Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11350 | A02 | 5122982 | C | T | splice_region_variant&synonymous_variant | LOW | c.3645G>A|p.Glu1215Glu |
S233 |
2 | BAA02g11350 | A02 | 5123628 | G | A | synonymous_variant | LOW | c.3264C>T|p.Arg1088Arg |
S37 |
3 | BAA02g11350 | A02 | 5124989 | C | T | missense_variant | MODERATE | c.2425G>A|p.Asp809Asn |
S195 |
4 | BAA02g11350 | A02 | 5128715 | G | A | synonymous_variant | LOW | c.771C>T|p.Cys257Cys |
S13 |
5 | BAA02g11350 | A02 | 5128965 | C | T | missense_variant | MODERATE | c.692G>A|p.Arg231Lys |
S267 |
6 | BAA02g11350 | A02 | 5129787 | G | A | missense_variant | MODERATE | c.202C>T|p.Pro68Ser |
S303 |
7 | BAA02g11350 | A02 | 5129922 | G | A | synonymous_variant | LOW | c.150C>T|p.Tyr50Tyr |
S12 |
8 | BAA02g11350 | A02 | 5129969 | C | T | missense_variant | MODERATE | c.103G>A|p.Glu35Lys |
S8 |
9 | BAA02g11350 | A02 | 5129981 | G | A | missense_variant | MODERATE | c.91C>T|p.Leu31Phe |
S36 |
10 | BAA02g11350 | A02 | 5130272 | G | A | upstream_gene_variant | MODIFIER | c.-115C>T| |
S303 |
11 | BAA02g11350 | A02 | 5131326 | G | A | upstream_gene_variant | MODIFIER | c.-1169C>T| |
S69 |
12 | BAA02g11350 | A02 | 5131380 | G | A | upstream_gene_variant | MODIFIER | c.-1223C>T| |
S143 |
13 | BAA02g11350 | A02 | 5131700 | C | T | upstream_gene_variant | MODIFIER | c.-1543G>A| |
S208 S219 |
14 | BAA02g11350 | A02 | 5131755 | C | T | upstream_gene_variant | MODIFIER | c.-1598G>A| |
S77 S82 |
15 | BAA02g11350 | A02 | 5132479 | C | T | upstream_gene_variant | MODIFIER | c.-2322G>A| |
S267 |
16 | BAA02g11350 | A02 | 5133109 | G | A | upstream_gene_variant | MODIFIER | c.-2952C>T| |
S11 |