Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g11040 | A01 | 5092658 | G | A | upstream_gene_variant | MODIFIER | c.-3923G>A| |
S153 |
2 | BAA01g11040 | A01 | 5092735 | G | A | upstream_gene_variant | MODIFIER | c.-3846G>A| |
S165 |
3 | BAA01g11040 | A01 | 5093707 | G | A | upstream_gene_variant | MODIFIER | c.-2874G>A| |
S178 |
4 | BAA01g11040 | A01 | 5094356 | C | T | upstream_gene_variant | MODIFIER | c.-2225C>T| |
S226 |
5 | BAA01g11040 | A01 | 5095068 | G | A | upstream_gene_variant | MODIFIER | c.-1513G>A| |
S72 |
6 | BAA01g11040 | A01 | 5095488 | T | G | upstream_gene_variant | MODIFIER | c.-1093T>G| |
S106 S109 S122 S143 S170 S257 S296 S35 S39 S67 S70 |
7 | BAA01g11040 | A01 | 5097392 | G | A | missense_variant | MODERATE | c.812G>A|p.Arg271Lys |
S133 |
8 | BAA01g11040 | A01 | 5097419 | C | T | missense_variant | MODERATE | c.839C>T|p.Pro280Leu |
S182 |
9 | BAA01g11040 | A01 | 5097580 | G | A | missense_variant | MODERATE | c.1000G>A|p.Asp334Asn |
S237 |
10 | BAA01g11040 | A01 | 5098011 | C | T | missense_variant | MODERATE | c.1318C>T|p.Arg440Cys |
S155 S211 |
11 | BAA01g11040 | A01 | 5099078 | G | A | synonymous_variant | LOW | c.1593G>A|p.Lys531Lys |
S257 |