Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g44440 | A03 | 21099235 | G | A | upstream_gene_variant | MODIFIER | c.-3643G>A| |
S153 S213 |
2 | BAA03g44440 | A03 | 21099436 | G | A | upstream_gene_variant | MODIFIER | c.-3442G>A| |
S226 |
3 | BAA03g44440 | A03 | 21099535 | G | A | upstream_gene_variant | MODIFIER | c.-3343G>A| |
S242 |
4 | BAA03g44440 | A03 | 21100485 | C | T | upstream_gene_variant | MODIFIER | c.-2393C>T| |
S299 |
5 | BAA03g44440 | A03 | 21100541 | C | T | upstream_gene_variant | MODIFIER | c.-2337C>T| |
S242 |
6 | BAA03g44440 | A03 | 21100805 | C | T | upstream_gene_variant | MODIFIER | c.-2073C>T| |
S40 S49 |
7 | BAA03g44440 | A03 | 21100903 | G | A | upstream_gene_variant | MODIFIER | c.-1975G>A| |
S17 |
8 | BAA03g44440 | A03 | 21103049 | C | T | missense_variant | MODERATE | c.172C>T|p.Pro58Ser |
S67 |
9 | BAA03g44440 | A03 | 21103286 | C | T | missense_variant | MODERATE | c.409C>T|p.Pro137Ser |
S179 |
10 | BAA03g44440 | A03 | 21103361 | C | T | missense_variant | MODERATE | c.484C>T|p.Pro162Ser |
S176 |
11 | BAA03g44440 | A03 | 21103365 | C | T | missense_variant | MODERATE | c.488C>T|p.Ser163Phe |
S264 |
12 | BAA03g44440 | A03 | 21105393 | G | A | downstream_gene_variant | MODIFIER | c.*1281G>A| |
S260 |
13 | BAA03g44440 | A03 | 21106056 | C | T | downstream_gene_variant | MODIFIER | c.*1944C>T| |
S279 |
14 | BAA03g44440 | A03 | 21106571 | C | T | downstream_gene_variant | MODIFIER | c.*2459C>T| |
S158 |
15 | BAA03g44440 | A03 | 21106930 | C | T | downstream_gene_variant | MODIFIER | c.*2818C>T| |
S181 S56 |
16 | BAA03g44440 | A03 | 21107474 | C | T | downstream_gene_variant | MODIFIER | c.*3362C>T| |
S216 |
17 | BAA03g44440 | A03 | 21108351 | G | A | downstream_gene_variant | MODIFIER | c.*4239G>A| |
S169 |
18 | BAA03g44440 | A03 | 21108644 | G | A | downstream_gene_variant | MODIFIER | c.*4532G>A| |
S70 |