Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g49490 | A09 | 52780636 | G | A | missense_variant | MODERATE | c.7G>A|p.Glu3Lys |
S234 |
2 | BAA09g49490 | A09 | 52780792 | G | A | missense_variant | MODERATE | c.163G>A|p.Asp55Asn |
S181 |
3 | BAA09g49490 | A09 | 52780809 | G | A | synonymous_variant | LOW | c.180G>A|p.Ser60Ser |
S281 |
4 | BAA09g49490 | A09 | 52781620 | G | A | missense_variant | MODERATE | c.991G>A|p.Asp331Asn |
S42 |
5 | BAA09g49490 | A09 | 52782730 | C | T | missense_variant | MODERATE | c.1945C>T|p.Arg649Cys |
S170 |
6 | BAA09g49490 | A09 | 52782853 | G | A | missense_variant | MODERATE | c.2068G>A|p.Ala690Thr |
S247 |
7 | BAA09g49490 | A09 | 52785082 | G | A | downstream_gene_variant | MODIFIER | c.*1695G>A| |
S240 |
8 | BAA09g49490 | A09 | 52786028 | T | A | downstream_gene_variant | MODIFIER | c.*2641T>A| |
S61 |
9 | BAA09g49490 | A09 | 52788159 | C | T | downstream_gene_variant | MODIFIER | c.*4772C>T| |
S241 |