Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g33250 | A02 | 28468352 | G | A | upstream_gene_variant | MODIFIER | c.-4468G>A| |
S208 |
2 | BAA02g33250 | A02 | 28469131 | G | A | upstream_gene_variant | MODIFIER | c.-3689G>A| |
S156 |
3 | BAA02g33250 | A02 | 28469178 | C | T | upstream_gene_variant | MODIFIER | c.-3642C>T| |
S46 |
4 | BAA02g33250 | A02 | 28469261 | G | A | upstream_gene_variant | MODIFIER | c.-3559G>A| |
S111 |
5 | BAA02g33250 | A02 | 28469764 | G | A | upstream_gene_variant | MODIFIER | c.-3056G>A| |
S80 |
6 | BAA02g33250 | A02 | 28469772 | G | A | upstream_gene_variant | MODIFIER | c.-3048G>A| |
S67 |
7 | BAA02g33250 | A02 | 28469906 | G | A | upstream_gene_variant | MODIFIER | c.-2914G>A| |
S288 |
8 | BAA02g33250 | A02 | 28470230 | G | A | upstream_gene_variant | MODIFIER | c.-2590G>A| |
S13 S140 S168 S279 S64 |
9 | BAA02g33250 | A02 | 28470306 | A | T | upstream_gene_variant | MODIFIER | c.-2514A>T| |
S13 |
10 | BAA02g33250 | A02 | 28470640 | C | A | upstream_gene_variant | MODIFIER | c.-2180C>A| |
S199 |
11 | BAA02g33250 | A02 | 28470655 | G | A | upstream_gene_variant | MODIFIER | c.-2165G>A| |
S251 |
12 | BAA02g33250 | A02 | 28470903 | G | A | upstream_gene_variant | MODIFIER | c.-1917G>A| |
S245 |
13 | BAA02g33250 | A02 | 28471449 | G | A | upstream_gene_variant | MODIFIER | c.-1371G>A| |
S275 |
14 | BAA02g33250 | A02 | 28473107 | C | T | intron_variant | MODIFIER | c.11-165C>T| |
S129 |
15 | BAA02g33250 | A02 | 28473272 | G | A | missense_variant&splice_region_variant | MODERATE | c.11G>A|p.Gly4Glu |
S228 |
16 | BAA02g33250 | A02 | 28473962 | C | T | missense_variant&splice_region_variant | MODERATE | c.550C>T|p.His184Tyr |
S299 |
17 | BAA02g33250 | A02 | 28474556 | C | T | intron_variant | MODIFIER | c.845-29C>T| |
S242 |
18 | BAA02g33250 | A02 | 28475071 | G | A | missense_variant | MODERATE | c.1331G>A|p.Arg444Lys |
S153 S213 |
19 | BAA02g33250 | A02 | 28475183 | C | T | synonymous_variant | LOW | c.1443C>T|p.Ser481Ser |
S165 |
20 | BAA02g33250 | A02 | 28475855 | C | T | missense_variant | MODERATE | c.2003C>T|p.Ser668Phe |
S2 S4 S6 |
21 | BAA02g33250 | A02 | 28476873 | C | T | downstream_gene_variant | MODIFIER | c.*231C>T| |
S255 |
22 | BAA02g33250 | A02 | 28476911 | G | A | downstream_gene_variant | MODIFIER | c.*269G>A| |
S265 |
23 | BAA02g33250 | A02 | 28477277 | C | T | downstream_gene_variant | MODIFIER | c.*635C>T| |
S292 |
24 | BAA02g33250 | A02 | 28477323 | C | T | downstream_gene_variant | MODIFIER | c.*681C>T| |
S208 S219 |
25 | BAA02g33250 | A02 | 28477621 | G | A | downstream_gene_variant | MODIFIER | c.*979G>A| |
S297 |