Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10670 | A02 | 4766026 | C | T | missense_variant | MODERATE | c.2831G>A|p.Arg944Lys |
S160 |
2 | BAA02g10670 | A02 | 4766183 | C | T | missense_variant | MODERATE | c.2674G>A|p.Gly892Arg |
S112 |
3 | BAA02g10670 | A02 | 4766642 | C | T | synonymous_variant | LOW | c.2379G>A|p.Arg793Arg |
S152 |
4 | BAA02g10670 | A02 | 4767176 | G | A | splice_region_variant&intron_variant | LOW | c.1933-4C>T| |
S85 |
5 | BAA02g10670 | A02 | 4767528 | C | T | missense_variant | MODERATE | c.1649G>A|p.Ser550Asn |
S144 |
6 | BAA02g10670 | A02 | 4768009 | C | T | missense_variant | MODERATE | c.1168G>A|p.Gly390Arg |
S8 |
7 | BAA02g10670 | A02 | 4768284 | C | T | missense_variant | MODERATE | c.893G>A|p.Gly298Asp |
S55 |
8 | BAA02g10670 | A02 | 4768416 | C | T | missense_variant | MODERATE | c.761G>A|p.Arg254Lys |
S46 |
9 | BAA02g10670 | A02 | 4769272 | G | A | synonymous_variant | LOW | c.261C>T|p.Phe87Phe |
S43 |
10 | BAA02g10670 | A02 | 4772631 | G | A | upstream_gene_variant | MODIFIER | c.-2738C>T| |
S296 |
11 | BAA02g10670 | A02 | 4773719 | G | A | upstream_gene_variant | MODIFIER | c.-3826C>T| |
S4 |