Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g00560 | A09 | 512603 | G | A | missense_variant | MODERATE | c.1279C>T|p.Pro427Ser |
S130 |
2 | BAA09g00560 | A09 | 513793 | G | A | missense_variant | MODERATE | c.394C>T|p.Pro132Ser |
S13 |
3 | BAA09g00560 | A09 | 513844 | C | T | missense_variant | MODERATE | c.343G>A|p.Asp115Asn |
S143 |
4 | BAA09g00560 | A09 | 514208 | G | A | synonymous_variant | LOW | c.66C>T|p.Asn22Asn |
S289 S290 |
5 | BAA09g00560 | A09 | 515626 | C | T | upstream_gene_variant | MODIFIER | c.-1353G>A| |
S40 S49 |
6 | BAA09g00560 | A09 | 515973 | C | T | upstream_gene_variant | MODIFIER | c.-1700G>A| |
S183 S198 |
7 | BAA09g00560 | A09 | 516423 | G | A | upstream_gene_variant | MODIFIER | c.-2150C>T| |
S90 |
8 | BAA09g00560 | A09 | 516926 | C | T | upstream_gene_variant | MODIFIER | c.-2653G>A| |
S242 |
9 | BAA09g00560 | A09 | 518149 | G | A | upstream_gene_variant | MODIFIER | c.-3876C>T| |
S98 |