Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g15090 | A02 | 7207187 | G | A | upstream_gene_variant | MODIFIER | c.-4813G>A| |
S87 |
2 | BAA02g15090 | A02 | 7207704 | C | T | upstream_gene_variant | MODIFIER | c.-4296C>T| |
S267 |
3 | BAA02g15090 | A02 | 7207711 | G | A | upstream_gene_variant | MODIFIER | c.-4289G>A| |
S125 |
4 | BAA02g15090 | A02 | 7208006 | C | T | upstream_gene_variant | MODIFIER | c.-3994C>T| |
S38 |
5 | BAA02g15090 | A02 | 7208886 | G | A | upstream_gene_variant | MODIFIER | c.-3114G>A| |
S203 |
6 | BAA02g15090 | A02 | 7209457 | G | A | upstream_gene_variant | MODIFIER | c.-2543G>A| |
S297 |
7 | BAA02g15090 | A02 | 7210197 | C | T | upstream_gene_variant | MODIFIER | c.-1803C>T| |
S63 |
8 | BAA02g15090 | A02 | 7211847 | C | T | upstream_gene_variant | MODIFIER | c.-153C>T| |
S71 |
9 | BAA02g15090 | A02 | 7212298 | G | A | missense_variant | MODERATE | c.299G>A|p.Arg100Lys |
S190 |
10 | BAA02g15090 | A02 | 7213832 | G | A | intron_variant | MODIFIER | c.400-36G>A| |
S23 |
11 | BAA02g15090 | A02 | 7213851 | C | T | intron_variant | MODIFIER | c.400-17C>T| |
S289 S290 |
12 | BAA02g15090 | A02 | 7213994 | G | A | missense_variant | MODERATE | c.526G>A|p.Ala176Thr |
S33 |
13 | BAA02g15090 | A02 | 7214512 | G | A | synonymous_variant | LOW | c.1044G>A|p.Lys348Lys |
S204 |
14 | BAA02g15090 | A02 | 7214707 | C | T | synonymous_variant | LOW | c.1239C>T|p.Leu413Leu |
S66 |
15 | BAA02g15090 | A02 | 7215020 | G | A | intron_variant | MODIFIER | c.1403-101G>A| |
S79 S91 |