Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g00430 | A05 | 232242 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.2754-1G>A| |
S13 |
2 | BAA05g00430 | A05 | 232434 | G | A | synonymous_variant | LOW | c.2640C>T|p.Asp880Asp |
S40 S49 |
3 | BAA05g00430 | A05 | 232531 | C | T | missense_variant | MODERATE | c.2543G>A|p.Arg848Lys |
S292 |
4 | BAA05g00430 | A05 | 232630 | C | T | missense_variant | MODERATE | c.2444G>A|p.Arg815Lys |
S188 |
5 | BAA05g00430 | A05 | 233557 | C | T | missense_variant | MODERATE | c.1765G>A|p.Gly589Arg |
S267 |
6 | BAA05g00430 | A05 | 235466 | G | A | intron_variant | MODIFIER | c.738+29C>T| |
|
7 | BAA05g00430 | A05 | 235576 | G | A | intron_variant | MODIFIER | c.667-10C>T| |
S157 S163 |
8 | BAA05g00430 | A05 | 236256 | C | T | synonymous_variant | LOW | c.204G>A|p.Thr68Thr |
S41 |
9 | BAA05g00430 | A05 | 237889 | G | A | upstream_gene_variant | MODIFIER | c.-1321C>T| |
S40 S49 |
10 | BAA05g00430 | A05 | 238112 | C | T | upstream_gene_variant | MODIFIER | c.-1544G>A| |
S4 |
11 | BAA05g00430 | A05 | 238120 | G | A | upstream_gene_variant | MODIFIER | c.-1552C>T| |
S223 |
12 | BAA05g00430 | A05 | 238279 | C | T | upstream_gene_variant | MODIFIER | c.-1711G>A| |
S184 |
13 | BAA05g00430 | A05 | 239163 | G | A | upstream_gene_variant | MODIFIER | c.-2595C>T| |
S206 S26 |
14 | BAA05g00430 | A05 | 240353 | G | A | upstream_gene_variant | MODIFIER | c.-3785C>T| |
S116 |