Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g17120 | A10 | 16633680 | G | A | upstream_gene_variant | MODIFIER | c.-3033G>A| |
S157 S163 |
2 | BAA10g17120 | A10 | 16633882 | G | A | upstream_gene_variant | MODIFIER | c.-2831G>A| |
S57 |
3 | BAA10g17120 | A10 | 16634676 | G | A | upstream_gene_variant | MODIFIER | c.-2037G>A| |
S293 |
4 | BAA10g17120 | A10 | 16635519 | C | T | upstream_gene_variant | MODIFIER | c.-1194C>T| |
S242 |
5 | BAA10g17120 | A10 | 16636481 | C | T | upstream_gene_variant | MODIFIER | c.-232C>T| |
S161 |
6 | BAA10g17120 | A10 | 16636609 | G | A | upstream_gene_variant | MODIFIER | c.-104G>A| |
S53 |
7 | BAA10g17120 | A10 | 16636693 | G | A | upstream_gene_variant | MODIFIER | c.-20G>A| |
S219 S72 |
8 | BAA10g17120 | A10 | 16636941 | G | A | missense_variant | MODERATE | c.229G>A|p.Glu77Lys |
S81 |
9 | BAA10g17120 | A10 | 16637140 | C | T | missense_variant | MODERATE | c.428C>T|p.Pro143Leu |
S95 |