Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g22670 | A10 | 19391410 | G | A | upstream_gene_variant | MODIFIER | c.-4880G>A| |
S252 S276 |
2 | BAA10g22670 | A10 | 19391427 | G | A | upstream_gene_variant | MODIFIER | c.-4863G>A| |
S192 |
3 | BAA10g22670 | A10 | 19392455 | G | A | upstream_gene_variant | MODIFIER | c.-3835G>A| |
S150 |
4 | BAA10g22670 | A10 | 19393602 | G | A | upstream_gene_variant | MODIFIER | c.-2688G>A| |
S69 |
5 | BAA10g22670 | A10 | 19394137 | G | A | upstream_gene_variant | MODIFIER | c.-2153G>A| |
S192 |
6 | BAA10g22670 | A10 | 19394273 | C | T | upstream_gene_variant | MODIFIER | c.-2017C>T| |
S269 |
7 | BAA10g22670 | A10 | 19394600 | C | T | upstream_gene_variant | MODIFIER | c.-1690C>T| |
S98 |
8 | BAA10g22670 | A10 | 19395928 | C | T | upstream_gene_variant | MODIFIER | c.-362C>T| |
S41 |
9 | BAA10g22670 | A10 | 19396633 | C | T | missense_variant | MODERATE | c.344C>T|p.Ala115Val |
S189 |
10 | BAA10g22670 | A10 | 19396898 | G | A | splice_donor_variant&intron_variant | HIGH | c.608+1G>A| |
S164 |