Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g29980 | A10 | 22371162 | C | T | missense_variant | MODERATE | c.691G>A|p.Asp231Asn |
S37 |
2 | BAA10g29980 | A10 | 22371374 | G | A | missense_variant | MODERATE | c.479C>T|p.Ala160Val |
S126 |
3 | BAA10g29980 | A10 | 22372271 | C | T | missense_variant | MODERATE | c.67G>A|p.Asp23Asn |
S152 |