Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g29490 | A02 | 16890032 | G | A | missense_variant | MODERATE | c.44C>T|p.Pro15Leu |
S36 |
2 | BAA02g29490 | A02 | 16890044 | G | A | missense_variant | MODERATE | c.32C>T|p.Thr11Ile |
S47 |
3 | BAA02g29490 | A02 | 16890321 | C | T | upstream_gene_variant | MODIFIER | c.-246G>A| |
S162 |
4 | BAA02g29490 | A02 | 16890396 | G | A | upstream_gene_variant | MODIFIER | c.-321C>T| |
S71 |
5 | BAA02g29490 | A02 | 16890958 | C | T | upstream_gene_variant | MODIFIER | c.-883G>A| |
S185 |
6 | BAA02g29490 | A02 | 16891485 | C | T | upstream_gene_variant | MODIFIER | c.-1410G>A| |
S84 S93 |
7 | BAA02g29490 | A02 | 16891667 | C | T | upstream_gene_variant | MODIFIER | c.-1592G>A| |
S32 |
8 | BAA02g29490 | A02 | 16894263 | C | T | upstream_gene_variant | MODIFIER | c.-4188G>A| |
S42 |
9 | BAA02g29490 | A02 | 16894748 | C | T | upstream_gene_variant | MODIFIER | c.-4673G>A| |
S177 |
10 | BAA02g29490 | A02 | 16894761 | C | T | upstream_gene_variant | MODIFIER | c.-4686G>A| |
S171 |
11 | BAA02g29490 | A02 | 16894773 | C | T | upstream_gene_variant | MODIFIER | c.-4698G>A| |
S92 |