Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g57150 | A09 | 56527040 | G | A | missense_variant | MODERATE | c.1292C>T|p.Thr431Ile |
S32 |
2 | BAA09g57150 | A09 | 56527222 | G | A | synonymous_variant | LOW | c.1110C>T|p.Leu370Leu |
S2 |
3 | BAA09g57150 | A09 | 56527709 | G | A | missense_variant | MODERATE | c.623C>T|p.Ala208Val |
S244 |
4 | BAA09g57150 | A09 | 56527943 | G | A | missense_variant | MODERATE | c.389C>T|p.Thr130Ile |
S193 |
5 | BAA09g57150 | A09 | 56528526 | C | A | upstream_gene_variant | MODIFIER | c.-156G>T| |
S296 |
6 | BAA09g57150 | A09 | 56528529 | G | A | upstream_gene_variant | MODIFIER | c.-159C>T| |
S144 |
7 | BAA09g57150 | A09 | 56529338 | C | T | upstream_gene_variant | MODIFIER | c.-968G>A| |
S208 |
8 | BAA09g57150 | A09 | 56531912 | G | A | upstream_gene_variant | MODIFIER | c.-3542C>T| |
S88 |
9 | BAA09g57150 | A09 | 56532749 | C | T | upstream_gene_variant | MODIFIER | c.-4379G>A| |
S19 |
10 | BAA09g57150 | A09 | 56532974 | G | A | upstream_gene_variant | MODIFIER | c.-4604C>T| |
S19 |