Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g51860 | A09 | 53952373 | C | T | missense_variant | MODERATE | c.1429G>A|p.Asp477Asn |
S163 |
2 | BAA09g51860 | A09 | 53952711 | C | T | missense_variant | MODERATE | c.1091G>A|p.Gly364Glu |
S237 |
3 | BAA09g51860 | A09 | 53953204 | G | A | synonymous_variant | LOW | c.918C>T|p.Leu306Leu |
S167 |
4 | BAA09g51860 | A09 | 53954356 | G | A | synonymous_variant | LOW | c.297C>T|p.Phe99Phe |
S284 |
5 | BAA09g51860 | A09 | 53954964 | C | T | upstream_gene_variant | MODIFIER | c.-312G>A| |
S256 |
6 | BAA09g51860 | A09 | 53955273 | C | T | upstream_gene_variant | MODIFIER | c.-621G>A| |
S149 |
7 | BAA09g51860 | A09 | 53955797 | C | T | upstream_gene_variant | MODIFIER | c.-1145G>A| |
S104 S52 |
8 | BAA09g51860 | A09 | 53956129 | G | A | upstream_gene_variant | MODIFIER | c.-1477C>T| |
S110 |
9 | BAA09g51860 | A09 | 53956835 | G | A | upstream_gene_variant | MODIFIER | c.-2183C>T| |
S257 |
10 | BAA09g51860 | A09 | 53957203 | G | A | upstream_gene_variant | MODIFIER | c.-2551C>T| |
S225 |