Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g20080 | A01 | 9889407 | C | T | upstream_gene_variant | MODIFIER | c.-3419C>T| |
S53 |
2 | BAA01g20080 | A01 | 9890420 | G | A | upstream_gene_variant | MODIFIER | c.-2406G>A| |
S86 |
3 | BAA01g20080 | A01 | 9890579 | A | C | upstream_gene_variant | MODIFIER | c.-2247A>C| |
S15 S3 |
4 | BAA01g20080 | A01 | 9891403 | C | T | upstream_gene_variant | MODIFIER | c.-1423C>T| |
S210 |
5 | BAA01g20080 | A01 | 9891753 | G | A | upstream_gene_variant | MODIFIER | c.-1073G>A| |
S172 S217 |
6 | BAA01g20080 | A01 | 9892309 | G | A | upstream_gene_variant | MODIFIER | c.-517G>A| |
S122 |
7 | BAA01g20080 | A01 | 9892412 | G | A | upstream_gene_variant | MODIFIER | c.-414G>A| |
S298 |
8 | BAA01g20080 | A01 | 9892441 | G | A | upstream_gene_variant | MODIFIER | c.-385G>A| |
S175 |
9 | BAA01g20080 | A01 | 9892924 | C | T | synonymous_variant | LOW | c.99C>T|p.Gly33Gly |
S247 |
10 | BAA01g20080 | A01 | 9896242 | G | A | splice_region_variant&intron_variant | LOW | c.2028-7G>A| |
S142 |
11 | BAA01g20080 | A01 | 9896274 | G | A | missense_variant | MODERATE | c.2053G>A|p.Glu685Lys |
S75 |
12 | BAA01g20080 | A01 | 9896454 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.2164-1G>A| |
S67 |