Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g08260 | A01 | 3613238 | G | A | missense_variant | MODERATE | c.28G>A|p.Glu10Lys |
|
2 | BAA01g08260 | A01 | 3614073 | C | T | intron_variant | MODIFIER | c.43-94C>T| |
S205 |
3 | BAA01g08260 | A01 | 3614236 | G | A | missense_variant | MODERATE | c.112G>A|p.Gly38Arg |
S251 |
4 | BAA01g08260 | A01 | 3615563 | G | A | missense_variant | MODERATE | c.1259G>A|p.Arg420Lys |
S234 |
5 | BAA01g08260 | A01 | 3615788 | G | A | synonymous_variant | LOW | c.1401G>A|p.Glu467Glu |
S187 |
6 | BAA01g08260 | A01 | 3615852 | C | T | missense_variant | MODERATE | c.1465C>T|p.Pro489Ser |
S153 S213 |
7 | BAA01g08260 | A01 | 3615922 | G | A | splice_donor_variant&intron_variant | HIGH | c.1534+1G>A| |
S69 |
8 | BAA01g08260 | A01 | 3616344 | C | T | missense_variant | MODERATE | c.1780C>T|p.Pro594Ser |
S263 |
9 | BAA01g08260 | A01 | 3616889 | G | T | missense_variant | MODERATE | c.2240G>T|p.Arg747Ile |
S149 |
10 | BAA01g08260 | A01 | 3616911 | G | A | missense_variant | MODERATE | c.2262G>A|p.Met754Ile |
S151 S202 |
11 | BAA01g08260 | A01 | 3617648 | G | A | missense_variant | MODERATE | c.2842G>A|p.Val948Ile |
S202 |
12 | BAA01g08260 | A01 | 3617671 | G | A | downstream_gene_variant | MODIFIER | c.*18G>A| |
S204 |
13 | BAA01g08260 | A01 | 3617831 | C | T | downstream_gene_variant | MODIFIER | c.*178C>T| |
S43 |
14 | BAA01g08260 | A01 | 3618034 | G | A | downstream_gene_variant | MODIFIER | c.*381G>A| |
S195 |
15 | BAA01g08260 | A01 | 3618205 | C | T | downstream_gene_variant | MODIFIER | c.*552C>T| |
S166 |
16 | BAA01g08260 | A01 | 3618347 | C | T | downstream_gene_variant | MODIFIER | c.*694C>T| |
S128 |
17 | BAA01g08260 | A01 | 3618850 | C | T | downstream_gene_variant | MODIFIER | c.*1197C>T| |
S18 |
18 | BAA01g08260 | A01 | 3619139 | G | A | downstream_gene_variant | MODIFIER | c.*1486G>A| |
S216 |