Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g34390 | A02 | 29455729 | G | A | synonymous_variant | LOW | c.1176C>T|p.Val392Val |
S25 |
2 | BAA02g34390 | A02 | 29455904 | C | T | missense_variant | MODERATE | c.1091G>A|p.Arg364Lys |
S32 |
3 | BAA02g34390 | A02 | 29456649 | G | A | synonymous_variant | LOW | c.693C>T|p.Gly231Gly |
S13 |
4 | BAA02g34390 | A02 | 29457568 | C | T | missense_variant&splice_region_variant | MODERATE | c.412G>A|p.Val138Ile |
S276 |
5 | BAA02g34390 | A02 | 29460561 | C | T | upstream_gene_variant | MODIFIER | c.-1076G>A| |
S181 |
6 | BAA02g34390 | A02 | 29461838 | G | A | upstream_gene_variant | MODIFIER | c.-2353C>T| |
S148 S210 |
7 | BAA02g34390 | A02 | 29461861 | G | A | upstream_gene_variant | MODIFIER | c.-2376C>T| |
S70 |
8 | BAA02g34390 | A02 | 29461866 | C | T | upstream_gene_variant | MODIFIER | c.-2381G>A| |
S175 |
9 | BAA02g34390 | A02 | 29463894 | G | A | upstream_gene_variant | MODIFIER | c.-4409C>T| |
S247 |
10 | BAA02g34390 | A02 | 29464093 | C | T | upstream_gene_variant | MODIFIER | c.-4608G>A| |
S139 |
11 | BAA02g34390 | A02 | 29464147 | C | T | upstream_gene_variant | MODIFIER | c.-4662G>A| |
S35 |
12 | BAA02g34390 | A02 | 29464229 | G | A | upstream_gene_variant | MODIFIER | c.-4744C>T| |
S251 |
13 | BAA02g34390 | A02 | 29464421 | G | A | upstream_gene_variant | MODIFIER | c.-4936C>T| |
S161 |
14 | BAA02g34390 | A02 | 29464480 | G | A | upstream_gene_variant | MODIFIER | c.-4995C>T| |
S211 S227 |