Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g05000 | A03 | 2111843 | C | T | upstream_gene_variant | MODIFIER | c.-4151C>T| |
S166 |
2 | BAA03g05000 | A03 | 2112410 | A | G | upstream_gene_variant | MODIFIER | c.-3584A>G| |
S270 |
3 | BAA03g05000 | A03 | 2112562 | C | T | upstream_gene_variant | MODIFIER | c.-3432C>T| |
S126 |
4 | BAA03g05000 | A03 | 2113821 | G | A | upstream_gene_variant | MODIFIER | c.-2173G>A| |
S162 |
5 | BAA03g05000 | A03 | 2114450 | C | T | upstream_gene_variant | MODIFIER | c.-1544C>T| |
S283 |
6 | BAA03g05000 | A03 | 2114886 | C | T | upstream_gene_variant | MODIFIER | c.-1108C>T| |
S263 |
7 | BAA03g05000 | A03 | 2115702 | G | A | upstream_gene_variant | MODIFIER | c.-292G>A| |
S139 |
8 | BAA03g05000 | A03 | 2116395 | C | T | missense_variant | MODERATE | c.197C>T|p.Ser66Phe |
S259 |
9 | BAA03g05000 | A03 | 2117137 | C | T | missense_variant | MODERATE | c.695C>T|p.Ala232Val |
S303 |
10 | BAA03g05000 | A03 | 2118568 | C | T | missense_variant | MODERATE | c.1918C>T|p.Pro640Ser |
S117 |
11 | BAA03g05000 | A03 | 2118695 | C | T | missense_variant | MODERATE | c.2045C>T|p.Ser682Phe |
S99 |
12 | BAA03g05000 | A03 | 2119361 | C | T | missense_variant | MODERATE | c.2711C>T|p.Ser904Phe |
S164 |
13 | BAA03g05000 | A03 | 2119765 | C | T | downstream_gene_variant | MODIFIER | c.*112C>T| |
S211 |
14 | BAA03g05000 | A03 | 2121753 | C | T | downstream_gene_variant | MODIFIER | c.*2100C>T| |
S131 |
15 | BAA03g05000 | A03 | 2122756 | G | A | downstream_gene_variant | MODIFIER | c.*3103G>A| |
S273 |
16 | BAA03g05000 | A03 | 2122966 | G | A | downstream_gene_variant | MODIFIER | c.*3313G>A| |
S175 |
17 | BAA03g05000 | A03 | 2123820 | C | T | downstream_gene_variant | MODIFIER | c.*4167C>T| |
S241 |