Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g48460 | A09 | 52261704 | C | T | missense_variant | MODERATE | c.1430G>A|p.Gly477Glu |
S168 |
2 | BAA09g48460 | A09 | 52265307 | G | A | synonymous_variant | LOW | c.390C>T|p.Asn130Asn |
S71 |
3 | BAA09g48460 | A09 | 52265854 | C | T | upstream_gene_variant | MODIFIER | c.-158G>A| |
S18 |
4 | BAA09g48460 | A09 | 52265985 | G | A | upstream_gene_variant | MODIFIER | c.-289C>T| |
S2 |
5 | BAA09g48460 | A09 | 52266365 | G | A | upstream_gene_variant | MODIFIER | c.-669C>T| |
S165 |
6 | BAA09g48460 | A09 | 52266592 | G | A | upstream_gene_variant | MODIFIER | c.-896C>T| |
S59 |
7 | BAA09g48460 | A09 | 52266975 | G | A | upstream_gene_variant | MODIFIER | c.-1279C>T| |
S236 |
8 | BAA09g48460 | A09 | 52268424 | C | T | upstream_gene_variant | MODIFIER | c.-2728G>A| |
S51 |
9 | BAA09g48460 | A09 | 52269563 | G | A | upstream_gene_variant | MODIFIER | c.-3867C>T| |
S202 |