Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g15130 | A10 | 15629994 | C | T | synonymous_variant | LOW | c.2616G>A|p.Glu872Glu |
S84 |
2 | BAA10g15130 | A10 | 15631505 | G | A | missense_variant | MODERATE | c.1598C>T|p.Ala533Val |
S295 |
3 | BAA10g15130 | A10 | 15631569 | G | A | missense_variant | MODERATE | c.1534C>T|p.Pro512Ser |
S125 |
4 | BAA10g15130 | A10 | 15631985 | C | T | missense_variant | MODERATE | c.1277G>A|p.Gly426Glu |
S70 |
5 | BAA10g15130 | A10 | 15632725 | G | A | synonymous_variant | LOW | c.646C>T|p.Leu216Leu |
S95 |
6 | BAA10g15130 | A10 | 15633103 | G | A | missense_variant | MODERATE | c.268C>T|p.Leu90Phe |
S9 |
7 | BAA10g15130 | A10 | 15635614 | C | T | upstream_gene_variant | MODIFIER | c.-2244G>A| |
S87 |
8 | BAA10g15130 | A10 | 15636274 | G | A | upstream_gene_variant | MODIFIER | c.-2904C>T| |
S166 |