Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g20850 | A04 | 23836223 | G | A | upstream_gene_variant | MODIFIER | c.-2887G>A| |
S278 |
2 | BAA04g20850 | A04 | 23837035 | C | T | upstream_gene_variant | MODIFIER | c.-2075C>T| |
S37 |
3 | BAA04g20850 | A04 | 23837375 | C | T | upstream_gene_variant | MODIFIER | c.-1735C>T| |
S64 |
4 | BAA04g20850 | A04 | 23837816 | C | G | upstream_gene_variant | MODIFIER | c.-1294C>G| |
S188 |
5 | BAA04g20850 | A04 | 23837856 | C | T | upstream_gene_variant | MODIFIER | c.-1254C>T| |
S286 |
6 | BAA04g20850 | A04 | 23838386 | G | A | upstream_gene_variant | MODIFIER | c.-724G>A| |
S206 S26 |
7 | BAA04g20850 | A04 | 23838756 | C | T | upstream_gene_variant | MODIFIER | c.-354C>T| |
S255 |
8 | BAA04g20850 | A04 | 23838791 | G | A | upstream_gene_variant | MODIFIER | c.-319G>A| |
S42 |
9 | BAA04g20850 | A04 | 23839226 | C | T | synonymous_variant | LOW | c.117C>T|p.Leu39Leu |
S136 S275 |
10 | BAA04g20850 | A04 | 23839359 | G | A | missense_variant | MODERATE | c.250G>A|p.Asp84Asn |
S179 |
11 | BAA04g20850 | A04 | 23839892 | A | G | missense_variant | MODERATE | c.629A>G|p.Asn210Ser |
S207 |
12 | BAA04g20850 | A04 | 23841609 | G | A | downstream_gene_variant | MODIFIER | c.*1617G>A| |
S13 |
13 | BAA04g20850 | A04 | 23842214 | G | A | downstream_gene_variant | MODIFIER | c.*2222G>A| |
S124 |
14 | BAA04g20850 | A04 | 23842271 | G | A | downstream_gene_variant | MODIFIER | c.*2279G>A| |
S231 |
15 | BAA04g20850 | A04 | 23843620 | C | T | downstream_gene_variant | MODIFIER | c.*3628C>T| |
S107 |