Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g39530 | A02 | 33581060 | C | T | upstream_gene_variant | MODIFIER | c.-3930C>T| |
S98 |
2 | BAA02g39530 | A02 | 33581417 | G | A | upstream_gene_variant | MODIFIER | c.-3573G>A| |
S35 |
3 | BAA02g39530 | A02 | 33582812 | C | T | upstream_gene_variant | MODIFIER | c.-2178C>T| |
S170 |
4 | BAA02g39530 | A02 | 33583201 | G | A | upstream_gene_variant | MODIFIER | c.-1789G>A| |
S69 |
5 | BAA02g39530 | A02 | 33584113 | C | T | upstream_gene_variant | MODIFIER | c.-877C>T| |
S40 S49 |
6 | BAA02g39530 | A02 | 33584198 | C | T | upstream_gene_variant | MODIFIER | c.-792C>T| |
S42 |
7 | BAA02g39530 | A02 | 33585178 | C | T | splice_region_variant&intron_variant | LOW | c.182+7C>T| |
S162 |
8 | BAA02g39530 | A02 | 33585311 | G | A | synonymous_variant | LOW | c.246G>A|p.Gln82Gln |
S281 |
9 | BAA02g39530 | A02 | 33585950 | G | A | missense_variant | MODERATE | c.583G>A|p.Val195Ile |
S274 S86 |
10 | BAA02g39530 | A02 | 33586159 | C | T | synonymous_variant | LOW | c.792C>T|p.Gly264Gly |
S202 |
11 | BAA02g39530 | A02 | 33586282 | G | A | synonymous_variant | LOW | c.915G>A|p.Gly305Gly |
S286 |
12 | BAA02g39530 | A02 | 33586322 | G | A | missense_variant | MODERATE | c.955G>A|p.Asp319Asn |
S174 S256 S27 |
13 | BAA02g39530 | A02 | 33586804 | G | A | missense_variant | MODERATE | c.1184G>A|p.Cys395Tyr |
S41 |
14 | BAA02g39530 | A02 | 33587616 | G | A | missense_variant | MODERATE | c.1996G>A|p.Glu666Lys |
S26 |
15 | BAA02g39530 | A02 | 33588799 | C | T | downstream_gene_variant | MODIFIER | c.*726C>T| |
S190 |
16 | BAA02g39530 | A02 | 33590448 | G | A | downstream_gene_variant | MODIFIER | c.*2375G>A| |
S69 |
17 | BAA02g39530 | A02 | 33590606 | G | A | downstream_gene_variant | MODIFIER | c.*2533G>A| |
S35 |
18 | BAA02g39530 | A02 | 33590962 | G | A | downstream_gene_variant | MODIFIER | c.*2889G>A| |
S71 |
19 | BAA02g39530 | A02 | 33591377 | C | T | downstream_gene_variant | MODIFIER | c.*3304C>T| |
S99 |