Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g10420 | A08 | 9422465 | C | T | upstream_gene_variant | MODIFIER | c.-1202C>T| |
S6 |
2 | BAA08g10420 | A08 | 9422555 | G | A | upstream_gene_variant | MODIFIER | c.-1112G>A| |
S289 S290 |
3 | BAA08g10420 | A08 | 9422858 | G | A | upstream_gene_variant | MODIFIER | c.-809G>A| |
S238 |
4 | BAA08g10420 | A08 | 9422926 | G | A | upstream_gene_variant | MODIFIER | c.-741G>A| |
S265 |
5 | BAA08g10420 | A08 | 9423036 | G | A | upstream_gene_variant | MODIFIER | c.-631G>A| |
S165 |
6 | BAA08g10420 | A08 | 9423179 | G | A | upstream_gene_variant | MODIFIER | c.-488G>A| |
S39 |
7 | BAA08g10420 | A08 | 9423340 | G | A | upstream_gene_variant | MODIFIER | c.-327G>A| |
S130 |
8 | BAA08g10420 | A08 | 9423480 | G | A | upstream_gene_variant | MODIFIER | c.-187G>A| |
S65 |
9 | BAA08g10420 | A08 | 9423855 | C | T | intron_variant | MODIFIER | c.176+13C>T| |
S174 S216 S241 |
10 | BAA08g10420 | A08 | 9424255 | C | T | missense_variant | MODERATE | c.506C>T|p.Ala169Val |
S295 |
11 | BAA08g10420 | A08 | 9424757 | C | T | downstream_gene_variant | MODIFIER | c.*489C>T| |
S121 |
12 | BAA08g10420 | A08 | 9425122 | G | A | downstream_gene_variant | MODIFIER | c.*854G>A| |
S260 |