Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g29650 | A01 | 18729770 | C | T | upstream_gene_variant | MODIFIER | c.-4296C>T| |
S183 |
2 | BAA01g29650 | A01 | 18730866 | C | T | upstream_gene_variant | MODIFIER | c.-3200C>T| |
S303 |
3 | BAA01g29650 | A01 | 18731178 | G | A | upstream_gene_variant | MODIFIER | c.-2888G>A| |
S61 |
4 | BAA01g29650 | A01 | 18731662 | G | A | upstream_gene_variant | MODIFIER | c.-2404G>A| |
S36 |
5 | BAA01g29650 | A01 | 18731957 | G | A | upstream_gene_variant | MODIFIER | c.-2109G>A| |
S122 |
6 | BAA01g29650 | A01 | 18732081 | G | A | upstream_gene_variant | MODIFIER | c.-1985G>A| |
S245 |
7 | BAA01g29650 | A01 | 18733112 | G | A | upstream_gene_variant | MODIFIER | c.-954G>A| |
S121 |
8 | BAA01g29650 | A01 | 18735126 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.370-1G>A| |
S163 |
9 | BAA01g29650 | A01 | 18738597 | G | A | intron_variant | MODIFIER | c.1477-157G>A| |
S187 |
10 | BAA01g29650 | A01 | 18738920 | C | T | intron_variant | MODIFIER | c.1619+24C>T| |
S128 |
11 | BAA01g29650 | A01 | 18739887 | G | A | missense_variant | MODERATE | c.2044G>A|p.Ala682Thr |
S163 |
12 | BAA01g29650 | A01 | 18741208 | G | A | missense_variant | MODERATE | c.2827G>A|p.Val943Ile |
S259 |