Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g13150 | A10 | 14389669 | G | A | synonymous_variant | LOW | c.834C>T|p.Phe278Phe |
S226 |
2 | BAA10g13150 | A10 | 14389688 | C | T | missense_variant | MODERATE | c.815G>A|p.Gly272Glu |
S42 |
3 | BAA10g13150 | A10 | 14389702 | G | A | splice_region_variant&synonymous_variant | LOW | c.801C>T|p.Leu267Leu |
S198 |
4 | BAA10g13150 | A10 | 14391927 | G | A | upstream_gene_variant | MODIFIER | c.-686C>T| |
S68 |
5 | BAA10g13150 | A10 | 14392033 | C | T | upstream_gene_variant | MODIFIER | c.-792G>A| |
S256 |
6 | BAA10g13150 | A10 | 14392066 | G | A | upstream_gene_variant | MODIFIER | c.-825C>T| |
S192 |
7 | BAA10g13150 | A10 | 14392440 | G | A | upstream_gene_variant | MODIFIER | c.-1199C>T| |
S184 |
8 | BAA10g13150 | A10 | 14393270 | G | A | upstream_gene_variant | MODIFIER | c.-2029C>T| |
S13 S140 S219 S279 S72 |
9 | BAA10g13150 | A10 | 14393851 | G | A | upstream_gene_variant | MODIFIER | c.-2610C>T| |
S105 S106 |