Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g38990 | A07 | 35201028 | C | T | synonymous_variant | LOW | c.2562G>A|p.Arg854Arg |
S56 |
2 | BAA07g38990 | A07 | 35201113 | G | A | missense_variant | MODERATE | c.2477C>T|p.Ser826Leu |
S283 |
3 | BAA07g38990 | A07 | 35201913 | C | T | missense_variant | MODERATE | c.1861G>A|p.Glu621Lys |
S60 |
4 | BAA07g38990 | A07 | 35202920 | C | T | missense_variant | MODERATE | c.1003G>A|p.Glu335Lys |
S245 |
5 | BAA07g38990 | A07 | 35203529 | G | A | stop_gained | HIGH | c.394C>T|p.Gln132* |
S169 |
6 | BAA07g38990 | A07 | 35203884 | G | A | synonymous_variant | LOW | c.39C>T|p.Leu13Leu |
S209 |
7 | BAA07g38990 | A07 | 35205754 | G | A | upstream_gene_variant | MODIFIER | c.-1832C>T| |
S135 |
8 | BAA07g38990 | A07 | 35207541 | C | T | upstream_gene_variant | MODIFIER | c.-3619G>A| |
S66 |
9 | BAA07g38990 | A07 | 35207600 | C | T | upstream_gene_variant | MODIFIER | c.-3678G>A| |
S161 |