Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02650 | A02 | 1203167 | C | T | downstream_gene_variant | MODIFIER | c.*3267G>A| |
S245 |
2 | BAA02g02650 | A02 | 1203177 | C | T | downstream_gene_variant | MODIFIER | c.*3257G>A| |
S61 |
3 | BAA02g02650 | A02 | 1204299 | G | A | downstream_gene_variant | MODIFIER | c.*2135C>T| |
S168 |
4 | BAA02g02650 | A02 | 1204345 | C | T | downstream_gene_variant | MODIFIER | c.*2089G>A| |
S100 |
5 | BAA02g02650 | A02 | 1204459 | G | A | downstream_gene_variant | MODIFIER | c.*1975C>T| |
S292 |
6 | BAA02g02650 | A02 | 1206559 | G | A | synonymous_variant | LOW | c.1255C>T|p.Leu419Leu |
S206 S26 |
7 | BAA02g02650 | A02 | 1206582 | G | A | missense_variant | MODERATE | c.1232C>T|p.Pro411Leu |
S276 |
8 | BAA02g02650 | A02 | 1207013 | G | A | missense_variant | MODERATE | c.977C>T|p.Pro326Leu |
S131 |
9 | BAA02g02650 | A02 | 1207992 | G | A | missense_variant | MODERATE | c.782C>T|p.Pro261Leu |
S204 |
10 | BAA02g02650 | A02 | 1208022 | G | A | missense_variant | MODERATE | c.752C>T|p.Ser251Phe |
S308 |
11 | BAA02g02650 | A02 | 1208520 | C | T | missense_variant | MODERATE | c.439G>A|p.Asp147Asn |
S13 |
12 | BAA02g02650 | A02 | 1210027 | C | T | upstream_gene_variant | MODIFIER | c.-1069G>A| |
S251 |
13 | BAA02g02650 | A02 | 1210074 | C | T | upstream_gene_variant | MODIFIER | c.-1116G>A| |
S56 |
14 | BAA02g02650 | A02 | 1211582 | C | T | upstream_gene_variant | MODIFIER | c.-2624G>A| |
S153 |
15 | BAA02g02650 | A02 | 1212992 | C | T | upstream_gene_variant | MODIFIER | c.-4034G>A| |
S61 |