Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g49620 | A09 | 52845812 | G | A | missense_variant | MODERATE | c.1678G>A|p.Gly560Arg |
S79 S84 |
2 | BAA09g49620 | A09 | 52846065 | G | A | intron_variant | MODIFIER | c.1854-77G>A| |
S10 |
3 | BAA09g49620 | A09 | 52846105 | C | T | intron_variant | MODIFIER | c.1854-37C>T| |
S223 |
4 | BAA09g49620 | A09 | 52846520 | C | T | synonymous_variant | LOW | c.2070C>T|p.Ile690Ile |
S18 |
5 | BAA09g49620 | A09 | 52848035 | C | T | downstream_gene_variant | MODIFIER | c.*1239C>T| |
S163 |
6 | BAA09g49620 | A09 | 52850235 | C | T | downstream_gene_variant | MODIFIER | c.*3439C>T| |
S175 |
7 | BAA09g49620 | A09 | 52850625 | C | T | downstream_gene_variant | MODIFIER | c.*3829C>T| |
S108 |
8 | BAA09g49620 | A09 | 52851139 | G | A | downstream_gene_variant | MODIFIER | c.*4343G>A| |
S178 |
9 | BAA09g49620 | A09 | 52851242 | C | T | downstream_gene_variant | MODIFIER | c.*4446C>T| |
S245 |