Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g03130 | A02 | 1379853 | G | A | missense_variant | MODERATE | c.212C>T|p.Ala71Val |
S168 |
2 | BAA02g03130 | A02 | 1379899 | C | T | missense_variant | MODERATE | c.166G>A|p.Glu56Lys |
S174 S175 |
3 | BAA02g03130 | A02 | 1380212 | G | A | upstream_gene_variant | MODIFIER | c.-148C>T| |
S269 |
4 | BAA02g03130 | A02 | 1380390 | C | T | upstream_gene_variant | MODIFIER | c.-326G>A| |
S54 |
5 | BAA02g03130 | A02 | 1380466 | G | A | upstream_gene_variant | MODIFIER | c.-402C>T| |
S236 |
6 | BAA02g03130 | A02 | 1380475 | C | T | upstream_gene_variant | MODIFIER | c.-411G>A| |
S200 |
7 | BAA02g03130 | A02 | 1381530 | G | A | upstream_gene_variant | MODIFIER | c.-1466C>T| |
S45 |
8 | BAA02g03130 | A02 | 1381625 | G | A | upstream_gene_variant | MODIFIER | c.-1561C>T| |
S125 |
9 | BAA02g03130 | A02 | 1382221 | G | A | upstream_gene_variant | MODIFIER | c.-2157C>T| |
S86 |
10 | BAA02g03130 | A02 | 1382694 | C | T | upstream_gene_variant | MODIFIER | c.-2630G>A| |
S287 |
11 | BAA02g03130 | A02 | 1383117 | G | A | upstream_gene_variant | MODIFIER | c.-3053C>T| |
S210 |
12 | BAA02g03130 | A02 | 1383768 | G | A | upstream_gene_variant | MODIFIER | c.-3704C>T| |
S289 |
13 | BAA02g03130 | A02 | 1383990 | G | A | upstream_gene_variant | MODIFIER | c.-3926C>T| |
S95 |
14 | BAA02g03130 | A02 | 1384125 | G | A | upstream_gene_variant | MODIFIER | c.-4061C>T| |
S57 |
15 | BAA02g03130 | A02 | 1384563 | C | T | upstream_gene_variant | MODIFIER | c.-4499G>A| |
S121 |