Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g12030 | A02 | 5428503 | G | A | downstream_gene_variant | MODIFIER | c.*182C>T| |
S53 S75 S81 S82 S92 |
2 | BAA02g12030 | A02 | 5428627 | G | A | downstream_gene_variant | MODIFIER | c.*58C>T| |
S256 |
3 | BAA02g12030 | A02 | 5429037 | G | A | missense_variant | MODERATE | c.1853C>T|p.Ala618Val |
S197 |
4 | BAA02g12030 | A02 | 5429139 | G | A | missense_variant | MODERATE | c.1751C>T|p.Thr584Ile |
S274 |
5 | BAA02g12030 | A02 | 5430793 | C | T | missense_variant | MODERATE | c.662G>A|p.Gly221Glu |
S211 S227 |
6 | BAA02g12030 | A02 | 5430797 | G | A | missense_variant | MODERATE | c.658C>T|p.Leu220Phe |
S246 |
7 | BAA02g12030 | A02 | 5431160 | G | A | synonymous_variant | LOW | c.393C>T|p.Asn131Asn |
S269 |
8 | BAA02g12030 | A02 | 5431228 | G | A | synonymous_variant | LOW | c.325C>T|p.Leu109Leu |
S57 |
9 | BAA02g12030 | A02 | 5431640 | G | A | missense_variant | MODERATE | c.148C>T|p.Pro50Ser |
S228 |
10 | BAA02g12030 | A02 | 5433141 | C | T | upstream_gene_variant | MODIFIER | c.-1245G>A| |
S66 |
11 | BAA02g12030 | A02 | 5433497 | G | A | upstream_gene_variant | MODIFIER | c.-1601C>T| |
S289 S290 |
12 | BAA02g12030 | A02 | 5433830 | G | A | upstream_gene_variant | MODIFIER | c.-1934C>T| |
S190 |
13 | BAA02g12030 | A02 | 5434638 | C | T | upstream_gene_variant | MODIFIER | c.-2742G>A| |
S135 |
14 | BAA02g12030 | A02 | 5434726 | C | T | upstream_gene_variant | MODIFIER | c.-2830G>A| |
S104 |
15 | BAA02g12030 | A02 | 5435091 | G | A | upstream_gene_variant | MODIFIER | c.-3195C>T| |
S197 |