Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g34550 | A01 | 23102522 | C | T | upstream_gene_variant | MODIFIER | c.-179C>T| |
S111 |
2 | BAA01g34550 | A01 | 23102776 | C | T | missense_variant | MODERATE | c.76C>T|p.Arg26Cys |
S238 |
3 | BAA01g34550 | A01 | 23103156 | G | A | synonymous_variant | LOW | c.456G>A|p.Lys152Lys |
S43 |
4 | BAA01g34550 | A01 | 23103808 | G | A | downstream_gene_variant | MODIFIER | c.*622G>A| |
S70 |
5 | BAA01g34550 | A01 | 23104231 | C | T | downstream_gene_variant | MODIFIER | c.*1045C>T| |
S75 |
6 | BAA01g34550 | A01 | 23104264 | G | A | downstream_gene_variant | MODIFIER | c.*1078G>A| |
S225 |
7 | BAA01g34550 | A01 | 23104292 | A | T | downstream_gene_variant | MODIFIER | c.*1106A>T| |
S278 |
8 | BAA01g34550 | A01 | 23104317 | C | T | downstream_gene_variant | MODIFIER | c.*1131C>T| |
S136 |
9 | BAA01g34550 | A01 | 23104351 | G | A | downstream_gene_variant | MODIFIER | c.*1165G>A| |
S132 S137 S215 S89 |
10 | BAA01g34550 | A01 | 23104472 | C | T | downstream_gene_variant | MODIFIER | c.*1286C>T| |
S55 |
11 | BAA01g34550 | A01 | 23105307 | G | A | downstream_gene_variant | MODIFIER | c.*2121G>A| |
S299 |
12 | BAA01g34550 | A01 | 23105360 | G | A | downstream_gene_variant | MODIFIER | c.*2174G>A| |
S105 S106 |
13 | BAA01g34550 | A01 | 23105371 | A | T | downstream_gene_variant | MODIFIER | c.*2185A>T| |
S126 |
14 | BAA01g34550 | A01 | 23105848 | G | A | downstream_gene_variant | MODIFIER | c.*2662G>A| |
S201 |
15 | BAA01g34550 | A01 | 23106090 | G | A | downstream_gene_variant | MODIFIER | c.*2904G>A| |
S207 |
16 | BAA01g34550 | A01 | 23106830 | G | A | downstream_gene_variant | MODIFIER | c.*3644G>A| |
S244 |
17 | BAA01g34550 | A01 | 23107044 | G | A | downstream_gene_variant | MODIFIER | c.*3858G>A| |
S308 |
18 | BAA01g34550 | A01 | 23107651 | C | T | downstream_gene_variant | MODIFIER | c.*4465C>T| |
S65 |
19 | BAA01g34550 | A01 | 23107989 | C | T | downstream_gene_variant | MODIFIER | c.*4803C>T| |
S178 |