Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g47890 | A02 | 38556805 | G | A | missense_variant | MODERATE | c.538G>A|p.Asp180Asn |
S280 |
2 | BAA02g47890 | A02 | 38556866 | A | T | missense_variant | MODERATE | c.599A>T|p.Gln200Leu |
S177 |
3 | BAA02g47890 | A02 | 38557876 | G | A | intron_variant | MODIFIER | c.1194-87G>A| |
S247 |
4 | BAA02g47890 | A02 | 38557990 | G | A | synonymous_variant | LOW | c.1221G>A|p.Ala407Ala |
S45 |
5 | BAA02g47890 | A02 | 38558018 | G | A | missense_variant | MODERATE | c.1249G>A|p.Glu417Lys |
S169 |
6 | BAA02g47890 | A02 | 38558663 | G | A | intron_variant | MODIFIER | c.1332+562G>A| |
S4 |
7 | BAA02g47890 | A02 | 38560439 | G | A | downstream_gene_variant | MODIFIER | c.*750G>A| |
S150 |
8 | BAA02g47890 | A02 | 38560580 | C | T | downstream_gene_variant | MODIFIER | c.*891C>T| |
S193 |
9 | BAA02g47890 | A02 | 38561079 | C | T | downstream_gene_variant | MODIFIER | c.*1390C>T| |
S295 |
10 | BAA02g47890 | A02 | 38561192 | C | T | downstream_gene_variant | MODIFIER | c.*1503C>T| |
S175 |
11 | BAA02g47890 | A02 | 38561699 | G | A | downstream_gene_variant | MODIFIER | c.*2010G>A| |
S30 |
12 | BAA02g47890 | A02 | 38563120 | C | T | downstream_gene_variant | MODIFIER | c.*3431C>T| |
S295 |
13 | BAA02g47890 | A02 | 38563409 | C | T | downstream_gene_variant | MODIFIER | c.*3720C>T| |
S295 |
14 | BAA02g47890 | A02 | 38563434 | T | C | downstream_gene_variant | MODIFIER | c.*3745T>C| |
S85 |
15 | BAA02g47890 | A02 | 38564143 | G | A | downstream_gene_variant | MODIFIER | c.*4454G>A| |
S66 |
16 | BAA02g47890 | A02 | 38564275 | G | A | downstream_gene_variant | MODIFIER | c.*4586G>A| |
S130 |
17 | BAA02g47890 | A02 | 38564420 | G | A | downstream_gene_variant | MODIFIER | c.*4731G>A| |
S211 |
18 | BAA02g47890 | A02 | 38564441 | G | A | downstream_gene_variant | MODIFIER | c.*4752G>A| |
S282 |