Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g28930 | A05 | 32643210 | C | T | upstream_gene_variant | MODIFIER | c.-793C>T| |
S115 |
2 | BAA05g28930 | A05 | 32644507 | G | A | missense_variant | MODERATE | c.505G>A|p.Glu169Lys |
S178 |
3 | BAA05g28930 | A05 | 32644810 | G | A | missense_variant | MODERATE | c.808G>A|p.Gly270Ser |
S257 |
4 | BAA05g28930 | A05 | 32644842 | G | A | missense_variant | MODERATE | c.840G>A|p.Met280Ile |
S40 S49 |
5 | BAA05g28930 | A05 | 32644978 | G | A | missense_variant | MODERATE | c.976G>A|p.Ala326Thr |
S249 |
6 | BAA05g28930 | A05 | 32645117 | G | A | missense_variant | MODERATE | c.1115G>A|p.Arg372Lys |
S61 |
7 | BAA05g28930 | A05 | 32645446 | G | A | missense_variant | MODERATE | c.1444G>A|p.Asp482Asn |
S15 S3 |
8 | BAA05g28930 | A05 | 32645629 | G | A | intron_variant | MODIFIER | c.1553+74G>A| |
S15 S3 |
9 | BAA05g28930 | A05 | 32646126 | C | T | intron_variant | MODIFIER | c.1707-18C>T| |
S261 |
10 | BAA05g28930 | A05 | 32647174 | G | A | downstream_gene_variant | MODIFIER | c.*382G>A| |
S187 |
11 | BAA05g28930 | A05 | 32648213 | C | T | downstream_gene_variant | MODIFIER | c.*1421C>T| |
S216 |
12 | BAA05g28930 | A05 | 32648712 | G | A | downstream_gene_variant | MODIFIER | c.*1920G>A| |
S257 |
13 | BAA05g28930 | A05 | 32648720 | G | A | downstream_gene_variant | MODIFIER | c.*1928G>A| |
S151 S166 S167 S236 S257 S263 |
14 | BAA05g28930 | A05 | 32648772 | G | A | downstream_gene_variant | MODIFIER | c.*1980G>A| |
S56 |
15 | BAA05g28930 | A05 | 32649178 | T | C | downstream_gene_variant | MODIFIER | c.*2386T>C| |
S149 |
16 | BAA05g28930 | A05 | 32649558 | G | A | downstream_gene_variant | MODIFIER | c.*2766G>A| |
S46 |
17 | BAA05g28930 | A05 | 32649757 | G | A | downstream_gene_variant | MODIFIER | c.*2965G>A| |
S77 S82 |
18 | BAA05g28930 | A05 | 32649786 | G | A | downstream_gene_variant | MODIFIER | c.*2994G>A| |
S262 |
19 | BAA05g28930 | A05 | 32650792 | C | T | downstream_gene_variant | MODIFIER | c.*4000C>T| |
S111 |