Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g44190 | A09 | 49965374 | C | T | downstream_gene_variant | MODIFIER | c.*4328G>A| |
S235 |
2 | BAA09g44190 | A09 | 49966078 | C | T | downstream_gene_variant | MODIFIER | c.*3624G>A| |
S297 |
3 | BAA09g44190 | A09 | 49966401 | G | A | downstream_gene_variant | MODIFIER | c.*3301C>T| |
S289 S290 |
4 | BAA09g44190 | A09 | 49966609 | G | A | downstream_gene_variant | MODIFIER | c.*3093C>T| |
S105 S106 |
5 | BAA09g44190 | A09 | 49967763 | C | T | downstream_gene_variant | MODIFIER | c.*1939G>A| |
S251 |
6 | BAA09g44190 | A09 | 49968097 | G | A | downstream_gene_variant | MODIFIER | c.*1605C>T| |
S71 |
7 | BAA09g44190 | A09 | 49968639 | G | A | downstream_gene_variant | MODIFIER | c.*1063C>T| |
S246 |
8 | BAA09g44190 | A09 | 49969341 | C | T | downstream_gene_variant | MODIFIER | c.*361G>A| |
S120 |
9 | BAA09g44190 | A09 | 49970091 | G | A | missense_variant | MODERATE | c.10C>T|p.Pro4Ser |
S156 S213 S34 S6 |
10 | BAA09g44190 | A09 | 49970672 | C | T | upstream_gene_variant | MODIFIER | c.-572G>A| |
S272 |
11 | BAA09g44190 | A09 | 49971307 | G | A | upstream_gene_variant | MODIFIER | c.-1207C>T| |
S201 |
12 | BAA09g44190 | A09 | 49971424 | G | A | upstream_gene_variant | MODIFIER | c.-1324C>T| |
S165 |
13 | BAA09g44190 | A09 | 49973697 | G | A | upstream_gene_variant | MODIFIER | c.-3597C>T| |
S265 |
14 | BAA09g44190 | A09 | 49973777 | G | A | upstream_gene_variant | MODIFIER | c.-3677C>T| |
S54 |
15 | BAA09g44190 | A09 | 49973841 | G | A | upstream_gene_variant | MODIFIER | c.-3741C>T| |
S235 S260 |
16 | BAA09g44190 | A09 | 49974692 | C | T | upstream_gene_variant | MODIFIER | c.-4592G>A| |
S247 |