Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g37760 | A07 | 34638248 | G | A | upstream_gene_variant | MODIFIER | c.-3543G>A| |
S120 |
2 | BAA07g37760 | A07 | 34640480 | C | T | upstream_gene_variant | MODIFIER | c.-1311C>T| |
S8 |
3 | BAA07g37760 | A07 | 34640661 | C | T | upstream_gene_variant | MODIFIER | c.-1130C>T| |
S274 |
4 | BAA07g37760 | A07 | 34641172 | C | T | upstream_gene_variant | MODIFIER | c.-619C>T| |
S68 |
5 | BAA07g37760 | A07 | 34642092 | C | T | missense_variant | MODERATE | c.302C>T|p.Ser101Phe |
S293 S36 |
6 | BAA07g37760 | A07 | 34642892 | G | A | missense_variant | MODERATE | c.670G>A|p.Val224Ile |
S11 |
7 | BAA07g37760 | A07 | 34643294 | G | A | missense_variant | MODERATE | c.1072G>A|p.Glu358Lys |
S240 |
8 | BAA07g37760 | A07 | 34643578 | G | A | synonymous_variant | LOW | c.1356G>A|p.Glu452Glu |
S163 |
9 | BAA07g37760 | A07 | 34643655 | C | T | missense_variant | MODERATE | c.1433C>T|p.Pro478Leu |
S134 |