Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g41760 | A05 | 39752078 | G | A | intron_variant | MODIFIER | c.805-28G>A| |
S82 S92 |
2 | BAA05g41760 | A05 | 39752887 | C | T | intron_variant | MODIFIER | c.1101+130C>T| |
S51 |
3 | BAA05g41760 | A05 | 39753483 | C | T | intron_variant | MODIFIER | c.1183-50C>T| |
S13 |
4 | BAA05g41760 | A05 | 39753979 | G | A | synonymous_variant | LOW | c.1254G>A|p.Gly418Gly |
S292 |
5 | BAA05g41760 | A05 | 39754795 | G | A | missense_variant | MODERATE | c.1685G>A|p.Arg562Lys |
S296 |
6 | BAA05g41760 | A05 | 39754800 | G | A | missense_variant | MODERATE | c.1690G>A|p.Glu564Lys |
S35 |
7 | BAA05g41760 | A05 | 39754911 | G | A | missense_variant | MODERATE | c.1801G>A|p.Ala601Thr |
S61 |
8 | BAA05g41760 | A05 | 39755361 | C | T | synonymous_variant | LOW | c.1911C>T|p.Ser637Ser |
S33 |
9 | BAA05g41760 | A05 | 39755490 | G | A | synonymous_variant | LOW | c.2040G>A|p.Glu680Glu |
S284 |
10 | BAA05g41760 | A05 | 39756099 | C | T | synonymous_variant | LOW | c.2289C>T|p.Arg763Arg |
S18 |
11 | BAA05g41760 | A05 | 39757218 | C | T | missense_variant | MODERATE | c.2966C>T|p.Ser989Phe |
S260 |
12 | BAA05g41760 | A05 | 39757224 | G | A | missense_variant | MODERATE | c.2972G>A|p.Gly991Glu |
S68 |