Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g25790 | A10 | 20693657 | C | T | missense_variant | MODERATE | c.101C>T|p.Pro34Leu |
S265 S39 |
2 | BAA10g25790 | A10 | 20695891 | G | A | synonymous_variant | LOW | c.2148G>A|p.Arg716Arg |
S278 |
3 | BAA10g25790 | A10 | 20695924 | C | T | synonymous_variant | LOW | c.2181C>T|p.Leu727Leu |
S294 |
4 | BAA10g25790 | A10 | 20695950 | C | T | splice_region_variant&intron_variant | LOW | c.2200+7C>T| |
S44 |
5 | BAA10g25790 | A10 | 20696538 | C | T | missense_variant | MODERATE | c.2710C>T|p.Pro904Ser |
S168 |
6 | BAA10g25790 | A10 | 20696997 | G | A | missense_variant | MODERATE | c.3169G>A|p.Glu1057Lys |
S39 |