Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g38450 | A02 | 32750172 | C | T | upstream_gene_variant | MODIFIER | c.-4878C>T| |
S256 S259 |
2 | BAA02g38450 | A02 | 32750186 | G | A | upstream_gene_variant | MODIFIER | c.-4864G>A| |
S8 |
3 | BAA02g38450 | A02 | 32751312 | C | T | upstream_gene_variant | MODIFIER | c.-3738C>T| |
S195 |
4 | BAA02g38450 | A02 | 32751362 | C | T | upstream_gene_variant | MODIFIER | c.-3688C>T| |
S167 |
5 | BAA02g38450 | A02 | 32752245 | C | T | upstream_gene_variant | MODIFIER | c.-2805C>T| |
S206 |
6 | BAA02g38450 | A02 | 32754734 | C | T | upstream_gene_variant | MODIFIER | c.-316C>T| |
S240 |
7 | BAA02g38450 | A02 | 32755021 | C | T | upstream_gene_variant | MODIFIER | c.-29C>T| |
S252 |
8 | BAA02g38450 | A02 | 32755176 | C | T | missense_variant | MODERATE | c.127C>T|p.Leu43Phe |
S32 |
9 | BAA02g38450 | A02 | 32755186 | C | T | missense_variant&splice_region_variant | MODERATE | c.137C>T|p.Pro46Leu |
S226 |
10 | BAA02g38450 | A02 | 32755216 | G | A | intron_variant | MODIFIER | c.137+30G>A| |
S146 |
11 | BAA02g38450 | A02 | 32755552 | G | A | missense_variant | MODERATE | c.217G>A|p.Asp73Asn |
S210 S279 |
12 | BAA02g38450 | A02 | 32756616 | C | T | missense_variant | MODERATE | c.740C>T|p.Ser247Leu |
S64 |
13 | BAA02g38450 | A02 | 32756722 | C | T | intron_variant | MODIFIER | c.775-17C>T| |
S273 |