Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g06860 | A07 | 16202120 | C | T | missense_variant | MODERATE | c.892G>A|p.Gly298Arg |
S232 |
2 | BAA07g06860 | A07 | 16202161 | C | T | missense_variant | MODERATE | c.851G>A|p.Gly284Asp |
S9 |
3 | BAA07g06860 | A07 | 16202690 | C | T | missense_variant | MODERATE | c.598G>A|p.Val200Ile |
S160 |
4 | BAA07g06860 | A07 | 16202775 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.514-1G>A| |
S166 |
5 | BAA07g06860 | A07 | 16204084 | C | T | upstream_gene_variant | MODIFIER | c.-371G>A| |
S120 |
6 | BAA07g06860 | A07 | 16204263 | C | T | upstream_gene_variant | MODIFIER | c.-550G>A| |
S293 |
7 | BAA07g06860 | A07 | 16205276 | C | T | upstream_gene_variant | MODIFIER | c.-1563G>A| |
S85 |
8 | BAA07g06860 | A07 | 16205374 | G | A | upstream_gene_variant | MODIFIER | c.-1661C>T| |
S88 |
9 | BAA07g06860 | A07 | 16205472 | G | A | upstream_gene_variant | MODIFIER | c.-1759C>T| |
S190 |
10 | BAA07g06860 | A07 | 16205532 | C | T | upstream_gene_variant | MODIFIER | c.-1819G>A| |
S18 |