Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g39770 | A07 | 35576746 | C | T | missense_variant | MODERATE | c.1985G>A|p.Arg662Gln |
S144 |
2 | BAA07g39770 | A07 | 35578740 | C | T | synonymous_variant | LOW | c.1398G>A|p.Leu466Leu |
S164 |
3 | BAA07g39770 | A07 | 35583826 | G | A | upstream_gene_variant | MODIFIER | c.-1441C>T| |
S169 |
4 | BAA07g39770 | A07 | 35583893 | C | T | upstream_gene_variant | MODIFIER | c.-1508G>A| |
S56 |
5 | BAA07g39770 | A07 | 35584089 | G | A | upstream_gene_variant | MODIFIER | c.-1704C>T| |
S133 |
6 | BAA07g39770 | A07 | 35584248 | G | A | upstream_gene_variant | MODIFIER | c.-1863C>T| |
S298 |
7 | BAA07g39770 | A07 | 35585940 | G | A | upstream_gene_variant | MODIFIER | c.-3555C>T| |
S117 |