Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g17040 | A05 | 9527938 | G | A | downstream_gene_variant | MODIFIER | c.*1562C>T| |
S144 |
2 | BAA05g17040 | A05 | 9528266 | C | T | downstream_gene_variant | MODIFIER | c.*1234G>A| |
S130 |
3 | BAA05g17040 | A05 | 9529778 | C | T | missense_variant | MODERATE | c.1393G>A|p.Glu465Lys |
S113 |
4 | BAA05g17040 | A05 | 9530130 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1042-1G>A| |
S51 |
5 | BAA05g17040 | A05 | 9530306 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.933-1G>A| |
S198 |
6 | BAA05g17040 | A05 | 9530479 | C | T | synonymous_variant | LOW | c.828G>A|p.Lys276Lys |
S236 |
7 | BAA05g17040 | A05 | 9530586 | C | T | missense_variant&splice_region_variant | MODERATE | c.721G>A|p.Ala241Thr |
S162 |
8 | BAA05g17040 | A05 | 9531030 | T | C | synonymous_variant | LOW | c.372A>G|p.Ala124Ala |
S190 |
9 | BAA05g17040 | A05 | 9533480 | C | T | upstream_gene_variant | MODIFIER | c.-1981G>A| |
S71 |
10 | BAA05g17040 | A05 | 9534050 | C | T | upstream_gene_variant | MODIFIER | c.-2551G>A| |
S201 |
11 | BAA05g17040 | A05 | 9534188 | G | A | upstream_gene_variant | MODIFIER | c.-2689C>T| |
S134 |
12 | BAA05g17040 | A05 | 9534212 | G | A | upstream_gene_variant | MODIFIER | c.-2713C>T| |
S262 |
13 | BAA05g17040 | A05 | 9534222 | C | T | upstream_gene_variant | MODIFIER | c.-2723G>A| |
S207 |
14 | BAA05g17040 | A05 | 9534624 | G | A | upstream_gene_variant | MODIFIER | c.-3125C>T| |
S68 |
15 | BAA05g17040 | A05 | 9534664 | G | A | upstream_gene_variant | MODIFIER | c.-3165C>T| |
S32 |
16 | BAA05g17040 | A05 | 9535076 | G | A | upstream_gene_variant | MODIFIER | c.-3577C>T| |
S56 |
17 | BAA05g17040 | A05 | 9535408 | G | A | upstream_gene_variant | MODIFIER | c.-3909C>T| |
S293 |
18 | BAA05g17040 | A05 | 9535508 | G | A | upstream_gene_variant | MODIFIER | c.-4009C>T| |
S294 |