Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g10660 | A05 | 5418057 | G | A | downstream_gene_variant | MODIFIER | c.*871C>T| |
S260 |
2 | BAA05g10660 | A05 | 5419764 | G | A | missense_variant | MODERATE | c.476C>T|p.Ser159Phe |
S173 |
3 | BAA05g10660 | A05 | 5419890 | G | A | missense_variant | MODERATE | c.350C>T|p.Ala117Val |
S274 |
4 | BAA05g10660 | A05 | 5420039 | C | T | missense_variant | MODERATE | c.293G>A|p.Cys98Tyr |
S169 S208 |
5 | BAA05g10660 | A05 | 5420154 | G | A | missense_variant | MODERATE | c.178C>T|p.Pro60Ser |
S252 |
6 | BAA05g10660 | A05 | 5421761 | C | A | upstream_gene_variant | MODIFIER | c.-1430G>T| |
S162 S234 |
7 | BAA05g10660 | A05 | 5423069 | C | T | upstream_gene_variant | MODIFIER | c.-2738G>A| |
S256 |
8 | BAA05g10660 | A05 | 5423117 | C | T | upstream_gene_variant | MODIFIER | c.-2786G>A| |
S12 |
9 | BAA05g10660 | A05 | 5423384 | G | A | upstream_gene_variant | MODIFIER | c.-3053C>T| |
S262 |
10 | BAA05g10660 | A05 | 5424399 | C | T | upstream_gene_variant | MODIFIER | c.-4068G>A| |
S295 |
11 | BAA05g10660 | A05 | 5424502 | C | T | upstream_gene_variant | MODIFIER | c.-4171G>A| |
S291 |