Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g08660 | A05 | 4310943 | C | T | upstream_gene_variant | MODIFIER | c.-1809C>T| |
S128 |
2 | BAA05g08660 | A05 | 4311431 | G | A | upstream_gene_variant | MODIFIER | c.-1321G>A| |
S242 |
3 | BAA05g08660 | A05 | 4311450 | C | T | upstream_gene_variant | MODIFIER | c.-1302C>T| |
S59 |
4 | BAA05g08660 | A05 | 4311808 | G | A | upstream_gene_variant | MODIFIER | c.-944G>A| |
S126 |
5 | BAA05g08660 | A05 | 4311968 | A | G | upstream_gene_variant | MODIFIER | c.-784A>G| |
S183 |
6 | BAA05g08660 | A05 | 4312691 | C | T | upstream_gene_variant | MODIFIER | c.-61C>T| |
S148 S30 S31 |
7 | BAA05g08660 | A05 | 4312725 | C | T | upstream_gene_variant | MODIFIER | c.-27C>T| |
S161 |
8 | BAA05g08660 | A05 | 4313094 | G | A | missense_variant | MODERATE | c.343G>A|p.Val115Ile |
S284 |
9 | BAA05g08660 | A05 | 4313342 | C | T | synonymous_variant | LOW | c.591C>T|p.His197His |
S292 |