Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g26390 | A02 | 14663106 | G | A | upstream_gene_variant | MODIFIER | c.-4551G>A| |
S70 |
2 | BAA02g26390 | A02 | 14663454 | C | T | upstream_gene_variant | MODIFIER | c.-4203C>T| |
S185 |
3 | BAA02g26390 | A02 | 14663709 | C | T | upstream_gene_variant | MODIFIER | c.-3948C>T| |
S280 |
4 | BAA02g26390 | A02 | 14665005 | C | T | upstream_gene_variant | MODIFIER | c.-2652C>T| |
S178 |
5 | BAA02g26390 | A02 | 14666113 | G | A | upstream_gene_variant | MODIFIER | c.-1544G>A| |
S36 |
6 | BAA02g26390 | A02 | 14666169 | G | A | upstream_gene_variant | MODIFIER | c.-1488G>A| |
S158 |
7 | BAA02g26390 | A02 | 14666459 | C | T | upstream_gene_variant | MODIFIER | c.-1198C>T| |
S139 |
8 | BAA02g26390 | A02 | 14667010 | A | T | upstream_gene_variant | MODIFIER | c.-647A>T| |
S186 |
9 | BAA02g26390 | A02 | 14668178 | G | A | intron_variant | MODIFIER | c.368-26G>A| |
S293 |
10 | BAA02g26390 | A02 | 14668483 | G | A | missense_variant | MODERATE | c.580G>A|p.Gly194Arg |
S125 |
11 | BAA02g26390 | A02 | 14668507 | C | T | missense_variant | MODERATE | c.604C>T|p.His202Tyr |
S192 |
12 | BAA02g26390 | A02 | 14669889 | A | T | intron_variant | MODIFIER | c.1461+40A>T| |
S58 |
13 | BAA02g26390 | A02 | 14670718 | C | T | missense_variant | MODERATE | c.1928C>T|p.Ala643Val |
S6 |
14 | BAA02g26390 | A02 | 14671110 | G | A | downstream_gene_variant | MODIFIER | c.*361G>A| |
S237 |
15 | BAA02g26390 | A02 | 14672449 | C | T | downstream_gene_variant | MODIFIER | c.*1700C>T| |
S163 |
16 | BAA02g26390 | A02 | 14675058 | G | A | downstream_gene_variant | MODIFIER | c.*4309G>A| |
S230 |
17 | BAA02g26390 | A02 | 14675126 | C | T | downstream_gene_variant | MODIFIER | c.*4377C>T| |
S38 |