Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g16850 | A04 | 21137634 | C | T | upstream_gene_variant | MODIFIER | c.-4916C>T| |
S100 |
2 | BAA04g16850 | A04 | 21137668 | G | A | upstream_gene_variant | MODIFIER | c.-4882G>A| |
S144 |
3 | BAA04g16850 | A04 | 21137690 | C | T | upstream_gene_variant | MODIFIER | c.-4860C>T| |
S107 |
4 | BAA04g16850 | A04 | 21138055 | G | A | upstream_gene_variant | MODIFIER | c.-4495G>A| |
S99 |
5 | BAA04g16850 | A04 | 21139377 | C | T | upstream_gene_variant | MODIFIER | c.-3173C>T| |
S9 |
6 | BAA04g16850 | A04 | 21139974 | G | A | upstream_gene_variant | MODIFIER | c.-2576G>A| |
S182 |
7 | BAA04g16850 | A04 | 21142929 | C | T | missense_variant | MODERATE | c.238C>T|p.Pro80Ser |
S225 |
8 | BAA04g16850 | A04 | 21143192 | C | T | synonymous_variant | LOW | c.501C>T|p.Ser167Ser |
S23 |
9 | BAA04g16850 | A04 | 21143588 | C | T | synonymous_variant | LOW | c.576C>T|p.Leu192Leu |
S81 S85 |
10 | BAA04g16850 | A04 | 21145130 | G | A | intron_variant | MODIFIER | c.904-553G>A| |
S91 |
11 | BAA04g16850 | A04 | 21146312 | G | A | downstream_gene_variant | MODIFIER | c.*564G>A| |
S165 |
12 | BAA04g16850 | A04 | 21147398 | G | A | downstream_gene_variant | MODIFIER | c.*1650G>A| |
S255 |
13 | BAA04g16850 | A04 | 21148282 | C | T | downstream_gene_variant | MODIFIER | c.*2534C>T| |
S137 |