Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g00930 | A10 | 438223 | G | A | upstream_gene_variant | MODIFIER | c.-4926G>A| |
S164 |
2 | BAA10g00930 | A10 | 438455 | C | T | upstream_gene_variant | MODIFIER | c.-4694C>T| |
S152 |
3 | BAA10g00930 | A10 | 439768 | G | A | upstream_gene_variant | MODIFIER | c.-3381G>A| |
S134 |
4 | BAA10g00930 | A10 | 439821 | G | A | upstream_gene_variant | MODIFIER | c.-3328G>A| |
S128 |
5 | BAA10g00930 | A10 | 439927 | C | T | upstream_gene_variant | MODIFIER | c.-3222C>T| |
S119 |
6 | BAA10g00930 | A10 | 439940 | G | A | upstream_gene_variant | MODIFIER | c.-3209G>A| |
S184 |
7 | BAA10g00930 | A10 | 440109 | G | A | upstream_gene_variant | MODIFIER | c.-3040G>A| |
S18 |
8 | BAA10g00930 | A10 | 441404 | C | T | upstream_gene_variant | MODIFIER | c.-1745C>T| |
S6 |
9 | BAA10g00930 | A10 | 443881 | C | T | missense_variant | MODERATE | c.733C>T|p.Pro245Ser |
S139 |
10 | BAA10g00930 | A10 | 444105 | G | A | synonymous_variant | LOW | c.957G>A|p.Ser319Ser |
S130 |
11 | BAA10g00930 | A10 | 449038 | C | T | downstream_gene_variant | MODIFIER | c.*4855C>T| |
S149 |