Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g36080 | A07 | 33891876 | C | T | missense_variant | MODERATE | c.1675G>A|p.Ala559Thr |
S23 |
2 | BAA07g36080 | A07 | 33892271 | C | T | missense_variant | MODERATE | c.1280G>A|p.Gly427Glu |
S245 |
3 | BAA07g36080 | A07 | 33892462 | G | A | synonymous_variant | LOW | c.1089C>T|p.Ser363Ser |
S292 |
4 | BAA07g36080 | A07 | 33892803 | G | A | missense_variant | MODERATE | c.748C>T|p.Leu250Phe |
S47 S74 |
5 | BAA07g36080 | A07 | 33893014 | C | T | synonymous_variant | LOW | c.537G>A|p.Lys179Lys |
S229 |
6 | BAA07g36080 | A07 | 33894407 | C | T | synonymous_variant | LOW | c.144G>A|p.Glu48Glu |
S282 |
7 | BAA07g36080 | A07 | 33896729 | G | A | upstream_gene_variant | MODIFIER | c.-2179C>T| |
S138 |
8 | BAA07g36080 | A07 | 33897556 | C | T | upstream_gene_variant | MODIFIER | c.-3006G>A| |
S221 |