Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g40960 | A07 | 36127795 | G | A | missense_variant | MODERATE | c.938C>T|p.Ser313Leu |
S239 |
2 | BAA07g40960 | A07 | 36129197 | C | T | missense_variant&splice_region_variant | MODERATE | c.604G>A|p.Glu202Lys |
S195 |
3 | BAA07g40960 | A07 | 36129511 | C | T | synonymous_variant | LOW | c.375G>A|p.Arg125Arg |
S173 |
4 | BAA07g40960 | A07 | 36129578 | C | T | stop_gained | HIGH | c.308G>A|p.Trp103* |
S66 |
5 | BAA07g40960 | A07 | 36130264 | C | T | upstream_gene_variant | MODIFIER | c.-379G>A| |
S132 S137 S138 S237 S288 S89 |
6 | BAA07g40960 | A07 | 36130493 | C | T | upstream_gene_variant | MODIFIER | c.-608G>A| |
|
7 | BAA07g40960 | A07 | 36133991 | G | A | upstream_gene_variant | MODIFIER | c.-4106C>T| |
S171 |
8 | BAA07g40960 | A07 | 36134806 | G | A | upstream_gene_variant | MODIFIER | c.-4921C>T| |
S296 |
9 | BAA07g40960 | A07 | 36134843 | C | T | upstream_gene_variant | MODIFIER | c.-4958G>A| |
S32 |