Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g41190 | A03 | 19290247 | C | T | missense_variant | MODERATE | c.1043G>A|p.Gly348Asp |
S136 |
2 | BAA03g41190 | A03 | 19290482 | G | A | synonymous_variant | LOW | c.808C>T|p.Leu270Leu |
S265 |
3 | BAA03g41190 | A03 | 19290515 | C | T | missense_variant | MODERATE | c.775G>A|p.Gly259Arg |
S35 |
4 | BAA03g41190 | A03 | 19290566 | C | T | missense_variant | MODERATE | c.724G>A|p.Glu242Lys |
S201 |
5 | BAA03g41190 | A03 | 19290827 | C | T | missense_variant | MODERATE | c.463G>A|p.Val155Ile |
S19 |
6 | BAA03g41190 | A03 | 19291073 | G | A | missense_variant | MODERATE | c.290C>T|p.Ser97Phe |
S272 |
7 | BAA03g41190 | A03 | 19291251 | C | T | missense_variant | MODERATE | c.112G>A|p.Asp38Asn |
S240 |
8 | BAA03g41190 | A03 | 19295295 | G | A | upstream_gene_variant | MODIFIER | c.-3933C>T| |
S123 |
9 | BAA03g41190 | A03 | 19295859 | C | T | upstream_gene_variant | MODIFIER | c.-4497G>A| |
S144 |