Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g42960 | A05 | 40509295 | C | T | synonymous_variant | LOW | c.3075G>A|p.Leu1025Leu |
S48 |
2 | BAA05g42960 | A05 | 40509346 | C | T | synonymous_variant | LOW | c.3024G>A|p.Lys1008Lys |
S109 |
3 | BAA05g42960 | A05 | 40509506 | G | A | missense_variant | MODERATE | c.2864C>T|p.Pro955Leu |
S73 |
4 | BAA05g42960 | A05 | 40510389 | C | T | missense_variant | MODERATE | c.1981G>A|p.Val661Ile |
S275 |
5 | BAA05g42960 | A05 | 40511019 | G | A | synonymous_variant | LOW | c.1351C>T|p.Leu451Leu |
S8 |
6 | BAA05g42960 | A05 | 40511151 | C | T | missense_variant | MODERATE | c.1219G>A|p.Gly407Arg |
S135 |
7 | BAA05g42960 | A05 | 40511927 | C | T | missense_variant | MODERATE | c.443G>A|p.Ser148Asn |
S267 |
8 | BAA05g42960 | A05 | 40512010 | C | T | synonymous_variant | LOW | c.360G>A|p.Gln120Gln |
S247 |
9 | BAA05g42960 | A05 | 40512279 | C | T | missense_variant | MODERATE | c.91G>A|p.Val31Ile |
S226 |
10 | BAA05g42960 | A05 | 40513024 | G | A | upstream_gene_variant | MODIFIER | c.-655C>T| |
S130 |
11 | BAA05g42960 | A05 | 40513891 | G | A | upstream_gene_variant | MODIFIER | c.-1522C>T| |
S292 |