Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g25490 | A02 | 13986196 | G | A | upstream_gene_variant | MODIFIER | c.-4078G>A| |
S58 |
2 | BAA02g25490 | A02 | 13988042 | C | T | upstream_gene_variant | MODIFIER | c.-2232C>T| |
S201 |
3 | BAA02g25490 | A02 | 13988226 | G | A | upstream_gene_variant | MODIFIER | c.-2048G>A| |
S237 |
4 | BAA02g25490 | A02 | 13988733 | C | T | upstream_gene_variant | MODIFIER | c.-1541C>T| |
S241 |
5 | BAA02g25490 | A02 | 13988945 | G | A | upstream_gene_variant | MODIFIER | c.-1329G>A| |
S23 |
6 | BAA02g25490 | A02 | 13988961 | G | A | upstream_gene_variant | MODIFIER | c.-1313G>A| |
S259 |
7 | BAA02g25490 | A02 | 13989244 | C | T | upstream_gene_variant | MODIFIER | c.-1030C>T| |
S186 |
8 | BAA02g25490 | A02 | 13989591 | C | T | upstream_gene_variant | MODIFIER | c.-683C>T| |
S302 |
9 | BAA02g25490 | A02 | 13990090 | C | T | upstream_gene_variant | MODIFIER | c.-184C>T| |
S183 S198 |
10 | BAA02g25490 | A02 | 13990320 | C | T | missense_variant | MODERATE | c.47C>T|p.Pro16Leu |
S87 |
11 | BAA02g25490 | A02 | 13990706 | G | A | missense_variant | MODERATE | c.433G>A|p.Ala145Thr |
S134 |
12 | BAA02g25490 | A02 | 13990810 | C | T | synonymous_variant | LOW | c.537C>T|p.Ser179Ser |
S25 S264 |
13 | BAA02g25490 | A02 | 13991554 | G | A | downstream_gene_variant | MODIFIER | c.*639G>A| |
S136 |
14 | BAA02g25490 | A02 | 13992031 | G | A | downstream_gene_variant | MODIFIER | c.*1116G>A| |
S264 |
15 | BAA02g25490 | A02 | 13993459 | C | T | downstream_gene_variant | MODIFIER | c.*2544C>T| |
S84 S93 |
16 | BAA02g25490 | A02 | 13994141 | C | T | downstream_gene_variant | MODIFIER | c.*3226C>T| |
S265 S39 |
17 | BAA02g25490 | A02 | 13994199 | G | A | downstream_gene_variant | MODIFIER | c.*3284G>A| |
S259 |
18 | BAA02g25490 | A02 | 13994667 | C | T | downstream_gene_variant | MODIFIER | c.*3752C>T| |
S178 |
19 | BAA02g25490 | A02 | 13994872 | C | T | downstream_gene_variant | MODIFIER | c.*3957C>T| |
S182 |
20 | BAA02g25490 | A02 | 13995419 | C | A | downstream_gene_variant | MODIFIER | c.*4504C>A| |
S182 |
21 | BAA02g25490 | A02 | 13995698 | C | T | downstream_gene_variant | MODIFIER | c.*4783C>T| |
S183 S198 |