Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g08890 | A10 | 10896487 | C | T | upstream_gene_variant | MODIFIER | c.-521C>T| |
S149 |
2 | BAA10g08890 | A10 | 10897704 | C | T | intron_variant | MODIFIER | c.462+38C>T| |
S301 S304 |
3 | BAA10g08890 | A10 | 10898454 | G | A | intron_variant | MODIFIER | c.463-319G>A| |
S226 |
4 | BAA10g08890 | A10 | 10898717 | C | T | intron_variant | MODIFIER | c.463-56C>T| |
S260 |
5 | BAA10g08890 | A10 | 10900365 | C | T | downstream_gene_variant | MODIFIER | c.*994C>T| |
S17 |
6 | BAA10g08890 | A10 | 10900958 | C | T | downstream_gene_variant | MODIFIER | c.*1587C>T| |
S235 |
7 | BAA10g08890 | A10 | 10901663 | C | T | downstream_gene_variant | MODIFIER | c.*2292C>T| |
S73 |
8 | BAA10g08890 | A10 | 10902086 | C | T | downstream_gene_variant | MODIFIER | c.*2715C>T| |
S171 |
9 | BAA10g08890 | A10 | 10902734 | G | A | downstream_gene_variant | MODIFIER | c.*3363G>A| |
S241 |
10 | BAA10g08890 | A10 | 10903124 | C | T | downstream_gene_variant | MODIFIER | c.*3753C>T| |
S132 S137 S215 |