Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g12440 | A01 | 5868089 | G | A | upstream_gene_variant | MODIFIER | c.-2972G>A| |
S28 |
2 | BAA01g12440 | A01 | 5868924 | C | T | upstream_gene_variant | MODIFIER | c.-2137C>T| |
S61 |
3 | BAA01g12440 | A01 | 5868941 | C | T | upstream_gene_variant | MODIFIER | c.-2120C>T| |
S286 |
4 | BAA01g12440 | A01 | 5869151 | C | T | upstream_gene_variant | MODIFIER | c.-1910C>T| |
S182 |
5 | BAA01g12440 | A01 | 5869955 | C | T | upstream_gene_variant | MODIFIER | c.-1106C>T| |
S270 |
6 | BAA01g12440 | A01 | 5870057 | G | A | upstream_gene_variant | MODIFIER | c.-1004G>A| |
S272 |
7 | BAA01g12440 | A01 | 5870575 | G | A | upstream_gene_variant | MODIFIER | c.-486G>A| |
S272 |
8 | BAA01g12440 | A01 | 5871174 | G | A | synonymous_variant | LOW | c.114G>A|p.Gln38Gln |
S149 |
9 | BAA01g12440 | A01 | 5871236 | C | T | missense_variant | MODERATE | c.176C>T|p.Ser59Phe |
S4 |
10 | BAA01g12440 | A01 | 5871265 | G | A | missense_variant | MODERATE | c.205G>A|p.Asp69Asn |
S17 |
11 | BAA01g12440 | A01 | 5871787 | G | A | missense_variant | MODERATE | c.500G>A|p.Gly167Glu |
S60 |
12 | BAA01g12440 | A01 | 5873831 | G | A | downstream_gene_variant | MODIFIER | c.*1932G>A| |
S195 |
13 | BAA01g12440 | A01 | 5874618 | G | A | downstream_gene_variant | MODIFIER | c.*2719G>A| |
S209 |
14 | BAA01g12440 | A01 | 5875909 | G | A | downstream_gene_variant | MODIFIER | c.*4010G>A| |
S162 |
15 | BAA01g12440 | A01 | 5875916 | C | T | downstream_gene_variant | MODIFIER | c.*4017C>T| |
S265 S297 |
16 | BAA01g12440 | A01 | 5876507 | G | A | downstream_gene_variant | MODIFIER | c.*4608G>A| |
S232 |
17 | BAA01g12440 | A01 | 5876560 | C | T | downstream_gene_variant | MODIFIER | c.*4661C>T| |
S155 S211 |