Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g44280 | A09 | 50034126 | C | T | upstream_gene_variant | MODIFIER | c.-4743C>T| |
S117 |
2 | BAA09g44280 | A09 | 50034700 | C | T | upstream_gene_variant | MODIFIER | c.-4169C>T| |
S68 |
3 | BAA09g44280 | A09 | 50035911 | C | T | upstream_gene_variant | MODIFIER | c.-2958C>T| |
S68 |
4 | BAA09g44280 | A09 | 50036116 | C | T | upstream_gene_variant | MODIFIER | c.-2753C>T| |
S113 |
5 | BAA09g44280 | A09 | 50036309 | C | T | upstream_gene_variant | MODIFIER | c.-2560C>T| |
S135 |
6 | BAA09g44280 | A09 | 50036328 | C | T | upstream_gene_variant | MODIFIER | c.-2541C>T| |
S109 |
7 | BAA09g44280 | A09 | 50039449 | C | T | missense_variant | MODERATE | c.431C>T|p.Thr144Ile |
S87 |
8 | BAA09g44280 | A09 | 50039636 | C | T | synonymous_variant | LOW | c.618C>T|p.Val206Val |
S292 |
9 | BAA09g44280 | A09 | 50040004 | T | A | missense_variant | MODERATE | c.986T>A|p.Leu329Gln |
S239 |
10 | BAA09g44280 | A09 | 50040019 | C | T | missense_variant | MODERATE | c.1001C>T|p.Ser334Leu |
S206 S26 |