Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19050 | A02 | 9866648 | A | T | downstream_gene_variant | MODIFIER | c.*2694T>A| |
S191 |
2 | BAA02g19050 | A02 | 9867393 | G | T | downstream_gene_variant | MODIFIER | c.*1949C>A| |
S120 |
3 | BAA02g19050 | A02 | 9867476 | G | A | downstream_gene_variant | MODIFIER | c.*1866C>T| |
S293 |
4 | BAA02g19050 | A02 | 9867487 | C | T | downstream_gene_variant | MODIFIER | c.*1855G>A| |
S289 S290 |
5 | BAA02g19050 | A02 | 9867738 | G | A | downstream_gene_variant | MODIFIER | c.*1604C>T| |
S247 |
6 | BAA02g19050 | A02 | 9867863 | C | T | downstream_gene_variant | MODIFIER | c.*1479G>A| |
S246 |
7 | BAA02g19050 | A02 | 9867999 | G | A | downstream_gene_variant | MODIFIER | c.*1343C>T| |
S13 |
8 | BAA02g19050 | A02 | 9869003 | G | A | downstream_gene_variant | MODIFIER | c.*339C>T| |
S278 |
9 | BAA02g19050 | A02 | 9869247 | C | T | downstream_gene_variant | MODIFIER | c.*95G>A| |
S233 |
10 | BAA02g19050 | A02 | 9869398 | C | T | missense_variant | MODERATE | c.1810G>A|p.Glu604Lys |
S77 S82 |
11 | BAA02g19050 | A02 | 9870774 | G | A | missense_variant | MODERATE | c.1097C>T|p.Ser366Phe |
S76 |
12 | BAA02g19050 | A02 | 9872302 | C | T | missense_variant | MODERATE | c.247G>A|p.Glu83Lys |
S178 |
13 | BAA02g19050 | A02 | 9872313 | G | A | missense_variant | MODERATE | c.236C>T|p.Ser79Phe |
S238 |
14 | BAA02g19050 | A02 | 9873544 | C | T | upstream_gene_variant | MODIFIER | c.-731G>A| |
S202 |
15 | BAA02g19050 | A02 | 9877401 | T | C | upstream_gene_variant | MODIFIER | c.-4588A>G| |
S179 |
16 | BAA02g19050 | A02 | 9877732 | C | T | upstream_gene_variant | MODIFIER | c.-4919G>A| |
S233 |