Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g21850 | A10 | 19083404 | G | A | upstream_gene_variant | MODIFIER | c.-1657G>A| |
S18 |
2 | BAA10g21850 | A10 | 19083690 | G | A | upstream_gene_variant | MODIFIER | c.-1371G>A| |
S50 |
3 | BAA10g21850 | A10 | 19083792 | C | T | upstream_gene_variant | MODIFIER | c.-1269C>T| |
S11 |
4 | BAA10g21850 | A10 | 19083886 | C | T | upstream_gene_variant | MODIFIER | c.-1175C>T| |
S294 |
5 | BAA10g21850 | A10 | 19083974 | G | A | upstream_gene_variant | MODIFIER | c.-1087G>A| |
S62 |
6 | BAA10g21850 | A10 | 19084787 | G | A | upstream_gene_variant | MODIFIER | c.-274G>A| |
S93 |
7 | BAA10g21850 | A10 | 19085400 | C | T | synonymous_variant | LOW | c.261C>T|p.Phe87Phe |
S268 |
8 | BAA10g21850 | A10 | 19088664 | C | T | downstream_gene_variant | MODIFIER | c.*3222C>T| |
S199 |
9 | BAA10g21850 | A10 | 19089729 | G | A | downstream_gene_variant | MODIFIER | c.*4287G>A| |
S295 |
10 | BAA10g21850 | A10 | 19090138 | C | T | downstream_gene_variant | MODIFIER | c.*4696C>T| |
S48 |
11 | BAA10g21850 | A10 | 19090369 | C | T | downstream_gene_variant | MODIFIER | c.*4927C>T| |
S38 |