Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g01370 | A10 | 682262 | C | T | missense_variant | MODERATE | c.398C>T|p.Ala133Val |
S175 |
2 | BAA10g01370 | A10 | 682266 | G | A | synonymous_variant | LOW | c.402G>A|p.Ala134Ala |
S176 |
3 | BAA10g01370 | A10 | 683588 | G | A | missense_variant&splice_region_variant | MODERATE | c.999G>A|p.Met333Ile |
S13 |
4 | BAA10g01370 | A10 | 684030 | G | A | missense_variant | MODERATE | c.1441G>A|p.Gly481Arg |
S249 |
5 | BAA10g01370 | A10 | 684056 | G | A | synonymous_variant | LOW | c.1467G>A|p.Glu489Glu |
S95 |
6 | BAA10g01370 | A10 | 684157 | G | A | missense_variant | MODERATE | c.1568G>A|p.Gly523Glu |
S127 |
7 | BAA10g01370 | A10 | 684417 | G | A | missense_variant | MODERATE | c.1828G>A|p.Glu610Lys |
S230 |
8 | BAA10g01370 | A10 | 685394 | G | A | synonymous_variant | LOW | c.2733G>A|p.Ala911Ala |
S148 S30 |
9 | BAA10g01370 | A10 | 686525 | G | A | missense_variant | MODERATE | c.3571G>A|p.Ala1191Thr |
S45 |