Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g14590 | A10 | 15225119 | C | T | upstream_gene_variant | MODIFIER | c.-2319C>T| |
S185 |
2 | BAA10g14590 | A10 | 15225655 | C | T | upstream_gene_variant | MODIFIER | c.-1783C>T| |
S210 S225 |
3 | BAA10g14590 | A10 | 15227149 | C | T | upstream_gene_variant | MODIFIER | c.-289C>T| |
S229 |
4 | BAA10g14590 | A10 | 15228785 | G | A | missense_variant | MODERATE | c.677G>A|p.Arg226Lys |
S94 |
5 | BAA10g14590 | A10 | 15229370 | C | T | downstream_gene_variant | MODIFIER | c.*566C>T| |
S296 |
6 | BAA10g14590 | A10 | 15229581 | G | A | downstream_gene_variant | MODIFIER | c.*777G>A| |
S151 S167 S257 S262 S263 |
7 | BAA10g14590 | A10 | 15231344 | C | T | downstream_gene_variant | MODIFIER | c.*2540C>T| |
S197 |
8 | BAA10g14590 | A10 | 15231840 | C | T | downstream_gene_variant | MODIFIER | c.*3036C>T| |
S206 |
9 | BAA10g14590 | A10 | 15233226 | C | T | downstream_gene_variant | MODIFIER | c.*4422C>T| |
S268 |