Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g40120 | A09 | 47437961 | C | T | missense_variant | MODERATE | c.1061G>A|p.Gly354Glu |
S186 |
2 | BAA09g40120 | A09 | 47438491 | C | T | missense_variant | MODERATE | c.531G>A|p.Met177Ile |
S37 |
3 | BAA09g40120 | A09 | 47438494 | C | T | synonymous_variant | LOW | c.528G>A|p.Lys176Lys |
S54 |
4 | BAA09g40120 | A09 | 47438559 | C | T | missense_variant | MODERATE | c.463G>A|p.Ala155Thr |
S232 |
5 | BAA09g40120 | A09 | 47438723 | C | T | missense_variant | MODERATE | c.299G>A|p.Ser100Asn |
S242 |
6 | BAA09g40120 | A09 | 47438808 | C | T | missense_variant | MODERATE | c.214G>A|p.Glu72Lys |
S68 |
7 | BAA09g40120 | A09 | 47439102 | G | A | upstream_gene_variant | MODIFIER | c.-81C>T| |
S174 S216 S265 S27 |