Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g08760 | A06 | 4454112 | G | A | upstream_gene_variant | MODIFIER | c.-2311G>A| |
S69 |
2 | BAA06g08760 | A06 | 4457231 | C | T | missense_variant | MODERATE | c.544C>T|p.Leu182Phe |
S12 |
3 | BAA06g08760 | A06 | 4458749 | G | A | missense_variant | MODERATE | c.1381G>A|p.Asp461Asn |
S295 |
4 | BAA06g08760 | A06 | 4458867 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1416-1G>A| |
S100 |
5 | BAA06g08760 | A06 | 4458920 | C | T | missense_variant | MODERATE | c.1468C>T|p.Leu490Phe |
S56 |
6 | BAA06g08760 | A06 | 4459557 | G | A | missense_variant | MODERATE | c.1790G>A|p.Gly597Asp |
S112 |
7 | BAA06g08760 | A06 | 4459760 | G | A | synonymous_variant | LOW | c.1899G>A|p.Arg633Arg |
S75 S81 |
8 | BAA06g08760 | A06 | 4460908 | C | T | synonymous_variant | LOW | c.2706C>T|p.His902His |
S121 |