Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g01490 | A09 | 1076859 | G | A | upstream_gene_variant | MODIFIER | c.-239G>A| |
S130 |
2 | BAA09g01490 | A09 | 1077116 | G | A | missense_variant | MODERATE | c.19G>A|p.Asp7Asn |
S246 |
3 | BAA09g01490 | A09 | 1077237 | G | A | intron_variant | MODIFIER | c.46-42G>A| |
S124 |
4 | BAA09g01490 | A09 | 1077665 | G | A | synonymous_variant | LOW | c.339G>A|p.Ser113Ser |
S45 |
5 | BAA09g01490 | A09 | 1078589 | G | A | missense_variant | MODERATE | c.721G>A|p.Gly241Arg |
S275 |
6 | BAA09g01490 | A09 | 1080162 | C | T | synonymous_variant | LOW | c.1704C>T|p.Ser568Ser |
S125 |
7 | BAA09g01490 | A09 | 1080454 | C | T | missense_variant | MODERATE | c.1916C>T|p.Ala639Val |
S169 |
8 | BAA09g01490 | A09 | 1080477 | G | A | missense_variant | MODERATE | c.1939G>A|p.Asp647Asn |
S34 |
9 | BAA09g01490 | A09 | 1080805 | C | T | synonymous_variant | LOW | c.2095C>T|p.Leu699Leu |
S303 |