Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g02260 | A10 | 1075715 | G | A | missense_variant | MODERATE | c.850C>T|p.Pro284Ser |
S157 S163 |
2 | BAA10g02260 | A10 | 1075889 | G | A | splice_region_variant&intron_variant | LOW | c.792+7C>T| |
S13 |
3 | BAA10g02260 | A10 | 1076235 | C | T | synonymous_variant | LOW | c.453G>A|p.Gly151Gly |
S116 |
4 | BAA10g02260 | A10 | 1076684 | C | T | missense_variant | MODERATE | c.4G>A|p.Val2Ile |
S56 |