Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g41620 | A05 | 39694116 | G | A | downstream_gene_variant | MODIFIER | c.*4977C>T| |
S8 |
2 | BAA05g41620 | A05 | 39699360 | G | A | missense_variant | MODERATE | c.1337C>T|p.Ser446Phe |
S42 |
3 | BAA05g41620 | A05 | 39699530 | C | T | missense_variant | MODERATE | c.1277G>A|p.Gly426Asp |
S251 |
4 | BAA05g41620 | A05 | 39701397 | G | A | synonymous_variant | LOW | c.615C>T|p.Leu205Leu |
S127 |
5 | BAA05g41620 | A05 | 39702482 | C | T | synonymous_variant | LOW | c.252G>A|p.Lys84Lys |
S203 |
6 | BAA05g41620 | A05 | 39702666 | C | T | synonymous_variant | LOW | c.150G>A|p.Gln50Gln |
S239 |
7 | BAA05g41620 | A05 | 39703004 | G | A | synonymous_variant | LOW | c.24C>T|p.Leu8Leu |
S121 |
8 | BAA05g41620 | A05 | 39703006 | G | A | missense_variant | MODERATE | c.22C>T|p.Leu8Phe |
S182 |
9 | BAA05g41620 | A05 | 39704241 | T | A | upstream_gene_variant | MODIFIER | c.-1214A>T| |
S206 |
10 | BAA05g41620 | A05 | 39705806 | C | T | upstream_gene_variant | MODIFIER | c.-2779G>A| |
S20 |
11 | BAA05g41620 | A05 | 39707959 | C | T | upstream_gene_variant | MODIFIER | c.-4932G>A| |
S197 |