Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g17880 | A05 | 10146040 | C | T | upstream_gene_variant | MODIFIER | c.-3324C>T| |
S47 |
2 | BAA05g17880 | A05 | 10146838 | G | A | upstream_gene_variant | MODIFIER | c.-2526G>A| |
S231 |
3 | BAA05g17880 | A05 | 10149060 | G | A | upstream_gene_variant | MODIFIER | c.-304G>A| |
S110 |
4 | BAA05g17880 | A05 | 10149078 | G | A | upstream_gene_variant | MODIFIER | c.-286G>A| |
S279 |
5 | BAA05g17880 | A05 | 10149377 | G | A | missense_variant | MODERATE | c.14G>A|p.Arg5Lys |
S173 |
6 | BAA05g17880 | A05 | 10149494 | G | A | intron_variant | MODIFIER | c.44+87G>A| |
S260 |
7 | BAA05g17880 | A05 | 10149873 | C | T | missense_variant | MODERATE | c.142C>T|p.Pro48Ser |
S250 |
8 | BAA05g17880 | A05 | 10150007 | G | A | intron_variant | MODIFIER | c.179+97G>A| |
S296 |
9 | BAA05g17880 | A05 | 10150119 | C | T | intron_variant | MODIFIER | c.180-200C>T| |
S182 |
10 | BAA05g17880 | A05 | 10151642 | G | A | downstream_gene_variant | MODIFIER | c.*614G>A| |
S14 |
11 | BAA05g17880 | A05 | 10152259 | G | A | downstream_gene_variant | MODIFIER | c.*1231G>A| |
S274 |
12 | BAA05g17880 | A05 | 10152974 | G | A | downstream_gene_variant | MODIFIER | c.*1946G>A| |
S161 |
13 | BAA05g17880 | A05 | 10153069 | G | A | downstream_gene_variant | MODIFIER | c.*2041G>A| |
S138 |
14 | BAA05g17880 | A05 | 10153088 | G | A | downstream_gene_variant | MODIFIER | c.*2060G>A| |
S293 |
15 | BAA05g17880 | A05 | 10153100 | G | A | downstream_gene_variant | MODIFIER | c.*2072G>A| |
S218 |
16 | BAA05g17880 | A05 | 10155134 | C | T | downstream_gene_variant | MODIFIER | c.*4106C>T| |
S113 |
17 | BAA05g17880 | A05 | 10155602 | G | A | downstream_gene_variant | MODIFIER | c.*4574G>A| |
S272 |