Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g45650 | A01 | 30475314 | A | T | downstream_gene_variant | MODIFIER | c.*4862T>A| |
S153 S157 S262 S263 |
2 | BAA01g45650 | A01 | 30475672 | C | T | downstream_gene_variant | MODIFIER | c.*4504G>A| |
S275 |
3 | BAA01g45650 | A01 | 30477047 | G | A | downstream_gene_variant | MODIFIER | c.*3129C>T| |
S174 S216 S241 S27 |
4 | BAA01g45650 | A01 | 30477357 | G | A | downstream_gene_variant | MODIFIER | c.*2819C>T| |
S228 |
5 | BAA01g45650 | A01 | 30478330 | C | T | downstream_gene_variant | MODIFIER | c.*1846G>A| |
S289 S290 |
6 | BAA01g45650 | A01 | 30479506 | C | T | downstream_gene_variant | MODIFIER | c.*670G>A| |
S171 |
7 | BAA01g45650 | A01 | 30480661 | C | T | missense_variant | MODERATE | c.994G>A|p.Gly332Arg |
S279 |
8 | BAA01g45650 | A01 | 30480813 | G | A | missense_variant | MODERATE | c.842C>T|p.Ala281Val |
S55 |
9 | BAA01g45650 | A01 | 30481866 | G | A | upstream_gene_variant | MODIFIER | c.-55C>T| |
S151 |
10 | BAA01g45650 | A01 | 30481911 | C | T | upstream_gene_variant | MODIFIER | c.-100G>A| |
S303 |
11 | BAA01g45650 | A01 | 30482721 | C | T | upstream_gene_variant | MODIFIER | c.-910G>A| |
S50 |
12 | BAA01g45650 | A01 | 30483554 | G | A | upstream_gene_variant | MODIFIER | c.-1743C>T| |
S176 |
13 | BAA01g45650 | A01 | 30483742 | A | C | upstream_gene_variant | MODIFIER | c.-1931T>G| |
S159 |