Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g56930 | A09 | 56366558 | C | T | splice_region_variant&synonymous_variant | LOW | c.1215G>A|p.Gln405Gln |
S278 |
2 | BAA09g56930 | A09 | 56368781 | C | T | missense_variant | MODERATE | c.4G>A|p.Gly2Arg |
S61 |
3 | BAA09g56930 | A09 | 56369438 | C | T | upstream_gene_variant | MODIFIER | c.-654G>A| |
S130 |
4 | BAA09g56930 | A09 | 56369599 | G | A | upstream_gene_variant | MODIFIER | c.-815C>T| |
S42 |
5 | BAA09g56930 | A09 | 56370718 | C | T | upstream_gene_variant | MODIFIER | c.-1934G>A| |
S212 |
6 | BAA09g56930 | A09 | 56371627 | G | A | upstream_gene_variant | MODIFIER | c.-2843C>T| |
S98 |
7 | BAA09g56930 | A09 | 56371668 | C | T | upstream_gene_variant | MODIFIER | c.-2884G>A| |
S6 |