Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g16370 | A02 | 7978777 | C | T | missense_variant | MODERATE | c.1603G>A|p.Val535Ile |
S245 |
2 | BAA02g16370 | A02 | 7978929 | G | A | missense_variant | MODERATE | c.1451C>T|p.Ser484Phe |
S129 |
3 | BAA02g16370 | A02 | 7979159 | C | T | missense_variant | MODERATE | c.1304G>A|p.Gly435Glu |
S210 S225 |
4 | BAA02g16370 | A02 | 7979230 | T | A | synonymous_variant | LOW | c.1233A>T|p.Pro411Pro |
S238 |
5 | BAA02g16370 | A02 | 7979694 | C | T | missense_variant | MODERATE | c.910G>A|p.Asp304Asn |
S127 |
6 | BAA02g16370 | A02 | 7980015 | C | T | synonymous_variant | LOW | c.738G>A|p.Glu246Glu |
S275 |
7 | BAA02g16370 | A02 | 7980387 | C | T | missense_variant | MODERATE | c.531G>A|p.Met177Ile |
S15 S3 |
8 | BAA02g16370 | A02 | 7980572 | G | A | synonymous_variant | LOW | c.423C>T|p.His141His |
S180 |
9 | BAA02g16370 | A02 | 7981535 | G | A | missense_variant | MODERATE | c.137C>T|p.Thr46Ile |
S229 |
10 | BAA02g16370 | A02 | 7981555 | G | A | synonymous_variant | LOW | c.117C>T|p.Phe39Phe |
S50 |
11 | BAA02g16370 | A02 | 7982504 | G | A | upstream_gene_variant | MODIFIER | c.-833C>T| |
S149 S245 |
12 | BAA02g16370 | A02 | 7982800 | C | T | upstream_gene_variant | MODIFIER | c.-1129G>A| |
S99 |
13 | BAA02g16370 | A02 | 7983604 | G | A | upstream_gene_variant | MODIFIER | c.-1933C>T| |
S279 |
14 | BAA02g16370 | A02 | 7984448 | G | A | upstream_gene_variant | MODIFIER | c.-2777C>T| |
S33 |