Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g31690 | A08 | 21011671 | C | T | missense_variant | MODERATE | c.676G>A|p.Val226Ile |
S286 |
2 | BAA08g31690 | A08 | 21011768 | G | A | synonymous_variant | LOW | c.579C>T|p.Ile193Ile |
S42 |
3 | BAA08g31690 | A08 | 21011935 | G | A | splice_region_variant&intron_variant | LOW | c.486+6C>T| |
S200 |
4 | BAA08g31690 | A08 | 21016859 | G | A | upstream_gene_variant | MODIFIER | c.-4117C>T| |
S37 |