Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g44120 | A06 | 28318806 | C | T | missense_variant | MODERATE | c.1144G>A|p.Asp382Asn |
S176 |
2 | BAA06g44120 | A06 | 28320103 | G | A | synonymous_variant | LOW | c.501C>T|p.Tyr167Tyr |
S249 |
3 | BAA06g44120 | A06 | 28320447 | C | T | missense_variant | MODERATE | c.157G>A|p.Asp53Asn |
S15 S3 |
4 | BAA06g44120 | A06 | 28323238 | G | A | upstream_gene_variant | MODIFIER | c.-2521C>T| |
S249 |
5 | BAA06g44120 | A06 | 28324126 | C | T | upstream_gene_variant | MODIFIER | c.-3409G>A| |
S221 |
6 | BAA06g44120 | A06 | 28324351 | C | T | upstream_gene_variant | MODIFIER | c.-3634G>A| |
S149 |
7 | BAA06g44120 | A06 | 28325636 | C | T | upstream_gene_variant | MODIFIER | c.-4919G>A| |
S223 |