Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g27650 | A10 | 21479737 | C | T | missense_variant | MODERATE | c.3355G>A|p.Val1119Ile |
S2 |
2 | BAA10g27650 | A10 | 21480090 | C | T | missense_variant | MODERATE | c.3091G>A|p.Asp1031Asn |
S28 |
3 | BAA10g27650 | A10 | 21480357 | C | T | missense_variant | MODERATE | c.2824G>A|p.Asp942Asn |
S107 |
4 | BAA10g27650 | A10 | 21480531 | G | A | missense_variant | MODERATE | c.2650C>T|p.Pro884Ser |
S159 S243 |
5 | BAA10g27650 | A10 | 21481329 | C | T | missense_variant | MODERATE | c.1958G>A|p.Arg653Lys |
S295 |
6 | BAA10g27650 | A10 | 21481457 | G | A | synonymous_variant | LOW | c.1830C>T|p.Val610Val |
S39 |
7 | BAA10g27650 | A10 | 21482950 | C | T | missense_variant | MODERATE | c.940G>A|p.Ala314Thr |
S72 S78 |
8 | BAA10g27650 | A10 | 21483681 | C | T | synonymous_variant | LOW | c.480G>A|p.Glu160Glu |
S38 |
9 | BAA10g27650 | A10 | 21483700 | G | A | missense_variant | MODERATE | c.461C>T|p.Ser154Phe |
S62 |
10 | BAA10g27650 | A10 | 21484145 | G | A | synonymous_variant | LOW | c.132C>T|p.Ser44Ser |
S125 |