Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g26070 | A02 | 14440476 | G | A | missense_variant | MODERATE | c.364C>T|p.Leu122Phe |
S50 |
2 | BAA02g26070 | A02 | 14440546 | C | T | synonymous_variant | LOW | c.294G>A|p.Ser98Ser |
S182 |
3 | BAA02g26070 | A02 | 14440923 | G | A | missense_variant | MODERATE | c.8C>T|p.Ser3Leu |
S191 |
4 | BAA02g26070 | A02 | 14443200 | G | A | upstream_gene_variant | MODIFIER | c.-2270C>T| |
S25 |
5 | BAA02g26070 | A02 | 14443688 | G | A | upstream_gene_variant | MODIFIER | c.-2758C>T| |
S136 |
6 | BAA02g26070 | A02 | 14443900 | C | T | upstream_gene_variant | MODIFIER | c.-2970G>A| |
S274 |
7 | BAA02g26070 | A02 | 14444206 | G | A | upstream_gene_variant | MODIFIER | c.-3276C>T| |
S237 |
8 | BAA02g26070 | A02 | 14444362 | G | A | upstream_gene_variant | MODIFIER | c.-3432C>T| |
|
9 | BAA02g26070 | A02 | 14444452 | G | A | upstream_gene_variant | MODIFIER | c.-3522C>T| |
S37 |
10 | BAA02g26070 | A02 | 14444705 | G | A | upstream_gene_variant | MODIFIER | c.-3775C>T| |
S109 |
11 | BAA02g26070 | A02 | 14444786 | C | T | upstream_gene_variant | MODIFIER | c.-3856G>A| |
S123 |