Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g00990 | A07 | 679980 | C | T | downstream_gene_variant | MODIFIER | c.*1227G>A| |
S183 S198 |
2 | BAA07g00990 | A07 | 681017 | C | T | downstream_gene_variant | MODIFIER | c.*190G>A| |
S77 S82 |
3 | BAA07g00990 | A07 | 681606 | A | C | synonymous_variant | LOW | c.669T>G|p.Ser223Ser |
S159 S243 S299 |
4 | BAA07g00990 | A07 | 681679 | G | A | missense_variant | MODERATE | c.596C>T|p.Ala199Val |
S87 |
5 | BAA07g00990 | A07 | 682089 | C | T | synonymous_variant | LOW | c.186G>A|p.Ser62Ser |
S32 |
6 | BAA07g00990 | A07 | 682115 | C | T | missense_variant | MODERATE | c.160G>A|p.Asp54Asn |
S28 |
7 | BAA07g00990 | A07 | 682180 | C | T | missense_variant | MODERATE | c.95G>A|p.Ser32Asn |
S103 |
8 | BAA07g00990 | A07 | 683741 | C | T | upstream_gene_variant | MODIFIER | c.-1467G>A| |
S20 |
9 | BAA07g00990 | A07 | 686160 | C | T | upstream_gene_variant | MODIFIER | c.-3886G>A| |
S95 |