Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g19100 | A09 | 11620543 | C | T | upstream_gene_variant | MODIFIER | c.-3811C>T| |
S295 |
2 | BAA09g19100 | A09 | 11620878 | C | T | upstream_gene_variant | MODIFIER | c.-3476C>T| |
S255 |
3 | BAA09g19100 | A09 | 11620912 | G | A | upstream_gene_variant | MODIFIER | c.-3442G>A| |
S172 S217 |
4 | BAA09g19100 | A09 | 11621065 | G | A | upstream_gene_variant | MODIFIER | c.-3289G>A| |
S88 |
5 | BAA09g19100 | A09 | 11622217 | G | A | upstream_gene_variant | MODIFIER | c.-2137G>A| |
S131 |
6 | BAA09g19100 | A09 | 11622893 | C | T | upstream_gene_variant | MODIFIER | c.-1461C>T| |
S217 S248 |
7 | BAA09g19100 | A09 | 11622902 | G | A | upstream_gene_variant | MODIFIER | c.-1452G>A| |
S20 |
8 | BAA09g19100 | A09 | 11623115 | C | T | upstream_gene_variant | MODIFIER | c.-1239C>T| |
S245 |
9 | BAA09g19100 | A09 | 11624005 | C | T | upstream_gene_variant | MODIFIER | c.-349C>T| |
S41 |
10 | BAA09g19100 | A09 | 11624467 | A | C | missense_variant | MODERATE | c.114A>C|p.Lys38Asn |
S295 |
11 | BAA09g19100 | A09 | 11625550 | G | A | missense_variant | MODERATE | c.1045G>A|p.Ala349Thr |
S301 S304 |
12 | BAA09g19100 | A09 | 11626282 | G | A | downstream_gene_variant | MODIFIER | c.*253G>A| |
S87 |