Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g22850 | A02 | 12381192 | G | A | upstream_gene_variant | MODIFIER | c.-2522G>A| |
S187 |
2 | BAA02g22850 | A02 | 12382991 | C | T | upstream_gene_variant | MODIFIER | c.-723C>T| |
S157 S163 |
3 | BAA02g22850 | A02 | 12388889 | C | T | intron_variant | MODIFIER | c.43-1758C>T| |
S140 |
4 | BAA02g22850 | A02 | 12388994 | C | T | intron_variant | MODIFIER | c.43-1653C>T| |
S123 |
5 | BAA02g22850 | A02 | 12389370 | G | A | intron_variant | MODIFIER | c.43-1277G>A| |
S111 |
6 | BAA02g22850 | A02 | 12390427 | G | A | intron_variant | MODIFIER | c.43-220G>A| |
S232 |
7 | BAA02g22850 | A02 | 12390672 | G | A | missense_variant | MODERATE | c.68G>A|p.Ser23Asn |
S132 S137 S215 |
8 | BAA02g22850 | A02 | 12390741 | C | T | missense_variant | MODERATE | c.137C>T|p.Pro46Leu |
S207 |
9 | BAA02g22850 | A02 | 12391040 | C | T | missense_variant | MODERATE | c.436C>T|p.Arg146Trp |
S221 |
10 | BAA02g22850 | A02 | 12391109 | G | A | missense_variant | MODERATE | c.505G>A|p.Glu169Lys |
S28 |
11 | BAA02g22850 | A02 | 12391186 | G | A | synonymous_variant | LOW | c.582G>A|p.Val194Val |
S263 |
12 | BAA02g22850 | A02 | 12391299 | G | A | missense_variant | MODERATE | c.695G>A|p.Arg232Gln |
S166 |
13 | BAA02g22850 | A02 | 12391724 | C | T | downstream_gene_variant | MODIFIER | c.*394C>T| |
S73 S91 |
14 | BAA02g22850 | A02 | 12392287 | G | A | downstream_gene_variant | MODIFIER | c.*957G>A| |
S90 |
15 | BAA02g22850 | A02 | 12392636 | G | A | downstream_gene_variant | MODIFIER | c.*1306G>A| |
S294 |
16 | BAA02g22850 | A02 | 12392749 | C | T | downstream_gene_variant | MODIFIER | c.*1419C>T| |
S299 |