Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g17740 | A09 | 10677185 | G | A | synonymous_variant | LOW | c.2442C>T|p.Arg814Arg |
S178 |
2 | BAA09g17740 | A09 | 10678698 | C | T | missense_variant | MODERATE | c.1588G>A|p.Asp530Asn |
S187 |
3 | BAA09g17740 | A09 | 10679637 | G | A | synonymous_variant | LOW | c.786C>T|p.Gly262Gly |
S80 |
4 | BAA09g17740 | A09 | 10682097 | G | A | intron_variant | MODIFIER | c.474-2148C>T| |
S188 |
5 | BAA09g17740 | A09 | 10686596 | C | T | intron_variant | MODIFIER | c.473+4890G>A| |
S95 |
6 | BAA09g17740 | A09 | 10687402 | G | A | intron_variant | MODIFIER | c.473+4084C>T| |
S8 |
7 | BAA09g17740 | A09 | 10692641 | C | T | upstream_gene_variant | MODIFIER | c.-683G>A| |
S256 |
8 | BAA09g17740 | A09 | 10693206 | C | T | upstream_gene_variant | MODIFIER | c.-1248G>A| |
S124 |
9 | BAA09g17740 | A09 | 10694284 | G | A | upstream_gene_variant | MODIFIER | c.-2326C>T| |
S45 |
10 | BAA09g17740 | A09 | 10695145 | G | A | upstream_gene_variant | MODIFIER | c.-3187C>T| |
S169 |
11 | BAA09g17740 | A09 | 10695646 | G | A | upstream_gene_variant | MODIFIER | c.-3688C>T| |
S74 |