MODERATE | c.814C>T|p.Leu272Phe |
S299 |
6 | BAA05g00520 | A05 | 292512 | G | A | synonymous_variant | LOW | c.705C>T|p.Leu235Leu |
S67 |
7 | BAA05g00520 | A05 | 292944 | G | A | synonymous_variant | LOW | c.360C>T|p.Leu120Leu |
S184 |
8 | BAA05g00520 | A05 | 293088 | G | A | synonymous_variant | LOW | c.216C>T|p.Leu72Leu |
S166 S167 S257 S262 |
9 | BAA05g00520 | A05 | 295633 | T | A | upstream_gene_variant | MODIFIER | c.-2241A>T| |
S6 |
10 | BAA05g00520 | A05 | 296888 | C | T | upstream_gene_variant | MODIFIER | c.-3496G>A| |
S100 |