Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g28050 | A10 | 21625121 | G | A | upstream_gene_variant | MODIFIER | c.-4560G>A| |
S192 |
2 | BAA10g28050 | A10 | 21625506 | C | T | upstream_gene_variant | MODIFIER | c.-4175C>T| |
S104 S52 |
3 | BAA10g28050 | A10 | 21625814 | C | T | upstream_gene_variant | MODIFIER | c.-3867C>T| |
S204 |
4 | BAA10g28050 | A10 | 21626910 | G | A | upstream_gene_variant | MODIFIER | c.-2771G>A| |
S60 |
5 | BAA10g28050 | A10 | 21627060 | C | T | upstream_gene_variant | MODIFIER | c.-2621C>T| |
S189 |
6 | BAA10g28050 | A10 | 21627377 | C | T | upstream_gene_variant | MODIFIER | c.-2304C>T| |
S206 S26 |
7 | BAA10g28050 | A10 | 21628991 | G | A | upstream_gene_variant | MODIFIER | c.-690G>A| |
S42 |
8 | BAA10g28050 | A10 | 21629999 | C | T | missense_variant | MODERATE | c.319C>T|p.Pro107Ser |
S12 |
9 | BAA10g28050 | A10 | 21630340 | C | T | splice_region_variant&synonymous_variant | LOW | c.660C>T|p.Thr220Thr |
S203 |
10 | BAA10g28050 | A10 | 21631179 | C | T | synonymous_variant | LOW | c.724C>T|p.Leu242Leu |
S56 |