Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g33190 | A07 | 32250636 | C | T | missense_variant | MODERATE | c.706G>A|p.Asp236Asn |
S88 |
2 | BAA07g33190 | A07 | 32250960 | A | T | missense_variant | MODERATE | c.471T>A|p.Ser157Arg |
S43 |
3 | BAA07g33190 | A07 | 32250997 | C | T | missense_variant&splice_region_variant | MODERATE | c.434G>A|p.Gly145Glu |
S90 |
4 | BAA07g33190 | A07 | 32251669 | G | A | missense_variant | MODERATE | c.340C>T|p.Leu114Phe |
S228 |
5 | BAA07g33190 | A07 | 32251916 | G | A | missense_variant | MODERATE | c.182C>T|p.Ala61Val |
S129 |
6 | BAA07g33190 | A07 | 32256046 | C | T | upstream_gene_variant | MODIFIER | c.-3949G>A| |
S286 |
7 | BAA07g33190 | A07 | 32256242 | G | A | upstream_gene_variant | MODIFIER | c.-4145C>T| |
S225 S73 |
8 | BAA07g33190 | A07 | 32256545 | C | T | upstream_gene_variant | MODIFIER | c.-4448G>A| |
S229 |