Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44600 | A02 | 36708482 | G | A | upstream_gene_variant | MODIFIER | c.-2964G>A| |
S69 |
2 | BAA02g44600 | A02 | 36709128 | G | A | upstream_gene_variant | MODIFIER | c.-2318G>A| |
S282 |
3 | BAA02g44600 | A02 | 36709270 | C | T | upstream_gene_variant | MODIFIER | c.-2176C>T| |
S142 |
4 | BAA02g44600 | A02 | 36710399 | C | T | upstream_gene_variant | MODIFIER | c.-1047C>T| |
S283 |
5 | BAA02g44600 | A02 | 36711164 | C | T | upstream_gene_variant | MODIFIER | c.-282C>T| |
S92 |
6 | BAA02g44600 | A02 | 36712153 | C | T | missense_variant | MODERATE | c.353C>T|p.Ser118Leu |
S135 |
7 | BAA02g44600 | A02 | 36712672 | G | A | missense_variant | MODERATE | c.649G>A|p.Glu217Lys |
S67 |
8 | BAA02g44600 | A02 | 36712708 | C | T | missense_variant | MODERATE | c.685C>T|p.Leu229Phe |
S39 |
9 | BAA02g44600 | A02 | 36712776 | G | A | synonymous_variant | LOW | c.753G>A|p.Arg251Arg |
S4 |
10 | BAA02g44600 | A02 | 36713051 | G | A | synonymous_variant | LOW | c.948G>A|p.Glu316Glu |
S197 |
11 | BAA02g44600 | A02 | 36713149 | G | A | intron_variant | MODIFIER | c.966+80G>A| |
S230 |
12 | BAA02g44600 | A02 | 36714395 | C | T | missense_variant | MODERATE | c.1550C>T|p.Thr517Ile |
S203 |
13 | BAA02g44600 | A02 | 36715952 | C | T | synonymous_variant | LOW | c.1971C>T|p.Asp657Asp |
S301 S304 |
14 | BAA02g44600 | A02 | 36715986 | G | A | missense_variant | MODERATE | c.2005G>A|p.Gly669Arg |
S68 |
15 | BAA02g44600 | A02 | 36716928 | C | T | missense_variant | MODERATE | c.2368C>T|p.Pro790Ser |
S131 |
16 | BAA02g44600 | A02 | 36717696 | C | T | stop_gained | HIGH | c.3013C>T|p.Arg1005* |
S18 |
17 | BAA02g44600 | A02 | 36717752 | C | T | synonymous_variant | LOW | c.3069C>T|p.Phe1023Phe |
S181 |