Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g26990 | A03 | 12422707 | C | T | missense_variant | MODERATE | c.1668G>A|p.Met556Ile |
S278 |
2 | BAA03g26990 | A03 | 12424268 | G | A | missense_variant | MODERATE | c.1214C>T|p.Pro405Leu |
S143 |
3 | BAA03g26990 | A03 | 12424323 | C | T | missense_variant | MODERATE | c.1159G>A|p.Glu387Lys |
S278 |
4 | BAA03g26990 | A03 | 12426867 | C | T | intron_variant | MODIFIER | c.872+677G>A| |
S171 |
5 | BAA03g26990 | A03 | 12428060 | C | T | intron_variant | MODIFIER | c.488-132G>A| |
S82 S92 |
6 | BAA03g26990 | A03 | 12428374 | A | T | intron_variant | MODIFIER | c.488-446T>A| |
S301 |
7 | BAA03g26990 | A03 | 12428643 | G | A | intron_variant | MODIFIER | c.488-715C>T| |
S122 |
8 | BAA03g26990 | A03 | 12430332 | G | A | intron_variant | MODIFIER | c.487+721C>T| |
S280 |
9 | BAA03g26990 | A03 | 12431000 | C | T | intron_variant | MODIFIER | c.487+53G>A| |
S173 |
10 | BAA03g26990 | A03 | 12431815 | G | A | upstream_gene_variant | MODIFIER | c.-171C>T| |
S47 |
11 | BAA03g26990 | A03 | 12432269 | C | T | upstream_gene_variant | MODIFIER | c.-625G>A| |
S157 S163 |
12 | BAA03g26990 | A03 | 12433909 | G | A | upstream_gene_variant | MODIFIER | c.-2265C>T| |
S203 |
13 | BAA03g26990 | A03 | 12434165 | G | A | upstream_gene_variant | MODIFIER | c.-2521C>T| |
S286 |