Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g01830 | A04 | 1051454 | C | T | upstream_gene_variant | MODIFIER | c.-2817C>T| |
S301 S304 |
2 | BAA04g01830 | A04 | 1052398 | C | T | upstream_gene_variant | MODIFIER | c.-1873C>T| |
S119 |
3 | BAA04g01830 | A04 | 1053168 | C | T | upstream_gene_variant | MODIFIER | c.-1103C>T| |
S242 |
4 | BAA04g01830 | A04 | 1053445 | G | A | upstream_gene_variant | MODIFIER | c.-826G>A| |
S219 S72 |
5 | BAA04g01830 | A04 | 1055668 | G | A | synonymous_variant | LOW | c.1398G>A|p.Leu466Leu |
S158 |
6 | BAA04g01830 | A04 | 1055848 | G | A | missense_variant | MODERATE | c.1486G>A|p.Ala496Thr |
S34 |
7 | BAA04g01830 | A04 | 1056098 | C | T | missense_variant | MODERATE | c.1625C>T|p.Ala542Val |
S65 |
8 | BAA04g01830 | A04 | 1056353 | G | A | missense_variant | MODERATE | c.1783G>A|p.Val595Ile |
S151 |
9 | BAA04g01830 | A04 | 1056371 | C | T | missense_variant | MODERATE | c.1801C>T|p.Pro601Ser |
S294 |
10 | BAA04g01830 | A04 | 1057461 | C | T | splice_region_variant&intron_variant | LOW | c.2547+4C>T| |
S110 |
11 | BAA04g01830 | A04 | 1060694 | G | A | downstream_gene_variant | MODIFIER | c.*2972G>A| |
S4 |
12 | BAA04g01830 | A04 | 1060791 | C | T | downstream_gene_variant | MODIFIER | c.*3069C>T| |
S139 |
13 | BAA04g01830 | A04 | 1061329 | G | A | downstream_gene_variant | MODIFIER | c.*3607G>A| |
S229 |