Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g35760 | A09 | 44090451 | C | T | upstream_gene_variant | MODIFIER | c.-4492C>T| |
S139 |
2 | BAA09g35760 | A09 | 44090476 | C | T | upstream_gene_variant | MODIFIER | c.-4467C>T| |
S201 |
3 | BAA09g35760 | A09 | 44091188 | C | T | upstream_gene_variant | MODIFIER | c.-3755C>T| |
S152 |
4 | BAA09g35760 | A09 | 44095731 | G | A | synonymous_variant | LOW | c.234G>A|p.Gln78Gln |
S149 |
5 | BAA09g35760 | A09 | 44096218 | G | A | missense_variant | MODERATE | c.508G>A|p.Ala170Thr |
S51 |
6 | BAA09g35760 | A09 | 44096224 | G | A | missense_variant | MODERATE | c.514G>A|p.Glu172Lys |
S67 |
7 | BAA09g35760 | A09 | 44096226 | G | A | synonymous_variant | LOW | c.516G>A|p.Glu172Glu |
S51 |
8 | BAA09g35760 | A09 | 44097010 | C | T | missense_variant | MODERATE | c.958C>T|p.Leu320Phe |
S57 |
9 | BAA09g35760 | A09 | 44098272 | C | T | missense_variant&splice_region_variant | MODERATE | c.1816C>T|p.Pro606Ser |
S229 |
10 | BAA09g35760 | A09 | 44098417 | C | T | synonymous_variant | LOW | c.1875C>T|p.Ser625Ser |
S192 |
11 | BAA09g35760 | A09 | 44101377 | G | A | downstream_gene_variant | MODIFIER | c.*2016G>A| |
S156 |
12 | BAA09g35760 | A09 | 44101384 | C | T | downstream_gene_variant | MODIFIER | c.*2023C>T| |
S14 |
13 | BAA09g35760 | A09 | 44101583 | G | C | downstream_gene_variant | MODIFIER | c.*2222G>C| |
S204 |